DisGeNET - a database of gene-disease associations

PTPRQ, protein tyrosine phosphatase receptor type Q, 374462

N. diseases: 21; N. variants: 7

Disease: hearing impairment ×

Source: ALL

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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

Disease

Score _gda

Association Type

Type

Original DB

Sentence supporting the association

PMID

PMID Year

CUI:	C1384666
Disease:	hearing impairment

hearing impairment

0.100

CausalMutation

phenotype

CLINVAR

CUI:	C1384666
Disease:	hearing impairment

hearing impairment

0.100

Biomarker

phenotype

HPO