Homo sapiens (human): 201266 Help Entry 201266            CDS       T01001                                  Symbol SLC39A11, C17orf26, ZIP-11, ZIP11 Name (RefSeq) solute carrier family 39 member 11   KO K14717   solute carrier family 39 (zinc transporter), member 11 Organism hsa  Homo sapiens (human) Pathway hsa05010   Alzheimer disease hsa05012   Parkinson disease Brite KEGG Orthology (KO) [BR:hsa00001]  09160 Human Diseases   09164 Neurodegenerative disease    05010 Alzheimer disease     201266 (SLC39A11)    05012 Parkinson disease     201266 (SLC39A11)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     201266 (SLC39A11) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC39: Metal ion transporter    201266 (SLC39A11) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Zip Motif Other DBs NCBI-GeneID:  201266 NCBI-ProteinID:  NP_001153242 OMIM:  616508 HGNC:  14463 Ensembl:  ENSG00000133195 Pharos:  Q8N1S5(Tbio) UniProt:  Q8N1S5 LinkDB All DBs Position 17:complement(72645949..73092688) Genome browser AA seq 342 aa AA seqDB search MLQGHSSVFQALLGTFFTWGMTAAGAALVFVFSSGQRRILDGSLGFAAGVMLAASYWSLL APAVEMATSSGGFGAFAFFPVAVGFTLGAAFVYLADLLMPHLGAAEDPQTTLALNFGSTL MKKKSDPEGPALLFPESELSIRIGRAGLLSDKSENGEAYQRKKAAATGLPEGPAVPVPSR GNLAQPGGSSWRRIALLILAITIHNVPEGLAVGVGFGAIEKTASATFESARNLAIGIGIQ NFPEGLAVSLPLRGAGFSTWRAFWYGQLSGMVEPLAGVFGAFAVVLAEPILPYALAFAAG AMVYVVMDDIIPEAQISGNGKLASWASILGFVVMMSLDVGLG NT seq 1029 nt NT seq  +upstreamnt  +downstreamnt atgctccaaggccacagctctgtgttccaggccttgctggggaccttcttcacctggggg atgacagcagctggggcagctctcgtgttcgtattctctagtggacagaggcggatctta gatggaagtcttggctttgctgcaggggtcatgttggcagcttcctattggtctcttctg gccccagcagttgagatggccacgtcctctgggggcttcggtgcctttgccttcttccct gtggctgttggcttcacccttggagcggcttttgtctacttggctgacctcctgatgcct cacttgggtgcagcagaagacccccagacgaccctggcactgaacttcggctctacgttg atgaagaagaagtctgatcctgagggtcccgcgctgctcttccctgagagtgaactttcc atccggataggtagagctgggcttctttcagacaagagtgagaatggtgaggcatatcag agaaagaaggcggcagccactggccttccagagggtcctgctgtccctgtgccttctcga gggaatctggcacagcccggcggcagcagctggaggaggatcgcactgctcatcttggcc atcactatacacaacgttccagagggtctcgctgttggagttggatttggggctatagaa aagacggcatctgctacctttgagagtgccaggaatttggccattggaatcgggatccag aatttccccgagggcctggctgtcagccttcccttgcgaggggcaggcttctccacctgg agagctttctggtatgggcagctgagcggcatggtggagcccctggccggggtctttggt gcctttgccgtggtgctggctgagcccatcctgccctacgctctggcctttgctgccggt gccatggtctacgtggtcatggacgacatcatccccgaagcccagatcagtggtaatggg aaactggcatcctgggcctccatcctgggatttgtagtgatgatgtcactggacgttggc ctgggctag

Homo sapiens (human): 221074 Help Entry 221074            CDS       T01001                                  Symbol SLC39A12, LZT-Hs8, ZIP-12, ZIP12, bA570F3.1 Name (RefSeq) solute carrier family 39 member 12   KO K14718   solute carrier family 39 (zinc transporter), member 12 Organism hsa  Homo sapiens (human) Pathway hsa05010   Alzheimer disease hsa05012   Parkinson disease Brite KEGG Orthology (KO) [BR:hsa00001]  09160 Human Diseases   09164 Neurodegenerative disease    05010 Alzheimer disease     221074 (SLC39A12)    05012 Parkinson disease     221074 (SLC39A12)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     221074 (SLC39A12) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC39: Metal ion transporter    221074 (SLC39A12) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Zip ZIP4_domain Motif Other DBs NCBI-GeneID:  221074 NCBI-ProteinID:  NP_001138667 OMIM:  608734 HGNC:  20860 Ensembl:  ENSG00000148482 Pharos:  Q504Y0(Tdark) UniProt:  Q504Y0 LinkDB All DBs Position 10:17951918..18043285 Genome browser AA seq 691 aa AA seqDB search MCFRTKLSVSWVPLFLLLSRVFSTETDKPSAQDSRSRGSSGQPADLLQVLSAGDHPPHNH SRSLIKTLLEKTGCPRRRNGMQGDCNLCFEPDALLLIAGGNFEDQLREEVVQRVSLLLLY YIIHQEEICSSKLNMSNKEYKFYLHSLLSLRQDEDSSFLSQNETEDILAFTRQYFDTSQS QCMETKTLQKKSGIVSSEGANESTLPQLAAMIITLSLQGVCLGQGNLPSPDYFTEYIFSS LNRTNTLRLSELDQLLNTLWTRSTCIKNEKIHQFQRKQNNIITHDQDYSNFSSSMEKESE DGPVSWDQTCFSARQLVEIFLQKGLSLISKEDFKQMSPGIIQQLLSCSCHLPKDQQAKLP PTTLEKYGYSTVAVTLLTLGSMLGTALVLFHSCEENYRLILQLFVGLAVGTLSGDALLHL IPQVLGLHKQEAPEFGHFHESKGHIWKLMGLIGGIHGFFLIEKCFILLVSPNDKQGLSLV NGHVGHSHHLALNSELSDQAGRGKSASTIQLKSPEDSQAAEMPIGSMTASNRKCKAISLL AIMILVGDSLHNFADGLAIGAAFSSSSESGVTTTIAILCHEIPHEMGDFAVLLSSGLSMK TAILMNFISSLTAFMGLYIGLSVSADPCVQDWIFTVTAGMFLYLSLVEMLPEMTHVQTQR PWMMFLLQNFGLILGWLSLLLLAIYEQNIKI NT seq 2076 nt NT seq  +upstreamnt  +downstreamnt atgtgcttccggacaaagctctcagtatcctgggtgccattgtttcttctactcagccgt gttttttctactgagacagacaaaccctcagcccaggatagcagaagccgtgggagttca ggccaaccggcagacctgctacaggttctctctgctggtgaccacccaccccacaaccac tcaagaagcctcatcaaaacattgttggagaaaactgggtgcccacggaggagaaacgga atgcaaggagattgcaatctgtgctttgaaccagatgcactattactaatagctggagga aattttgaagatcagcttagagaagaagtggtccagagagtttctcttctccttctctat tacattattcatcaggaagagatctgttcttcaaagctcaacatgagtaataaagagtat aaattttacctacacagcctactgagcctcaggcaggatgaagattcctctttcctttca cagaatgagacagaagatatcttggctttcaccaggcagtactttgacacttctcaaagc cagtgtatggaaaccaaaacgctgcagaaaaaatctggaatagtgagcagtgaaggtgct aatgaaagtacgcttcctcagttggcagccatgatcattactttgtccctccagggtgtt tgtctgggacaaggaaacttgccttccccagactactttacagaatatattttcagttcc ttgaatcgtacgaataccctccgcctatcagaactagaccaactcctcaacactctctgg accagaagtacttgtatcaaaaatgagaaaatccatcaatttcaaaggaaacaaaacaac ataataacccatgatcaggactattctaatttctcttcatccatggaaaaagagtctgag gatggtccagtttcctgggatcagacctgcttctctgctaggcagctggtggagatattt ctacagaagggcctctcactcatttctaaggaggactttaagcaaatgagtccagggatc atccagcagctcctcagctgctcctgccacttacccaaggaccaacaagcaaagctgcca cctaccactctggagaaatacggctacagcacggtggctgtcacccttctcacactgggc