DisGeNET - a database of gene-disease associations

Source: MGD

Disease: Sensorineural hearing loss, bilateral ×

Gene: MARVELD2 ×

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:	153562
Gene Symbol:	MARVELD2

MARVELD2

CUI:	C0452138
Disease:	Sensorineural hearing loss, bilateral

Sensorineural hearing loss, bilateral

0.200

Biomarker

MGD

Deletion of Tricellulin Causes Progressive Hearing Loss Associated with Degeneration of Cochlear Hair Cells.

26677943

2015

Entrez Id:	153562
Gene Symbol:	MARVELD2

MARVELD2

CUI:	C0452138
Disease:	Sensorineural hearing loss, bilateral

Sensorineural hearing loss, bilateral

0.200

Biomarker

MGD

Tricellulin deficiency affects tight junction architecture and cochlear hair cells.

23979167

2013