Homo sapiens (human): 6507 Help Entry 6507              CDS       T01001                                  Symbol SLC1A3, EA6, EAAT1, GLAST, GLAST1 Name (RefSeq) solute carrier family 1 member 3   KO K05614   solute carrier family 1 (glial high affinity glutamate transporter), member 3 Organism hsa  Homo sapiens (human) Pathway hsa04082   Neuroactive ligand signaling hsa04721   Synaptic vesicle cycle hsa04724   Glutamatergic synapse hsa05016   Huntington disease Network nt06544  Neuroactive ligand signaling   Element N01884   Transport of glutamate, EAAT Disease H00749   Episodic ataxias Brite KEGG Orthology (KO) [BR:hsa00001]  09130 Environmental Information Processing   09133 Signaling molecules and interaction    04082 Neuroactive ligand signaling     6507 (SLC1A3)  09150 Organismal Systems   09156 Nervous system    04724 Glutamatergic synapse     6507 (SLC1A3)    04721 Synaptic vesicle cycle     6507 (SLC1A3)  09160 Human Diseases   09164 Neurodegenerative disease    05016 Huntington disease     6507 (SLC1A3)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     6507 (SLC1A3)    04147 Exosome [BR:hsa04147]     6507 (SLC1A3) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC1: High-affinity glutamate and neutral amino acid transporter    6507 (SLC1A3) Exosome [BR:hsa04147]  Exosomal proteins   Exosomal proteins of cortical neuronal cells    6507 (SLC1A3) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  SDF MT Motif Other DBs NCBI-GeneID:  6507 NCBI-ProteinID:  NP_004163 OMIM:  600111 HGNC:  10941 Ensembl:  ENSG00000079215 UniProt:  P43003 Q8N169 Structure PDBPDBj LinkDB All DBs Position 5:36596588..36688334 Genome browser AA seq 542 aa AA seqDB search MTKSNGEEPKMGGRMERFQQGVRKRTLLAKKKVQNITKEDVKSYLFRNAFVLLTVTAVIV GTILGFTLRPYRMSYREVKYFSFPGELLMRMLQMLVLPLIISSLVTGMAALDSKASGKMG MRAVVYYMTTTIIAVVIGIIIVIIIHPGKGTKENMHREGKIVRVTAADAFLDLIRNMFPP NLVEACFKQFKTNYEKRSFKVPIQANETLVGAVINNVSEAMETLTRITEELVPVPGSVNG VNALGLVVFSMCFGFVIGNMKEQGQALREFFDSLNEAIMRLVAVIMWYAPVGILFLIAGK IVEMEDMGVIGGQLAMYTVTVIVGLLIHAVIVLPLLYFLVTRKNPWVFIGGLLQALITAL GTSSSSATLPITFKCLEENNGVDKRVTRFVLPVGATINMDGTALYEALAAIFIAQVNNFE LNFGQIITISITATAASIGAAGIPQAGLVTMVIVLTSVGLPTDDITLIIAVDWFLDRLRT TTNVLGDSLGAGIVEHLSRHELKNRDVEMGNSVIEENEMKKPYQLIAQDNETEKPIDSET KM NT seq 1629 nt NT seq  +upstreamnt  +downstreamnt atgactaaaagcaatggagaagagcccaagatggggggcaggatggagagattccagcag ggagtccgtaaacgcacacttttggccaagaagaaagtgcagaacattacaaaggaggat gttaaaagttacctgtttcggaatgcttttgtgctgctcacagtcaccgctgtcattgtg ggtacaatccttggatttaccctccgaccatacagaatgagctaccgggaagtcaagtac ttctcctttcctggggaacttctgatgaggatgttacagatgctggtcttaccacttatc atctccagtcttgtcacaggaatggcggcgctagatagtaaggcatcagggaagatggga atgcgagctgtagtctattatatgactaccaccatcattgctgtggtgattggcataatc attgtcatcatcatccatcctgggaagggcacaaaggaaaacatgcacagagaaggcaaa