tccatgctggggacagcgctggtccttttccatagctgtgaggagaactacaggcttatc ttacagctgtttgtgggcttggccgtcgggacactgtctggggacgctctgctccacctt atccctcaggttcttggtttacataagcaggaagccccagaatttgggcatttccatgaa agcaaaggtcatatttggaaactgatgggattaattggaggcatccatggatttttcttg atagaaaaatgttttattcttcttgtatcaccaaatgacaagcagggcctgtcattggtt aatgggcacgtgggtcattcccaccatcttgcactcaactctgaattaagtgaccaggca ggcagaggcaaatctgcttcaactatccagttgaaaagcccagaagattcacaggcagct gaaatgcctataggcagtatgacagcctccaacagaaaatgtaaagccattagcttgtta gcaatcatgattctggttggggacagcctgcataattttgcagatggcctagccatagga gcagccttctcatcatcatccgagtcaggagtgaccactacgattgctatcttgtgtcat gaaatcccacatgaaatgggagactttgccgtgctcttaagctctggactttctatgaag actgccatcctgatgaattttataagctccctaactgccttcatgggattatacattggc ctttccgtgtcagctgatccatgtgttcaagactggatcttcacagtcactgctgggatg ttcttatatttatccttggttgaaatgcttcctgaaatgactcatgttcaaacacaacga ccctggatgatgtttctcctgcaaaactttggattgatcctaggttggctttctctcctg ctcttggctatatatgagcaaaatattaaaatataa

Homo sapiens (human): 23516 Help Entry 23516             CDS       T01001                                  Symbol SLC39A14, HCIN, HMNDYT2, LZT-Hs4, NET34, ZIP14, cig19 Name (RefSeq) solute carrier family 39 member 14   KO K14720   solute carrier family 39 (zinc transporter), member 14 Organism hsa  Homo sapiens (human) Pathway hsa04216   Ferroptosis hsa05010   Alzheimer disease hsa05012   Parkinson disease Disease H01938   Hypermanganesemia with dystonia Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09143 Cell growth and death    04216 Ferroptosis     23516 (SLC39A14)  09160 Human Diseases   09164 Neurodegenerative disease    05010 Alzheimer disease     23516 (SLC39A14)    05012 Parkinson disease     23516 (SLC39A14)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     23516 (SLC39A14) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC39: Metal ion transporter    23516 (SLC39A14) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Zip DUF808 Motif Other DBs NCBI-GeneID:  23516 NCBI-ProteinID:  NP_001121903 OMIM:  608736 HGNC:  20858 Ensembl:  ENSG00000104635 Pharos:  Q15043(Tbio) UniProt:  Q15043 LinkDB All DBs Position 8:22367278..22434129 Genome browser AA seq 492 aa AA seqDB search MKLLLLHPAFQSCLLLTLLGLWRTTPEAHASSLGAPAISAASFLQDLIHRYGEGDSLTLQ QLKALLNHLDVGVGRGNVTQHVQGHRNLSTCFSSGDLFTAHNFSEQSRIGSSELQEFCPT ILQQLDSRACTSENQENEENEQTEEGRPSAVEVWGYGLLCVTVISLCSLLGASVVPFMKK TFYKRLLLYFIALAIGTLYSNALFQLIPEAFGFNPLEDYYVSKSAVVFGGFYLFFFTEKI LKILLKQKNEHHHGHSHYASESLPSKKDQEEGVMEKLQNGDLDHMIPQHCSSELDGKAPM VDEKVIVGSLSVQDLQASQSACYWLKGVRYSDIGTLAWMITLSDGLHNFIDGLAIGASFT VSVFQGISTSVAILCEEFPHELGDFVILLNAGMSIQQALFFNFLSACCCYLGLAFGILAG SHFSANWIFALAGGMFLYISLADMFPEMNEVCQEDERKGSILIPFIIQNLGLLTGFTIMV VLTMYSGQIQIG NT seq 1479 nt NT seq  +upstreamnt  +downstreamnt atgaagctgctgctgctgcacccggccttccagagctgcctcctgctgaccctgcttggc ttatggagaaccacccctgaggctcacgcttcatccctgggtgcaccagctatcagcgct gcctccttcctgcaggatctaatacatcggtatggcgagggtgacagcctcactctgcag cagctgaaggccctactcaaccacctggatgtgggagtgggccggggtaatgtcacccag cacgtgcaaggacacaggaacctctccacgtgctttagttctggagacctcttcactgcc cacaatttcagcgagcagtcgcggattgggagcagcgagctccaggagttctgccccacc atcctccagcagctggattcccgggcctgcacctcggagaaccaggaaaacgaggagaat gagcagacggaggaggggcggccaagcgctgttgaagtgtggggatacggtctcctctgt gtgaccgtcatctccctctgctccctcctgggggccagcgtggtgcccttcatgaagaag accttttacaagaggctgctgctctacttcatagctctggcgattggaaccctctactcc aacgccctcttccagctcatcccggaggcatttggtttcaaccctctggaagattattat gtctccaagtctgcagtggtgtttgggggcttttatcttttctttttcacagagaagatc ttgaagattcttcttaagcagaaaaatgagcatcatcatggacacagccattatgcctct gagtcgcttccctccaagaaggaccaggaggagggggtgatggagaagctgcagaacggg gacctggaccacatgattcctcagcactgcagcagtgagctggacggcaaggcgcccatg gtggacgagaaggtcattgtgggctcgctctctgtgcaggacctgcaggcttcccagagt gcttgctactggctgaaaggtgtccgctactctgatatcggcactctggcctggatgatc actctgagcgacggcctccataatttcatcgatggcctggccatcggtgcttccttcact gtgtcagttttccaaggcatcagcacctcggtggccatcctctgtgaggagttcccacat gagctaggagactttgtcatcctgctcaacgctgggatgagcatccaacaagctctcttc ttcaacttcctttctgcctgctgctgctacctgggtctggcctttggcatcctggccggc agccacttctctgccaactggatttttgcgctagctggaggaatgttcttgtatatttct ctggctgatatgttccctgagatgaatgaggtctgtcaagaggatgaaaggaagggcagc atcttgattccatttatcatccagaacctgggcctcctgactggattcaccatcatggtg gtcctcaccatgtattcaggacagatccagattgggtag

Homo sapiens (human): 25800 Help Entry 25800             CDS       T01001                                  Symbol SLC39A6, LIV-1, LIV1, ZIP6 Name (RefSeq) solute carrier family 39 member 6   KO K14712   solute carrier family 39 (zinc transporter), member 6 Organism hsa  Homo sapiens (human) Pathway hsa05010   Alzheimer disease hsa05012   Parkinson disease Brite KEGG Orthology (KO) [BR:hsa00001]  09160 Human Diseases   09164 Neurodegenerative disease    05010 Alzheimer disease     25800 (SLC39A6)    05012 Parkinson disease     25800 (SLC39A6)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     25800 (SLC39A6) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC39: Metal ion transporter    25800 (SLC39A6) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Zip Phage_Mu_Gp48 Motif Other DBs NCBI-GeneID:  25800 NCBI-ProteinID:  NP_036451 OMIM:  608731 HGNC:  18607 Ensembl:  ENSG00000141424 Pharos:  Q13433(Tbio) UniProt:  Q13433 LinkDB All DBs Position 18:complement(36108531..36129340) Genome browser AA seq 755 aa AA seqDB search MARKLSVILILTFALSVTNPLHELKAAAFPQTTEKISPNWESGINVDLAISTRQYHLQQL FYRYGENNSLSVEGFRKLLQNIGIDKIKRIHIHHDHDHHSDHEHHSDHERHSDHEHHSEH EHHSDHDHHSHHNHAASGKNKRKALCPDHDSDSSGKDPRNSQGKGAHRPEHASGRRNVKD SVSASEVTSTVYNTVSEGTHFLETIETPRPGKLFPKDVSSSTPPSVTSKSRVSRLAGRKT