Entity Details

Primary name MEI1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ5TIA1
EntryNameMEI1_HUMAN
FullNameMeiosis inhibitor protein 1
TaxID9606
Evidenceevidence at transcript level
Length1274
SequenceStatuscomplete
DateCreated2008-09-02
DateModified2021-06-02

Ontological Relatives

GenesMEI1

GO terms

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GOName
GO:0007127 meiosis I

Subcellular Location

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Domains

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DomainNameCategoryType
IPR011989 Armadillo-like helicalFamilyHomologous superfamily
IPR016024 Armadillo-type foldFamilyHomologous superfamily

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

1 interaction

InteractorPartnerSourcesPublicationsLink
MEI1_HUMANNEDD8_HUMANBioGRID16503656 details