DisGeNET - a database of gene-disease associations

Source: CLINVAR

Disease: Nasopharyngeal Neoplasms ×

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:	7157
Gene Symbol:	TP53

TP53

CUI:	C0027439
Disease:	Nasopharyngeal Neoplasms

Nasopharyngeal Neoplasms

0.410

GeneticVariation

CLINVAR

Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.

26619011

2016

Entrez Id:	5290
Gene Symbol:	PIK3CA

PIK3CA

CUI:	C0027439
Disease:	Nasopharyngeal Neoplasms

Nasopharyngeal Neoplasms

0.100

GeneticVariation

CLINVAR

Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.

26619011

2016

Entrez Id:	2263
Gene Symbol:	FGFR2

FGFR2

CUI:	C0027439
Disease:	Nasopharyngeal Neoplasms

Nasopharyngeal Neoplasms

0.100

GeneticVariation

CLINVAR

Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.

26619011

2016

Entrez Id:	3265
Gene Symbol:	HRAS

HRAS

CUI:	C0027439
Disease:	Nasopharyngeal Neoplasms

Nasopharyngeal Neoplasms

0.100

GeneticVariation

CLINVAR

Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.

26619011

2016

Entrez Id:	4893
Gene Symbol:	NRAS

NRAS

CUI:	C0027439
Disease:	Nasopharyngeal Neoplasms

Nasopharyngeal Neoplasms

0.100

GeneticVariation

CLINVAR

Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.

26619011

2016

Entrez Id:	79728
Gene Symbol:	PALB2

PALB2

CUI:	C0027439
Disease:	Nasopharyngeal Neoplasms

Nasopharyngeal Neoplasms

0.100

CausalMutation

CLINVAR