TCTN1 Chromosome 12

Tectonic family member 1
60 variants 60 Health Risk

Upload your DNA to see your personal genotypes for variants in TCTN1.

What This Gene Does
This gene encodes a member of a family of secreted and transmembrane proteins. The orthologous gene in mouse functions downstream of smoothened and rab23 to modulate hedgehog signal transduction. This protein is a component of the tectonic-like complex, which forms a barrier between the ciliary axoneme and the basal body. A mutation in this gene was found in a family with Joubert syndrome-13. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]
Gene Info
Gene Group
"Tectonic proteins|MKS complex"
Locus Type
gene with protein product
Location
12q24.11
Ensembl
ENSG00000204852
Associated Conditions (12)
Joubert syndrome 13
Meckel-Gruber syndrome
Joubert syndrome
Inborn genetic diseases
TCTN1-related disorder
Developmental disorder
Joubert syndrome and related disorders
Malignant tumor of urinary bladder
Clear cell carcinoma of kidney
Global developmental delay
Typical Joubert syndrome MRI findings
Lung cancer
Key Variants
RS118057448
Conflicting classifications of pathogenicity
Joubert syndrome 13, Meckel-Gruber syndrome, Joubert syndrome
Health Risk
RS1415245710
Conflicting classifications of pathogenicity
Meckel-Gruber syndrome, Joubert syndrome, Inborn genetic diseases
Health Risk
RS145478892
Conflicting classifications of pathogenicity
Joubert syndrome 13, Joubert syndrome, Meckel-Gruber syndrome
Health Risk
RS145970332
Conflicting classifications of pathogenicity
Joubert syndrome 13, Meckel-Gruber syndrome, Joubert syndrome
Health Risk
RS188817098
Conflicting classifications of pathogenicity
Joubert syndrome, Meckel-Gruber syndrome, Joubert syndrome 13
Health Risk
RS199529768
Conflicting classifications of pathogenicity
Joubert syndrome 13, Meckel-Gruber syndrome, Joubert syndrome
Health Risk
RS201894544
Conflicting classifications of pathogenicity
Joubert syndrome, Meckel-Gruber syndrome, Joubert syndrome 13
Health Risk
RS368907353
Conflicting classifications of pathogenicity
Joubert syndrome, Meckel-Gruber syndrome, TCTN1-related disorder
Health Risk
RS370336923
Conflicting classifications of pathogenicity
Joubert syndrome, Meckel-Gruber syndrome, Joubert syndrome
Health Risk
RS371066430
Conflicting classifications of pathogenicity
Joubert syndrome 13, Meckel-Gruber syndrome, Joubert syndrome
Health Risk
RS371899538
Conflicting classifications of pathogenicity
Meckel-Gruber syndrome, Joubert syndrome, Joubert syndrome 13
Health Risk
RS754017886
Conflicting classifications of pathogenicity
Joubert syndrome, Meckel-Gruber syndrome, Joubert syndrome
Health Risk
All Variants (60)
RSID Category Clinical Significance Conditions
RS118057448 Health Risk Conflicting classifications of pathogenicity Joubert syndrome 13, Meckel-Gruber syndrome, Joubert syndrome
RS1415245710 Health Risk Conflicting classifications of pathogenicity Meckel-Gruber syndrome, Joubert syndrome, Inborn genetic diseases
RS145478892 Health Risk Conflicting classifications of pathogenicity Joubert syndrome 13, Joubert syndrome, Meckel-Gruber syndrome
RS145970332 Health Risk Conflicting classifications of pathogenicity Joubert syndrome 13, Meckel-Gruber syndrome, Joubert syndrome
RS188817098 Health Risk Conflicting classifications of pathogenicity Joubert syndrome, Meckel-Gruber syndrome, Joubert syndrome 13
RS199529768 Health Risk Conflicting classifications of pathogenicity Joubert syndrome 13, Meckel-Gruber syndrome, Joubert syndrome
RS201894544 Health Risk Conflicting classifications of pathogenicity Joubert syndrome, Meckel-Gruber syndrome, Joubert syndrome 13
RS368907353 Health Risk Conflicting classifications of pathogenicity Joubert syndrome, Meckel-Gruber syndrome, TCTN1-related disorder
RS370336923 Health Risk Conflicting classifications of pathogenicity Joubert syndrome, Meckel-Gruber syndrome, Joubert syndrome
RS371066430 Health Risk Conflicting classifications of pathogenicity Joubert syndrome 13, Meckel-Gruber syndrome, Joubert syndrome
