FHOD1

FHOD1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesFHOD1, FHOS, formin homology 2 domain containing 1
External IDsOMIM: 606881; MGI: 2679008; HomoloGene: 40860; GeneCards: FHOD1; OMA:FHOD1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

29109

234686

Ensembl

ENSG00000135723

ENSMUSG00000014778

UniProt

Q9Y613

Q6P9Q4

RefSeq (mRNA)

NM_013241
NM_001318202

NM_177699

RefSeq (protein)

NP_001305131
NP_037373

NP_808367

Location (UCSC)Chr 16: 67.23 – 67.25 MbChr 8: 106.06 – 106.07 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

FH1/FH2 domain-containing protein 1 is a protein that in humans is encoded by the FHOD1 gene.

This gene encodes a protein which is a member of the formin/diaphanous family of proteins. The gene is ubiquitously expressed but is found in abundance in the spleen. The encoded protein has sequence homology to diaphanous and formin proteins within the Formin Homology (FH)1 and FH2 domains. It also contains a coiled-coil domain, a collagen-like domain, two nuclear localization signals, and several potential PKC and PKA phosphorylation sites. It is a predominantly cytoplasmic protein and is expressed in a variety of human cell lines.