DisGeNET - a database of gene-disease associations

HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA, C3554021

Gene: SEMA3A ×

Source: UNIPROT ×

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

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs137871935

SEMA3A

0.700

GeneticVariation

UNIPROT

The prevalence of CHD7 missense versus truncating mutations is higher in patients with Kallmann syndrome than in typical CHARGE patients.

25077900

2014

dbSNP:

rs139295139

SEMA3A

0.700

GeneticVariation

UNIPROT

The prevalence of CHD7 missense versus truncating mutations is higher in patients with Kallmann syndrome than in typical CHARGE patients.

25077900

2014

dbSNP:

rs318240751

SEMA3A

0.700

GeneticVariation

UNIPROT

The prevalence of CHD7 missense versus truncating mutations is higher in patients with Kallmann syndrome than in typical CHARGE patients.

25077900

2014

dbSNP:

rs318240752

SEMA3A

0.700

GeneticVariation

UNIPROT

The prevalence of CHD7 missense versus truncating mutations is higher in patients with Kallmann syndrome than in typical CHARGE patients.

25077900

2014

dbSNP:

rs318240753

SEMA3A

0.700

GeneticVariation

UNIPROT

The prevalence of CHD7 missense versus truncating mutations is higher in patients with Kallmann syndrome than in typical CHARGE patients.

25077900

2014

dbSNP:

rs36026860

SEMA3A

0.700

GeneticVariation

UNIPROT

The prevalence of CHD7 missense versus truncating mutations is higher in patients with Kallmann syndrome than in typical CHARGE patients.

25077900

2014

dbSNP:

rs748219597

SEMA3A

0.700

GeneticVariation

UNIPROT

The prevalence of CHD7 missense versus truncating mutations is higher in patients with Kallmann syndrome than in typical CHARGE patients.

25077900

2014

dbSNP:

rs761486957

SEMA3A

0.700

GeneticVariation

UNIPROT

The prevalence of CHD7 missense versus truncating mutations is higher in patients with Kallmann syndrome than in typical CHARGE patients.

25077900

2014

dbSNP:

rs137871935

SEMA3A

0.700

GeneticVariation

UNIPROT

SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development.

22416012

2012

dbSNP:

rs137871935

SEMA3A

0.700

GeneticVariation

UNIPROT

SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome.

22927827

2012

dbSNP:

rs139295139

SEMA3A

0.700

GeneticVariation

UNIPROT

SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome.

22927827

2012

dbSNP:

rs139295139

SEMA3A

0.700

GeneticVariation

UNIPROT

SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development.

22416012

2012

dbSNP:

rs318240751

SEMA3A

0.700

GeneticVariation

UNIPROT

SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome.

22927827

2012

dbSNP:

rs318240751

SEMA3A

0.700

GeneticVariation

UNIPROT

SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development.

22416012

2012

dbSNP:

rs318240752

SEMA3A

0.700

GeneticVariation

UNIPROT

SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome.

22927827

2012

dbSNP:

rs318240752

SEMA3A

0.700

GeneticVariation

UNIPROT

SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development.

22416012

2012

dbSNP:

rs318240753

SEMA3A

0.700

GeneticVariation

UNIPROT

SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome.

22927827

2012

dbSNP:

rs318240753

SEMA3A

0.700

GeneticVariation

UNIPROT

SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development.

22416012

2012

dbSNP:

rs36026860

SEMA3A

0.700

GeneticVariation

UNIPROT

SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome.

22927827

2012

dbSNP:

rs36026860

SEMA3A

0.700

GeneticVariation

UNIPROT

SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development.

22416012

2012

dbSNP:

rs748219597

SEMA3A

0.700

GeneticVariation

UNIPROT

SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development.

22416012

2012

dbSNP:

rs748219597

SEMA3A

0.700

GeneticVariation

UNIPROT

SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome.

22927827

2012

dbSNP:

rs761486957

SEMA3A

0.700

GeneticVariation

UNIPROT

SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development.

22416012

2012

dbSNP:

rs761486957

SEMA3A

0.700

GeneticVariation

UNIPROT

SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome.

22927827

2012

dbSNP:

rs199979628

SEMA3A

0.700

GeneticVariation

UNIPROT