KEGG   Homo sapiens (human): 3769
Entry
3769              CDS       T01001                                 
Symbol
KCNJ13, KIR1.4, KIR7.1, LCA16, SVD
Name
(RefSeq) potassium inwardly rectifying channel subfamily J member 13
  KO
K05006  potassium inwardly-rectifying channel subfamily J member 13
Organism
hsa  Homo sapiens (human)
Pathway
hsa04974  Protein digestion and absorption
Disease
H00805  Vitreoretinal degeneration
H00837  Leber congenital amaurosis
H02077  Snowflake vitreoretinal degeneration
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09150 Organismal Systems
  09154 Digestive system
   04974 Protein digestion and absorption
    3769 (KCNJ13)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:hsa04040]
    3769 (KCNJ13)
Ion channels [BR:hsa04040]
 Voltage-gated cation channels
  Potassium channel, inwardly-rectifying (Kir)
   3769 (KCNJ13)
SSDB
Motif
Pfam: IRK IRK_C Ion_trans_2 DUF3324
Other DBs
NCBI-GeneID: 3769
NCBI-ProteinID: NP_002233
OMIM: 603208
HGNC: 6259
Ensembl: ENSG00000115474
UniProt: O60928
Position
2:complement(232765802..232776565)
AA seq 360 aa
MDSSNCKVIAPLLSQRYRRMVTKDGHSTLQMDGAQRGLAYLRDAWGILMDMRWRWMMLVF
SASFVVHWLVFAVLWYVLAEMNGDLELDHDAPPENHTICVKYITSFTAAFSFSLETQLTI
GYGTMFPSGDCPSAIALLAIQMLLGLMLEAFITGAFVAKIARPKNRAFSIRFTDTAVVAH
MDGKPNLIFQVANTRPSPLTSVRVSAVLYQERENGKLYQTSVDFHLDGISSDECPFFIFP
LTYYHSITPSSPLATLLQHENPSHFELVVFLSAMQEGTGEICQRRTSYLPSEIMLHHCFA
SLLTRGSKGEYQIKMENFDKTVPEFPTPLVSKSPNRTDLDIHINGQSIDNFQISETGLTE
NT seq 1083 nt   +upstreamnt  +downstreamnt
atggacagcagtaattgcaaagttattgctcctctcctaagtcaaagataccggaggatg
gtcaccaaggatggccacagcacacttcaaatggatggcgctcaaagaggtcttgcatat
cttcgagatgcttggggaatcctaatggacatgcgctggcgttggatgatgttggtcttt
tctgcttcttttgttgtccactggcttgtctttgcagtgctctggtatgttctggctgag
atgaatggtgatctggaactagatcatgatgccccacctgaaaaccacactatctgtgtc
aagtatatcaccagtttcacagctgcattctccttctccctggagacacaactcacaatt
ggttatggtaccatgttccccagtggtgactgtccaagtgcaatcgccttacttgccata
caaatgctcctaggcctcatgctagaggcttttatcacaggtgcttttgtggcgaagatt
gcccggccaaaaaatcgagctttttcaattcgctttactgacacagcagtagtagctcac
atggatggcaaacctaatcttatcttccaagtggccaacacccgacctagccctctaacc
agtgtccgggtctcagctgtactctatcaggaaagagaaaatggcaaactctaccagacc
agtgtggatttccaccttgatggcatcagttctgacgaatgtccattcttcatctttcca
ctaacgtactatcactccattacaccatcaagtcctctggctactctgctccagcatgaa
aatccttctcactttgaattagttgtattcctttcagcaatgcaggagggcactggagaa
atatgccaaaggaggacatcctacctaccgtctgaaatcatgttacatcactgttttgca
tctctgttgacccgaggttccaaaggtgaatatcaaatcaagatggagaattttgacaag
actgtccctgaatttccaactcctctggtttctaaaagcccaaacaggactgacctggat
atccacatcaatggacaaagcattgacaattttcagatctctgaaacaggactgacagaa
taa

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Pathway (1)   
   KEGG PATHWAY (1)   
Disease (6)   
   KEGG DISEASE (3)   
   OMIM (3)   
Genome (1)   
   KEGG GENOME (1)   
Gene (13)   
   KEGG ORTHOLOGY (1)   
   RefGene (3)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (4)   
   OC (1)   
Protein sequence (7)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (5)   
DNA sequence (29)   
   RefSeq(nuc) (5)   
   GenBank (12)   
   EMBL (12)   
Protein domain (4)   
   Pfam (4)   
All databases (63)   

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