IFT140 Chromosome 16

Intraflagellar transport 140
355 variants 355 Health Risk

Upload your DNA to see your personal genotypes for variants in IFT140.

What This Gene Does
This gene encodes one of the subunits of the intraflagellar transport (IFT) complex A. Intraflagellar transport is involved in the genesis, resorption and signaling of primary cilia. The primary cilium is a microtubule-based sensory organelle at the surface of most quiescent mammalian cells, that receives signals from its environment, such as the flow of fluid, light or odors, and transduces those signals to the nucleus. Loss of the corresponding protein in mouse results in renal cystic disease. [provided by RefSeq, Jun 2012]
Gene Info
Gene Group
"WD repeat domain containing|IFT-A complex"
Locus Type
gene with protein product
Location
16p13.3
Ensembl
ENSG00000187535
Associated Conditions (35)
Saldino-Mainzer syndrome
Inborn genetic diseases
Nephronophthisis
Retinal dystrophy
IFT140-related disorder
Retinitis pigmentosa 80
Ovarian serous cystadenocarcinoma
Cleft palate
Gastric cancer
Familial cancer of breast
Retinitis pigmentosa
Microcephaly
Cranioectodermal dysplasia 5
See cases
Sarcoma
Nonpapillary renal cell carcinoma
Thyroid cancer
nonmedullary
1
Thymoma
+15 more conditions
Key Variants
RS1019259823
Conflicting classifications of pathogenicity
Saldino-Mainzer syndrome, Inborn genetic diseases, Saldino-Mainzer syndrome
Health Risk
RS1049601354
Conflicting classifications of pathogenicity
Saldino-Mainzer syndrome, Inborn genetic diseases, Saldino-Mainzer syndrome
Health Risk
RS1057518064
Conflicting classifications of pathogenicity
Saldino-Mainzer syndrome, Nephronophthisis, Saldino-Mainzer syndrome
Health Risk
RS112545558
Conflicting classifications of pathogenicity
Saldino-Mainzer syndrome, Retinal dystrophy, IFT140-related disorder
Health Risk
RS113216558
Conflicting classifications of pathogenicity
Saldino-Mainzer syndrome, Retinitis pigmentosa 80, Saldino-Mainzer syndrome
Health Risk
RS1276436237
Conflicting classifications of pathogenicity
Saldino-Mainzer syndrome, Inborn genetic diseases, Saldino-Mainzer syndrome
Health Risk
RS1323647622
Conflicting classifications of pathogenicity
Retinal dystrophy, Saldino-Mainzer syndrome, Retinitis pigmentosa 80
Health Risk
RS1330112951
Conflicting classifications of pathogenicity
Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
Health Risk
RS1339640657
Conflicting classifications of pathogenicity
Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
Health Risk
RS1372854875
Conflicting classifications of pathogenicity
Retinal dystrophy, Saldino-Mainzer syndrome, Retinal dystrophy
Health Risk
RS137925718
Conflicting classifications of pathogenicity
Saldino-Mainzer syndrome, IFT140-related disorder, Saldino-Mainzer syndrome
Health Risk
RS138166567
Conflicting classifications of pathogenicity
Saldino-Mainzer syndrome, IFT140-related disorder, Saldino-Mainzer syndrome
Health Risk
All Variants (355)
RSID Category Clinical Significance Conditions
RS778404277 Health Risk Conflicting classifications of pathogenicity Saldino-Mainzer syndrome, Retinitis pigmentosa 80, Saldino-Mainzer syndrome
RS778960409 Health Risk Conflicting classifications of pathogenicity Saldino-Mainzer syndrome, Retinitis pigmentosa 80, Inborn genetic diseases
RS780540683 Health Risk Conflicting classifications of pathogenicity Saldino-Mainzer syndrome, Retinitis pigmentosa 80, Saldino-Mainzer syndrome
RS780666037 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Saldino-Mainzer syndrome, Retinal dystrophy
RS886043802 Health Risk Conflicting classifications of pathogenicity Saldino-Mainzer syndrome, Retinitis pigmentosa 80, Saldino-Mainzer syndrome
RS894474570 Health Risk Conflicting classifications of pathogenicity Saldino-Mainzer syndrome, Retinitis pigmentosa 80, Saldino-Mainzer syndrome
RS900599017 Health Risk Conflicting classifications of pathogenicity Saldino-Mainzer syndrome, Retinitis pigmentosa 80, Saldino-Mainzer syndrome