NESVSEPRKGFMYSRNTNENPQECFNASKLLTSHGMGIQVPLNATEFNYLCPAIINQIDA RSCLIHTSEKKAEIPPKTYSLQIAWVGGFIAISIISFLSLLGVILVPLMNRVFFKFLLSF LVALAVGTLSGDAFLHLLPHSHASHHHSHSHEEPAMEMKRGPLFSHLSSQNIEESAYFDS TWKGLTALGGLYFMFLVEHVLTLIKQFKDKKKKNQKKPENDDDVEIKKQLSKYESQLSTN EEKVDTDDRTEGYLRADSQEPSHFDSQQPAVLEEEEVMIAHAHPQEVYNEYVPRGCKNKC HSHFHDTLGQSDDLIHHHHDYHHILHHHHHQNHHPHSHSQRYSREELKDAGVATLAWMVI MGDGLHNFSDGLAIGAAFTEGLSSGLSTSVAVFCHELPHELGDFAVLLKAGMTVKQAVLY NALSAMLAYLGMATGIFIGHYAENVSMWIFALTAGLFMYVALVDMVPEMLHNDASDHGCS RWGYFFLQNAGMLLGFGIMLLISIFEHKIVFRINF NT seq 2268 nt NT seq  +upstreamnt  +downstreamnt atggcgaggaagttatctgtaatcttgatcctgacctttgccctctctgtcacaaatccc cttcatgaactaaaagcagctgctttcccccagaccactgagaaaattagtccgaattgg gaatctggcattaatgttgacttggcaatttccacacggcaatatcatctacaacagctt ttctaccgctatggagaaaataattctttgtcagttgaagggttcagaaaattacttcaa aatataggcatagataagattaaaagaatccatatacaccatgaccacgaccatcactca gaccacgagcatcactcagaccatgagcgtcactcagaccatgagcatcactcagagcac gagcatcactctgaccatgatcatcactctcaccataatcatgctgcttctggtaaaaat aagcgaaaagctctttgcccagaccatgactcagatagttcaggtaaagatcctagaaac agccaggggaaaggagctcaccgaccagaacatgccagtggtagaaggaatgtcaaggac agtgttagtgctagtgaagtgacctcaactgtgtacaacactgtctctgaaggaactcac tttctagagacaatagagactccaagacctggaaaactcttccccaaagatgtaagcagc tccactccacccagtgtcacatcaaagagccgggtgagccggctggctggtaggaaaaca aatgaatctgtgagtgagccccgaaaaggctttatgtattccagaaacacaaatgaaaat cctcaggagtgtttcaatgcatcaaagctactgacatctcatggcatgggcatccaggtt ccgctgaatgcaacagagttcaactatctctgtccagccatcatcaaccaaattgatgct agatcttgtctgattcatacaagtgaaaagaaggctgaaatccctccaaagacctattca ttacaaatagcctgggttggtggttttatagccatttccatcatcagtttcctgtctctg ctgggggttatcttagtgcctctcatgaatcgggtgtttttcaaatttctcctgagtttc cttgtggcactggccgttgggactttgagtggtgatgcttttttacaccttcttccacat tctcatgcaagtcaccaccatagtcatagccatgaagaaccagcaatggaaatgaaaaga ggaccacttttcagtcatctgtcttctcaaaacatagaagaaagtgcctattttgattcc acgtggaagggtctaacagctctaggaggcctgtatttcatgtttcttgttgaacatgtc ctcacattgatcaaacaatttaaagataagaagaaaaagaatcagaagaaacctgaaaat gatgatgatgtggagattaagaagcagttgtccaagtatgaatctcaactttcaacaaat gaggagaaagtagatacagatgatcgaactgaaggctatttacgagcagactcacaagag ccctcccactttgattctcagcagcctgcagtcttggaagaagaagaggtcatgatagct catgctcatccacaggaagtctacaatgaatatgtacccagagggtgcaagaataaatgc cattcacatttccacgatacactcggccagtcagacgatctcattcaccaccatcatgac taccatcatattctccatcatcaccaccaccaaaaccaccatcctcacagtcacagccag cgctactctcgggaggagctgaaagatgccggcgtcgccactctggcctggatggtgata atgggtgatggcctgcacaatttcagcgatggcctagcaattggtgctgcttttactgaa ggcttatcaagtggtttaagtacttctgttgctgtgttctgtcatgagttgcctcatgaa ttaggtgactttgctgttctactaaaggctggcatgaccgttaagcaggctgtcctttat aatgcattgtcagccatgctggcgtatcttggaatggcaacaggaattttcattggtcat tatgctgaaaatgtttctatgtggatatttgcacttactgctggcttattcatgtatgtt gctctggttgatatggtacctgaaatgctgcacaatgatgctagtgaccatggatgtagc cgctgggggtatttctttttacagaatgctgggatgcttttgggttttggaattatgtta cttatttccatatttgaacataaaatcgtgtttcgtataaatttctag

Homo sapiens (human): 27173 Help Entry 27173             CDS       T01001                                  Symbol SLC39A1, ZIP1, ZIRTL Name (RefSeq) solute carrier family 39 member 1   KO K14709   solute carrier family 39 (zinc transporter), member 1/2/3 Organism hsa  Homo sapiens (human) Pathway hsa05010   Alzheimer disease hsa05012   Parkinson disease Brite KEGG Orthology (KO) [BR:hsa00001]  09160 Human Diseases   09164 Neurodegenerative disease    05010 Alzheimer disease     27173 (SLC39A1)    05012 Parkinson disease     27173 (SLC39A1)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     27173 (SLC39A1) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC39: Metal ion transporter    27173 (SLC39A1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Zip YLATT Motif Other DBs NCBI-GeneID:  27173 NCBI-ProteinID:  NP_001258886 OMIM:  604740 HGNC:  12876 Ensembl:  ENSG00000143570 Pharos:  Q9NY26(Tbio) UniProt:  Q9NY26 LinkDB All DBs Position 1:complement(153959110..153968184) Genome browser AA seq 324 aa AA seqDB search MGPWGEPELLVWRPEAVASEPPVPVGLEVKLGALVLLLVLTLLCSLVPICVLRRPGANHE GSASRQKALSLVSCFAGGVFLATCLLDLLPDYLAAIDEALAALHVTLQFPLQEFILAMGF FLVLVMEQITLAYKEQSGPSPLEETRALLGTVNGGPQHWHDGPGVPQASGAPATPSALRA CVLVFSLALHSVFEGLAVGLQRDRARAMELCLALLLHKGILAVSLSLRLLQSHLRAQVVA GCGILFSCMTPLGIGLGAALAESAGPLHQLAQSVLEGMAAGTFLYITFLEILPQELASSE QRILKVILLLAGFALLTGLLFIQI NT seq 975 nt NT seq  +upstreamnt  +downstreamnt atggggccctggggagagccagagctcctggtgtggcgccccgaggcggtagcttcagag cctccagtgcctgtggggctggaggtgaagttgggggccctggtgctgctgctggtgctc accctcctctgcagcctggtgcccatctgtgtgctgcgccggccaggagctaaccatgaa ggctcagcttcccgccagaaagccctgagcctagtaagctgtttcgcggggggcgtcttt ttggccacttgtctcctggacctgctgcctgactacctggctgccatagatgaggccctg gcagccttgcacgtgacgctccagttcccactgcaagagttcatcctggccatgggcttc ttcctggtcctggtgatggagcagatcacactggcttacaaggagcagtcagggccgtca cctctggaggaaacaagggctctgctgggaacagtgaatggtgggccgcagcattggcat gatgggccaggggtcccacaggcgagtggagccccagcaaccccctcagccttgcgtgcc tgtgtactggtgttctccctggccctccactccgtgttcgaggggctggcggtagggctg cagcgagaccgggctcgggccatggagctgtgcctggctttgctgctccacaagggcatc ctggctgtcagcctgtccctgcggctgttgcagagccaccttagggcacaggtggtggct ggctgtgggatcctcttctcatgcatgacacctctaggcatcgggctgggtgcagctctg gcagagtcggcaggacctctgcaccagctggcccagtctgtgctagagggcatggcagct ggcacctttctctatatcacctttctggaaatcctgccccaggagctggccagttctgag caaaggatcctcaaggtcattctgctcctagcaggctttgccctgctcactggcctgctc ttcatccaaatctag

