DisGeNET - a database of gene-disease associations

Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome, C4014821

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

Gene

UniProt

Gene Full Name

Protein Class

N. diseases_g

DSI _g

DPI _g

pLI

Score _gda

EL _gda

EI _gda

N. PMIDs

N. SNPs _gda

First Ref.

Last Ref.

Entrez Id:	284217
Gene Symbol:	LAMA1

LAMA1

P25391

laminin subunit alpha 1

107

0.582

0.808

3.2E-32

0.610

strong

1.000

2

12

2011

2014