Homo sapiens (human): 81539 Help Entry 81539             CDS       T01001                                  Symbol SLC38A1, ATA1, NAT2, SAT1, SNAT1 Name (RefSeq) solute carrier family 38 member 1   KO K14990   solute carrier family 38 (sodium-coupled neutral amino acid transporter), member 1 Organism hsa  Homo sapiens (human) Pathway hsa04724   Glutamatergic synapse hsa04727   GABAergic synapse Network nt06544  Neuroactive ligand signaling   Element N01885   Transport of glutamine, SNAT Brite KEGG Orthology (KO) [BR:hsa00001]  09150 Organismal Systems   09156 Nervous system    04724 Glutamatergic synapse     81539 (SLC38A1)    04727 GABAergic synapse     81539 (SLC38A1)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     81539 (SLC38A1) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC38: System A and System N sodium-coupled neutral amino acid transporter    81539 (SLC38A1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Aa_trans Cation_ATPase_C Motif Other DBs NCBI-GeneID:  81539 NCBI-ProteinID:  NP_001070952 OMIM:  608490 HGNC:  13447 Ensembl:  ENSG00000111371 UniProt:  Q9H2H9 LinkDB All DBs Position 12:complement(46183063..46269043) Genome browser AA seq 487 aa AA seqDB search MMHFKSGLELTELQNMTVPEDDNISNDSNDFTEVENGQINSKFISDRESRRSLTNSHLEK KKCDEYIPGTTSLGMSVFNLSNAIMGSGILGLAFALANTGILLFLVLLTSVTLLSIYSIN LLLICSKETGCMVYEKLGEQVFGTTGKFVIFGATSLQNTGAMLSYLFIVKNELPSAIKFL MGKEETFSAWYVDGRVLVVIVTFGIILPLCLLKNLGYLGYTSGFSLSCMVFFLIVVIYKK FQIPCIVPELNSTISANSTNADTCTPKYVTFNSKTVYALPTIAFAFVCHPSVLPIYSELK DRSQKKMQMVSNISFFAMFVMYFLTAIFGYLTFYDNVQSDLLHKYQSKDDILILTVRLAV IVAVILTVPVLFFTVRSSLFELAKKTKFNLCRHTVVTCILLVVINLLVIFIPSMKDIFGV VGVTSANMLIFILPSSLYLKITDQDGDKGTQRIWAALFLGLGVLFSLVSIPLVIYDWACS SSSDEGH NT seq 1464 nt NT seq  +upstreamnt  +downstreamnt atgatgcatttcaaaagtggactcgaattaactgagttgcaaaacatgacagtgcccgag gatgataacattagcaatgactccaatgatttcaccgaagtagaaaatggtcagataaat agcaagtttatttctgatcgtgaaagtagaagaagtctcacaaacagccatttggaaaaa aagaagtgtgatgagtatattccaggtacaacctccttaggcatgtctgtttttaaccta agcaacgccattatgggcagtgggattttgggactcgcctttgccctggcaaacactgga atcctactttttctggtacttttgacttcagtgacattgctgtctatatattcaataaac ctcctattgatctgttcaaaagaaacaggctgcatggtgtatgaaaagctgggggaacaa gtctttggcaccacagggaagttcgtaatctttggagccacctctctacagaacactgga gcaatgctgagctacctcttcatcgtaaaaaatgaactaccctctgccataaagtttcta atgggaaaggaagagacattttcagcctggtacgtggatggccgcgttctggtggtgata gttacctttggcataattctccctctgtgtctcttgaagaacttagggtatcttggctat actagtggattttccttgagctgtatggtttttttcctaattgtggttatttacaagaaa tttcaaattccctgcattgttccagagctaaattcaacaataagtgctaattcaacaaat gctgacacgtgtacgccaaaatatgttaccttcaattcaaagaccgtgtatgctttaccc accattgcatttgcatttgtttgccacccgtcagtcctgccaatttacagtgagcttaaa gaccgatcacagaaaaaaatgcagatggtttcaaacatctcctttttcgccatgtttgtt