HFM1

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
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RefSeq (mRNA)

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RefSeq (protein)

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Location (UCSC)n/an/a
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HFM1 is a gene that in humans encodes a protein necessary for homologous recombination of chromosomes.[1] Biallelic mutations in HFM1 cause recessive primary ovarian insufficiency.[1]

References

  1. 1.0 1.1 Wang J, Zhang W, Jiang H, Wu BL (March 2014). "Mutations in HFM1 in recessive primary ovarian insufficiency". The New England Journal of Medicine. 370 (10): 972–4. doi:10.1056/NEJMc1310150. PMID 24597873.