KEGG   Homo sapiens (human): 3773
Entry
3773              CDS       T01001                                 
Symbol
KCNJ16, BIR9, HKTD, KIR5.1
Name
(RefSeq) potassium inwardly rectifying channel subfamily J member 16
  KO
K05009  potassium inwardly-rectifying channel subfamily J member 16
Organism
hsa  Homo sapiens (human)
Pathway
hsa04971  Gastric acid secretion
Disease
H02790  Hypokalemic tubulopathy and deafness
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09150 Organismal Systems
  09154 Digestive system
   04971 Gastric acid secretion
    3773 (KCNJ16)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:hsa04040]
    3773 (KCNJ16)
Ion channels [BR:hsa04040]
 Voltage-gated cation channels
  Potassium channel, inwardly-rectifying (Kir)
   3773 (KCNJ16)
SSDB
Motif
Pfam: IRK_C IRK Ion_trans_2 Ion_trans
Other DBs
NCBI-GeneID: 3773
NCBI-ProteinID: NP_001257351
OMIM: 605722
HGNC: 6262
Ensembl: ENSG00000153822
UniProt: Q9NPI9
Position
17:70075225..70135608
AA seq 418 aa
MSYYGSSYHIINADAKYPGYPPEHIIAEKRRARRRLLHKDGSCNVYFKHIFGEWGSYVVD
IFTTLVDTKWRHMFVIFSLSYILSWLIFGSVFWLIAFHHGDLLNDPDITPCVDNVHSFTG
AFLFSLETQTTIGYGYRCVTEECSVAVLMVILQSILSCIINTFIIGAALAKMATARKRAQ
TIRFSYFALIGMRDGKLCLMWRIGDFRPNHVVEGTVRAQLLRYTEDSEGRMTMAFKDLKL
VNDQIILVTPVTIVHEIDHESPLYALDRKAVAKDNFEILVTFIYTGDSTGTSHQSRSSYV
PREILWGHRFNDVLEVKRKYYKVNCLQFEGSVEVYAPFCSAKQLDWKDQQLHIEKAPPVR
ESCTSDTKARRRSFSAVAIVSSCENPEETTTSATHEYRETPYQKALLTLNRISVESQM
NT seq 1257 nt   +upstreamnt  +downstreamnt
atgagctattacggcagcagctatcatattatcaatgcggacgcaaaatacccaggctac
ccgccagagcacattatagctgagaagagaagagcaagaagacgattacttcacaaagat
ggcagctgtaatgtctacttcaagcacatttttggagaatggggaagctatgtggttgac
atcttcaccactcttgtggacaccaagtggcgccatatgtttgtgatattttctttatct
tatattctctcgtggttgatatttggctctgtcttttggctcatagcctttcatcatggc
gatctattaaatgatccagacatcacaccttgtgttgacaacgtccattctttcacaggg
gcctttttgttctccctagagacccaaaccaccataggatatggttatcgctgtgttact
gaagaatgttctgtggccgtgctcatggtgatcctccagtccatcttaagttgcatcata
aatacctttatcattggagctgccttggccaaaatggcaactgctcgaaagagagcccaa
accattcgtttcagctactttgcacttataggtatgagagatgggaagctttgcctcatg
tggcgcattggtgattttcggccaaaccacgtggtagaaggaacagttagagcccaactt
ctccgctatacagaagacagtgaagggaggatgacgatggcatttaaagacctcaaatta
gtcaacgaccaaatcatcctggtcaccccggtaactattgtccatgaaattgaccatgag
agccctctgtatgcccttgaccgcaaagcagtagccaaagataactttgagattttggtg
acatttatctatactggtgattccactggaacatctcaccaatctagaagctcctatgtt
ccccgagaaattctctggggccataggtttaatgatgtcttggaagttaagaggaagtat
tacaaagtgaactgcttacagtttgaaggaagtgtggaagtatatgcccccttttgcagt
gccaagcaattggactggaaagaccagcagctccacatagaaaaagcaccaccagttcga
gaatcctgcacgtcggacaccaaggcgagacgaaggtcatttagtgcagttgccattgtc
agcagctgtgaaaaccctgaggagaccaccacttccgccacacatgaatatagggaaaca
ccttatcagaaagctctcctgactttaaacagaatctctgtagaatcccaaatgtag

  All links  
Disease (2)   
   OMIM (2)   
Gene (8)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (3)   
   OC (1)   
Protein sequence (40)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (38)   
DNA sequence (66)   
   RefSeq(nuc) (38)   
   GenBank (14)   
   EMBL (14)   
Protein domain (4)   
   Pfam (4)   
All databases (120)   

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