DisGeNET - a database of gene-disease associations

Source: MGD

Disease: Congenital atresia of nasopharynx ×

Gene: CCDC39 ×

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

Gene Full Name

DSI _g

DPI _g

pLI

Disease

Type

Score _gda

EL_gda

EI _gda

N.PMIDs

N.SNPs _gda

First Ref.

LastRef.

Entrez Id:	339829
Gene Symbol:	CCDC39

CCDC39

coiled-coil domain containing 39

0.641

0.615

7.9E-12

CUI:	C0265747
Disease:	Congenital atresia of nasopharynx

Congenital atresia of nasopharynx

disease

0.200

None

0