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FLASH GENE
Symbol MEIOB contributors: mct - updated : 13-04-2021
HGNC name meiosis-specific with OB domain-containing protein
HGNC id 28569
ASSOCIATED DISORDERS
corresponding disease(s) SPGF22
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional germinal mutation      
a truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22
Susceptibility
Variant & Polymorphism
Candidate gene
Marker
Therapy target
ANIMAL & CELL MODELS
Meiob-null mouse mutants exhibit a failure in meiosis and sterility in both sexes