Homo sapiens (human): 10991
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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
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Aa_trans
Motif
Other DBs
NCBI-GeneID:
10991
NCBI-ProteinID:
NP_006832
OMIM:
604437
HGNC:
18044
Ensembl:
ENSG00000188338
UniProt:
Q99624
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All DBs
Position
3:50205271..50221486
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AA seq
504 aa
AA seq
DB search
MEAPLQTEMVELVPNGKHSEGLLPVITPMAGNQRVEDPARSCMEGKSFLQKSPSKEPHFT
DFEGKTSFGMSVFNLSNAIMGSGILGLAYAMANTGIILFLFLLTAVALLSSYSIHLLLKS
SGVVGIRAYEQLGYRAFGTPGKLAAALAITLQNIGAMSSYLYIIKSELPLVIQTFLNLEE
KTSDWYMNGNYLVILVSVTIILPLALMRQLGYLGYSSGFSLSCMVFFLIAVIYKKFHVPC
PLPPNFNNTTGNFSHVEIVKEKVQLQVEPEASAFCTPSYFTLNSQTAYTIPIMAFAFVCH
PEVLPIYTELKDPSKKKMQHISNLSIAVMYIMYFLAALFGYLTFYNGVESELLHTYSKVD
PFDVLILCVRVAVLTAVTLTVPIVLFPVRRAIQQMLFPNQEFSWLRHVLIAVGLLTCINL
LVIFAPNILGIFGVIGATSAPFLIFIFPAIFYFRIMPTEKEPARSTPKILALCFAMLGFL
LMTMSLSFIIIDWASGTSRHGGNH
NT seq
1515 nt
NT seq
+upstream
nt +downstream
nt
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
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