Human (GRCh38.p14)
Description

formin homology 2 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:26178]

Gene Synonyms

FHOS2, FLJ22297, FLJ22717, KIAA1695

Location

Chromosome 18: 36,297,713-36,780,220 forward strand.

GRCh38:CM000680.2

About this gene

This gene has 9 transcripts (splice variants), 347 orthologues, 18 paralogues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000590592.6FHOD3-20656821622aaENSP00000466937.1
 
Protein coding
CCDS62418Q2V2M9-4 NM_001281740.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS ALT2TSL:1
ENST00000257209.8FHOD3-20149671439aaENSP00000257209.3
 
Protein coding
CCDS32816Q2V2M9-3 -GENCODE basicAPPRIS P4TSL:1
ENST00000359247.8FHOD3-20245181422aaENSP00000352186.3
 
Protein coding
CCDS62419Q2V2M9-1 -GENCODE basicAPPRIS ALT2TSL:1
ENST00000592930.5FHOD3-20941261200aaENSP00000468163.1
 
Protein coding
K7ER94 -TSL:1CDS 5' incomplete
ENST00000591635.5FHOD3-2073035635aaENSP00000467195.1
 
Protein coding
K7EP24 -GENCODE basicTSL:5
ENST00000592128.5FHOD3-2082112528aaENSP00000467462.2
 
Protein coding
A0A0A0MTS9 -TSL:1CDS 5' incomplete
ENST00000585579.2FHOD3-2031720375aaENSP00000465843.1
 
Protein coding
K7EKZ0 -TSL:1CDS 5' incomplete
ENST00000589114.5FHOD3-2054154No protein-
 
Retained intron
--TSL:2
ENST00000587493.1FHOD3-204885No protein-
 
Retained intron
--TSL:1