DisGeNET - a database of gene-disease associations

Source: ORPHANET

Disease: DIABETES MELLITUS, PERMANENT NEONATAL ×

Gene: INS ×

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:	3630
Gene Symbol:	INS

INS

insulin

0.445

0.923

0.30

CUI:	C1833104
Disease:	DIABETES MELLITUS, PERMANENT NEONATAL

DIABETES MELLITUS, PERMANENT NEONATAL

disease

1.000

strong

0.955

0

1998

2019