atgtacttcttgactgccatttttggctacttgacattctatgacaacgtgcagtccgac ctccttcacaaatatcagagtaaagatgacattctcatcctgacagtgcggctggctgtc attgttgctgtgatcctcacagtgccggtgttatttttcacggttcgttcatctttattt gaactggctaagaaaacaaagtttaatttatgtcgtcataccgtggttacctgcatactc ttggttgttatcaacttgttggtgatcttcataccctccatgaaggatatttttggagtc gtaggagttacatctgctaacatgcttattttcattcttccttcatctctttatttaaaa atcacagaccaggatggagataaaggaactcaaagaatttgggctgcccttttcttgggc ctgggggtgttgttctccttggtcagcattcccttggtcatctatgactgggcctgctca tcgagtagtgacgaaggccactga

Homo sapiens (human): 54407 Help Entry 54407             CDS       T01001                                  Symbol SLC38A2, ATA2, PRO1068, SAT2, SNAT2 Name (RefSeq) solute carrier family 38 member 2   KO K14207   solute carrier family 38 (sodium-coupled neutral amino acid transporter), member 2 Organism hsa  Homo sapiens (human) Pathway hsa04724   Glutamatergic synapse hsa04727   GABAergic synapse hsa04974   Protein digestion and absorption Network nt06544  Neuroactive ligand signaling   Element N01885   Transport of glutamine, SNAT Brite KEGG Orthology (KO) [BR:hsa00001]  09150 Organismal Systems   09154 Digestive system    04974 Protein digestion and absorption     54407 (SLC38A2)   09156 Nervous system    04724 Glutamatergic synapse     54407 (SLC38A2)    04727 GABAergic synapse     54407 (SLC38A2)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     54407 (SLC38A2) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC38: System A and System N sodium-coupled neutral amino acid transporter    54407 (SLC38A2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Aa_trans Motif Other DBs NCBI-GeneID:  54407 NCBI-ProteinID:  NP_061849 OMIM:  605180 HGNC:  13448 Ensembl:  ENSG00000134294 UniProt:  Q96QD8 LinkDB All DBs Position 12:complement(46358188..46372773) Genome browser AA seq 506 aa AA seqDB search MKKAEMGRFSISPDEDSSSYSSNSDFNYSYPTKQAALKSHYADVDPENQNFLLESNLGKK KYETEFHPGTTSFGMSVFNLSNAIVGSGILGLSYAMANTGIALFIILLTFVSIFSLYSVH LLLKTANEGGSLLYEQLGYKAFGLVGKLAASGSITMQNIGAMSSYLFIVKYELPLVIQAL TNIEDKTGLWYLNGNYLVLLVSLVVILPLSLFRNLGYLGYTSGLSLLCMVFFLIVVICKK FQVPCPVEAALIINETINTTLTQPTALVPALSHNVTENDSCRPHYFIFNSQTVYAVPILI FSFVCHPAVLPIYEELKDRSRRRMMNVSKISFFAMFLMYLLAALFGYLTFYEHVESELLH TYSSILGTDILLLIVRLAVLMAVTLTVPVVIFPIRSSVTHLLCASKDFSWWRHSLITVSI LAFTNLLVIFVPTIRDIFGFIGASAASMLIFILPSAFYIKLVKKEPMKSVQKIGALFFLL SGVLVMTGSMALIVLDWVHNAPGGGH NT seq 1521 nt NT seq  +upstreamnt  +downstreamnt atgaagaaggccgaaatgggacgattcagtatttccccggatgaagacagcagcagctac agttccaacagcgacttcaactactcctaccccaccaagcaagctgctctgaaaagccat tatgcagatgtagatcctgaaaaccagaactttttacttgaatcgaatttggggaagaag aagtatgaaacagaatttcatccaggtactacttcctttggaatgtcagtatttaatctg agcaatgcgattgtgggcagtggaatccttgggctttcttatgccatggctaatactgga