Entity Details

Primary name C11orf80
Entity type gene
Source Source Link

Details

PrimaryID79703
RefseqGene
SymbolC11orf80
Namechromosome 11 open reading frame 80
Chromosome11
Location11q13.2
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-03-12
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsTO6BL_HUMAN

GO terms

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GOName
GO:0005694 chromosome
GO:0007131 reciprocal meiotic recombination
GO:0042138 meiotic DNA double-strand break formation

Diseases

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Disease IDSourceNameDescription
618432 OMIMHydatidiform mole, recurrent, 4 (HYDM4)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 may be caused by variants affecting the gene represented in this entry.

Interactions

1 interaction

InteractorPartnerSourcesPublicationsLink
C11orf80BRCA2BioGRID27433848 details