DisGeNET - a database of gene-disease associations

MYD88, MYD88 innate immune signal transduction adaptor, 4615

N. diseases: 480; N. variants: 9

Disease: Dermatitis, Atopic ×

Source: ALL

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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

Disease

Score _gda

Association Type

Type

Original DB

Sentence supporting the association

PMID

PMID Year

CUI:	C0011615
Disease:	Dermatitis, Atopic

Dermatitis, Atopic

0.020

Biomarker

disease

BEFREE

Taken together, the data demonstrate a critical role of MyD88 in DCs and of IL-33 signaling via ST2 in MC903-induced AD.

28383552

2017

CUI:	C0011615
Disease:	Dermatitis, Atopic

Dermatitis, Atopic

0.020

GeneticVariation

disease

BEFREE

Genetic variations in MyD88 adaptor-like are associated with atopic dermatitis.

21399862

2011