DisGeNET - a database of gene-disease associations

Source: ALL

Gene: IFT80 ×

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:	57560
Gene Symbol:	IFT80

IFT80

intraflagellar transport 80

0.575

0.692

1.4E-19

CUI:	C1970005
Disease:	Asphyxiating Thoracic Dystrophy 2

Asphyxiating Thoracic Dystrophy 2

disease

0.900

strong

1.000

2007

2011

Entrez Id:	57560
Gene Symbol:	IFT80

IFT80

intraflagellar transport 80

0.575

0.692

1.4E-19

CUI:	C0265275
Disease:	Jeune thoracic dystrophy

Jeune thoracic dystrophy

disease

0.610

strong

1.000

2007

Entrez Id:	57560
Gene Symbol:	IFT80

IFT80

intraflagellar transport 80

0.575

0.692

1.4E-19

CUI:	C0432197
Disease:	Short rib-polydactyly syndrome, Verma-Naumoff type

Short rib-polydactyly syndrome, Verma-Naumoff type

disease

0.500

None

1.000

2011

2012

Entrez Id:	57560
Gene Symbol:	IFT80

IFT80

intraflagellar transport 80

0.575

0.692

1.4E-19

CUI:	C0152427
Disease:	Polydactyly

Polydactyly

disease

0.500

None

1.000

2007

Entrez Id:	57560
Gene Symbol:	IFT80

IFT80

intraflagellar transport 80

0.575

0.692

1.4E-19

CUI:	C0432198
Disease:	Short rib-polydactyly syndrome, Beemer type

Short rib-polydactyly syndrome, Beemer type

disease

0.400

None

1.000

2019

Entrez Id:	57560
Gene Symbol:	IFT80

IFT80

intraflagellar transport 80

0.575

0.692

1.4E-19

CUI:	C0035229
Disease:	Respiratory Insufficiency

Respiratory Insufficiency

phenotype

0.400

None

1.000

2007

Entrez Id:	57560
Gene Symbol:	IFT80

IFT80

intraflagellar transport 80

0.575

0.692

1.4E-19

CUI:	C4277690
Disease:	Ciliopathies

Ciliopathies

disease

0.320

None

1.000

2018

2019

Entrez Id:	57560
Gene Symbol:	IFT80

IFT80

intraflagellar transport 80

0.575

0.692

1.4E-19

CUI:	C0022679
Disease:	Cystic kidney

Cystic kidney

disease

0.310

None

1.000

2007

Entrez Id:	57560
Gene Symbol:	IFT80

IFT80

intraflagellar transport 80

0.575

0.692

1.4E-19

CUI:	C0035304
Disease:	Retinal Degeneration

Retinal Degeneration

phenotype

0.300

None

1.000

2007

Entrez Id:	57560
Gene Symbol:	IFT80

IFT80

intraflagellar transport 80

0.575

0.692

1.4E-19

CUI:	C0039978
Disease:	Thoracic Diseases

Thoracic Diseases

group

0.300

None

1.000

2007

Entrez Id:	57560
Gene Symbol:	IFT80

IFT80

intraflagellar transport 80

0.575

0.692

1.4E-19

CUI:	C0235063
Disease:	Respiratory Depression

Respiratory Depression

phenotype

0.300

None

1.000

2007

Entrez Id:	57560
Gene Symbol:	IFT80

IFT80

intraflagellar transport 80

0.575

0.692

1.4E-19

CUI:	C1691228
Disease:	Cystic Kidney Diseases

Cystic Kidney Diseases

group

0.300

None

1.000

2007

Entrez Id:	57560
Gene Symbol:	IFT80

IFT80

intraflagellar transport 80

0.575

0.692

1.4E-19

CUI:	C0004044
Disease:	Asphyxia

Asphyxia

phenotype

0.300

None

1.000

2007

Entrez Id:	57560
Gene Symbol:	IFT80

IFT80

intraflagellar transport 80

0.575

0.692

1.4E-19

CUI:	C1145670
Disease:	Respiratory Failure

Respiratory Failure

disease

0.300

None

1.000

2007

Entrez Id:	57560
Gene Symbol:	IFT80

IFT80

intraflagellar transport 80

0.575

0.692

1.4E-19

CUI:	C0005941
Disease:	Bone Diseases, Developmental

Bone Diseases, Developmental

group

0.300

None

1.000

2007

Entrez Id:	57560
Gene Symbol:	IFT80

IFT80

intraflagellar transport 80

0.575

0.692

1.4E-19

CUI:	C1879645
Disease:	Adverse Event by CTCAE Category

Adverse Event by CTCAE Category

phenotype

0.300

moderate

Entrez Id:	57560
Gene Symbol:	IFT80

IFT80

intraflagellar transport 80

0.575

0.692

1.4E-19

CUI:	C0878659
Disease:	Disproportionate short stature

Disproportionate short stature

phenotype

0.300

None

Entrez Id:	57560
Gene Symbol:	IFT80

IFT80

intraflagellar transport 80

0.575

0.692

1.4E-19

CUI:	C0337443
Disease:	Sodium measurement

Sodium measurement

phenotype

0.300

moderate

Entrez Id:	57560
Gene Symbol:	IFT80

IFT80

intraflagellar transport 80

0.575

0.692

1.4E-19

CUI:	C2910340
Disease:	Asphyxiating thoracic dysplasia [Jeune]

Asphyxiating thoracic dysplasia [Jeune]

disease

0.200

None

1.000

2011

Entrez Id:	57560
Gene Symbol:	IFT80

IFT80

intraflagellar transport 80

0.575

0.692

1.4E-19

CUI:	C0432195
Disease:	Short rib dysplasia

Short rib dysplasia

disease

0.200

None

1.000

2011

Entrez Id:	57560
Gene Symbol:	IFT80

IFT80

intraflagellar transport 80

0.575

0.692

1.4E-19

CUI:	C0036069
Disease:	Saldino-Noonan Syndrome

Saldino-Noonan Syndrome

disease

0.200

None

1.000

2011

Entrez Id:	57560
Gene Symbol:	IFT80

IFT80

intraflagellar transport 80

0.575

0.692

1.4E-19

CUI:	C0202117
Disease:	Low density lipoprotein cholesterol measurement

Low density lipoprotein cholesterol measurement

phenotype

0.100

None

1.000

2018

Entrez Id:	57560
Gene Symbol:	IFT80

IFT80

intraflagellar transport 80

0.575

0.692

1.4E-19

CUI:	C0149745
Disease:	Oral Ulcer

Oral Ulcer

disease

0.100

None

1.000

2019

Entrez Id:	57560
Gene Symbol:	IFT80

IFT80

intraflagellar transport 80

0.575

0.692

1.4E-19

CUI:	C0426790
Disease:	Narrow thorax

Narrow thorax

phenotype

0.100

None

Entrez Id:	57560
Gene Symbol:	IFT80

IFT80

intraflagellar transport 80

0.575

0.692

1.4E-19

CUI:	C0426789
Disease:	Short thorax

Short thorax

phenotype

0.100

None