FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term spermatogenic failure 54 ID (Ontology) DOID:0112335 (Human Disease)
Definition A spermatogenic failure characterized by male infertility due to oligoteratoasthenozoospermia, with markedly reduced sperm counts and severely reduced or absent sperm motility that has_material_basis_in homozygous or compound heterozygous mutation in the CATIP gene on chromosome 2q35.
Also Known As "SPGF54"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
    Results list data from multiple species. Click on a button above and use the 'Filter by species' options on the resulting HitList to retrieve species-specific data.
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Genes
 spermatogenic failure 54       1
 for disease ribbon | spermatogenic failure 54       1
 model of | spermatogenic failure 54       1
Spanning Tree (Parents/Children)
Only view relationship: 
autosomal genetic disease
 |__autosomal recessive disease__
male infertility                 |
 |__spermatogenic failure________|
                                 spermatogenic failure 54  1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a autosomal recessive disease
spermatogenic failure
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "SPGF54" EXACT OMO:0003012
Secondary IDs
hide External Crossreferences & Linkouts
MIM:619379