KEGG   Homo sapiens (human): 6509
Entry
6509              CDS       T01001                                 
Symbol
SLC1A4, ASCT1, SATT, SPATCCM
Name
(RefSeq) solute carrier family 1 member 4
  KO
K05615  solute carrier family 1 (neutral amino acid transporter), member 4
Organism
hsa  Homo sapiens (human)
Disease
H02282  Spastic tetraplegia, thin corpus callosum, and progressive microcephaly
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    6509 (SLC1A4)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC1: High-affinity glutamate and neutral amino acid transporter
   6509 (SLC1A4)
SSDB
Motif
Pfam: SDF
Other DBs
NCBI-GeneID: 6509
NCBI-ProteinID: NP_003029
OMIM: 600229
HGNC: 10942
Ensembl: ENSG00000115902
Position
2:64988479..65023865
AA seq 532 aa
MEKSNETNGYLDSAQAGPAAGPGAPGTAAGRARRCAGFLRRQALVLLTVSGVLAGAGLGA
ALRGLSLSRTQVTYLAFPGEMLLRMLRMIILPLVVCSLVSGAASLDASCLGRLGGIAVAY
FGLTTLSASALAVALAFIIKPGSGAQTLQSSDLGLEDSGPPPVPKETVDSFLDLARNLFP
SNLVVAAFRTYATDYKVVTQNSSSGNVTHEKIPIGTEIEGMNILGLVLFALVLGVALKKL
GSEGEDLIRFFNSLNEATMVLVSWIMWYVPVGIMFLVGSKIVEMKDIIVLVTSLGKYIFA
SILGHVIHGGIVLPLIYFVFTRKNPFRFLLGLLAPFATAFATCSSSATLPSMMKCIEENN
GVDKRISRFILPIGATVNMDGAAIFQCVAAVFIAQLNNVELNAGQIFTILVTATASSVGA
AGVPAGGVLTIAIILEAIGLPTHDLPLILAVDWIVDRTTTVVNVEGDALGAGILHHLNQK
ATKKGEQELAEVKVEAIPNCKSEEETSPLVTHQNPAGPVASAPELESKESVL
NT seq 1599 nt   +upstreamnt  +downstreamnt
atggagaagagcaacgagaccaacggctaccttgacagcgctcaggcggggcctgcggcc
gggcccggagctccggggaccgcggcgggacgcgcacggcgttgcgcgggcttcctgcgg
cgccaagcgctggtgctgctcaccgtgtccggggtgctggcgggcgcgggcctgggcgcg
gcgttgcgcgggctcagcctgagccgcacgcaggtcacctacctggccttccccggcgag
atgctgctccgcatgctgcgcatgatcatcctgccgctggtggtctgcagcctggtgtcg
ggcgccgcctcgctcgatgccagctgcctcgggcgtctgggcggcatcgctgtcgcctac
tttggcctcaccacactgagtgcctcggcgctcgccgtggccttggcgttcatcatcaag
ccaggatccggtgcgcagacccttcagtccagcgacctggggctggaggactcggggcct
cctcctgtccccaaagagacggtggactctttcctcgacctggccagaaacctgtttccc
tccaatcttgtggttgcagctttccgtacgtatgcaaccgattataaagtcgtgacccag
aacagcagctctggaaatgtaacccatgaaaagatccccataggcactgagatagaaggg
atgaacattttaggattggtcctgtttgctctggtgttaggagtggccttaaagaaacta
ggctccgaaggagaagacctcatccgtttcttcaattccctcaacgaggcgacgatggtg
ctggtgtcctggattatgtggtacgtacctgtgggcatcatgttccttgttggaagcaag
atcgtggaaatgaaagacatcatcgtgctggtgaccagcctggggaaatacatcttcgca
tctatattgggccatgttattcatggaggaattgttctgccacttatttattttgttttc
acacgaaaaaacccattcagattcctcctgggcctcctcgccccatttgcgacagcattt
gctacctgctccagctcagcgacccttccctctatgatgaagtgcattgaagagaacaat
ggtgtggacaagaggatcagcaggtttattctccccatcggggccaccgtgaacatggac
ggagcagccatcttccagtgtgtggccgcggtgttcattgcgcaactcaacaacgtagag
ctcaacgcaggacagattttcaccattctagtgactgccacagcgtccagtgttggagca
gcaggcgtgccagctggaggggtcctcaccattgccattatcctggaggccattgggctg
cctactcatgacctgcctctgatcctggctgtggactggattgtggaccggaccaccacg
gtggtgaatgtggaaggggatgccctgggtgcaggcattctccaccacctgaatcagaag
gcaacaaagaaaggcgagcaggaacttgctgaggtgaaagtggaagccatccccaactgc
aagtctgaggaggagacatcgcccctggtgacacaccagaaccccgctggccccgtggcc
agtgccccagaactggaatccaaggagtcggttctgtga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (10)   
   KEGG ORTHOLOGY (1)   
   RefGene (1)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (3)   
   OC (1)   
Protein sequence (6)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (4)   
DNA sequence (37)   
   RefSeq(nuc) (5)   
   GenBank (16)   
   EMBL (16)   
Protein domain (1)   
   Pfam (1)   
All databases (60)   

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