Human (GRCh38.p14)
Description

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

Gene Synonyms

FHOS

Location
About this transcript

This transcript has 22 exons, is annotated with 32 domains and features, is associated with 9014 variant alleles and maps to 670 oligo probes.

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

Protein domains for ENSP00000258201.4