IFT172 Chromosome 2

Intraflagellar transport 172
196 variants 196 Health Risk

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What This Gene Does
This gene encodes a subunit of the intraflagellar transport subcomplex IFT-B. Subcomplexes IFT-A and IFT-B are necessary for ciliary assembly and maintenance. Mutations in this gene have been associated with skeletal ciliopathies, with or without polydactyly, such as such short-rib thoracic dysplasias 1, 9 or 10. [provided by RefSeq, Mar 2014]
Gene Info
Gene Group
"WD repeat domain containing|IFT-B2 complex"
Locus Type
gene with protein product
Location
2p23.3
Ensembl
ENSG00000138002
Associated Conditions (21)
Short-rib thoracic dysplasia 10 with or without polydactyly
Retinitis pigmentosa 71
Bardet-Biedl syndrome 20
IFT172-related disorder
Retinal dystrophy
Inborn genetic diseases
Optic atrophy
Cervical cancer
Familial cancer of breast
Asphyxiating thoracic dystrophy 1
Intellectual disability
Short-rib thoracic dysplasia 10 without polydactyly
Malignant tumor of esophagus
Ovarian serous cystadenocarcinoma
Acute myeloid leukemia
Anophthalmia-microphthalmia syndrome
Bardet-Biedl syndrome
Retinitis pigmentosa
Short-rib thoracic dysplasia 10 with polydactyly
Joubert syndrome
+1 more conditions
Key Variants
RS1011923461
Conflicting classifications of pathogenicity
Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Bardet-Biedl syndrome 20
Health Risk
RS115716101
Conflicting classifications of pathogenicity
Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Bardet-Biedl syndrome 20
Health Risk
RS1238278691
Conflicting classifications of pathogenicity
Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Retinal dystrophy
Health Risk
RS1259207198
Conflicting classifications of pathogenicity
Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Bardet-Biedl syndrome 20
Health Risk
RS1270472738
Conflicting classifications of pathogenicity
Retinal dystrophy, Retinitis pigmentosa 71, Short-rib thoracic dysplasia 10 with or without polydactyly
Health Risk
RS1346517687
Conflicting classifications of pathogenicity
Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Retinal dystrophy
Health Risk
RS137868356
Conflicting classifications of pathogenicity
Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Bardet-Biedl syndrome 20
Health Risk
RS137906877
Conflicting classifications of pathogenicity
Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Inborn genetic diseases
Health Risk
RS138511988
Conflicting classifications of pathogenicity
Retinitis pigmentosa 71, Short-rib thoracic dysplasia 10 with or without polydactyly, IFT172-related disorder
Health Risk
RS138604630
Conflicting classifications of pathogenicity
Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, IFT172-related disorder
Health Risk
RS139229844
Conflicting classifications of pathogenicity
Inborn genetic diseases, Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71
Health Risk
RS139560074
Conflicting classifications of pathogenicity
Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, IFT172-related disorder
Health Risk
All Variants (196)
RSID Category Clinical Significance Conditions
RS1011923461 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Bardet-Biedl syndrome 20
RS115716101 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Bardet-Biedl syndrome 20
RS1238278691 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Retinal dystrophy
RS1259207198 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Bardet-Biedl syndrome 20
RS1270472738 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinitis pigmentosa 71, Short-rib thoracic dysplasia 10 with or without polydactyly
RS1346517687 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Retinal dystrophy
RS137868356 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Bardet-Biedl syndrome 20
RS137906877 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Inborn genetic diseases
RS138511988 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 71, Short-rib thoracic dysplasia 10 with or without polydactyly, IFT172-related disorder
RS138604630 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, IFT172-related disorder
RS139229844 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71
RS139560074 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, IFT172-related disorder
RS140967266 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Inborn genetic diseases
RS141086523 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 71, Short-rib thoracic dysplasia 10 with or without polydactyly, Inborn genetic diseases
RS141098495 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Bardet-Biedl syndrome 20
RS141440865 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 71, Short-rib thoracic dysplasia 10 with or without polydactyly, Bardet-Biedl syndrome 20
RS142409945 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 71, Short-rib thoracic dysplasia 10 with or without polydactyly, Inborn genetic diseases
RS143520040 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, IFT172-related disorder
RS144868723 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Retinal dystrophy
RS145541911 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 without polydactyly, Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71
RS146332658 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Bardet-Biedl syndrome 20
RS146615936 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Bardet-Biedl syndrome 20
RS147303046 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, IFT172-related disorder
RS147394910 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Inborn genetic diseases
RS147744868 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Bardet-Biedl syndrome 20
RS149065251 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, IFT172-related disorder
RS150739354 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Bardet-Biedl syndrome 20
RS150882197 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Short-rib thoracic dysplasia 10 with or without polydactyly
RS184506506 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Retinal dystrophy
RS186020523 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, IFT172-related disorder
RS187728607 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 71, Short-rib thoracic dysplasia 10 with or without polydactyly, Bardet-Biedl syndrome 20
RS189236939 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, IFT172-related disorder
RS190366845 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71
RS200884031 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 71, Short-rib thoracic dysplasia 10 with or without polydactyly, IFT172-related disorder
RS201231401 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Bardet-Biedl syndrome 20
RS201356906 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 71, Short-rib thoracic dysplasia 10 with or without polydactyly, IFT172-related disorder
RS201840472 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 71, Short-rib thoracic dysplasia 10 with or without polydactyly, Bardet-Biedl syndrome 20
RS201921339 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 71, Short-rib thoracic dysplasia 10 with or without polydactyly, Bardet-Biedl syndrome 20
RS202089120 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Bardet-Biedl syndrome 20
RS367930028 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Bardet-Biedl syndrome 20
RS368343162 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 71, Short-rib thoracic dysplasia 10 with or without polydactyly, Inborn genetic diseases
RS368373262 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Bardet-Biedl syndrome 20
RS369191459 Health Risk Conflicting classifications of pathogenicity Anophthalmia-microphthalmia syndrome, Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71
RS369466577 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Inborn genetic diseases
RS370097039 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, Bardet-Biedl syndrome 20
RS370108416 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 71, Short-rib thoracic dysplasia 10 with or without polydactyly, IFT172-related disorder
RS370407165 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 71, Short-rib thoracic dysplasia 10 with or without polydactyly, IFT172-related disorder
RS370903625 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 71, Short-rib thoracic dysplasia 10 with or without polydactyly, Inborn genetic diseases
RS371658303 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 71, Short-rib thoracic dysplasia 10 with or without polydactyly, Bardet-Biedl syndrome 20
RS373382907 Health Risk Conflicting classifications of pathogenicity Short-rib thoracic dysplasia 10 with or without polydactyly, Retinitis pigmentosa 71, IFT172-related disorder
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