RS914258252 Health Risk Conflicting classifications of pathogenicity Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS939722027 Health Risk Conflicting classifications of pathogenicity Jeune thoracic dystrophy, Saldino-Mainzer syndrome, Jeune thoracic dystrophy
RS986239975 Health Risk Conflicting classifications of pathogenicity Saldino-Mainzer syndrome, Retinitis pigmentosa 80, Saldino-Mainzer syndrome
RS1085307074 Health Risk Likely pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS1221367358 Health Risk Likely pathogenic Saldino-Mainzer syndrome, IFT140-related disorder, Retinitis pigmentosa
RS145549969 Health Risk Likely pathogenic Retinitis pigmentosa 80, Saldino-Mainzer syndrome, Retinitis pigmentosa 80
RS1489989834 Health Risk Likely pathogenic Saldino-Mainzer syndrome, Retinitis pigmentosa 80, Saldino-Mainzer syndrome
RS1567386464 Health Risk Likely pathogenic Saldino-Mainzer syndrome, Retinitis pigmentosa 80, IFT140-related disorder
RS1567407044 Health Risk Likely pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS1596419766 Health Risk Likely pathogenic Saldino-Mainzer syndrome, Retinitis pigmentosa 80, Saldino-Mainzer syndrome
RS2033706353 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS2033836650 Health Risk Likely pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2034681207 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS2034739931 Health Risk Likely pathogenic Retinal dystrophy, Saldino-Mainzer syndrome, Retinal dystrophy
RS2035236903 Health Risk Likely pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2040683256 Health Risk Likely pathogenic Retinitis pigmentosa 80, Retinitis pigmentosa 80
RS2040685752 Health Risk Likely pathogenic Saldino-Mainzer syndrome, Retinitis pigmentosa 80, Saldino-Mainzer syndrome
RS2141171226 Health Risk Likely pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2141172226 Health Risk Likely pathogenic Saldino-Mainzer syndrome, Retinitis pigmentosa 80, Saldino-Mainzer syndrome
RS2141180025 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS2142041186 Health Risk Likely pathogenic
RS2142099151 Health Risk Likely pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2506064268 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS2506103002 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS2506113603 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS2506115439 Health Risk Likely pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2506115448 Health Risk Likely pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2506121441 Health Risk Likely pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2506136762 Health Risk Likely pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2507094576 Health Risk Likely pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2507094628 Health Risk Likely pathogenic Retinitis pigmentosa 80, Retinitis pigmentosa 80
RS2507641936 Health Risk Likely pathogenic Retinitis pigmentosa 80, Retinitis pigmentosa 80
RS2507642161 Health Risk Likely pathogenic IFT140-related disorder, IFT140-related disorder
RS2507835305 Health Risk Likely pathogenic Retinitis pigmentosa 80, Retinitis pigmentosa 80
RS2507865187 Health Risk Likely pathogenic Retinitis pigmentosa 80, Retinitis pigmentosa 80
RS2507935242 Health Risk Likely pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2508713536 Health Risk Likely pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2508719279 Health Risk Likely pathogenic Retinitis pigmentosa 80, Retinitis pigmentosa 80
RS375910993 Health Risk Likely pathogenic Saldino-Mainzer syndrome, Retinitis pigmentosa 80, Saldino-Mainzer syndrome
RS559371453 Health Risk Likely pathogenic Saldino-Mainzer syndrome, Retinitis pigmentosa 80, Saldino-Mainzer syndrome
RS574450870 Health Risk Likely pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS748523056 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS749330035 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
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