Human (GRCh38.p14)
Description

formin homology 2 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:17905]

Gene Synonyms

FHOS

Location

Chromosome 16: 67,229,387-67,247,481 reverse strand.

GRCh38:CM000678.2

About this gene

This gene has 10 transcripts (splice variants), 224 orthologues and 18 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000258201.9FHOD1-20138131164aaENSP00000258201.4
 
Protein coding
CCDS10834Q9Y613 NM_013241.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000561922.1FHOD1-2022069157aaENSP00000458085.1
 
Nonsense mediated decay
H3BVE7 -TSL:2
ENST00000567561.1FHOD1-20677322aaENSP00000462807.1
 
Nonsense mediated decay
J3KT53 -TSL:3CDS 5' incomplete
ENST00000567509.1FHOD1-205563108aaENSP00000462988.1
 
Nonsense mediated decay
J3KTH7 -TSL:4CDS 5' incomplete
ENST00000568595.1FHOD1-20852028aaENSP00000464011.1
 
Nonsense mediated decay
J3QR24 -TSL:4CDS 5' incomplete
ENST00000567752.5FHOD1-2074321No protein-
 
Retained intron
--TSL:2
ENST00000569888.1FHOD1-210780No protein-
 
Retained intron
--TSL:2
ENST00000569085.1FHOD1-209735No protein-
 
Retained intron
--TSL:2
ENST00000566006.1FHOD1-204673No protein-
 
Retained intron
--TSL:3
ENST00000562266.1FHOD1-203486No protein-
 
Retained intron
--TSL:2