KEGG   Homo sapiens (human): 388662
Entry
388662            CDS       T01001                                 
Symbol
SLC6A17, MRT48, NTT4
Name
(RefSeq) solute carrier family 6 member 17
  KO
K05048  solute carrier family 6 (neurotransmitter transporter, amino acid/orphan) member 15/16/17/18/20
Organism
hsa  Homo sapiens (human)
Disease
H00768  Autosomal recessive intellectual developmental disorder
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    388662 (SLC6A17)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC6: Sodium- and chloride-dependent neurotransmitter transporter
   388662 (SLC6A17)
SSDB
Motif
Pfam: SNF Gate Tmemb_18A Spindle_Spc25
Other DBs
NCBI-GeneID: 388662
NCBI-ProteinID: NP_001010898
OMIM: 610299
HGNC: 31399
Ensembl: ENSG00000197106
Pharos: Q9H1V8(Tbio)
UniProt: Q9H1V8
Position
1:110150494..110202202
AA seq 727 aa
MPKNSKVTQREHSSEHVTESVADLLALEEPVDYKQSVLNVAGEAGGKQKAVEEELDAEDR
PAWNSKLQYILAQIGFSVGLGNIWRFPYLCQKNGGGAYLVPYLVLLIIIGIPLFFLELAV
GQRIRRGSIGVWHYICPRLGGIGFSSCIVCLFVGLYYNVIIGWSIFYFFKSFQYPLPWSE
CPVVRNGSVAVVEAECEKSSATTYFWYREALDISDSISESGGLNWKMTLCLLVAWSIVGM
AVVKGIQSSGKVMYFSSLFPYVVLACFLVRGLLLRGAVDGILHMFTPKLDKMLDPQVWRE
AATQVFFALGLGFGGVIAFSSYNKQDNNCHFDAALVSFINFFTSVLATLVVFAVLGFKAN
IMNEKCVVENAEKILGYLNTNVLSRDLIPPHVNFSHLTTKDYMEMYNVIMTVKEDQFSAL
GLDPCLLEDELDKSVQGTGLAFIAFTEAMTHFPASPFWSVMFFLMLINLGLGSMIGTMAG
ITTPIIDTFKVPKEMFTVGCCVFAFLVGLLFVQRSGNYFVTMFDDYSATLPLTLIVILEN
IAVAWIYGTKKFMQELTEMLGFRPYRFYFYMWKFVSPLCMAVLTTASIIQLGVTPPGYSA
WIKEEAAERYLYFPNWAMALLITLIVVATLPIPVVFVLRHFHLLSDGSNTLSVSYKKGRM
MKDISNLEENDETRFILSKVPSEAPSPMPTHRSYLGPGSTSPLETSGNPNGRYGSGYLLA
STPESEL
NT seq 2184 nt   +upstreamnt  +downstreamnt
atgccgaagaacagcaaagtgacccagcgtgagcacagcagtgagcatgtcactgagtcc
gtggccgacctgctggccctcgaggagcctgtggactataagcagagtgtactgaatgtg
gctggtgaggcaggcggcaagcagaaggcggtggaggaggagctggatgcagaggaccgg
ccggcctggaacagtaagctgcagtacatcctggcccagattggcttctctgtgggcctc
ggcaacatctggaggttcccctacctgtgccagaaaaatggaggaggtgcttacctggtg
ccctacctggtgctgctgatcatcatcgggatccccctcttcttcctggagctggctgtg
ggtcagaggatccgccgcggcagcatcggtgtgtggcactatatatgtccccgcctgggg
ggcatcggcttctccagctgcatagtctgtctctttgtggggctgtattataatgtgatc
atcgggtggagcatcttctatttcttcaagtccttccagtacccgctgccctggagtgaa
tgtcctgtcgtcaggaatgggagcgtggcagtggtggaggcagagtgtgaaaagagctca
gccactacctacttctggtaccgagaggccttggacatctctgactccatctcggagagt
gggggcctcaactggaagatgaccctgtgcctcctcgtggcctggagcatcgtggggatg
gctgtcgttaagggcatccagtcctcggggaaggtgatgtatttcagctccctcttcccc
tacgtggtgctggcctgcttcctggtccgggggctgttgctgcgaggggcagttgatggc
atcctacacatgttcactcccaagctggacaagatgctggacccccaggtgtggcgggag
gcagctacccaggtcttctttgccttgggcctgggctttggtggtgtcattgccttctcc
agctacaataagcaggacaacaactgccacttcgatgccgccctggtgtccttcatcaac
ttcttcacgtcagtgttggccaccctcgtggtgtttgctgtgctgggcttcaaggccaac
atcatgaatgagaagtgtgtggtcgagaatgctgagaaaatcctagggtaccttaacacc
aacgtcctgagccgggacctcatcccaccccacgtcaacttctcccacctgaccacaaag
gactacatggagatgtacaatgtcatcatgaccgtgaaggaggaccagttctcagccctg
ggccttgacccctgccttctggaggacgagctggacaagtccgtgcagggcacaggcctg
gccttcatcgccttcactgaggccatgacgcacttccccgcctccccgttctggtccgtc
atgttcttcttgatgcttatcaacctgggcctgggcagcatgatcgggaccatggcaggc
atcaccacgcccatcatcgacaccttcaaggtgcccaaggagatgttcacagtgggctgc
tgtgtctttgcattcctcgtggggctgttgttcgtccagcgctccggaaactactttgtc
accatgttcgatgactactcggccaccctgccactcactctcatcgtcatccttgagaac
atcgctgtggcctggatttatggaaccaagaagttcatgcaggagctgacggagatgctg
ggcttccgcccctaccgcttctatttctacatgtggaagttcgtgtctccactatgcatg
gctgtgctcaccacagccagcatcatccagctgggggtcacgcccccgggctacagcgcc
tggatcaaggaggaggctgccgagcgctacctgtatttccccaactgggccatggcactc
ctgatcaccctcatcgtcgtggcgacgctgcccatccctgtggtgttcgtcctgcggcac
ttccacctgctctctgatggctccaacaccctctccgtgtcctacaagaagggccgcatg
atgaaggacatctccaacctggaggagaacgatgagacccgcttcatcctcagcaaggtg
cccagtgaggcaccttcccccatgcccactcaccgttcctatctggggcccggcagcaca
tcacccctggagaccagcggtaaccccaatggacgctatgggagcggctacctgctggcc
agcacccctgagtcggagctgtga

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Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (14)   
   KEGG ORTHOLOGY (1)   
   RefGene (7)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
   PHAROS (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (21)   
   RefSeq(nuc) (1)   
   GenBank (10)   
   EMBL (10)   
Protein domain (4)   
   Pfam (4)   
All databases (48)   

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