attgctctttttataattctcttgacatttgtgtcaatattttccctgtattctgttcat ctccttttgaagactgccaatgaaggagggtctttattatatgaacaattgggatataag gcatttggattagttggaaagcttgcagcatctggatcaattacaatgcagaacattgga gctatgtcaagctacctcttcatagtgaaatatgagttgcctttggtgatccaggcatta acgaacattgaagataaaactggattgtggtatctgaacgggaactatttggttctgttg gtgtcattggtggtcattcttcctttgtcgctgtttagaaatttaggatatttgggatat accagtggcctttccttgttgtgtatggtgttctttctgattgtggtcatttgcaagaaa tttcaggttccgtgtcctgtggaagctgctttgataattaacgaaacaataaacaccacc ttaacacagccaacagctcttgtacctgctttgtcacataacgtgactgaaaatgactct tgcagacctcactattttattttcaactcacagactgtctatgctgtgccaattctgatc ttttcatttgtctgtcatcctgctgttcttcccatctatgaagaactgaaagaccgcagc cgtagaagaatgatgaatgtgtccaagatttcattttttgctatgtttctcatgtatctg cttgccgccctctttggatacctaacattttacgaacatgttgagtcagaattgcttcat acctactcttctatcttgggaactgatattcttcttctcattgtccgtctggctgtgtta atggctgtgaccctgacagtaccagtagttattttcccaatccggagttctgtaactcac ttgttgtgtgcatcaaaagatttcagttggtggcgtcatagtctcattacagtgtctatc ttggcatttaccaatttacttgtcatctttgtcccaactattagggatatctttggtttt attggtgcatctgcagcttctatgttgatttttattcttccttctgccttctatatcaag ttggtgaagaaagaacctatgaaatctgtacaaaagattggggctttgttcttcctgtta agtggtgtactggtgatgaccggaagcatggccttgattgttttggattgggtacacaat gcacctggaggtggccattaa

Homo sapiens (human): 10991 Help Entry 10991             CDS       T01001                                  Symbol SLC38A3, DEE102, G17, NAT1, SN1, SNAT3 Name (RefSeq) solute carrier family 38 member 3   KO K13576   solute carrier family 38 (sodium-coupled neutral amino acid transporter), member 3 Organism hsa  Homo sapiens (human) Pathway hsa04724   Glutamatergic synapse hsa04727   GABAergic synapse hsa04964   Proximal tubule bicarbonate reclamation Network nt06544  Neuroactive ligand signaling   Element N01885   Transport of glutamine, SNAT N01892   GABA metabolism and transport in glia Disease H00606   Early infantile epileptic encephalopathy Brite KEGG Orthology (KO) [BR:hsa00001]  09150 Organismal Systems   09155 Excretory system    04964 Proximal tubule bicarbonate reclamation     10991 (SLC38A3)   09156 Nervous system    04724 Glutamatergic synapse     10991 (SLC38A3)    04727 GABAergic synapse     10991 (SLC38A3)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     10991 (SLC38A3) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC38: System A and System N sodium-coupled neutral amino acid transporter    10991 (SLC38A3) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Aa_trans Motif Other DBs NCBI-GeneID:  10991 NCBI-ProteinID:  NP_006832 OMIM:  604437 HGNC:  18044 Ensembl:  ENSG00000188338 UniProt:  Q99624 LinkDB All DBs Position 3:50205271..50221486 Genome browser AA seq 504 aa AA seqDB search MEAPLQTEMVELVPNGKHSEGLLPVITPMAGNQRVEDPARSCMEGKSFLQKSPSKEPHFT