FHOD1
Sign in to saveAlso known as FHOS, formin homology 2 domain containing 1
FH1/FH2 domain-containing protein 1 is a protein that in humans is encoded by the FHOD1 gene.
In the Vinony graph
Vinony's link graph records 4 inbound references to FHOD1, and connects out to PubMed, human chromosome 16 and Ensembl genome database project.
It is catalogued under the topic Genes on human chromosome 16.
Vinony links it to 5 Wikipedia language editions.
Gene data
FHOD1- Name
- formin homology 2 domain containing 1
- Type
- protein-coding
- Position
- 67,229,387–67,247,539 (−)
- Aliases
- FHOS
- Ensembl
- ENSG00000135723
- RefSeq RNA
- NM_001318202.2, NM_013241.3, XM_011523043.3, XM_011523044.2, XM_047433999.1
- RefSeq protein
- NP_001305131.1, NP_037373.2, XP_011521345.1, XP_011521346.1, XP_047289955.1
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. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015].
Gene Ontology
Biological process
Molecular function
via MyGene.info
Gene · Ensembl
formin homology 2 domain containing 1
- Symbol
- FHOD1
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 16:67,229,387-67,247,539
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 7 more facts
- HomoloGene ID
- 40860
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/29109
- genomic end
- 67247481
- genomic start
- 67263290
- chromosome
- human chromosome 16
- cytogenetic location
- 16q22.1
Sources (4)
via Wikidata · CC0
~1 min read
Encyclopedic overview
3 sectionsContents
- Interactions
- References
- Further reading
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.
Excerpted from Wikipedia’s “FHOD1” article, available under the CC BY-SA 4.0 licence.