DisGeNET - a database of gene-disease associations

Source: ORPHANET

Disease: Partial chromosome Y deletion ×

Gene: USP9Y ×

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	8287
Gene Symbol:	USP9Y

USP9Y

CUI:	C1507149
Disease:	Partial chromosome Y deletion

Partial chromosome Y deletion

0.300

ChromosomalRearrangement

ORPHANET

Screening for partial AZFa microdeletions in the Y chromosome of infertile men: is it of clinical relevance?

22537385

2012

Entrez Id:	8287
Gene Symbol:	USP9Y

USP9Y

CUI:	C1507149
Disease:	Partial chromosome Y deletion

Partial chromosome Y deletion

0.300

ChromosomalRearrangement

ORPHANET

Genetic dissection of the AZF regions of the human Y chromosome: thriller or filler for male (in)fertility?

20671934

2010

Entrez Id:	8287
Gene Symbol:	USP9Y

USP9Y

CUI:	C1507149
Disease:	Partial chromosome Y deletion

Partial chromosome Y deletion

0.300

ChromosomalRearrangement

ORPHANET

An azoospermic man with a de novo point mutation in the Y-chromosomal gene USP9Y.

10581029

1999