KEGG   Homo sapiens (human): 56660
Entry
56660             CDS       T01001                                 
Symbol
KCNK12, K2p12.1, THIK-2, THIK2
Name
(RefSeq) potassium two pore domain channel subfamily K member 12
  KO
K04921  potassium channel subfamily K member 12
Organism
hsa  Homo sapiens (human)
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:hsa04040]
    56660 (KCNK12)
Ion channels [BR:hsa04040]
 Voltage-gated cation channels
  Potassium channel, two-pore domain (K2P)
   56660 (KCNK12)
SSDB
Motif
Pfam: Ion_trans_2 Ion_trans
Other DBs
NCBI-GeneID: 56660
NCBI-ProteinID: NP_071338
OMIM: 607366
HGNC: 6274
Ensembl: ENSG00000184261
UniProt: Q9HB15
Position
2:complement(47509290..47570985)
AA seq 430 aa
MSSRSPRPPPRRSRRRLPRPSCCCCCCRRSHLNEDTGRFVLLAALIGLYLVAGATVFSAL
ESPGEAEARARWGATLRNFSAAHGVAEPELRAFLRHYEAALAAGVRADALRPRWDFPGAF
YFVGTVVSTIGFGMTTPATVGGKAFLIAYGLFGCAGTILFFNLFLERIISLLAFIMRACR
ERQLRRSGLLPATFRRGSALSEADSLAGWKPSVYHVLLILGLFAVLLSCCASAMYTSVEG
WDYVDSLYFCFVTFSTIGFGDLVSSQHAAYRNQGLYRLGNFLFILLGVCCIYSLFNVISI
LIKQVLNWMLRKLSCRCCARCCPAPGAPLARRNAITPGSRLRRRLAALGADPAARDSDAE
GRRLSGELISMRDLTASNKVSLALLQKQLSETANGYPRSVCVNTRQNGFSGGVGALGIMN
NRLAETSASR
NT seq 1293 nt   +upstreamnt  +downstreamnt
atgtcctcccgcagcccccggcccccgccccgccgtagccgccgccgcctgccgcgcccc
tcctgctgctgctgctgctgccgccgttcgcacctcaacgaggacaccggccgcttcgtg
ctgctggcggcgctcatcggcctctacctggtggcgggtgccacagtcttctcggcgctc
gagagccccggcgaggcggaggcgcgggcgcgctggggcgccacgctgcgcaacttcagc
gctgcgcacggcgtggccgagccagagctgcgcgccttcctccggcactacgaggccgcg
ctggccgccggcgtccgcgccgacgcgctgcgcccgcgctgggacttccccggcgccttc
tacttcgtgggcaccgtggtgtcaaccataggtttcggcatgaccacccccgcgacggtg
ggcgggaaggccttcctcatcgcctacgggctgttcggctgcgctgggaccatcctgttc
ttcaacctcttcctggagcgcatcatctcgctgctggccttcatcatgcgcgcctgccgg
gagcgccagctgcgccgcagcggcctgctgcccgccaccttccgccgcggctccgcgctc
tcggaggccgacagcctggcgggctggaagccctcggtgtaccacgtgctgctcatcctg
ggcctgttcgccgtgctgctgtcctgctgcgcctcggccatgtacaccagcgtggagggc
tgggactacgtggactcgctctacttctgcttcgtcaccttcagcaccatcggcttcggg
gacctggtgagcagccagcacgccgcctaccggaaccaggggctctaccgcctgggcaac
ttcctcttcatcctgctcggcgtgtgctgcatttactcgctcttcaacgtcatctccatc
ctcatcaagcaggtgctcaactggatgctgcgcaagctgagctgccgctgctgcgcgcgc
tgctgcccggctcctggcgcgcccctggcccggcgcaatgccatcaccccaggctcccgg
ctgcgccgccgcctggccgcgctcggtgccgaccccgcggcccgcgacagcgacgccgag
ggccgccgcctctcgggcgagctcatctccatgcgcgacctcacggcctccaacaaggtg
tcgctggcgctgctgcagaagcagctgtcggagacggccaacggctacccgcgcagcgtg
tgcgtcaacacgcgccagaacggcttctcgggcggcgtgggcgcgctgggcatcatgaac
aaccggctggccgagaccagcgcctccaggtag

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Ontology (2)   
   KEGG BRITE (2)   
Disease (1)   
   OMIM (1)   
Genome (1)   
   KEGG GENOME (1)   
Gene (47)   
   KEGG ORTHOLOGY (1)   
   RefGene (30)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (11)   
   OC (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (5)   
   RefSeq(nuc) (1)   
   GenBank (2)   
   EMBL (2)   
Protein domain (2)   
   Pfam (2)   
All databases (61)   

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