DisGeNET - a database of gene-disease associations

Gene: FAM160B1 ×

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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:	57700
Gene Symbol:	FAM160B1

FAM160B1

CUI:	C0557874
Disease:	Global developmental delay

Global developmental delay

0.300

Biomarker

GENOMICS_ENGLAND

FAM160B1 deficit associated with microcephaly, severe intellectual disability, ataxia, behavioral abnormalities and speech problems.

2019