DFEGKTSFGMSVFNLSNAIMGSGILGLAYAMANTGIILFLFLLTAVALLSSYSIHLLLKS SGVVGIRAYEQLGYRAFGTPGKLAAALAITLQNIGAMSSYLYIIKSELPLVIQTFLNLEE KTSDWYMNGNYLVILVSVTIILPLALMRQLGYLGYSSGFSLSCMVFFLIAVIYKKFHVPC PLPPNFNNTTGNFSHVEIVKEKVQLQVEPEASAFCTPSYFTLNSQTAYTIPIMAFAFVCH PEVLPIYTELKDPSKKKMQHISNLSIAVMYIMYFLAALFGYLTFYNGVESELLHTYSKVD PFDVLILCVRVAVLTAVTLTVPIVLFPVRRAIQQMLFPNQEFSWLRHVLIAVGLLTCINL LVIFAPNILGIFGVIGATSAPFLIFIFPAIFYFRIMPTEKEPARSTPKILALCFAMLGFL LMTMSLSFIIIDWASGTSRHGGNH NT seq 1515 nt NT seq  +upstreamnt  +downstreamnt atggaggcgcctttgcagacagagatggtggagctggtgcccaatggcaaacactcagag gggctgctcccggtcatcacccccatggcaggcaaccagagggtcgaggaccctgcacgg agctgtatggagggcaagagcttcctacagaaaagtcccagcaaggagccacacttcact gacttcgaggggaagacatcattcgggatgtcagtgttcaacctcagcaatgccatcatg ggcagcggcatcctgggactcgcctatgccatggccaatacgggcattatccttttcctg ttcctgttgacagctgtcgccttgctctccagctactccatccacctgctactcaagtcc tcaggggtcgtgggcatccgtgcctatgagcagctgggctaccgtgcctttgggacccca ggaaagctggcagcagccctggccatcacgctccagaacatcggagccatgtccagctac ctgtacatcatcaagtctgagctgccacttgtcatacagaccttcctgaacctggaggag aaaacctcggactggtacatgaacgggaactacctggtaatccttgtctctgtcaccatc attctgcccctggcactgatgcggcagcttggctacctgggctactccagcggcttctct cttagctgcatggtgttcttcctaattgcagtcatctacaaaaagttccacgtgccctgc ccactgccccccaacttcaacaacaccacaggcaacttcagccacgtggagatcgtgaag gagaaggtgcagctgcaggtcgagcctgaggcttcagccttctgcactcccagctacttc acgctcaactcacagacagcatacaccatccccatcatggccttcgccttcgtctgccac cccgaggtgctgcccatctatactgagctcaaggacccctccaagaagaagatgcagcac atctccaacctgtccatcgctgtcatgtacatcatgtacttcctggctgccctcttcggc tacctcaccttctacaacggggtggagtcggagctgctgcacacctacagcaaggtggac ccgtttgacgtcctgatcctgtgtgtgcgcgtggccgtgctgacagcagtcacgctcaca gtgcccatcgttctgttcccggtgcgccgcgccatccagcagatgctgtttccaaaccag gagttcagctggctgcggcatgtgcttattgccgttggcctgctcacttgtatcaacctg ctggtcatctttgcccccaacatcctgggcatctttggggtcatcggtgccacatctgcc ccattcctcatcttcatcttccctgccatcttctacttccgaatcatgcccacggagaag gagcctgcaagatccacccccaaaatcctggccctgtgttttgctatgcttggcttcttg ctgatgaccatgagcttgagcttcatcatcattgactgggcctcagggaccagccggcat ggaggaaaccactag

Homo sapiens (human): 92745 Help Entry 92745             CDS       T01001                                  Symbol SLC38A5, JM24, SN2, SNAT5, pp7194 Name (RefSeq) solute carrier family 38 member 5   KO K14992   solute carrier family 38 (sodium-coupled neutral amino acid transporter), member 5 Organism hsa  Homo sapiens (human) Pathway hsa04727   GABAergic synapse Network nt06544  Neuroactive ligand signaling   Element N01885   Transport of glutamine, SNAT N01892   GABA metabolism and transport in glia Brite KEGG Orthology (KO) [BR:hsa00001]  09150 Organismal Systems   09156 Nervous system    04727 GABAergic synapse     92745 (SLC38A5)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     