attgtacgagtgacagctgcagatgccttcctggacttgatcaggaacatgttccctcca aatctggtagaagcctgctttaaacagtttaaaaccaactatgagaagagaagctttaaa gtgcccatccaggccaacgaaacgcttgtgggtgctgtgataaacaatgtgtctgaggcc atggagactcttacccgaatcacagaggagctggtcccagttccaggatctgtgaatgga gtcaatgccctgggtctagttgtcttctccatgtgcttcggttttgtgattggaaacatg aaggaacaggggcaggccctgagagagttctttgattctcttaacgaagccatcatgaga ctggtagcagtaataatgtggtatgcccccgtgggtattctcttcctgattgctgggaag attgtggagatggaagacatgggtgtgattggggggcagcttgccatgtacaccgtgact gtcattgttggcttactcattcacgcagtcatcgtcttgccactcctctacttcttggta acacggaaaaacccttgggtttttattggagggttgctgcaagcactcatcaccgctctg gggacctcttcaagttctgccaccctacccatcaccttcaagtgcctggaagagaacaat ggcgtggacaagcgcgtcaccagattcgtgctccccgtaggagccaccattaacatggat gggactgccctctatgaggctttggctgccattttcattgctcaagttaacaactttgaa ctgaacttcggacaaattattacaatcagcatcacagccacagctgccagtattggggca gctggaattcctcaggcgggcctggtcactatggtcattgtgctgacatctgtcggcctg cccactgacgacatcacgctcatcatcgcggtggactggttcctggatcgcctccggacc accaccaacgtactgggagactccctgggagctgggattgtggagcacttgtcacgacat gaactgaagaacagagatgttgaaatgggtaactcagtgattgaagagaatgaaatgaag aaaccatatcaactgattgcacaggacaatgaaactgagaaacccatcgacagtgaaacc aagatgtag

Homo sapiens (human): 6506 Help Entry 6506              CDS       T01001                                  Symbol SLC1A2, DEE41, EAAT2, EIEE41, GLT-1, GLT1, HBGT Name (RefSeq) solute carrier family 1 member 2   KO K05613   solute carrier family 1 (glial high affinity glutamate transporter), member 2 Organism hsa  Homo sapiens (human) Pathway hsa04082   Neuroactive ligand signaling hsa04721   Synaptic vesicle cycle hsa04724   Glutamatergic synapse hsa05014   Amyotrophic lateral sclerosis hsa05016   Huntington disease Network nt06544  Neuroactive ligand signaling   Element N01884   Transport of glutamate, EAAT Disease H00606   Early infantile epileptic encephalopathy H01819   Early myoclonic encephalopathy Brite KEGG Orthology (KO) [BR:hsa00001]  09130 Environmental Information Processing   09133 Signaling molecules and interaction    04082 Neuroactive ligand signaling     6506 (SLC1A2)  09150 Organismal Systems   09156 Nervous system    04724 Glutamatergic synapse     6506 (SLC1A2)    04721 Synaptic vesicle cycle     6506 (SLC1A2)  09160 Human Diseases   09164 Neurodegenerative disease    05014 Amyotrophic lateral sclerosis     6506 (SLC1A2)    05016 Huntington disease     6506 (SLC1A2)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     6506 (SLC1A2) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC1: High-affinity glutamate and neutral amino acid transporter    6506 (SLC1A2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  SDF BPD_transp_1_N Motif Other DBs NCBI-GeneID:  6506 NCBI-ProteinID:  NP_004162 OMIM:  600300 HGNC:  10940 Ensembl:  ENSG00000110436 UniProt:  P43004 Structure PDBPDBj LinkDB All DBs Position 11:complement(35251205..35420507) Genome browser AA seq 574 aa AA seqDB search MASTEGANNMPKQVEVRMHDSHLGSEEPKHRHLGLRLCDKLGKNLLLTLTVFGVILGAVC GGLLRLASPIHPDVVMLIAFPGDILMRMLKMLILPLIISSLITGLSGLDAKASGRLGTRA MVYYMSTTIIAAVLGVILVLAIHPGNPKLKKQLGPGKKNDEVSSLDAFLDLIRNLFPENL VQACFQQIQTVTKKVLVAPPPDEEANATSAVVSLLNETVTEVPEETKMVIKKGLEFKDGM NVLGLIGFFIAFGIAMGKMGDQAKLMVDFFNILNEIVMKLVIMIMWYSPLGIACLICGKI IAIKDLEVVARQLGMYMVTVIIGLIIHGGIFLPLIYFVVTRKNPFSFFAGIFQAWITALG TASSAGTLPVTFRCLEENLGIDKRVTRFVLPVGATINMDGTALYEAVAAIFIAQMNGVVL DGGQIVTVSLTATLASVGAASIPSAGLVTMLLILTAVGLPTEDISLLVAVDWLLDRMRTS VNVVGDSFGAGIVYHLSKSELDTIDSQHRVHEDIEMTKTQSIYDDMKNHRESNSNQCVYA AHNSVIVDECKVTLAANGKSADCSVEEEPWKREK NT seq 1725 nt NT seq  +upstreamnt  +downstreamnt atggcatctacggaaggtgccaacaatatgcccaagcaggtggaagtgcgaatgcacgac agtcatcttggctcagaggaacccaagcaccggcacctgggcctgcgcctgtgtgacaag ctggggaagaatctgctgctcaccctgacggtgtttggtgtcatcctgggagcagtgtgt ggagggcttcttcgcttggcatctcccatccaccctgatgtggttatgttaatagccttc ccaggggatatactcatgaggatgctaaaaatgctcattctccctctaatcatctccagc ttaatcacagggttgtcaggcctggatgctaaggctagtggccgcttgggcacgagagcc atggtgtattacatgtccacgaccatcattgctgcagtactgggggtcattctggtcttg gctatccatccaggcaatcccaagctcaagaagcagctggggcctgggaagaagaatgat gaagtgtccagcctggatgccttcctggaccttattcgaaatctcttccctgaaaacctt gtccaagcctgctttcaacagattcaaacagtgacgaagaaagtcctggttgcaccaccg ccggacgaggaggccaacgcaaccagcgctgttgtctctctgttgaacgagactgtgact gaggtgccggaggagactaagatggttatcaagaagggcctggagttcaaggatgggatg aacgtcttaggtctgatagggtttttcattgcttttggcatcgctatggggaagatggga gatcaggccaagctgatggtggatttcttcaacattttgaatgagattgtaatgaagtta gtgatcatgatcatgtggtactctcccctgggtatcgcctgcctgatctgtggaaagatc attgcaatcaaggacttagaagtggttgctaggcaactggggatgtacatggtaacagtg atcataggcctcatcatccacgggggcatctttctccccttgatttactttgtagtgacc aggaaaaaccccttctccttttttgctggcattttccaagcttggatcactgccctgggc accgcttccagtgctggaactttgcctgtcacctttcgttgcctggaagaaaatctgggg attgataagcgtgtgactagattcgtccttcctgttggagcaaccattaacatggatggt acagccctttatgaagcggtagccgccatctttatagcccaaatgaatggtgttgtcctg gatggaggacagattgtgactgtaagcctcacagccaccctggcaagcgtcggcgcggcc agtatccccagtgccgggctggtcaccatgctcctcattctgacagccgtgggcctgcca acagaggacatcagcctgctggtggctgtggactggctgctggacaggatgagaacttca gtcaatgttgtgggtgactcttttggggctgggatagtctatcacctctccaagtctgag ctggataccattgactcccagcatcgagtgcatgaagatattgaaatgaccaagactcaa tccatttatgatgacatgaagaaccacagggaaagcaactctaatcaatgtgtctatgct gcacacaactctgtcatagtagatgaatgcaaggtaactctggcagccaatggaaagtca gccgactgcagtgttgaggaagaaccttggaaacgtgagaaataa

