DisGeNET - a database of gene-disease associations

Source: ALL

Disease: Congenital small ears ×

Gene: ORC1 ×

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

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	4998
Gene Symbol:	ORC1

ORC1

CUI:	C0152423
Disease:	Congenital small ears

Congenital small ears

0.400

Biomarker

GENOMICS_ENGLAND

Expression of the HsOrc1 gene, a human ORC1 homolog, is regulated by cell proliferation via the E2F transcription factor.

8943353

1996

Entrez Id:	4998
Gene Symbol:	ORC1

ORC1

CUI:	C0152423
Disease:	Congenital small ears

Congenital small ears

0.400

Biomarker

HPO