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Human (GRCh37.p13)
Description

forkhead box G1 [Source:HGNC Symbol;Acc:3811]

Gene Synonyms

BF1, BF2, FHKL3, FKH2, FKHL1, FKHL2, FKHL3, FKHL4, FOXG1A, FOXG1B, FOXG1C, HBF-1, HBF-2, HBF-3, HBF-G2, HBF2, HFK1, HFK2, HFK3, KHL2, QIN

Location

Chromosome 14: 29,235,050-29,238,870 forward strand.

GRCh37:CM000676.1

About this gene

This gene has 2 transcripts (splice variants), 15 paralogues and is associated with 5 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000382535.3FOXG1-2012754489aaENSP00000371975.3
 
Protein coding
CCDS9636P55316 -Ensembl CanonicalGENCODE basic
ENST00000313071.4FOXG1-0012584489aaENSP00000339004.3
 
Protein coding
CCDS9636P55316 NM_005249.4GENCODE basic