Homo sapiens (human): 6505 Help Entry 6505              CDS       T01001                                  Symbol SLC1A1, DCBXA, EAAC1, EAAT3, SCZD18, hEAAC1 Name (RefSeq) solute carrier family 1 member 1   KO K05612   solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter), member 1 Organism hsa  Homo sapiens (human) Pathway hsa04082   Neuroactive ligand signaling hsa04721   Synaptic vesicle cycle hsa04724   Glutamatergic synapse hsa04974   Protein digestion and absorption Network nt06544  Neuroactive ligand signaling   Element N01884   Transport of glutamate, EAAT Disease H00911   Dicarboxylic aminoaciduria H01649   Schizophrenia Brite KEGG Orthology (KO) [BR:hsa00001]  09130 Environmental Information Processing   09133 Signaling molecules and interaction    04082 Neuroactive ligand signaling     6505 (SLC1A1)  09150 Organismal Systems   09154 Digestive system    04974 Protein digestion and absorption     6505 (SLC1A1)   09156 Nervous system    04724 Glutamatergic synapse     6505 (SLC1A1)    04721 Synaptic vesicle cycle     6505 (SLC1A1)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     6505 (SLC1A1) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC1: High-affinity glutamate and neutral amino acid transporter    6505 (SLC1A1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  SDF Motif Other DBs NCBI-GeneID:  6505 NCBI-ProteinID:  NP_004161 OMIM:  133550 HGNC:  10939 Ensembl:  ENSG00000106688 UniProt:  P43005 Structure PDBPDBj LinkDB All DBs Position 9:4490468..4587469 Genome browser AA seq 524 aa AA seqDB search MGKPARKGCEWKRFLKNNWVLLSTVAAVVLGITTGVLVREHSNLSTLEKFYFAFPGEILM RMLKLIILPLIISSMITGVAALDSNVSGKIGLRAVVYYFCTTLIAVILGIVLVVSIKPGV TQKVGEIARTGSTPEVSTVDAMLDLIRNMFPENLVQACFQQYKTKREEVKPPSDPEMNMT EESFTAVMTTAISKNKTKEYKIVGMYSDGINVLGLIVFCLVFGLVIGKMGEKGQILVDFF NALSDATMKIVQIIMCYMPLGILFLIAGKIIEVEDWEIFRKLGLYMATVLTGLAIHSIVI LPLIYFIVVRKNPFRFAMGMAQALLTALMISSSSATLPVTFRCAEENNQVDKRITRFVLP VGATINMDGTALYEAVAAVFIAQLNDLDLGIGQIITISITATSASIGAAGVPQAGLVTMV IVLSAVGLPAEDVTLIIAVDWLLDRFRTMVNVLGDAFGTGIVEKLSKKELEQMDVSSEVN IVNPFALESTILDNEDSDTKKSYVNGGFAVDKSDTISFTQTSQF NT seq 1575 nt NT seq  +upstreamnt  +downstreamnt atggggaaaccggcgaggaaaggatgcgagtggaagcgcttcctgaagaataactgggtg ttgctgtccaccgtggccgcggtggtgctaggcattaccacaggagtcttggttcgagaa cacagcaacctctcaactctagagaaattctactttgcttttcctggagaaattctaatg cggatgctgaaactcatcattttgccattaattatatccagcatgattacaggtgttgct gcactggattccaacgtatccggaaaaattggtctgcgcgctgtcgtgtattatttctgt accactctcattgctgttattctaggtattgtgctggtggtgagcatcaagcctggtgtc acccagaaagtgggtgaaattgcgaggacaggcagcacccctgaagtcagtacggtggat gccatgttagatctcatcaggaatatgttccctgagaatcttgtccaggcctgttttcag cagtacaaaactaagcgtgaagaagtgaagcctcccagcgatccagagatgaacatgaca gaagagtccttcacagctgtcatgacaactgcaatttccaagaacaaaacaaaggaatac aaaattgttggcatgtattcagatggcataaacgtcctgggcttgattgtcttttgcctt gtctttggacttgtcattggaaaaatgggagaaaagggacaaattctggtggatttcttc aatgctttgagtgatgcaaccatgaaaatcgttcagatcatcatgtgttatatgccacta ggtattttgttcctgattgctgggaagatcatagaagttgaagactgggaaatattccgc aagctgggcctttacatggccacagtcctgactgggcttgcaatccactccattgtaatt