DisGeNET - a database of gene-disease associations

USP9X, ubiquitin specific peptidase 9 X-linked, 8239

N. diseases: 255; N. variants: 14

Source: ALL

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Variant

Gene

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs1569165417

Entrez Id:	8239
Gene Symbol:	USP9X

USP9X

CUI:	C4225416
Disease:

MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED

0.700

GeneticVariation

CLINVAR

dbSNP:

rs1569165417

Entrez Id:	8239
Gene Symbol:	USP9X

USP9X

CUI:	C3806746
Disease:

MENTAL RETARDATION, X-LINKED 99

0.700

GeneticVariation

CLINVAR

dbSNP:

rs587777318

Entrez Id:	8239
Gene Symbol:	USP9X

USP9X

CUI:	C3806746
Disease:

MENTAL RETARDATION, X-LINKED 99

0.700

CausalMutation

CLINVAR

dbSNP:

rs869025588

Entrez Id:	8239
Gene Symbol:	USP9X

USP9X

CUI:	C4225416
Disease:

MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED

0.700

CausalMutation

CLINVAR

dbSNP:

rs869025589

Entrez Id:	8239
Gene Symbol:	USP9X

USP9X

CUI:	C4225416
Disease:

MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED

0.700

CausalMutation

CLINVAR

dbSNP:

rs869025590

Entrez Id:	8239
Gene Symbol:	USP9X

USP9X

CUI:	C4225416
Disease:

MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED

0.700

CausalMutation

CLINVAR

dbSNP:

rs869025591

Entrez Id:	8239
Gene Symbol:	USP9X

USP9X

CUI:	C4225416
Disease:

MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED

0.700

CausalMutation

CLINVAR

dbSNP:

rs869025592

Entrez Id:	8239
Gene Symbol:	USP9X

USP9X

CUI:	C4225416
Disease:

MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED

0.700

CausalMutation

CLINVAR