DisGeNET - a database of gene-disease associations

Source: HPO

Gene: RPS6KA3 ×

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:	6197
Gene Symbol:	RPS6KA3

RPS6KA3

CUI:	C3714756
Disease:	Intellectual Disability

Intellectual Disability

0.170

Biomarker

HPO

Entrez Id:	6197
Gene Symbol:	RPS6KA3

RPS6KA3

CUI:	C0011581
Disease:	Depressive disorder

Depressive disorder

0.110

Biomarker

HPO

Entrez Id:	6197
Gene Symbol:	RPS6KA3

RPS6KA3

CUI:	C0013336
Disease:	Dwarfism

Dwarfism

0.110

Biomarker

HPO

Entrez Id:	6197
Gene Symbol:	RPS6KA3

RPS6KA3

CUI:	C0033975
Disease:	Psychotic Disorders

Psychotic Disorders

0.110

Biomarker

HPO

Entrez Id:	6197
Gene Symbol:	RPS6KA3

RPS6KA3

CUI:	C0036572
Disease:	Seizures

Seizures

0.110

Biomarker

HPO

Entrez Id:	6197
Gene Symbol:	RPS6KA3

RPS6KA3

CUI:	C0036857
Disease:	Severe intellectual disability

Severe intellectual disability

0.110

Biomarker

HPO

Entrez Id:	6197
Gene Symbol:	RPS6KA3

RPS6KA3

CUI:	C0005586
Disease:	Bipolar Disorder

Bipolar Disorder

0.100

Biomarker

HPO

Entrez Id:	6197
Gene Symbol:	RPS6KA3

RPS6KA3

CUI:	C0010495
Disease:	Cutis Laxa

Cutis Laxa

0.100

Biomarker

HPO

Entrez Id:	6197
Gene Symbol:	RPS6KA3

RPS6KA3

CUI:	C0013132
Disease:	Drooling

Drooling

0.100

Biomarker

HPO

Entrez Id:	6197
Gene Symbol:	RPS6KA3

RPS6KA3

CUI:	C0015469
Disease:	Facial paralysis

Facial paralysis

0.100

Biomarker

HPO

Entrez Id:	6197
Gene Symbol:	RPS6KA3

RPS6KA3

CUI:	C0016202
Disease:	Flatfoot

Flatfoot

0.100

Biomarker

HPO

Entrez Id:	6197
Gene Symbol:	RPS6KA3

RPS6KA3

CUI:	C0016842
Disease:	Congenital pectus excavatum

Congenital pectus excavatum

0.100

Biomarker

HPO

Entrez Id:	6197
Gene Symbol:	RPS6KA3

RPS6KA3

CUI:	C0018784
Disease:	Sensorineural Hearing Loss (disorder)

Sensorineural Hearing Loss (disorder)

0.100

Biomarker

HPO

Entrez Id:	6197
Gene Symbol:	RPS6KA3

RPS6KA3

CUI:	C0019294
Disease:	Hernia, Inguinal

Hernia, Inguinal

0.100

Biomarker

HPO

Entrez Id:	6197
Gene Symbol:	RPS6KA3

RPS6KA3

CUI:	C0020534
Disease:	Orbital separation excessive

Orbital separation excessive

0.100

Biomarker

HPO

Entrez Id:	6197
Gene Symbol:	RPS6KA3

RPS6KA3

CUI:	C0020608
Disease:	Hypodontia

Hypodontia

0.100

Biomarker

HPO

Entrez Id:	6197
Gene Symbol:	RPS6KA3

RPS6KA3

CUI:	C0022821
Disease:	Kyphosis deformity of spine

Kyphosis deformity of spine

0.100

Biomarker

HPO

Entrez Id:	6197
Gene Symbol:	RPS6KA3

RPS6KA3

CUI:	C0024433
Disease:	Macrostomia

Macrostomia

0.100

Biomarker

HPO

Entrez Id:	6197
Gene Symbol:	RPS6KA3

RPS6KA3

CUI:	C0024636
Disease:	Malocclusion

Malocclusion

0.100

Biomarker

HPO

Entrez Id:	6197
Gene Symbol:	RPS6KA3

RPS6KA3

CUI:	C0025037
Disease:	Meckel Diverticulum

Meckel Diverticulum

0.100

Biomarker

HPO

Entrez Id:	6197
Gene Symbol:	RPS6KA3

RPS6KA3

CUI:	C0025958
Disease:	Microcephaly

Microcephaly

0.100

Biomarker

HPO

Entrez Id:	6197
Gene Symbol:	RPS6KA3

RPS6KA3

CUI:	C0026266
Disease:	Mitral Valve Insufficiency

Mitral Valve Insufficiency

0.100

Biomarker

HPO

Entrez Id:	6197
Gene Symbol:	RPS6KA3

RPS6KA3

CUI:	C0026351
Disease:	Moderate intellectual disability

Moderate intellectual disability

0.100

Biomarker

HPO

Entrez Id:	6197
Gene Symbol:	RPS6KA3

RPS6KA3

CUI:	C0026827
Disease:	Muscle hypotonia

Muscle hypotonia

0.100

Biomarker

HPO

Entrez Id:	6197
Gene Symbol:	RPS6KA3

RPS6KA3

CUI:	C0028754
Disease:	Obesity

Obesity

0.100

Biomarker

HPO