DisGeNET - a database of gene-disease associations

TMEM99, transmembrane protein 99 (putative), 147184

N. diseases: 4; N. variants: 22

Disease: Congenital reticular ichthyosiform erythroderma ×

Source: ALL

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Variant

Gene

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs267607384

Entrez Id:	3858;147184
Gene Symbol:	KRT10;TMEM99

KRT10;TMEM99

CUI:	C3665704
Disease:

Congenital reticular ichthyosiform erythroderma

0.700

CausalMutation

CLINVAR

dbSNP:

rs587776815

Entrez Id:	3858;147184
Gene Symbol:	KRT10;TMEM99

KRT10;TMEM99

CUI:	C3665704
Disease:

Congenital reticular ichthyosiform erythroderma

0.700

CausalMutation

CLINVAR

dbSNP:

rs587776816

Entrez Id:	3858;147184
Gene Symbol:	KRT10;TMEM99

KRT10;TMEM99

CUI:	C3665704
Disease:

Congenital reticular ichthyosiform erythroderma

0.700

CausalMutation

CLINVAR

dbSNP:

rs587776817

Entrez Id:	3858;147184
Gene Symbol:	KRT10;TMEM99

KRT10;TMEM99

CUI:	C3665704
Disease:

Congenital reticular ichthyosiform erythroderma

0.700

CausalMutation

CLINVAR

dbSNP:

rs58852768

Entrez Id:	3858;147184
Gene Symbol:	KRT10;TMEM99

KRT10;TMEM99

CUI:	C3665704
Disease:

Congenital reticular ichthyosiform erythroderma

0.700

CausalMutation

CLINVAR