92745 (SLC38A5) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC38: System A and System N sodium-coupled neutral amino acid transporter    92745 (SLC38A5) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Aa_trans Motif Other DBs NCBI-GeneID:  92745 NCBI-ProteinID:  NP_277053 OMIM:  300649 HGNC:  18070 Ensembl:  ENSG00000017483 UniProt:  Q8WUX1 LinkDB All DBs Position X:complement(48458544..48470260) Genome browser AA seq 472 aa AA seqDB search MELQDPKMNGALPSDAVGYRQEREGFLPSRGPAPGSKPVQFMDFEGKTSFGMSVFNLSNA IMGSGILGLAYAMAHTGVIFFLALLLCIALLSSYSIHLLLTCAGIAGIRAYEQLGQRAFG PAGKVVVATVICLHNVGAMSSYLFIIKSELPLVIGTFLYMDPEGDWFLKGNLLIIIVSVL IILPLALMKHLGYLGYTSGLSLTCMLFFLVSVIYKKFQLGCAIGHNETAMESEALVGLPS QGLNSSCEAQMFTVDSQMSYTVPIMAFAFVCHPEVLPIYTELCRPSKRRMQAVANVSIGA MFCMYGLTATFGYLTFYSSVKAEMLHMYSQKDPLILCVRLAVLLAVTLTVPVVLFPIRRA LQQLLFPGKAFSWPRHVAIALILLVLVNVLVICVPTIRDIFGVIGSTSAPSLIFILPSIF YLRIVPSEVEPFLSWPKIQALCFGVLGVLFMAVSLGFMFANWATGQSRMSGH NT seq 1419 nt NT seq  +upstreamnt  +downstreamnt atggaactgcaggatccaaagatgaatggagccctcccttcggatgctgtgggctacagg caagaacgtgagggcttcctgcccagtcgtggtcctgctcctgggagcaagccggtccag ttcatggatttcgaggggaagacatcgtttggaatgtcagtgttcaacctcagcaacgcc atcatgggcagcggcatcctggggctggcctatgccatggcccacacgggggtcatcttc ttcctggccctgctgctgtgcattgcgcttctgtcgtcctactccatccacctcctgctg acctgtgctggtattgcaggcatccgagcctatgagcagctgggacagagggcattcggg cctgcggggaaggtagtggtggccacagtcatctgtctgcacaatgttggggccatgtcc agttacctgttcatcatcaaatctgagctccccctggttatcggcaccttcctgtacatg gaccccgagggggactggttcttgaagggaaacctcctcatcatcatcgtcagtgtgtta atcatcctgcccctcgccctcatgaaacacttgggctacctggggtacaccagtggtctc tctctgacctgcatgctgtttttccttgtttcggtcatctacaagaagttccaacttggc tgtgctataggccacaatgaaacagcaatggagagtgaagctctcgtgggactccccagc caaggactcaacagcagctgtgaggcccagatgttcacagttgactcacagatgtcctac acagtgcccattatggcttttgcttttgtctgccaccctgaggtgctgcccatctatacg gagctctgccggccctccaagcgcaggatgcaggccgtggccaacgtgtccattggggcc atgttctgcatgtatgggctcacagcaacctttggatacctcaccttctacagcagtgtg aaggcggagatgctgcacatgtacagccagaaggacccgctcatcctctgtgtgcgcctg gccgtgctgctcgcggtgaccctcactgtgccagtcgtgctgttccctatccgccgggcc ctgcagcagctgcttttcccaggcaaggccttcagctggccacgacatgtggccatagct ctgatcctgcttgttttggtcaatgtccttgtcatctgtgtgccaaccatccgggatatc tttggagttatcgggtccacctcagcccccagcctcatcttcatcctccccagcatcttc tacctccgcattgtaccctctgaggtggagcctttcttatcctggcccaagatccaggcc ctgtgctttggagtcctgggagtcctcttcatggccgtcagtctaggctttatgtttgcc aactgggccacaggccagagccgcatgtctggacactga

