spermatogenic failure 19 Disease Ontology Browser

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Disease Ontology Browser

spermatogenic failure 19 (DOID:0070170)
Alliance: disease page
Synonyms: SPGF19
Alt IDs: OMIM:617592
Definition: A spermatogenic failure that is characterized by autosomal recessive inheritance of sperm flagellar morphological abnormalities that has_material_basis_in mutation in the CFAP43 gene on chromosome 10q25.

Disease References using Mouse Models (1)

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/16/2024 MGI 6.23

Allelic Composition	Genetic Background	Reference	Phenotypes
Cfap43em1Fzh/Cfap43em1Fzh	involves: C57BL/6	J:258613	View
Cfap43em2Fzh/Cfap43em2Fzh	involves: C57BL/6	J:258613	View