Entity Details

Primary name MEI1
Entity type gene
Source Source Link

Details

PrimaryID150365
RefseqGene
SymbolMEI1
Namemeiotic double-stranded break formation protein 1
Chromosome22
Location22q13.2
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2002-01-22
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsMEI1_HUMAN

GO terms

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GOName
GO:0007127 meiosis I

Diseases

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Disease IDSourceNameDescription
618431 OMIMHydatidiform mole, recurrent, 3 (HYDM3)A disorder characterized by excessive trophoblast development that produces a growing mass of tissue inside the uterus at the beginning of a pregnancy. It leads to abnormal pregnancies with no embryo, and cystic degeneration of the chorionic villi. The disease is caused by variants affecting the gene represented in this entry.

Interactions

3 interactions

InteractorPartnerSourcesPublicationsLink
MEI1NEDD8BioGRID16503656 details
MEI1APBB1UniProt24284412 details
MEI1DDX58BioGRID32513696 details