DisGeNET - a database of gene-disease associations

Source: HPO

Disease: Feeding difficulties in infancy ×

Gene: BCS1L ×

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:	617
Gene Symbol:	BCS1L

BCS1L

BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone

0.534

0.808

4.7E-13

CUI:	C2674608
Disease:	Feeding difficulties in infancy

Feeding difficulties in infancy

phenotype

0.100

None

0