DisGeNET - a database of gene-disease associations

Source: INFERRED

Gene: PEX6 ×

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

Gene Full Name

DSI _g

DPI _g

pLI

Disease

Type

Score _gda

EL_gda

EI _gda

N.PMIDs

N.SNPs _gda

First Ref.

LastRef.

Entrez Id:	5190
Gene Symbol:	PEX6

PEX6

peroxisomal biogenesis factor 6

0.547

0.731

6.3E-06

CUI:	C3553936
Disease:	PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER)

PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER)

disease

0.700

None

1.000

1996

2016

Entrez Id:	5190
Gene Symbol:	PEX6

PEX6

peroxisomal biogenesis factor 6

0.547

0.731

6.3E-06

CUI:	C1832200
Disease:	Peroxisome biogenesis disorders

Peroxisome biogenesis disorders

group

0.680

strong

1.000

1996

2019

Entrez Id:	5190
Gene Symbol:	PEX6

PEX6

peroxisomal biogenesis factor 6

0.547

0.731

6.3E-06

CUI:	C3553937
Disease:	PEROXISOME BIOGENESIS DISORDER 4B

PEROXISOME BIOGENESIS DISORDER 4B

disease

0.600

None

1.000

1996

2016

Entrez Id:	5190
Gene Symbol:	PEX6

PEX6

peroxisomal biogenesis factor 6

0.547

0.731

6.3E-06

CUI:	C4225267
Disease:	HEIMLER SYNDROME 2

HEIMLER SYNDROME 2

disease

0.600

strong

1.000

2002

2016

Entrez Id:	5190
Gene Symbol:	PEX6

PEX6

peroxisomal biogenesis factor 6

0.547

0.731

6.3E-06

CUI:	C4721541
Disease:	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)

PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)

disease

0.400

strong

Entrez Id:	5190
Gene Symbol:	PEX6

PEX6

peroxisomal biogenesis factor 6

0.547

0.731

6.3E-06

CUI:	C3714756
Disease:	Intellectual Disability

Intellectual Disability

group

0.400

None

1.000

2011

Entrez Id:	5190
Gene Symbol:	PEX6

PEX6

peroxisomal biogenesis factor 6

0.547

0.731

6.3E-06

CUI:	C0025958
Disease:	Microcephaly

Microcephaly

disease

0.110

None

1.000

2016

Entrez Id:	5190
Gene Symbol:	PEX6

PEX6

peroxisomal biogenesis factor 6

0.547

0.731

6.3E-06

CUI:	C0432072
Disease:	Dysmorphic features

Dysmorphic features

disease

0.100

None

1.000

1996

2016

Entrez Id:	5190
Gene Symbol:	PEX6

PEX6

peroxisomal biogenesis factor 6

0.547

0.731

6.3E-06

CUI:	C0026827
Disease:	Muscle hypotonia

Muscle hypotonia

phenotype

0.100

None

1.000

1996

2016

Entrez Id:	5190
Gene Symbol:	PEX6

PEX6

peroxisomal biogenesis factor 6

0.547

0.731

6.3E-06

CUI:	C2985280
Disease:	Blood Protein Measurement

Blood Protein Measurement

phenotype

0.100

None

1.000

2018

Entrez Id:	5190
Gene Symbol:	PEX6

PEX6

peroxisomal biogenesis factor 6

0.547

0.731

6.3E-06

CUI:	C0200635
Disease:	Lymphocyte Count measurement

Lymphocyte Count measurement

phenotype

0.100

None

1.000

2012

Entrez Id:	5190
Gene Symbol:	PEX6

PEX6

peroxisomal biogenesis factor 6

0.547

0.731

6.3E-06

CUI:	C1849367
Disease:	Nasal bridge wide

Nasal bridge wide

phenotype

0.100

None

Entrez Id:	5190
Gene Symbol:	PEX6

PEX6

peroxisomal biogenesis factor 6

0.547

0.731

6.3E-06

CUI:	C1849134
Disease:	Impaired vibration sensation in the lower limbs

Impaired vibration sensation in the lower limbs

phenotype

0.100

None

Entrez Id:	5190
Gene Symbol:	PEX6

PEX6

peroxisomal biogenesis factor 6

0.547

0.731

6.3E-06

CUI:	C1849095
Disease:	Cochlear degeneration

Cochlear degeneration

phenotype

0.100

None

Entrez Id:	5190
Gene Symbol:	PEX6

PEX6

peroxisomal biogenesis factor 6

0.547

0.731

6.3E-06

CUI:	C1850573
Disease:	Slender build

Slender build

phenotype

0.100

None

Entrez Id:	5190
Gene Symbol:	PEX6

PEX6

peroxisomal biogenesis factor 6

0.547

0.731

6.3E-06

CUI:	C1843108
Disease:	Short palm

Short palm

phenotype

0.100

None

Entrez Id:	5190
Gene Symbol:	PEX6

PEX6

peroxisomal biogenesis factor 6

0.547

0.731

6.3E-06

CUI:	C1850794
Disease:	Proximal amyotrophy

Proximal amyotrophy

disease

0.100

None

Entrez Id:	5190
Gene Symbol:	PEX6

PEX6

peroxisomal biogenesis factor 6

0.547

0.731

6.3E-06

CUI:	C1849025
Disease:	Oval face

Oval face

phenotype

0.100

None

Entrez Id:	5190
Gene Symbol:	PEX6

PEX6

peroxisomal biogenesis factor 6

0.547

0.731

6.3E-06

CUI:	C1853241
Disease:	Flat face

Flat face

phenotype

0.100

None

Entrez Id:	5190
Gene Symbol:	PEX6

PEX6

peroxisomal biogenesis factor 6

0.547

0.731

6.3E-06

CUI:	C1854114
Disease:	Short nose

Short nose

phenotype

0.100

None

Entrez Id:	5190
Gene Symbol:	PEX6

PEX6

peroxisomal biogenesis factor 6

0.547

0.731

6.3E-06

CUI:	C1861324
Disease:	Short philtrum

Short philtrum

phenotype

0.100

None

Entrez Id:	5190
Gene Symbol:	PEX6

PEX6

peroxisomal biogenesis factor 6

0.547

0.731

6.3E-06

CUI:	C1859126
Disease:	Stippled epiphyses

Stippled epiphyses

phenotype

0.100

None

Entrez Id:	5190
Gene Symbol:	PEX6

PEX6

peroxisomal biogenesis factor 6

0.547

0.731

6.3E-06

CUI:	C1858430
Disease:	Death in infancy

Death in infancy

phenotype

0.100

None

Entrez Id:	5190
Gene Symbol:	PEX6

PEX6

peroxisomal biogenesis factor 6

0.547

0.731

6.3E-06

CUI:	C1858120
Disease:	Generalized hypotonia

Generalized hypotonia

phenotype

0.100

None

Entrez Id:	5190
Gene Symbol:	PEX6

PEX6

peroxisomal biogenesis factor 6

0.547

0.731

6.3E-06

CUI:	C1857790
Disease:	Thoracic scoliosis

Thoracic scoliosis

phenotype

0.100

None