Homo sapiens (human): 283375 Help Entry 283375            CDS       T01001                                  Symbol SLC39A5, LZT-Hs7, MYP24, ZIP5 Name (RefSeq) solute carrier family 39 member 5   KO K14711   solute carrier family 39 (zinc transporter), member 5 Organism hsa  Homo sapiens (human) Pathway hsa05010   Alzheimer disease hsa05012   Parkinson disease Disease H02041   Myopia Brite KEGG Orthology (KO) [BR:hsa00001]  09160 Human Diseases   09164 Neurodegenerative disease    05010 Alzheimer disease     283375 (SLC39A5)    05012 Parkinson disease     283375 (SLC39A5)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     283375 (SLC39A5) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC39: Metal ion transporter    283375 (SLC39A5) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Zip Motif Other DBs NCBI-GeneID:  283375 NCBI-ProteinID:  NP_001128667 OMIM:  608730 HGNC:  20502 Ensembl:  ENSG00000139540 Pharos:  Q6ZMH5(Tbio) UniProt:  Q6ZMH5 A0A024RB24 LinkDB All DBs Position 12:56230051..56237846 Genome browser AA seq 540 aa AA seqDB search MMGSPVSHLLAGFCVWVVLGWVGGSVPNLGPAEQEQNHYLAQLFGLYGENGTLTAGGLAR LLHSLGLGRVQGLRLGQHGPLTGRAASPAADNSTHRPQNPELSVDVWAGMPLGPSGWGDL EESKAPHLPRGPAPSGLDLLHRLLLLDHSLADHLNEDCLNGSQLLVNFGLSPAAPLTPRQ FALLCPALLYQIDSRVCIGAPAPAPPGDLLSALLQSALAVLLLSLPSPLSLLLLRLLGPR LLRPLLGFLGALAVGTLCGDALLHLLPHAQEGRHAGPGGLPEKDLGPGLSVLGGLFLLFV LENMLGLLRHRGLRPRCCRRKRRNLETRNLDPENGSGMALQPLQAAPEPGAQGQREKNSQ HPPALAPPGHQGHSHGHQGGTDITWMVLLGDGLHNLTDGLAIGAAFSDGFSSGLSTTLAV FCHELPHELGDFAMLLQSGLSFRRLLLLSLVSGALGLGGAVLGVGLSLGPVPLTPWVFGV TAGVFLYVALVDMLPALLRPPEPLPTPHVLLQGLGLLLGGGLMLAITLLEERLLPVTTEG NT seq 1623 nt NT seq  +upstreamnt  +downstreamnt atgatggggtccccagtgagtcatctgctggccggcttctgtgtgtgggtcgtcttgggc tgggtagggggctcagtccccaacctgggccctgctgagcaggagcagaaccattacctg gcccagctgtttggcctgtacggcgagaatgggacgctgactgcagggggcttggcgcgg cttctccacagcctggggctaggccgagttcaggggcttcgcctgggacagcatgggcct ctgactggacgggctgcatccccagctgcagacaattccacacacaggccacagaaccct gagctgagtgtggatgtctgggcagggatgcctctgggtccctcagggtggggtgacctg gaagagtcaaaggcccctcacctaccccgtgggccagccccctcgggcctggacctcctt cacaggcttctgttgctggaccactcattggctgaccacctgaatgaggattgtctgaac ggctcccagctgctggtcaattttggcttgagccccgctgctcctctgacccctcgtcag tttgctctgctgtgcccagccctgctttatcagatcgacagccgcgtctgcatcggcgct ccggcccctgcacccccaggggatctactatctgccctgcttcagagtgccctggcagtc ctgttgctcagcctcccttctcccctatccctgctgctgctgcggctcctgggacctcgt ctactacggcccttgctgggcttcctgggggccctggcggtgggcactctttgtggggat gcactgctacatctgctaccgcatgcacaagaagggcggcacgcaggacctggcggacta ccagagaaggacctgggcccggggctgtcagtgctcggaggcctcttcctgctctttgtg ctggagaacatgctggggcttttgcggcaccgagggctcaggccaagatgctgcaggcga aaacgaaggaatctcgaaacacgcaacttggatccggagaatggcagtgggatggccctt cagcccctacaggcagctccagagccaggggctcagggccagagggagaagaacagccag cacccaccagctctggcccctcctgggcaccaaggccacagtcatgggcaccagggtggc actgatatcacgtggatggtcctcctgggagatggtctacacaacctcactgatgggctg gccataggtgctgccttctctgatggcttctccagcggcctcagtaccaccttagcggtc ttctgccatgagctgccccacgaactgggtgactttgccatgctgctccagtcagggctg tcctttcggcggctgctgctgctgagcctcgtgtctggagccctgggattggggggtgca gtcctgggggtggggctcagcctgggccctgtccccctcactccctgggtgtttggggtc actgctggggtcttcctctatgtggcccttgtggacatgctaccagccctgcttcgtcct ccggagcccctgcctacgccccatgtgctcctgcaggggctggggctgctgctggggggc ggcctcatgcttgccataaccctgctggaggagcggctactgcccgtgaccactgagggc tga

Homo sapiens (human): 29985 Help Entry 29985             CDS       T01001                                  Symbol SLC39A3, ZIP-3, ZIP3 Name (RefSeq) solute carrier family 39 member 3   KO K14709   solute carrier family 39 (zinc transporter), member 1/2/3 Organism hsa  Homo sapiens (human) Pathway hsa05010   Alzheimer disease hsa05012   Parkinson disease Brite KEGG Orthology (KO) [BR:hsa00001]  09160 Human Diseases   09164 Neurodegenerative disease    05010 Alzheimer disease     29985 (SLC39A3)    05012 Parkinson disease     29985 (SLC39A3)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     29985 (SLC39A3) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC39: Metal ion transporter    29985 (SLC39A3) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Zip IF2_N Motif Other DBs NCBI-GeneID:  29985 NCBI-ProteinID:  NP_653165 OMIM:  612168 HGNC:  17128 Ensembl:  ENSG00000141873 Pharos:  Q9BRY0(Tbio) UniProt:  Q9BRY0 LinkDB All DBs Position 19:complement(2732524..2740076) Genome browser AA seq 314 aa AA seqDB search MVKLLVAKILCMVGVFFFMLLGSLLPVKIIETDFEKAHRSKKILSLCNTFGGGVFLATCF NALLPAVREKLQKVLSLGHISTDYPLAETILLLGFFMTVFLEQLILTFRKEKPSFIDLET FNAGSDVGSDSEYESPFMGGARGHALYVEPHGHGPSLSVQGLSRASPVRLLSLAFALSAH SVFEGLALGLQEEGEKVVSLFVGVAVHETLVAVALGISMARSAMPLRDAAKLAVTVSAMI PLGIGLGLGIESAQGVPGSVASVLLQGLAGGTFLFITFLEILAKELEEKSDRLLKVLFLV LGYTVLAGMVFLKW NT seq 945 nt NT seq  +upstreamnt  +downstreamnt atggtgaaattgctagtggccaaaatcctgtgcatggtgggcgtgttcttcttcatgctg ctcggctccctgctccccgtgaagatcatcgagacagattttgagaaggcccatcgctcg aaaaagatcctctctctctgcaacacctttggaggaggggtgtttctggccacgtgcttc aacgctctgctgcccgctgtgagggaaaagctccagaaggtcctgagcctcggccacatc agcaccgactacccgctggccgaaaccatcctcctgctgggcttcttcatgaccgtcttc ctggagcagctgatcctgaccttccgcaaggagaagccgtccttcatcgacctggagacc ttcaacgccggatcggacgtgggcagcgactcggagtatgagagccccttcatggggggc gcgcggggccacgcgctgtacgtggagccccacggccacggccccagcctgagcgtgcag ggcctctcgcgcgccagccccgtgcgcctgctcagcctggccttcgcgctgtcggcccac tcggtctttgagggcctggccctgggcctgcaggaggagggggagaaagtggtgagcctg ttcgtgggggtggccgtccacgagacactggtggccgtggccctgggcatcagcatggcc cggagtgccatgcccctgcgggacgcggccaagctggcggtcaccgtaagcgccatgatc cccctgggcatcggcctgggcctgggcattgagagcgcccagggcgtgccgggcagcgtg gcgtccgtgctgctgcagggcctggcgggcggcaccttcctcttcatcaccttcctggag atcctggccaaggagctggaggagaagagtgaccgtctgctcaaggtcctcttcctggtg ctgggctacaccgtcctggccgggatggtcttcctcaagtggtga

