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ECB-GENEPAGE-23193262
???displayGene.symbol??? nr2f2
![]() Symbol Status
![]() ???displayGene.name??? nuclear receptor subfamily 2 group F member 2
![]() Name Status
![]() ???displayGene.synonyms???
COUP transcription factor-like
,
LOC110987311
,
NR2F3
,
seven up homolog
,
Sp-Couptf
,
Sp-Couptf1
[+]
(
???displayGene.geneFunction??? Protein Function
![]() ???displayGene.geneInteractants???
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Diseases: MIM:
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 4; CHTD4
External Links:
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Symbol legend:



