DisGeNET - a database of gene-disease associations

Source: ALL

Disease: Fingerprints, Absence of ×

Gene: SMARCAD1 ×

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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:	56916
Gene Symbol:	SMARCAD1

SMARCAD1

CUI:	C1852150
Disease:	Fingerprints, Absence of

Fingerprints, Absence of

0.600

GermlineCausalMutation

ORPHANET

A mutation in a skin-specific isoform of SMARCAD1 causes autosomal-dominant adermatoglyphia.

21820097

2011

Entrez Id:	56916
Gene Symbol:	SMARCAD1

SMARCAD1

CUI:	C1852150
Disease:	Fingerprints, Absence of

Fingerprints, Absence of

0.600

Biomarker

CTD_human

Entrez Id:	56916
Gene Symbol:	SMARCAD1

SMARCAD1

CUI:	C1852150
Disease:	Fingerprints, Absence of

Fingerprints, Absence of

0.600

Biomarker

HPO

Entrez Id:	56916
Gene Symbol:	SMARCAD1

SMARCAD1

CUI:	C1852150
Disease:	Fingerprints, Absence of

Fingerprints, Absence of

0.600

CausalMutation

CLINVAR