AZF1

Gene name: ubiquitin specific peptidase 9, Y-linked
OMIM ID: 400005
Chromosome location: Yq11.21

Mutations

Disease/Phenotype	Spermatogenic failure, Y-linked, 2
DNA Change	AZFb+AZFc deletion
A.A. Change
Exon/Intron
Mutation Type	deletion
Reference	Imken L, El Houate B, Chafik A, Nahili H, Boulouiz R, Abidi O, Chadli E, Louanjli N, Elfath A, Hassar M, McElreavey K, Barakat A, Rouba H.AZF microdeletions and partial deletions of AZFc region on the Y chromosome in Moroccan men. Asian J Androl. 2007 Sep;9(5):674-8.

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Disease/Phenotype	Spermatogenic failure, Y-linked, 2
DNA Change	AZFc deletion
A.A. Change
Exon/Intron
Mutation Type	deletion
Reference	Imken L, El Houate B, Chafik A, Nahili H, Boulouiz R, Abidi O, Chadli E, Louanjli N, Elfath A, Hassar M, McElreavey K, Barakat A, Rouba H.AZF microdeletions and partial deletions of AZFc region on the Y chromosome in Moroccan men. Asian J Androl. 2007 Sep;9(5):674-8.

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  Variant not named according to HGVS recommendations