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 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 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

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