Homo sapiens (human): 29986 Help Entry 29986             CDS       T01001                                  Symbol SLC39A2, 6A1, ETI-1, ZIP-2, ZIP2 Name (RefSeq) solute carrier family 39 member 2   KO K14709   solute carrier family 39 (zinc transporter), member 1/2/3 Organism hsa  Homo sapiens (human) Pathway hsa05010   Alzheimer disease hsa05012   Parkinson disease Brite KEGG Orthology (KO) [BR:hsa00001]  09160 Human Diseases   09164 Neurodegenerative disease    05010 Alzheimer disease     29986 (SLC39A2)    05012 Parkinson disease     29986 (SLC39A2)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     29986 (SLC39A2) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC39: Metal ion transporter    29986 (SLC39A2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Zip Motif Other DBs NCBI-GeneID:  29986 NCBI-ProteinID:  NP_055394 OMIM:  612166 HGNC:  17127 Ensembl:  ENSG00000165794 Pharos:  Q9NP94(Tbio) UniProt:  Q9NP94 LinkDB All DBs Position 14:20999293..21001871 Genome browser AA seq 309 aa AA seqDB search MEQLLGIKLGCLFALLALTLGCGLTPICFKWFQIDAARGHHRLVLRLLGCISAGVFLGAG FMHMTAEALEEIESQIQKFMVQNRSASERNSSGDADSAHMEYPYGELIISLGFFFVFFLE SLALQCCPGAAGGSTVQDEEWGGAHIFELHSHGHLPSPSKGPLRALVLLLSLSFHSVFEG LAVGLQPTVAATVQLCLAVLAHKGLVVFGVGMRLVHLGTSSRWAVFSILLLALMSPLGLA VGLAVTGGDSEGGRGLAQAVLEGVAAGTFLYVTFLEILPRELASPEAPLAKWSCVAAGFA FMAFIALWA NT seq 930 nt NT seq  +upstreamnt  +downstreamnt atggagcaactactaggaataaaacttggctgcctgtttgccctgttggctctcactctg ggctgtggccttactcccatctgcttcaaatggttccagattgatgcagccagaggtcat caccggctagtcctcagactcctgggctgtatttctgctggtgttttcctgggagcaggg ttcatgcatatgactgctgaagccctggaggaaattgaatcacagattcagaagttcatg gtgcagaacagatcagcaagtgagagaaattcttctggtgatgctgattcagctcatatg gagtatccctatggagagctcatcatctccctgggcttcttttttgtcttctttttggag tcgctggcattgcagtgctgtcctggggctgctggaggatcgacagtgcaggacgaagaa tggggtggggctcatatcttcgaactccacagccatggacatttaccctcaccctcaaag ggtcccctccgagcccttgtcctcttgctgtcactctcctttcactcagtgtttgaaggg ctagctgtggggctgcagccgacagtagcagctaccgtgcagctctgccttgctgtcctg gctcataaggggcttgtggtgtttggtgtaggaatgcggctagtgcatttaggtaccagc tcacgatgggcagtgttctccatactattattagctctcatgtcccccctgggcctagcc gtagggctggctgtgactggaggggactctgaaggagggcggggcttagcccaggctgtg ttagagggtgtggcagctggtaccttcctgtatgtcaccttcctagaaattcttccacgg gagctagctagtcctgaggcccctctagctaagtggagctgtgtagccgctggttttgcc ttcatggcctttattgccttgtgggcctga

Homo sapiens (human): 55334 Help Entry 55334             CDS       T01001                                  Symbol SLC39A9, ZIP-9, ZIP9 Name (RefSeq) solute carrier family 39 member 9   KO K14715   solute carrier family 39 (zinc transporter), member 9 Organism hsa  Homo sapiens (human) Pathway hsa05010   Alzheimer disease hsa05012   Parkinson disease Brite KEGG Orthology (KO) [BR:hsa00001]  09160 Human Diseases   09164 Neurodegenerative disease    05010 Alzheimer disease     55334 (SLC39A9)    05012 Parkinson disease     55334 (SLC39A9)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     55334 (SLC39A9) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC39: Metal ion transporter    55334 (SLC39A9) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Zip Motif Other DBs NCBI-GeneID:  55334 NCBI-ProteinID:  NP_060845 OMIM:  619116 HGNC:  20182 Ensembl:  ENSG00000029364 Pharos:  Q9NUM3(Tbio) UniProt:  Q9NUM3 C4N9M8 LinkDB All DBs Position 14:69398384..69462390 Genome browser AA seq 307 aa AA seqDB search MDDFISISLLSLAMLVGCYVAGIIPLAVNFSEERLKLVTVLGAGLLCGTALAVIVPEGVH ALYEDILEGKHHQASETHNVIASDKAAEKSVVHEHEHSHDHTQLHAYIGVSLVLGFVFML LVDQIGNSHVHSTDDPEAARSSNSKITTTLGLVVHAAADGVALGAAASTSQTSVQLIVFV AIMLHKAPAAFGLVSFLMHAGLERNRIRKHLLVFALAAPVMSMVTYLGLSKSSKEALSEV NATGVAMLFSAGTFLYVATVHVLPEVGGIGHSHKPDATGGRGLSRLEVAALVLGCLIPLI LSVGHQH NT seq 924 nt NT seq  +upstreamnt  +downstreamnt atggatgatttcatctccattagcctgctgtctctggctatgttggtgggatgttacgtg gccggaatcattcccttggctgttaatttctcagaggaacgactgaagctggtgactgtt ttgggtgctggccttctctgtggaactgctctggcagtcatcgtgcctgaaggagtacat gccctttatgaagatattcttgagggaaaacaccaccaagcaagtgaaacacataatgtg attgcatcagacaaagcagcagaaaaatcagttgtccatgaacatgagcacagccacgac cacacacagctgcatgcctatattggtgtttccctcgttctgggcttcgttttcatgttg ctggtggaccagattggtaactcccatgtgcattctactgacgatccagaagcagcaagg tctagcaattccaaaatcaccaccacgctgggtctggttgtccatgctgcagctgatggt gttgctttgggagcagcagcatctacttcacagaccagtgtccagttaattgtgtttgtg gcaatcatgctacataaggcaccagctgcttttggactggtttccttcttgatgcatgct ggcttagagcggaatcgaatcagaaagcacttgctggtctttgcattggcagcaccagtt atgtccatggtgacatacttaggactgagtaagagcagtaaagaagccctttcagaggtg aacgccacgggagtggccatgcttttctctgccgggacatttctttatgttgccacagta catgtcctccctgaggtgggcggaatagggcacagccacaagcccgatgccacgggaggg agaggcctcagccgcctggaagtggcagccctggttctgggttgcctcatccctctcatc ctgtcagtaggacaccagcattaa

Homo sapiens (human): 55630 Help Entry 55630             CDS       T01001                                  Symbol SLC39A4, AEZ, AWMS2, ZIP4 Name (RefSeq) solute carrier family 39 member 4   KO K14710   solute carrier family 39 (zinc transporter), member 4 Organism hsa  Homo sapiens (human) Pathway hsa04978   Mineral absorption hsa05010   Alzheimer disease hsa05012   Parkinson disease Disease H00212   Acrodermatitis enteropathica Brite KEGG Orthology (KO) [BR:hsa00001]  09150 Organismal Systems   09154 Digestive system    04978 Mineral absorption     55630 (SLC39A4)  09160 Human Diseases   09164 Neurodegenerative disease    05010 Alzheimer disease     55630 (SLC39A4)    05012 Parkinson disease     55630 (SLC39A4)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     55630 (SLC39A4) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC39: Metal ion transporter    55630 (SLC39A4) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Zip ZIP4_domain Motif Other DBs NCBI-GeneID:  55630 NCBI-ProteinID:  NP_570901 OMIM:  607059 HGNC:  17129 Ensembl:  ENSG00000147804 Pharos:  Q6P5W5(Tbio) UniProt:  Q6P5W5 LinkDB All DBs Position 8:complement(144412414..144416844) Genome browser AA seq 647 aa AA seqDB search MASLVSLELGLLLAVLVVTATASPPAGLLSLLTSGQGALDQEALGGLLNTLADRVHCANG PCGKCLSVEDALGLGEPEGSGLPPGPVLEARYVARLSAAAVLYLSNPEGTCEDARAGLWA SHADHLLALLESPKALTPGLSWLLQRMQARAAGQTPKMACVDIPQLLEEAVGAGAPGSAG GVLAALLDHVRSGSCFHALPSPQYFVDFVFQQHSSEVPMTLAELSALMQRLGVGREAHSD HSHRHRGASSRDPVPLISSSNSSSVWDTVCLSARDVMAAYGLSEQAGVTPEAWAQLSPAL LQQQLSGACTSQSRPPVQDQLSQSERYLYGSLATLLICLCAVFGLLLLTCTGCRGVTHYI LQTFLSLAVGAVTGDAVLHLTPKVLGLHTHSEEGLSPQPTWRLLAMLAGLYAFFLFENLF NLLLPRDPEDLEDGPCGHSSHSHGGHSHGVSLQLAPSELRQPKPPHEGSRADLVAEESPE LLNPEPRRLSPELRLLPYMITLGDAVHNFADGLAVGAAFASSWKTGLATSLAVFCHELPH ELGDFAALLHAGLSVRQALLLNLASALTAFAGLYVALAVGVSEESEAWILAVATGLFLYV ALCDMLPAMLKVRDPRPWLLFLLHNVGLLGGWTVLLLLSLYEDDITF NT seq 1944 nt NT seq  +upstreamnt  +downstreamnt atggcgtccctggtctcgctggagctggggctgcttctggctgtgctggtggtgacggcg acggcgtccccgcctgctggtctgctgagcctgctcacctctggccagggcgctctggat caagaggctctgggcggcctgttaaatacgctggcggaccgtgtgcactgcgccaacggg ccgtgtggaaagtgcctgtctgtggaggacgccctgggcctgggcgagcctgaggggtca gggctgcccccgggcccggtcctggaggccaggtacgtcgcccgcctcagtgccgccgcc gtcctgtacctcagcaaccccgagggcacctgtgaggacgctcgggctggcctctgggcc tctcatgcagaccacctcctggccctgctcgagagccccaaggccctgaccccgggcctg agctggctgctgcagaggatgcaggcccgggctgccggccagacccccaagatggcctgc gtagatatccctcagctgctggaggaggcggtgggggcgggggctccgggcagtgctggc ggcgtcctggctgccctgctggaccatgtcaggagcgggtcttgcttccacgccttgccg agccctcagtacttcgtggactttgtgttccagcagcacagcagcgaggtccctatgacg ctggccgagctgtcagccttgatgcagcgcctgggggtgggcagggaggcccacagtgac cacagtcatcggcacaggggagccagcagccgggaccctgtgcccctcatcagctccagc aacagctccagtgtgtgggacacggtatgcctgagtgccagggacgtgatggctgcatat ggactgtcggaacaggctggggtgaccccggaggcctgggcccaactgagccctgccctg ctccaacagcagctgagtggagcctgcacctcccagtccaggccccccgtccaggaccag ctcagccagtcagagaggtatctgtacggctccctggccacgctgctcatctgcctctgc gcggtctttggcctcctgctgctgacctgcactggctgcaggggggtcacccactacatc ctgcagaccttcctgagcctggcagtgggtgcagtcactggggacgctgtcctgcatctg acgcccaaggtgctggggctgcatacacacagcgaagagggcctcagcccacagcccacc tggcgcctcctggctatgctggccgggctctacgccttcttcctgtttgagaacctcttc aatctcctgctgcccagggacccggaggacctggaggacgggccctgcggccacagcagc catagccacgggggccacagccacggtgtgtccctgcagctggcacccagcgagctccgg cagcccaagcccccccacgagggctcccgcgcagacctggtggcggaggagagcccggag ctgctgaaccctgagcccaggagactgagcccagagttgaggctactgccctatatgatc actctgggcgacgccgtgcacaacttcgccgacgggctggccgtgggcgccgccttcgcg tcctcctggaagaccgggctggccacctcgctggccgtgttctgccacgagttgccacac gagctgggggacttcgccgccttgctgcacgcggggctgtccgtgcgccaagcactgctg ctgaacctggcctccgcgctcacggccttcgctggtctctacgtggcactcgcggttgga gtcagcgaggagagcgaggcctggatcctggcagtggccaccggcctgttcctctacgta gcactctgcgacatgctcccggcgatgttgaaagtacgggacccgcggccctggctcctc ttcctgctgcacaacgtgggcctgctgggcggctggaccgtcctgctgctgctgtccctg tacgaggatgacatcaccttctga

Homo sapiens (human): 57181 Help Entry 57181             CDS       T01001                                  Symbol SLC39A10, LZT-Hs2 Name (RefSeq) solute carrier family 39 member 10   KO K14716   solute carrier family 39 (zinc transporter), member 10 Organism hsa  Homo sapiens (human) Pathway hsa05010   Alzheimer disease hsa05012   Parkinson disease Brite KEGG Orthology (KO) [BR:hsa00001]  09160 Human Diseases   09164 Neurodegenerative disease    05010 Alzheimer disease     57181 (SLC39A10)    05012 Parkinson disease     57181 (SLC39A10)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     57181 (SLC39A10) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC39: Metal ion transporter    57181 (SLC39A10) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Zip Mntp Motif Other DBs NCBI-GeneID:  57181 NCBI-ProteinID:  NP_001120729 OMIM:  608733 HGNC:  20861 Ensembl:  ENSG00000196950 Pharos:  Q9ULF5(Tbio) UniProt:  Q9ULF5 A0A024R3W5 Q05C42 LinkDB All DBs Position 2:195613029..195737700 Genome browser AA seq 831 aa AA seqDB search MKVHMHTKFCLICLLTFIFHHCNHCHEEHDHGPEALHRQHRGMTELEPSKFSKQAAENEK KYYIEKLFERYGENGRLSFFGLEKLLTNLGLGERKVVEINHEDLGHDHVSHLDILAVQEG KHFHSHNHQHSHNHLNSENQTVTSVSTKRNHKCDPEKETVEVSVKSDDKHMHDHNHRLRH HHRLHHHLDHNNTHHFHNDSITPSERGEPSNEPSTETNKTQEQSDVKLPKGKRKKKGRKS NENSEVITPGFPPNHDQGEQYEHNRVHKPDRVHNPGHSHVHLPERNGHDPGRGHQDLDPD NEGELRHTRKREAPHVKNNAIISLRKDLNEDDHHHECLNVTQLLKYYGHGANSPISTDLF TYLCPALLYQIDSRLCIEHFDKLLVEDINKDKNLVPEDEANIGASAWICGIISITVISLL SLLGVILVPIINQGCFKFLLTFLVALAVGTMSGDALLHLLPHSQGGHDHSHQHAHGHGHS HGHESNKFLEEYDAVLKGLVALGGIYLLFIIEHCIRMFKHYKQQRGKQKWFMKQNTEEST IGRKLSDHKLNNTPDSDWLQLKPLAGTDDSVVSEDRLNETELTDLEGQQESPPKNYLCIE EEKIIDHSHSDGLHTIHEHDLHAAAHNHHGENKTVLRKHNHQWHHKHSHHSHGPCHSGSD LKETGIANIAWMVIMGDGIHNFSDGLAIGAAFSAGLTGGISTSIAVFCHELPHELGDFAV LLKAGMTVKQAIVYNLLSAMMAYIGMLIGTAVGQYANNITLWIFAVTAGMFLYVALVDML PEMLHGDGDNEEHGFCPVGQFILQNLGLLFGFAIMLVIALYEDKIVFDIQF NT seq 2496 nt NT seq  +upstreamnt  +downstreamnt atgaaggtacatatgcacacaaaattttgcctcatttgtttgctgacatttatttttcat cattgcaaccattgccatgaagaacatgaccatggccctgaagcgcttcacagacagcat cgtggaatgacagaattggagccaagcaaattttcaaagcaagctgctgaaaatgaaaaa aaatactatattgaaaaactttttgagcgttatggtgaaaatggaagattatcctttttt ggtttggagaaacttttaacaaacttgggccttggagagagaaaagtagttgagattaat catgaggatcttggccacgatcatgtttctcatttagatattttggcagttcaagaggga aagcattttcactcacataaccaccagcattcccataatcatttaaattcagaaaatcaa actgtgaccagtgtatccacaaaaagaaaccataaatgtgatccagagaaagagacagtt