Homo sapiens (human): 388662
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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)
BRITE hierarchy
SSDB
Ortholog
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Gene cluster
GFIT
Motif
Pfam:
SNF
Gate
Tmemb_18A
Spindle_Spc25
Motif
Other DBs
NCBI-GeneID:
388662
NCBI-ProteinID:
NP_001010898
OMIM:
610299
HGNC:
31399
Ensembl:
ENSG00000197106
UniProt:
Q9H1V8
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Position
1:110150494..110202202
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AA seq
727 aa
AA seq
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MPKNSKVTQREHSSEHVTESVADLLALEEPVDYKQSVLNVAGEAGGKQKAVEEELDAEDR
PAWNSKLQYILAQIGFSVGLGNIWRFPYLCQKNGGGAYLVPYLVLLIIIGIPLFFLELAV
GQRIRRGSIGVWHYICPRLGGIGFSSCIVCLFVGLYYNVIIGWSIFYFFKSFQYPLPWSE
CPVVRNGSVAVVEAECEKSSATTYFWYREALDISDSISESGGLNWKMTLCLLVAWSIVGM
AVVKGIQSSGKVMYFSSLFPYVVLACFLVRGLLLRGAVDGILHMFTPKLDKMLDPQVWRE
AATQVFFALGLGFGGVIAFSSYNKQDNNCHFDAALVSFINFFTSVLATLVVFAVLGFKAN
IMNEKCVVENAEKILGYLNTNVLSRDLIPPHVNFSHLTTKDYMEMYNVIMTVKEDQFSAL
GLDPCLLEDELDKSVQGTGLAFIAFTEAMTHFPASPFWSVMFFLMLINLGLGSMIGTMAG
ITTPIIDTFKVPKEMFTVGCCVFAFLVGLLFVQRSGNYFVTMFDDYSATLPLTLIVILEN
IAVAWIYGTKKFMQELTEMLGFRPYRFYFYMWKFVSPLCMAVLTTASIIQLGVTPPGYSA
WIKEEAAERYLYFPNWAMALLITLIVVATLPIPVVFVLRHFHLLSDGSNTLSVSYKKGRM
MKDISNLEENDETRFILSKVPSEAPSPMPTHRSYLGPGSTSPLETSGNPNGRYGSGYLLA
STPESEL
NT seq
2184 nt
NT seq
+upstream
nt +downstream
nt
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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