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
RS749563050 Health Risk Likely pathogenic Saldino-Mainzer syndrome, Retinitis pigmentosa 80, Saldino-Mainzer syndrome
RS772603273 Health Risk Likely pathogenic Retinitis pigmentosa 80, Saldino-Mainzer syndrome, Retinitis pigmentosa 80
RS773555716 Health Risk Likely pathogenic
RS775682083 Health Risk Likely pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS780965515 Health Risk Likely pathogenic Retinitis pigmentosa, Renal cyst, Saldino-Mainzer syndrome
RS1166261279 Health Risk Pathogenic Saldino-Mainzer syndrome, Retinitis pigmentosa 80, Renal cyst
RS1221627009 Health Risk Pathogenic Saldino-Mainzer syndrome, Retinal dystrophy, Retinitis pigmentosa 80
RS1229896671 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS1253188873 Health Risk Pathogenic IFT140-related disorder, Renal cyst, Retinitis pigmentosa
RS1263308663 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS1404356337 Health Risk Pathogenic IFT140-related disorder, Renal cyst, IFT140-related disorder
RS1415763185 Health Risk Pathogenic Saldino-Mainzer syndrome, Retinitis pigmentosa 80, Saldino-Mainzer syndrome
RS1417500285 Health Risk Pathogenic Saldino-Mainzer syndrome, Cranioectodermal dysplasia, Saldino-Mainzer syndrome
RS1424099914 Health Risk Pathogenic Saldino-Mainzer syndrome, IFT140-related disorder, Saldino-Mainzer syndrome
RS1555474009 Health Risk Pathogenic Retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene, Retinitis pigmentosa 80, Retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene
RS1555486629 Health Risk Pathogenic Saldino-Mainzer syndrome, Retinitis pigmentosa 80, Saldino-Mainzer syndrome
RS1555487977 Health Risk Pathogenic Retinitis pigmentosa 80, Retinitis pigmentosa 80
RS1555491448 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS1567328510 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS1567330535 Health Risk Pathogenic Saldino-Mainzer syndrome, IFT140-related disorder, Saldino-Mainzer syndrome
RS1567413573 Health Risk Pathogenic Renal cyst, Renal cyst
RS2035218747 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2035852852 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2040631802 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2141144931 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2141145188 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2141147087 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2141148172 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2141172134 Health Risk Pathogenic Retinal dystrophy, Saldino-Mainzer syndrome, Retinal dystrophy
RS2141541431 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2141570994 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2141634877 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2141800223 Health Risk Pathogenic Retinitis pigmentosa 80, Cystic renal disease, Saldino-Mainzer syndrome
RS2141882563 Health Risk Pathogenic Retinitis pigmentosa 80, Retinitis pigmentosa 80
RS2142100542 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2506102659 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2507089875 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2507758369 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2507833751 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2507868188 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2508077781 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2508572306 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS2508572820 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS372746686 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS376586707 Health Risk Pathogenic Saldino-Mainzer syndrome, Retinitis pigmentosa 80, Retinal dystrophy
RS387907192 Health Risk Pathogenic Saldino-Mainzer syndrome, Retinitis pigmentosa 80, Saldino-Mainzer syndrome
RS387907193 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS431905506 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS431905520 Health Risk Pathogenic Saldino-Mainzer syndrome, Saldino-Mainzer syndrome
RS431905522 Health Risk Pathogenic Saldino-Mainzer syndrome, Retinitis pigmentosa 80, Renal cyst
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