RS371899538 Health Risk Conflicting classifications of pathogenicity Meckel-Gruber syndrome, Joubert syndrome, Joubert syndrome 13
RS754017886 Health Risk Conflicting classifications of pathogenicity Joubert syndrome, Meckel-Gruber syndrome, Joubert syndrome
RS762612208 Health Risk Conflicting classifications of pathogenicity Joubert syndrome 13, Joubert syndrome 13
RS762957362 Health Risk Conflicting classifications of pathogenicity Joubert syndrome, Meckel-Gruber syndrome, Joubert syndrome
RS765199264 Health Risk Conflicting classifications of pathogenicity Joubert syndrome, Meckel-Gruber syndrome, Developmental disorder
RS797046038 Health Risk Conflicting classifications of pathogenicity Joubert syndrome, Meckel-Gruber syndrome, Inborn genetic diseases
RS1165243207 Health Risk Likely pathogenic Joubert syndrome 13, Joubert syndrome, Meckel-Gruber syndrome
RS1303964272 Health Risk Likely pathogenic Joubert syndrome, Meckel-Gruber syndrome, Joubert syndrome
RS1307879089 Health Risk Likely pathogenic
RS1475200635 Health Risk Likely pathogenic Joubert syndrome, Meckel-Gruber syndrome, Joubert syndrome
RS1566003392 Health Risk Likely pathogenic Joubert syndrome and related disorders, Joubert syndrome and related disorders
RS200241085 Health Risk Likely pathogenic Meckel-Gruber syndrome, Joubert syndrome, Joubert syndrome 13
RS200863258 Health Risk Likely pathogenic Joubert syndrome and related disorders, Meckel-Gruber syndrome, Joubert syndrome
RS2066300090 Health Risk Likely pathogenic Meckel-Gruber syndrome, Joubert syndrome, Meckel-Gruber syndrome
RS2066444872 Health Risk Likely pathogenic Joubert syndrome, Meckel-Gruber syndrome, Joubert syndrome
RS2067211703 Health Risk Likely pathogenic Joubert syndrome and related disorders, Meckel-Gruber syndrome, Joubert syndrome
RS2136006298 Health Risk Likely pathogenic Joubert syndrome 13, Joubert syndrome 13
RS2136045792 Health Risk Likely pathogenic TCTN1-related disorder, TCTN1-related disorder
RS2548884767 Health Risk Likely pathogenic TCTN1-related disorder, TCTN1-related disorder
RS2548929536 Health Risk Likely pathogenic Joubert syndrome, Meckel-Gruber syndrome, Joubert syndrome
RS749481321 Health Risk Likely pathogenic Joubert syndrome and related disorders, Joubert syndrome and related disorders
RS756402483 Health Risk Likely pathogenic Joubert syndrome, Meckel-Gruber syndrome, Joubert syndrome
RS760922371 Health Risk Likely pathogenic Joubert syndrome 13, Clear cell carcinoma of kidney, Joubert syndrome 13
RS769457761 Health Risk Likely pathogenic Joubert syndrome, Meckel-Gruber syndrome, Joubert syndrome
RS886044606 Health Risk Likely pathogenic
RS1275375836 Health Risk Pathogenic Joubert syndrome 13, Joubert syndrome, Meckel-Gruber syndrome
RS1353535488 Health Risk Pathogenic Meckel-Gruber syndrome, Joubert syndrome, Meckel-Gruber syndrome
RS1420275854 Health Risk Pathogenic Meckel-Gruber syndrome, Joubert syndrome, Meckel-Gruber syndrome
RS1456431690 Health Risk Pathogenic Joubert syndrome, Meckel-Gruber syndrome, Joubert syndrome
RS1593376626 Health Risk Pathogenic Joubert syndrome 13, Joubert syndrome 13
RS2065847886 Health Risk Pathogenic Joubert syndrome, Meckel-Gruber syndrome, Joubert syndrome
RS2066579666 Health Risk Pathogenic Meckel-Gruber syndrome, Joubert syndrome, Meckel-Gruber syndrome
RS2066879614 Health Risk Pathogenic Meckel-Gruber syndrome, Joubert syndrome, Meckel-Gruber syndrome
RS2136171586 Health Risk Pathogenic Joubert syndrome 13, Joubert syndrome, Meckel-Gruber syndrome
RS2136172776 Health Risk Pathogenic Joubert syndrome, Meckel-Gruber syndrome, Joubert syndrome
RS2136195903 Health Risk Pathogenic Joubert syndrome, Meckel-Gruber syndrome, Joubert syndrome
RS2548754386 Health Risk Pathogenic Joubert syndrome, Meckel-Gruber syndrome, Joubert syndrome
RS2548796089 Health Risk Pathogenic Joubert syndrome, Meckel-Gruber syndrome, Joubert syndrome
RS2548832773 Health Risk Pathogenic Joubert syndrome 13, Joubert syndrome 13
RS2548901989 Health Risk Pathogenic Joubert syndrome, Meckel-Gruber syndrome, Joubert syndrome
Sign Up to Analyze Your DNA Log In