ctcccgctgatatatttcatagtcgtacgaaagaaccctttccgatttgccatgggaatg gcccaggctctcctgacagctctcatgatctcttccagttcagcaacactgcctgtcacc ttccgctgtgctgaagaaaataaccaggtggacaagaggatcactcgattcgtgttaccc gttggtgcaacaatcaacatggatgggactgcgctctatgaagcagtggcagcggtgttt attgcacagttgaatgacctggacttgggcattgggcagatcatcaccatcagtatcacg gccacatctgccagcatcggagctgctggcgtgccccaggctggcctggtgaccatggtg attgtgctgagtgccgtgggcctgcccgccgaggatgtcaccctgatcattgctgtcgac tggctcctggaccggttcaggaccatggtcaacgtccttggtgatgcttttgggacgggc attgtggaaaagctctccaagaaggagctggagcagatggatgtttcatctgaagtcaac attgtgaatccctttgccttggaatccacaatccttgacaacgaagactcagacaccaag aagtcttatgtcaatggaggctttgcagtagacaagtctgacaccatctcattcacccag acctcacagttctag

Homo sapiens (human): 6511 Help Entry 6511              CDS       T01001                                  Symbol SLC1A6, EAAT4 Name (RefSeq) solute carrier family 1 member 6   KO K05617   solute carrier family 1 (high affinity glutamate/aspartate transporter), member 6 Organism hsa  Homo sapiens (human) Pathway hsa04082   Neuroactive ligand signaling hsa04721   Synaptic vesicle cycle hsa04724   Glutamatergic synapse hsa05017   Spinocerebellar ataxia Network nt06462  Spinocerebellar ataxia nt06544  Neuroactive ligand signaling   Element N00965   RORA-mediated transcription N00966   Mutation-caused aberrant ATXN1 to RORA-mediated transcription N01884   Transport of glutamate, EAAT Brite KEGG Orthology (KO) [BR:hsa00001]  09130 Environmental Information Processing   09133 Signaling molecules and interaction    04082 Neuroactive ligand signaling     6511 (SLC1A6)  09150 Organismal Systems   09156 Nervous system    04724 Glutamatergic synapse     6511 (SLC1A6)    04721 Synaptic vesicle cycle     6511 (SLC1A6)  09160 Human Diseases   09164 Neurodegenerative disease    05017 Spinocerebellar ataxia     6511 (SLC1A6)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     6511 (SLC1A6) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC1: High-affinity glutamate and neutral amino acid transporter    6511 (SLC1A6) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  SDF Motif Other DBs NCBI-GeneID:  6511 NCBI-ProteinID:  NP_001371598 OMIM:  600637 HGNC:  10944 Ensembl:  ENSG00000105143 UniProt:  P48664 LinkDB All DBs Position 19:complement(14950033..15010643) Genome browser AA seq 564 aa AA seqDB search MSSHGNSLFLRESGQRLGRVGWLQRLQESLQQRALRTRLRLQTMTLEHVLRFLRRNAFIL LTVSAVVIGVSLAFALRPYQLTYRQIKYFSFPGELLMRMLQMLVLPLIVSSLVTGMASLD NKATGRMGMRAAVYYMVTTIIAVFIGILMVTIIHPGKGSKEGLHREGRIETIPTADAFMD LIRNMFPPNLVEACFKQFKTQYSTRVVTRTMVRTENGSEPGASMPPPFSVENGTSFLENV TRALGTLQEMLSFEETVPVPGSANGINALGLVVFSVAFGLVIGGMKHKGRVLRDFFDSLN EAIMRLVGIIIWYAPVGILFLIAGKILEMEDMAVLGGQLGMYTLTVIVGLFLHAGIVLPL IYFLVTHRNPFPFIGGMLQALITAMGTSSSSATLPITFRCLEEGLGVDRRITRFVLPVGA TVNMDGTALYEALAAIFIAQVNNYELNLGQITTISITATAASVGAAGIPQAGLVTMVIVL