Entity Details

Primary name HFM1
Entity type gene
Source Source Link

Details

PrimaryID164045
RefseqGeneNG_034120
SymbolHFM1
Namehelicase for meiosis 1
Chromosome1
Location1p22.2
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2002-01-26
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsHFM1_HUMAN

GO terms

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GOName
GO:0000712 resolution of meiotic recombination intermediates
GO:0003676 nucleic acid binding
GO:0003678 DNA helicase activity
GO:0005524 ATP binding
GO:0005634 nucleus

Diseases

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Disease IDSourceNameDescription
615724 OMIMPremature ovarian failure 9 (POF9)An ovarian disorder defined as the cessation of ovarian function under the age of 40 years. It is characterized by oligomenorrhea or amenorrhea, in the presence of elevated levels of serum gonadotropins and low estradiol. The disease may be caused by variants affecting the gene represented in this entry.

Interactions

4 interactions

InteractorPartnerSourcesPublicationsLink
HFM1FAM107ABioGRID28604741 details
HFM1NR3C1BioGRID31182584 details
HFM1TRIM25BioGRID29117863 details
HFM1DDX58BioGRID32513696 details