KEGG   Homo sapiens (human): 81615
Entry
81615             CDS       T01001                                 
Symbol
TMEM163, DC29, HLD25, SLC30A11, SV31
Name
(RefSeq) transmembrane protein 163
  KO
K14694  solute carrier family 30 (zinc transporter), member 11
Organism
hsa  Homo sapiens (human)
Disease
H00679  Hypomyelinating leukodystrophy
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    81615 (TMEM163)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC30: Zinc efflux transporter
   81615 (TMEM163)
SSDB
Other DBs
NCBI-GeneID: 81615
NCBI-ProteinID: NP_112185
OMIM: 618978
HGNC: 25380
Ensembl: ENSG00000152128
UniProt: Q8TC26
Position
2:complement(134455759..134719000)
AA seq 289 aa
MEPAAGIQRRSSQGPTVPPPPRGHAPPAAAPGPAPLSSPVREPPQLEEERQVRISESGQF
SDGLEDRGLLESSTRLKPHEAQNYRKKALWVSWFSIIVTLALAVAAFTVSVMRYSASAFG
FAFDAILDVLSSAIVLWRYSNAAAVHSAHREYIACVILGVIFLLSSICIVVKAIHDLSTR
LLPEVDDFLFSVSILSGILCSILAVLKFMLGKVLTSRALITDGFNSLVGGVMGFSILLSA
EVFKHDSAVWYLDGSIGVLIGLTIFAYGVKLLIDMVPRVRQTRHYEMFE
NT seq 870 nt   +upstreamnt  +downstreamnt
atggagccggccgcgggcatccagcgccgcagctcccaggggcccaccgtcccgccgccg
ccccggggccacgcgccaccggctgccgcccccggcccggccccgctgagctccccggtg
cgcgagccgccccagctggaggaggagcggcaggtgcggatcagcgagagcggccagttc
agcgacgggctggaggaccgaggcttactagaaagcagcacccgcctgaaacctcacgaa
gcccagaactacaggaagaaggcattgtgggtgtcctggttctccatcattgtcaccctg
gccctcgcggtggctgcctttactgtctccgttatgaggtacagcgcctctgcttttggg
tttgcatttgatgccatcctggacgtcctgtcatcggcgattgtcctgtggcgttacagc
aacgcggccgctgtgcactctgcccatagggagtacatagcctgtgtcatcttgggggtg
atattccttctgtcatccatatgtatagtggtcaaagccatccatgacctctcaactagg
ctgctcccagaagtggacgatttcctgttcagtgtctccattttaagtgggattctttgc
agcatcctggccgtgttgaagttcatgctggggaaggttctgaccagtagagcactcata
acagatgggtttaactccctcgtgggtggcgtgatgggcttctccattcttctgagcgcg
gaagtgttcaagcatgactcggcggtctggtacctggacggcagcataggcgttctgatc
ggcctcaccatatttgcctatggggtcaaactcctcatcgacatggtgccgagggtgagg
cagacacgtcactacgagatgtttgagtga

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