Source: INFERRED

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		intraflagellar transport 172 0.582 0.654 3.3E-33
CUI: C4225342
Disease: RETINITIS PIGMENTOSA 71
RETINITIS PIGMENTOSA 71 		disease 0.700 strong 1.000 0 7 2013 2015
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		intraflagellar transport 172 0.582 0.654 3.3E-33
CUI: C3810175
Disease: SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY
SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY 		disease 0.600 strong 1.000 0 6 2013 2013
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		intraflagellar transport 172 0.582 0.654 3.3E-33
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		disease 0.410 None 1.000 0 0 2015 2019
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		intraflagellar transport 172 0.582 0.654 3.3E-33
CUI: C0024507
Disease: Majewski Syndrome
Majewski Syndrome 		disease 0.400 None 0 1
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		intraflagellar transport 172 0.582 0.654 3.3E-33
CUI: C0456909
Disease: Blindness
Blindness 		phenotype 0.110 None 1.000 0 0 2018 2018
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		intraflagellar transport 172 0.582 0.654 3.3E-33
CUI: C1406921
Disease: Thoracic dysplasia
Thoracic dysplasia 		disease 0.110 None 1.000 0 0 2019 2019
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		intraflagellar transport 172 0.582 0.654 3.3E-33
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		disease 0.100 None 1.000 2 10 2010 2013
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		intraflagellar transport 172 0.582 0.654 3.3E-33
CUI: C0018099
Disease: Gout
Gout 		disease 0.100 None 1.000 2 10 2010 2013
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		intraflagellar transport 172 0.582 0.654 3.3E-33
CUI: C1261430
Disease: Fasting blood sugar result
Fasting blood sugar result 		phenotype 0.100 None 1.000 1 1 2012 2012
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		intraflagellar transport 172 0.582 0.654 3.3E-33
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis 		disease 0.100 None 1.000 1 1 2015 2015
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		intraflagellar transport 172 0.582 0.654 3.3E-33
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement 		phenotype 0.100 None 1.000 1 1 2012 2012
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		intraflagellar transport 172 0.582 0.654 3.3E-33
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		intraflagellar transport 172 0.582 0.654 3.3E-33
CUI: C1844562
Disease: Medial flaring of the eyebrow
Medial flaring of the eyebrow 		disease 0.100 None 0 0
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		intraflagellar transport 172 0.582 0.654 3.3E-33
CUI: C1848673
Disease: Hypoplastic feet
Hypoplastic feet 		phenotype 0.100 None 0 0
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		intraflagellar transport 172 0.582 0.654 3.3E-33
CUI: C1848701
Disease: Elevated hepatic transaminase
Elevated hepatic transaminase 		phenotype 0.100 None 0 0
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		intraflagellar transport 172 0.582 0.654 3.3E-33
CUI: C1849211
Disease: Generalized hirsutism
Generalized hirsutism 		phenotype 0.100 None 0 0
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		intraflagellar transport 172 0.582 0.654 3.3E-33
CUI: C1849367
Disease: Nasal bridge wide
Nasal bridge wide 		phenotype 0.100 None 0 0
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		intraflagellar transport 172 0.582 0.654 3.3E-33
CUI: C1854113
Disease: Prominent nasal bridge
Prominent nasal bridge 		phenotype 0.100 None 0 0
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		intraflagellar transport 172 0.582 0.654 3.3E-33
CUI: C1854912
Disease: Short long bone
Short long bone 		phenotype 0.100 None 0 0
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		intraflagellar transport 172 0.582 0.654 3.3E-33
CUI: C0576226
Disease: Short foot
Short foot 		phenotype 0.100 None 0 0
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		intraflagellar transport 172 0.582 0.654 3.3E-33
CUI: C0685840
Disease: Congenital hypoplasia of ovary
Congenital hypoplasia of ovary 		disease 0.100 None 0 0
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		intraflagellar transport 172 0.582 0.654 3.3E-33
CUI: C1842083
Disease: Abnormality of the ribs
Abnormality of the ribs 		disease 0.100 None 0 0
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		intraflagellar transport 172 0.582 0.654 3.3E-33
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril 		phenotype 0.100 None 0 0
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		intraflagellar transport 172 0.582 0.654 3.3E-33
CUI: C0687120
Disease: Nephronophthisis
Nephronophthisis 		disease 0.100 None 0 0
Entrez Id: 26160
Gene Symbol: IFT172
IFT172 		intraflagellar transport 172 0.582 0.654 3.3E-33
CUI: C1260959
Disease: Drusen
Drusen 		disease 0.100 None 0 0