DisGeNET - a database of gene-disease associations

FLRT3, fibronectin leucine rich transmembrane protein 3, 23767

N. diseases: 63; N. variants: 4

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:

rs398124654

Entrez Id:	23767;140733
Gene Symbol:	FLRT3;MACROD2

FLRT3;MACROD2

CUI:	C3808986
Disease:

HYPOGONADOTROPIC HYPOGONADISM 21 WITH OR WITHOUT ANOSMIA

0.800

GeneticVariation

UNIPROT

Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism.

23643382

2013

dbSNP:

rs398124654

Entrez Id:	23767;140733
Gene Symbol:	FLRT3;MACROD2

FLRT3;MACROD2

CUI:	C3808986
Disease:

HYPOGONADOTROPIC HYPOGONADISM 21 WITH OR WITHOUT ANOSMIA

0.800

CausalMutation

CLINVAR

dbSNP:

rs398124651

Entrez Id:	23767;140733
Gene Symbol:	FLRT3;MACROD2

FLRT3;MACROD2

CUI:	C3808986
Disease:

HYPOGONADOTROPIC HYPOGONADISM 21 WITH OR WITHOUT ANOSMIA

0.700

GeneticVariation

UNIPROT

Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism.

23643382

2013

dbSNP:

rs398124652

Entrez Id:	23767;140733
Gene Symbol:	FLRT3;MACROD2

FLRT3;MACROD2

CUI:	C3808986
Disease:

HYPOGONADOTROPIC HYPOGONADISM 21 WITH OR WITHOUT ANOSMIA

0.700

GeneticVariation

UNIPROT

Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism.

23643382

2013

dbSNP:

rs398124653

Entrez Id:	23767;140733
Gene Symbol:	FLRT3;MACROD2

FLRT3;MACROD2

CUI:	C3808986
Disease:

HYPOGONADOTROPIC HYPOGONADISM 21 WITH OR WITHOUT ANOSMIA

0.700

GeneticVariation

UNIPROT

Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism.

23643382

2013

dbSNP:

rs398124651

Entrez Id:	23767;140733
Gene Symbol:	FLRT3;MACROD2

FLRT3;MACROD2

CUI:	C4016902
Disease:

HYPOGONADOTROPIC HYPOGONADISM 21 WITH ANOSMIA, SUSCEPTIBILITY TO

0.700

SusceptibilityMutation

CLINVAR

dbSNP:

rs398124652

Entrez Id:	23767;140733
Gene Symbol:	FLRT3;MACROD2

FLRT3;MACROD2

CUI:	C4016902
Disease:

HYPOGONADOTROPIC HYPOGONADISM 21 WITH ANOSMIA, SUSCEPTIBILITY TO

0.700

SusceptibilityMutation

CLINVAR

dbSNP:

rs398124653

Entrez Id:	23767;140733
Gene Symbol:	FLRT3;MACROD2

FLRT3;MACROD2

CUI:	C4016902
Disease:

HYPOGONADOTROPIC HYPOGONADISM 21 WITH ANOSMIA, SUSCEPTIBILITY TO

0.700

SusceptibilityMutation

CLINVAR