gaagtgtctgtaaaatctgatgataaacatatgcatgaccataatcaccgcctacgtcat caccatcgtttgcatcatcatcttgatcataacaacactcaccattttcataatgattcc attactcccagtgagcgtggggagcctagcaatgaaccttcaacagagaccaataaaacc caggaacaatctgatgttaaactaccgaaaggaaagaggaagaaaaaagggaggaaaagt aatgaaaattctgaggttattacaccaggttttccccctaaccatgatcagggtgaacag tatgagcataatcgggtccacaaacctgatcgtgtacataacccaggtcattctcatgta catcttccagaacgtaatggtcatgatcctggtcgtggacaccaagatcttgatcctgat aatgaaggtgaacttcgacatactagaaagagagaagcaccacatgttaaaaataatgca ataatttctttgagaaaagatctaaatgaagatgaccatcatcatgaatgtttgaacgtc actcagttattaaaatactatggtcatggtgccaactctcccatctcaactgatttattt acatacctttgccctgcattgttatatcaaatcgacagcagactttgtattgagcatttt gacaaacttttagttgaagatataaataaggataaaaacctggttcctgaagatgaggca aatataggggcatcagcctggatttgtggtatcatttctatcactgtcattagcctgctt tccttgctaggcgtgatcttggttcctatcattaaccaaggatgcttcaaattccttctt acattccttgttgcattagctgtaggaacaatgagtggagacgcccttcttcatctactg ccccattctcagggtggacatgatcacagtcaccaacatgcacatgggcatggacattct catggacatgaatctaacaagtttttggaagaatatgatgctgtattgaaaggacttgtt gctctaggaggcatttacttgctatttatcattgaacactgcattagaatgtttaagcac tacaaacaacaaagaggaaaacagaaatggtttatgaaacagaacacagaagaatcaact attggaagaaagctttcagatcacaagttaaacaatacaccagattctgactggcttcaa ctcaagcctcttgccggaactgatgactcggttgtttctgaagatcgacttaatgaaact gaactgacagatttagaaggccaacaagaatcccctcctaaaaattacctttgtatagaa gaggagaaaatcatagaccattctcacagtgatggattacataccattcatgagcatgat ctccatgctgctgcacataaccaccacggcgagaacaaaactgtgctgaggaagcataat caccagtggcaccacaagcattctcatcattcccatggcccctgtcattctggatccgat ctgaaagaaacaggaatagctaatatagcctggatggtgatcatgggggatggcatccac aacttcagtgatgggctcgcaattggtgcagctttcagtgctggattgacaggaggaatc agtacttctatagccgtcttctgtcatgaactgccacatgaattaggagattttgcagtt cttcttaaagcaggcatgactgtaaagcaagcaattgtatacaacctcctctctgccatg atggcttacataggcatgctcataggcacagctgttggtcagtatgccaataacatcaca ctttggatctttgcagtcactgcaggcatgttcctctatgtagccttggtggatatgctt ccagaaatgttgcatggtgatggtgacaatgaagaacatggcttttgtcctgtggggcaa ttcatccttcagaatttaggattgctctttggatttgccattatgctggtgattgccctc tatgaagataaaattgtgtttgacatccagttttga

Homo sapiens (human): 64116 Help Entry 64116             CDS       T01001                                  Symbol SLC39A8, BIGM103, CDG2N, LZT-Hs6, PP3105, ZIP8 Name (RefSeq) solute carrier family 39 member 8   KO K14714   solute carrier family 39 (zinc transporter), member 8 Organism hsa  Homo sapiens (human) Pathway hsa04216   Ferroptosis hsa05010   Alzheimer disease hsa05012   Parkinson disease Disease H00119   Congenital disorders of glycosylation type II Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09143 Cell growth and death    04216 Ferroptosis     64116 (SLC39A8)  09160 Human Diseases   09164 Neurodegenerative disease    05010 Alzheimer disease     64116 (SLC39A8)    05012 Parkinson disease     64116 (SLC39A8)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     64116 (SLC39A8) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC39: Metal ion transporter    64116 (SLC39A8) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Zip DUF4271 Motif Other DBs NCBI-GeneID:  64116 NCBI-ProteinID:  NP_001128618 OMIM:  608732 HGNC:  20862 Ensembl:  ENSG00000138821 Pharos:  Q9C0K1(Tbio) UniProt:  Q9C0K1 A0A024RDG0 LinkDB All DBs Position 4:complement(102251041..102345482) Genome browser AA seq 460 aa AA seqDB search MAPGRAVAGLLLLAAAGLGGVAEGPGLAFSEDVLSVFGANLSLSAAQLQHLLEQMGAASR VGVPEPGQLHFNQCLTAEEIFSLHGFSNATQITSSKFSVICPAVLQQLNFHPCEDRPKHK TRPSHSEVWGYGFLSVTIINLASLLGLILTPLIKKSYFPKILTFFVGLAIGTLFSNAIFQ LIPEAFGFDPKVDSYVEKAVAVFGGFYLLFFFERMLKMLLKTYGQNGHTHFGNDNFGPQE KTHQPKALPAINGVTCYANPAVTEANGHIHFDNVSVVSLQDGKKEPSSCTCLKGPKLSEI GTIAWMITLCDALHNFIDGLAIGASCTLSLLQGLSTSIAILCEEFPHELGDFVILLNAGM STRQALLFNFLSACSCYVGLAFGILVGNNFAPNIIFALAGGMFLYISLADMFPEMNDMLR EKVTGRKTDFTFFMIQNAGMLTGFTAILLITLYAGEIELE NT seq 1383 nt NT seq  +upstreamnt  +downstreamnt atggccccgggtcgcgcggtggccgggctcctgttgctggcggccgccggcctcggagga gtggcggaggggccagggctagccttcagcgaggatgtgctgagcgtgttcggcgcgaat ctgagcctgtcggcggcgcagctccagcacttgctggagcagatgggagccgcctcccgc gtgggcgtcccggagcctggccagctgcacttcaaccagtgtttaactgctgaagagatc ttttcccttcatggcttttcaaatgctacccaaataaccagctccaaattctctgtcatc tgtccagcagtcttacagcaattgaactttcacccatgtgaggatcggcccaagcacaaa acaagaccaagtcattcagaagtttggggatatggattcctgtcagtgacgattattaat ctggcatctctcctcggattgattttgactccactgataaagaaatcttatttcccaaag attttgaccttttttgtggggctggctattgggactcttttttcaaatgcaattttccaa cttattccagaggcatttggatttgatcccaaagtcgacagttatgttgagaaggcagtt gctgtgtttggtggattttacctacttttcttttttgaaagaatgctaaagatgttatta aagacatatggtcagaatggtcatacccactttggaaatgataactttggtcctcaagaa aaaactcatcaacctaaagcattacctgccatcaatggtgtgacatgctatgcaaatcct gctgtcacagaagctaatggacatatccattttgataatgtcagtgtggtatctctacag gatggaaaaaaagagccaagttcatgtacctgtttgaaggggcccaaactgtcagaaata gggacgattgcctggatgataacgctctgcgatgccctccacaatttcatcgatggcctg gcgattggggcttcctgcaccttgtctctccttcagggactcagtacttccatagcaatc ctatgtgaggagtttccccacgagttaggagactttgtgatcctactcaatgcagggatg agcactcgacaagccttgctattcaacttcctttctgcatgttcctgctatgttgggcta gcttttggcattttggtgggcaacaatttcgctccaaatattatatttgcacttgctgga ggcatgttcctctatatttctctggcagatatgtttccagagatgaatgatatgctgaga gaaaaggtaactggaagaaaaaccgatttcaccttcttcatgattcagaatgctggaatg ttaactggattcacagccattctactcattaccttgtatgcaggagaaatcgaattggag taa

