HFM1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

HFM1 is a gene that in humans encodes a protein necessary for homologous recombination of chromosomes.[5] Biallelic mutations in HFM1 cause recessive primary ovarian insufficiency.[5]

AliasesHFM1, MER3, POF9, SEC63D1, Si-11, Si-11-6, helicase, ATP-dependent DNA helicase homolog, ATP dependent DNA helicase homolog, helicase for meiosis 1
End91,404,856 bp[1]
Quick facts Identifiers, Aliases ...
HFM1
Identifiers
AliasesHFM1, MER3, POF9, SEC63D1, Si-11, Si-11-6, helicase, ATP-dependent DNA helicase homolog, ATP dependent DNA helicase homolog, helicase for meiosis 1
External IDsOMIM: 615684; MGI: 3036246; HomoloGene: 87103; GeneCards: HFM1; OMA:HFM1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001017975

NM_001252516
NM_177873

RefSeq (protein)

NP_001017975

NP_001239445
NP_808541

Location (UCSC)Chr 1: 91.26 – 91.4 MbChr 5: 106.84 – 106.93 Mb
PubMed search[3][4]
Wikidata
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