potassium inwardly rectifying channel subfamily J member 11

Summary
Gene Symbol
  • KCNJ11
Organism
Homo sapiens (human)
External Links
NCBI Gene
3767
PubChem
3767
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Diabetes mellitus
  • Disease variant
  • Phosphoprotein
  • Potassium transport
  • Proteomics identification
  • Reference proteome
  • Transmembrane helix
  • Voltage-gated channel
Proteins
Displaying all 3 entries
UniProt Protein Name
Q14654
  • IKATP
  • Inward rectifier K(+) channel Kir6.2
  • Potassium channel, inwardly rectifying subfamily J member 11
A0A804HHV7
  • Inward rectifier K(+) channel Kir6.2
  • Potassium channel, inwardly rectifying subfamily J member 11
B2RC52
  • Inward rectifier K(+) channel Kir6.2
  • Potassium channel, inwardly rectifying subfamily J member 11
Gene Ontology (GO)
GO Hierarchy
Displaying entries 1 - 5 of 12 in total
GO Term Evidence Code PMID
nuclear envelope
axolemma
glutamatergic synapse
endosome
T-tubule
GO Hierarchy
GO Hierarchy
Disease
Disease Ontology
Displaying entries 1 - 10 of 12 in total
DO ID Disease Name Source
DOID:0060639 permanent neonatal diabetes mellitus
DOID:0070218 familial hyperinsulinemic hypoglycemia 2
DOID:0080855 Parkinsonism
DOID:0111110 maturity-onset diabetes of the young type 13
DOID:10763 hypertension
DOID:11446 sciatic neuropathy
DOID:11716 prediabetes syndrome
DOID:11832 visual epilepsy
DOID:1824 status epilepticus
DOID:2018 hyperinsulinism

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024