KEGG   Homo sapiens (human): 3766
Entry
3766              CDS       T01001                                 
Symbol
KCNJ10, BIRK-10, KCNJ13-PEN, KIR1.2, KIR4.1, SESAME
Name
(RefSeq) potassium inwardly rectifying channel subfamily J member 10
  KO
K05003  potassium inwardly-rectifying channel subfamily J member 10
Organism
hsa  Homo sapiens (human)
Pathway
hsa04971  Gastric acid secretion
hsa05016  Huntington disease
Disease
H00605  Deafness, autosomal recessive
H00803  Seizures-sensorineural deafness-ataxia-mental retardation-electrolyte imbalance (SESAME)
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09150 Organismal Systems
  09154 Digestive system
   04971 Gastric acid secretion
    3766 (KCNJ10)
 09160 Human Diseases
  09164 Neurodegenerative disease
   05016 Huntington disease
    3766 (KCNJ10)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:hsa04040]
    3766 (KCNJ10)
Ion channels [BR:hsa04040]
 Voltage-gated cation channels
  Potassium channel, inwardly-rectifying (Kir)
   3766 (KCNJ10)
SSDB
Motif
Pfam: IRK_C IRK DUF2182 Ion_trans_2
Other DBs
NCBI-GeneID: 3766
NCBI-ProteinID: NP_002232
OMIM: 602208
HGNC: 6256
Ensembl: ENSG00000177807
UniProt: P78508
Position
1:complement(160037467..160070160)
AA seq 379 aa
MTSVAKVYYSQTTQTESRPLMGPGIRRRRVLTKDGRSNVRMEHIADKRFLYLKDLWTTFI
DMQWRYKLLLFSATFAGTWFLFGVVWYLVAVAHGDLLELDPPANHTPCVVQVHTLTGAFL
FSLESQTTIGYGFRYISEECPLAIVLLIAQLVLTTILEIFITGTFLAKIARPKKRAETIR
FSQHAVVASHNGKPCLMIRVANMRKSLLIGCQVTGKLLQTHQTKEGENIRLNQVNVTFQV
DTASDSPFLILPLTFYHVVDETSPLKDLPLRSGEGDFELVLILSGTVESTSATCQVRTSY
LPEEILWGYEFTPAISLSASGKYIADFSLFDQVVKVASPSGLRDSTVRYGDPEKLKLEES
LREQAEKEGSALSVRISNV
NT seq 1140 nt   +upstreamnt  +downstreamnt
atgacgtcagttgccaaggtgtattacagtcagaccactcagacagaaagccggccccta
atgggcccagggatacgacggcggagagtcctgacaaaagatggtcgcagcaacgtgaga
atggagcacattgccgacaagcgcttcctctacctcaaggacctgtggacaaccttcatt
gacatgcagtggcgctacaagcttctgctcttctctgcgacctttgcaggcacatggttc
ctctttggcgtggtgtggtatctggtagctgtggcacatggggacctgctggagctggac
cccccggccaaccacaccccctgtgtggtacaggtgcacacactcactggagccttcctc
ttctcccttgaatcccaaaccaccattggctatggcttccgctacatcagtgaggaatgt
ccactggccattgtgcttcttattgcccagctggtgctcaccaccatcctggaaatcttc
atcacaggtaccttcctggcgaagattgcccggcccaagaagcgggctgagaccattcgt
ttcagccagcatgcagttgtggcctcccacaatggcaagccctgcctcatgatccgagtt
gccaatatgcgcaaaagcctcctcattggctgccaggtgacaggaaaactgcttcagacc
caccaaaccaaggaaggggagaacatccggctcaaccaggtcaatgtgactttccaagta
gacacagcctctgacagccccttccttattctaccccttaccttctatcatgtggtagat
gagaccagtcccttgaaagatctccctcttcgcagtggtgagggtgactttgagctggtg
ctgatcctaagtgggacagtggagtccaccagtgccacctgtcaggtgcgcacttcctac
ctgccagaggagatcctttggggctacgagttcacacctgccatctcactgtcagccagt
ggtaaatacatagctgactttagcctttttgaccaagttgtgaaagtggcctctcctagt
ggcctccgtgacagcactgtacgctacggagaccctgaaaagctcaagttggaggagtca
ttaagggagcaagctgagaaggagggcagtgcccttagtgtgcgcatcagcaatgtctga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Pathway (2)   
   KEGG PATHWAY (2)   
Disease (6)   
   KEGG DISEASE (2)   
   OMIM (4)   
Genome (1)   
   KEGG GENOME (1)   
Gene (9)   
   KEGG ORTHOLOGY (1)   
   RefGene (1)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (2)   
   OC (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (19)   
   RefSeq(nuc) (1)   
   GenBank (9)   
   EMBL (9)   
Protein domain (4)   
   Pfam (4)   
All databases (46)   

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