Homo sapiens (human): 7922 Help Entry 7922              CDS       T01001                                  Symbol SLC39A7, AGM9, D6S115E, D6S2244E, H2-KE4, HKE4, KE4, RING5, ZIP7 Name (RefSeq) solute carrier family 39 member 7   KO K14713   solute carrier family 39 (zinc transporter), member 7 Organism hsa  Homo sapiens (human) Pathway hsa05010   Alzheimer disease hsa05012   Parkinson disease Disease H00085   Agammaglobulinemias Brite KEGG Orthology (KO) [BR:hsa00001]  09160 Human Diseases   09164 Neurodegenerative disease    05010 Alzheimer disease     7922 (SLC39A7)    05012 Parkinson disease     7922 (SLC39A7)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     7922 (SLC39A7) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC39: Metal ion transporter    7922 (SLC39A7) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Zip Motif Other DBs NCBI-GeneID:  7922 NCBI-ProteinID:  NP_001070984 OMIM:  601416 HGNC:  4927 Ensembl:  ENSG00000112473 Pharos:  Q92504(Tbio) UniProt:  Q92504 A0A024RCX7 LinkDB All DBs Position 6:33200867..33204437 Genome browser AA seq 469 aa AA seqDB search MARGLGAPHWVAVGLLTWATLGLLVAGLGGHDDLHDDLQEDFHGHSHRHSHEDFHHGHSH AHGHGHTHESIWHGHTHDHDHGHSHEDLHHGHSHGYSHESLYHRGHGHDHEHSHGGYGES GAPGIKQDLDAVTLWAYALGATVLISAAPFFVLFLIPVESNSPRHRSLLQILLSFASGGL LGDAFLHLIPHALEPHSHHTLEQPGHGHSHSGQGPILSVGLWVLSGIVAFLVVEKFVRHV KGGHGHSHGHGHAHSHTRGSHGHGRQERSTKEKQSSEEEEKETRGVQKRRGGSTVPKDGP VRPQNAEEEKRGLDLRVSGYLNLAADLAHNFTDGLAIGASFRGGRGLGILTTMTVLLHEV PHEVGDFAILVQSGCSKKQAMRLQLLTAVGALAGTACALLTEGGAVGSEIAGGAGPGWVL PFTAGGFIYVATVSVLPELLREASPLQSLLEVLGLLGGVIMMVLIAHLE NT seq 1410 nt NT seq  +upstreamnt  +downstreamnt atggccagaggcctgggggccccccactgggtggccgtgggactgctgacctgggcgacc ttggggcttctggtggctggactcgggggtcatgacgacctgcacgacgatctgcaagag gacttccatggccacagccacaggcactcacatgaagatttccaccatggccacagccat gcccatggccatggccacactcacgagagcatctggcatggacatacccacgatcacgac catggacattcacatgaggatttacaccatggccatagccatggctactcccatgagagc ctctaccacagaggacatggacatgaccatgagcatagccatggaggctatggggagtct ggggctccaggcatcaagcaggacctggatgctgtcactctctgggcttatgcactgggg gccacagtgctgatctcagcagctccattttttgtcctcttccttatccccgtggagtcg aactctccccggcatcgctctctacttcagatcttgctcagttttgcttccggtgggctc ctgggagatgctttcctgcacctcattcctcatgctcttgaacctcattctcaccacact ctggagcaacccggacatggacactcccacagtggccagggccccattctgtctgtggga ctgtgggttctcagtggaattgttgcctttcttgtcgtggagaaatttgtgagacatgtg aaaggaggacatggtcacagtcatggacatggacacgctcacagtcatacacgtggaagt catggacatggaagacaagagcgttctaccaaggagaagcagagctcagaggaagaagaa aaggaaacaagaggggttcagaagaggcgaggagggagcacagtacccaaagatgggcca gtgagacctcagaacgctgaagaagaaaaaagaggcttagacctgcgtgtgtcggggtac ctgaatctggctgctgacttggcacacaacttcactgatggtctggccattggggcttcc tttcgagggggccggggactagggatcctgaccacaatgactgtcctgctacatgaagtg ccccacgaggtcggagactttgccatcttggtccagtctggctgcagcaaaaagcaggcg atgcgtctgcaactactgacagcagtaggggcactggcaggcacagcctgtgcccttctc actgaaggaggagcagtgggcagtgaaattgcaggtggtgcaggtcctggctgggtcctg ccatttactgcaggtggctttatctacgtagcaacagtgtctgtgttgcccgagctgctg agggaggcatcaccattgcaatcacttctggaggtgctggggctgctggggggagttatc atgatggtgctgattgcccaccttgagtga

Homo sapiens (human): 91252 Help Entry 91252             CDS       T01001                                  Symbol SLC39A13, EDSSPD3, LZT-Hs9, SCDEDS, ZIP13 Name (RefSeq) solute carrier family 39 member 13   KO K14719   solute carrier family 39 (zinc transporter), member 13 Organism hsa  Homo sapiens (human) Pathway hsa05010   Alzheimer disease hsa05012   Parkinson disease Disease H02239   Ehlers-Danlos syndrome, spondylodysplastic type Brite KEGG Orthology (KO) [BR:hsa00001]  09160 Human Diseases   09164 Neurodegenerative disease    05010 Alzheimer disease     91252 (SLC39A13)    05012 Parkinson disease     91252 (SLC39A13)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     91252 (SLC39A13) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC39: Metal ion transporter    91252 (SLC39A13) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Zip Motif Other DBs NCBI-GeneID:  91252 NCBI-ProteinID:  NP_001121697 OMIM:  608735 HGNC:  20859 Ensembl:  ENSG00000165915 Pharos:  Q96H72(Tbio) UniProt:  Q96H72 LinkDB All DBs Position 11:47407276..47416500 Genome browser AA seq 371 aa AA seqDB search MPGCPCPGCGMAGPRLLFLTALALELLERAGGSQPALRSRGTATACRLDNKESESWGALL SGERLDTWICSLLGSLMVGLSGVFPLLVIPLEMGTMLRSEAGAWRLKQLLSFALGGLLGN VFLHLLPEAWAYTCSASPGGEGQSLQQQQQLGLWVIAGILTFLALEKMFLDSKEEGTSQA PNKDPTAAAAALNGGHCLAQPAAEPGLGAVVRSIKVSGYLNLLANTIDNFTHGLAVAASF LVSKKIGLLTTMAILLHEIPHEVGDFAILLRAGFDRWSAAKLQLSTALGGLLGAGFAICT QSPKGVVGCSPAAEETAAWVLPFTSGGFLYIALVNVLPDLLEEEDPWRSLQQLLLLCAGI VVMVLFSLFVD NT seq 1116 nt NT seq  +upstreamnt  +downstreamnt atgcctggatgtccctgccctggctgtggcatggcgggcccaaggctcctcttcctcact gcccttgccctggagctcttggaaagggctgggggttcccagccggccctccggagccgg gggactgcgacggcctgtcgcctggacaacaaggaaagcgagtcctggggggctctgctg agcggagagcggctggacacctggatctgctccctcctgggttccctcatggtggggctc agtggggtcttcccgttgcttgtcattcccctagagatggggaccatgctgcgctcagaa gctggggcctggcgcctgaagcagctgctcagcttcgccctggggggactcttgggcaat gtgtttctgcatctgctgcccgaagcctgggcctacacgtgcagcgccagccctggtggt gaggggcagagcctgcagcagcagcaacagctggggctgtgggtcattgctggcatcctg accttcctggcgttggagaagatgttcctggacagcaaggaggaggggaccagccaggcc cccaacaaagaccccactgctgctgccgccgcgctcaatggaggccactgtctggcccag ccggctgcagagcccggcctcggtgccgtggtccggagcatcaaagtcagcggctacctc aacctgctggccaacaccatcgataacttcacccacgggctggctgtggctgccagcttc cttgtgagcaagaagatcgggctcctgacaaccatggccatcctcctgcatgagatcccc catgaggtgggcgactttgccatcctgctccgggccggctttgaccgatggagcgcagcc aagctgcaactctcaacagcgctggggggcctactgggcgctggcttcgccatctgtacc cagtcccccaagggagtagttgggtgttctcccgctgcagaggagacggcagcctgggtc ctgcccttcacctctggcggctttctctacatcgccttggtgaacgtgctccctgacctc ttggaagaagaggacccgtggcgctccctgcagcagctgcttctgctctgtgcgggcatc gtggtaatggtgctgttctcgctcttcgtggattaa

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