KCNMB2

Description potassium calcium-activated channel subfamily M regulatory beta subunit 2
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GO Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Acute lymphoblastic leukemia (childhood) ( 19684603)
  • Amyotrophic lateral sclerosis (sporadic) ( 24529757)
  • Bipolar disorder and schizophrenia ( 22688191)
  • Chin dimples ( 27182965)
  • Corneal structure ( 23291589)
  • Cough in response to angiotensin-converting enzyme inhibitor drugs ( 28084903)
  • Hippocampal sclerosis ( 25188341)
  • Left ventricular obstructive tract defect (inherited effect) ( 28468790)
  • Response to lamotrigine in genetic generalized epilepsy ( 32308125)
  • Suicide attempts ( 30145303)
Interacting Genes 1 interacting genes: APP
Entrez ID 10242
HPRD ID 05557
Ensembl ID ENSG00000197584
Uniprot IDs B5BNW5 B7Z513 Q9Y691
PDB IDs 1JO6
Enriched GO Terms of Interacting Partners?
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