Terminology Service for NFDI4Health

Kcnv2

Go to external page https://identifiers.org/rgd:1309271


INVOLVED IN protein homooligomerization (inferred); regulation of ion transmembrane transport (inferred); ASSOCIATED WITH cone dystrophy (ortholog); cone-rod dystrophy 14 (ortholog); fundus dystrophy (ortholog); INTERACTS WITH bisphenol A; endosulfan; 1,1,1-trichloroethane (ortholog)

Term info

Label

Kcnv2

Synonyms
  • LOC294065
  • potassium voltage-gated channel modifier subfamily V member 2
database cross reference
MARKER RGD ID

5075418, 5073390, 5029721

MARKER SYMBOL

RH138582, BE096685, RH137408

OLD NAME

potassium channel, subfamily V, member 2;potassium channel, voltage-gated modifier subfamily V, member 2;potassium voltage-gated channel subfamily V member 2

UNIGENE ID

Rn.168638

Term relations

Subclass of: