ZFIN Human Disease: spermatogenic failure 27

OBO ID: DOID:0111928

Term Name:	spermatogenic failure 27		Search Ontology:
Synonyms:	SPGF27
Definition:	A spermatogenic failure characterized by multiple morphologic abnormalities of the sperm flagella, loss of the central pair of microtubules, loss of the inner dynein arms, and peripheral doublet disorganization of the flagella that has_material_basis_in homozygous or compound heterozygous mutation in AK7 on chromosome 14q32.2. https://pubmed.ncbi.nlm.nih.gov/29365104/
References:	OMIM:617965
Ontology:	Human Disease ( DOID:0111928 )

Relationships

is a type of:	autosomal recessive disease spermatogenic failure autosomal recessive disease spermatogenic failure Show first 5 Terms

OTHER spermatogenic failure 27 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
AK7	ak7a ak7b	?Spermatogenic failure 27	617965

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None