TSVGLPTEDITLIIAVDWFLDRLRTMTNVLGDSIGAAVIEHLSQRELELQEAELTLPSLG KPYKSLMAQEKGASRGRGGNESAM NT seq 1695 nt NT seq  +upstreamnt  +downstreamnt atgagcagccatggcaacagcctgttcctgcgggagagcggccagcggctgggccgggtg ggctggctgcagcggctgcaggaaagcctgcagcagagagcactgcgcacgcgcctgcgc ctgcagaccatgaccctcgagcacgtgctgcgcttcctgcgccgaaacgccttcattctg ctgacggtcagcgccgtggtcattggggtcagcctggcctttgccctgcgcccatatcag ctcacctaccgccagatcaagtacttctcttttcctggagagcttctgatgaggatgctg cagatgctggtgttacctctcattgtctccagcctggtcacaggtatggcatccctggac aacaaggccacggggcggatggggatgcgggcagctgtgtactacatggtgaccaccatc atcgcggtcttcatcggcatcctcatggtcaccatcatccatcccgggaagggctccaag gaggggctgcaccgggagggccggatcgagaccatccccacagctgatgccttcatggac ctgatcagaaatatgtttccaccaaaccttgtggaggcctgcttcaaacagttcaagacg cagtacagcacgagggtggtaaccaggaccatggtgaggacagagaacgggtctgagccg ggtgcctccatgcctcctccattctcagtggagaacggaaccagcttcctggaaaatgtc actcgggccttgggtaccctgcaggagatgctgagctttgaggagactgtacccgtgcct ggctccgccaatggcatcaacgccctgggcctcgtggtcttctctgtggcctttgggctg gtcattggtggcatgaaacacaagggcagagtcctcagggacttcttcgacagcctcaat gaggctattatgaggctggtgggcatcattatctggtatgcacctgtgggcatcctgttc ctgattgctgggaagattctggagatggaagacatggccgtcctggggggtcagctgggc atgtacaccctgaccgtcatcgtgggcctgttcctccatgccggcattgtccttcccctc atctacttcctcgtcactcaccggaaccccttccccttcattgggggcatgctacaagcc ctcatcaccgctatgggcacgtcttccagctcggcaacgctgcccatcaccttccgctgc ctggaggagggcctgggtgtggaccgccgcatcaccaggttcgtcctgcccgtgggcgcc acggtcaacatggatggcactgccctctacgaggccctggctgccatcttcattgctcaa gttaacaactacgagctcaacctgggtcagatcacaaccatcagcatcacggccacagca gccagtgttggggctgctggcatcccccaggcgggtctggtcaccatggtcattgtgctt acgtcggtcggcttgcccacggaagacatcacgctcatcattgccgtggactggttcctt gaccggcttcgcacaatgaccaacgtactgggggactcaattggagcggccgtcatcgag cacttgtctcagcgggagctggagcttcaggaagctgagcttaccctccccagcctgggg aaaccctacaagtccctcatggcacaggagaagggggcatcccggggacggggaggcaac gagagtgctatgtga

Homo sapiens (human): 6512 Help Entry 6512              CDS       T01001                                  Symbol SLC1A7, AAAT, EAAT5 Name (RefSeq) solute carrier family 1 member 7   KO K05618   solute carrier family 1 (glutamate transporter), member 7 Organism hsa  Homo sapiens (human) Pathway hsa04082   Neuroactive ligand signaling hsa04721   Synaptic vesicle cycle hsa04724   Glutamatergic synapse Network nt06544  Neuroactive ligand signaling   Element N01884   Transport of glutamate, EAAT Brite KEGG Orthology (KO) [BR:hsa00001]  09130 Environmental Information Processing   09133 Signaling molecules and interaction    04082 Neuroactive ligand signaling     6512 (SLC1A7)  09150 Organismal Systems   09156 Nervous system    04724 Glutamatergic synapse     6512 (SLC1A7)    04721 Synaptic vesicle cycle     6512 (SLC1A7)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     6512 (SLC1A7) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC1: High-affinity glutamate and neutral amino acid transporter    6512 (SLC1A7) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  SDF Motif Other DBs NCBI-GeneID:  6512 NCBI-ProteinID:  NP_006662 OMIM:  604471 HGNC:  10945 Ensembl:  ENSG00000162383 UniProt:  O00341 F1T0D3 LinkDB All DBs Position 1:complement(53087183..53142638) Genome browser AA seq 560 aa AA seqDB search MVPHAILARGRDVCRRNGLLILSVLSVIVGCLLGFFLRTRRLSPQEISYFQFPGELLMRM LKMMILPLVVSSLMSGLASLDAKTSSRLGVLTVAYYLWTTFMAVIVGIFMVSIIHPGSAA QKETTEQSGKPIMSSADALLDLIRNMFPANLVEATFKQYRTKTTPVVKSPKVAPEEAPPR RILIYGVQEENGSHVQNFALDLTPPPEVVYKSEPGTSDGMNVLGIVFFSATMGIMLGRMG DSGAPLVSFCQCLNESVMKIVAVAVWYFPFGIVFLIAGKILEMDDPRAVGKKLGFYSVTV VCGLVLHGLFILPLLYFFITKKNPIVFIRGILQALLIALATSSSSATLPITFKCLLENNH IDRRIARFVLPVGATINMDGTALYEAVAAIFIAQVNNYELDFGQIITISITATAASIGAA GIPQAGLVTMVIVLTSVGLPTDDITLIIAVDWALDRFRTMINVLGDALAAGIMAHICRKD FARDTGTEKLLPCETKPVSLQEIVAAQQNGCVKSVAEASELTLGPTCPHHVPVQVEQDEE LPAASLNHCTIQISELETNV NT seq 1683 nt NT seq  +upstreamnt  +downstreamnt atggtgccgcatgccatcttggcacgggggagggacgtgtgcaggcggaatggactcctc atcctgtctgtgctgtctgtcatcgtgggctgcctcctcggcttcttcttgaggacccgg cgcctctcaccacaggaaattagttacttccagttccctggagagctcctgatgaggatg ctgaagatgatgatcctgccactggtggtctccagcttgatgtccggacttgcctccctg gatgccaagacctctagccgcctgggcgtcctcaccgtggcgtactacctgtggaccacc ttcatggctgtcatcgtgggcatcttcatggtctccatcatccacccaggcagcgcggcc cagaaggagaccacggagcagagtgggaagcccatcatgagctcagccgatgccctgttg gacctcatccggaacatgttcccagccaacctagtagaagccacattcaaacagtaccgc accaagaccaccccagttgtcaagtcccccaaggtggcaccagaggaggcccctcctcgg cggatcctcatctacggggtccaggaggagaatggctcccatgtgcagaacttcgccctg gacctgaccccgccgcccgaggtcgtttacaagtcagagccgggcaccagcgatggcatg aatgtgctgggcatcgtcttcttctctgccaccatgggcatcatgctgggccgcatgggt gacagcggggcccccctggtcagcttctgccagtgcctcaatgagtcggtcatgaagatc gtggcggtggctgtgtggtatttccccttcggcattgtgttcctcattgcgggtaagatc ctggagatggacgaccccagggccgtcggcaagaagctgggcttctactcagtcaccgtg gtgtgcgggctggtgctccacgggctctttatcctgcccctgctctacttcttcatcacc aagaagaatcccatcgtcttcatccgtggcatcctgcaggctctgctcatcgcgctggcc acctcctccagctcagccacactgcccatcaccttcaagtgcctgctggagaacaaccac atcgaccggcgcatcgctcgcttcgtgctgcccgtgggtgccaccatcaacatggacggc actgcgctctacgaggctgtggccgccatcttcatcgcccaggtcaacaactacgagctg gactttggccagatcatcaccatcagtatcacagccactgcagccagcattggggcagct ggcatcccccaggccggcctcgtcaccatggtcatcgtgctcacctccgtgggactgccc accgatgacatcaccctcatcattgccgttgactgggctctggaccgtttccgcaccatg attaacgtgctgggtgatgcgctggcagcggggatcatggcccatatatgtcggaaggat tttgcccgggacacaggcaccgagaaactgctgccctgcgagaccaagccagtgagcctc caggagatcgtggcagcccagcagaatggctgtgtgaagagtgtagccgaggcctccgag ctcaccctgggccccacctgcccccaccacgtccccgttcaagtggagcaggatgaggag ctgcccgctgcgagtctgaaccactgcaccatccagatcagtgagctggagaccaatgtc tga

DBGET integrated database retrieval system