Homo sapiens (human): 55238 Help Entry 55238             CDS       T01001                                  Symbol SLC38A7, SNAT7 Name (RefSeq) solute carrier family 38 member 7   KO K14994   solute carrier family 38 (sodium-coupled neutral amino acid transporter), member 7/8 Organism hsa  Homo sapiens (human) Network nt06544  Neuroactive ligand signaling   Element N01885   Transport of glutamine, SNAT Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     55238 (SLC38A7) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC38: System A and System N sodium-coupled neutral amino acid transporter    55238 (SLC38A7) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Aa_trans Trp_Tyr_perm Spore_permease T4SS_pilin Motif Other DBs NCBI-GeneID:  55238 NCBI-ProteinID:  NP_001356537 OMIM:  614236 HGNC:  25582 Ensembl:  ENSG00000103042 UniProt:  Q9NVC3 LinkDB All DBs Position 16:complement(58665109..58684770) Genome browser AA seq 462 aa AA seqDB search MAQVSINNDYSEWDLSTDAGERARLLQSPCVDTAPKSEWEASPGGLDRGTTSTLGAIFIV VNACLGAGLLNFPAAFSTAGGVAAGIALQMGMLVFIISGLVILAYCSQASNERTYQEVVW AVCGKLTGVLCEVAIAVYTFGTCIAFLIIIGDQQDKIIAVMAKEPEGASGPWYTDRKFTI SLTAFLFILPLSIPREIGFQKYASFLSVVGTWYVTAIVIIKYIWPDKEMTPGNILTRPAS WMAVFNAMPTICFGFQCHVSSVPVFNSMQQPEVKTWGGVVTAAMVIALAVYMGTGICGFL TFGAAVDPDVLLSYPSEDMAVAVARAFIILSVLTSYPILHFCGRAVVEGLWLRYQGVPVE EDVGRERRRRVLQTLVWFLLTLLLALFIPDIGKVISVIGGLAACFIFVFPGLCLIQAKLS EMEEVKPASWWVLVSYGVLLVTLGAFIFGQTTANAIFVDLLA NT seq 1389 nt NT seq  +upstreamnt  +downstreamnt atggcccaggtcagcatcaacaatgactacagcgagtgggacttgagcacggatgccggg gagcgggctcggctgctgcagagtccctgtgtggacacagcccccaagagtgagtgggaa gcctctcctgggggtctggacagaggcaccacttccacacttggggccatcttcatcgtc gtcaacgcgtgcctgggtgcagggttactcaacttcccagcagccttcagcactgcgggg ggcgtggcagcaggcatcgcactgcagatgggtatgctggttttcatcatcagtggcctt gtcatcctggcctactgctcccaggccagcaatgagaggacctaccaggaggtggtatgg gctgtgtgtggcaagctgacaggtgtgctatgtgaggtggccatcgctgtctacaccttt ggcacctgcattgccttcctaatcatcattggcgaccagcaggacaagattatagctgtg atggcgaaagagccggagggggccagcggcccttggtacacagaccgcaagttcaccatc agcctcactgccttcctcttcatcctgcccctctccatccccagggagattggtttccag aaatatgccagcttcctgagcgtcgtgggtacctggtacgtcacagccatcgttatcatc aagtacatctggccagataaagagatgaccccagggaacatcctgaccaggccggcttcc tggatggctgtgttcaatgccatgcccaccatctgcttcggatttcagtgccacgtcagc agtgtgcccgtcttcaacagcatgcagcagcctgaagtgaagacctggggtggagtggtg acagctgccatggtcatagccctcgctgtctacatggggacaggcatctgtggcttcctg acctttggagctgctgtggatcctgacgtgctcctgtcctatccctcggaggacatggcc gtggccgttgcccgagccttcatcatcctgagcgtgctcacctcctaccctatcctgcac ttctgtgggcgggcggtggtggaaggcctgtggctgcgctaccagggggtgccagtggag gaggacgtggggcgggagcggcggcggcgagtgctgcagacgctggtctggttcctgctc accctgctgctggcgctcttcatccctgacatcggcaaggtgatctcagtcattggaggc ctggccgcctgcttcatcttcgtcttcccagggctgtgcctcattcaagccaaactctct gagatggaagaggtcaaaccagccagctggtgggtgctggtcagctacggagtcctcttg gtcaccctgggagccttcatcttcggccagaccacagccaacgccatctttgtggatctc ttggcataa

