Entity Details

Primary name MEIOB
Entity type gene
Source Source Link

Details

PrimaryID254528
RefseqGene
SymbolMEIOB
Namemeiosis specific with OB-fold
Chromosome16
Location16p13.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2002-07-27
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsMEIOB_HUMAN

GO terms

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GOName
GO:0000712 resolution of meiotic recombination intermediates
GO:0000724 double-strand break repair via homologous recombination
GO:0003682 chromatin binding
GO:0003697 single-stranded DNA binding
GO:0005634 nucleus
GO:0005694 chromosome
GO:0005737 cytoplasm
GO:0007129 homologous chromosome pairing at meiosis
GO:0007140 male meiotic nuclear division
GO:0007141 male meiosis I
GO:0007144 female meiosis I
GO:0008310 single-stranded DNA 3'-5' exodeoxyribonuclease activity
GO:0009566 fertilization

Diseases

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Disease IDSourceNameDescription
617706 OMIMSpermatogenic failure 22 (SPGF22)An infertility disorder caused by spermatogenesis defects that result in non-obstructive azoospermia. The disease is caused by variants affecting the gene represented in this entry.

Interactions

3 interactions

InteractorPartnerSourcesPublicationsLink
MEIOBFAM107ABioGRID28604741 details
MEIOBGAPDHSBioGRID, IntAct26186194 28514442 details
MEIOBHECW2BioGRID24163370 details