primary ovarian insufficiency 5

Summary
Definition
A primary ovarian insufficiency that has_material_basis_in heterozygous mutation in the NOBOX gene on chromosome 7q35.
Super Class
autosomal dominant disease primary ovarian insufficiency
Disease Ontology
DOID:0080862
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
135935 NOBOX NOBOX oogenesis homeobox
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
O60393 Homeobox protein NOBOX

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 6, 2026