Homo sapiens (human): 146167 Help Entry 146167            CDS       T01001                                  Symbol SLC38A8, FHASD, FVH2, SNAT8 Name (RefSeq) solute carrier family 38 member 8   KO K14994   solute carrier family 38 (sodium-coupled neutral amino acid transporter), member 7/8 Organism hsa  Homo sapiens (human) Network nt06544  Neuroactive ligand signaling   Element N01885   Transport of glutamine, SNAT Disease H01256   Foveal hypoplasia Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     146167 (SLC38A8) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC38: System A and System N sodium-coupled neutral amino acid transporter    146167 (SLC38A8) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Aa_trans Trp_Tyr_perm YSIRK_signal Motif Other DBs NCBI-GeneID:  146167 NCBI-ProteinID:  NP_001073911 OMIM:  615585 HGNC:  32434 Ensembl:  ENSG00000166558 UniProt:  A6NNN8 LinkDB All DBs Position 16:complement(84009667..84043372) Genome browser AA seq 435 aa AA seqDB search MEGQTPGSRGLPEKPHPATAAATLSSMGAVFILMKSALGAGLLNFPWAFSKAGGVVPAFL VELVSLVFLISGLVILGYAAAVSGQATYQGVVRGLCGPAIGKLCEACFLLNLLMISVAFL RVIGDQLEKLCDSLLSGTPPAPQPWYADQRFTLPLLSVLVILPLSAPREIAFQKYTSILG TLAACYLALVITVQYYLWPQGLVRESHPSLSPASWTSVFSVFPTICFGFQCHEAAVSIYC SMRKRSLSHWALVSVLSLLACCLIYSLTGVYGFLTFGTEVSADVLMSYPGNDMVIIVARV LFAVSIVTVYPIVLFLGRSVMQDFWRRSCLGGWGPSALADPSGLWVRMPLTILWVTVTLA MALFMPDLSEIVSIIGGISSFFIFIFPGLCLICAMGVEPIGPRVKCCLEVWGVVSVLVGT FIFGQSTAAAVWEMF NT seq 1308 nt NT seq  +upstreamnt  +downstreamnt atggagggacagaccccaggaagcaggggccttccagaaaagcctcaccctgccacggct gctgccactctgtcctcgatgggcgctgtcttcatcctcatgaagtccgcgctgggagct ggcctgctcaacttcccctgggccttctccaaagcgggcggagtggtccctgccttcctg gtggagctggtctcgttggtcttcctgatcagcgggctggtcatcctgggctatgctgct gctgtcagtggccaggccacctaccagggtgtggtcagggggctgtgtggccctgccatt gggaagctgtgtgaggcctgcttcctcctcaacctgctcatgatctccgtggccttcctc agggtgatcggggaccagctggagaagctgtgtgactccctcctgtctggcaccccgccc gccccgcagccgtggtacgcagaccagcgcttcaccctgcccctgctctccgtgctggtc atcctgcccctgtctgccccgcgggagatcgccttccagaaatacacaagcatcctaggc actctggctgcctgttacctggccctggtcatcaccgtgcagtactacctctggccccag ggcctcgtgcgtgagtcccatccttcactgagccctgcctcctggacctctgtgttcagt gtcttccccaccatctgcttcgggtttcagtgtcacgaagctgccgtctccatctactgc agcatgcgcaaacggagcctctcccactgggccctggtgtctgtgctgtccttgctggcc tgctgcctcatctattcactgacgggggtttatggcttcctgacttttgggacagaagtt tctgctgacgtcttgatgtcctacccaggcaatgatatggtcatcattgtggcccgggtc ctttttgctgtctccatcgtaactgtctaccccatcgtgctcttcctggggaggtcagtg atgcaggacttctggaggaggagctgcttggggggatgggggcccagcgccctggccgac ccctcagggctgtgggtccggatgccgctgaccatcctgtgggtcaccgtgacgctcgcc atggcgctgtttatgcctgacctcagcgagatcgtcagcatcatcggaggcatcagttcc ttcttcatcttcatcttcccaggtttgtgcctcatctgtgcaatgggtgtcgagcctata ggaccaagagtcaagtgctgcctggaggtctggggagtggtctctgtgctggtcggcacc ttcatctttgggcagagcacggcggcagcggtctgggagatgttctga

DBGET integrated database retrieval system