DisGeNET - a database of gene-disease associations

Source: ALL

Disease: Craniofacial Abnormalities ×

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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

Gene

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	2260
Gene Symbol:	FGFR1

FGFR1

CUI:	C0376634
Disease:	Craniofacial Abnormalities

Craniofacial Abnormalities

0.300

Biomarker

CTD_human

Fgfr1 regulates patterning of the pharyngeal region.

2003