TCTN1 (tectonic family member 1)

2015-03-01  

Identity

HGNC
LOCATION
12q24.11
LOCUSID
ALIAS
JBTS13,TECT1
FUSION GENES

Other Information

Locus ID:

NCBI: 79600
MIM: 609863
HGNC: 26113
Ensembl: ENSG00000204852

Variants:

dbSNP: 79600
ClinVar: 79600
TCGA: ENSG00000204852
COSMIC: TCTN1

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000204852ENST00000377654A0A0A0MRU7
ENSG00000204852ENST00000397655Q2MV58
ENSG00000204852ENST00000397656J3KPW2
ENSG00000204852ENST00000397659Q2MV58
ENSG00000204852ENST00000464809E9PIB8
ENSG00000204852ENST00000471804S4R339
ENSG00000204852ENST00000478122E9PIB8
ENSG00000204852ENST00000480648E9PNE4
ENSG00000204852ENST00000481720S4R3G2
ENSG00000204852ENST00000490514E9PR69
ENSG00000204852ENST00000495659E9PIB8
ENSG00000204852ENST00000498072S4R3M8
ENSG00000204852ENST00000546643S4R2Y1
ENSG00000204852ENST00000547461F8VSB8
ENSG00000204852ENST00000549123F8VQ12
ENSG00000204852ENST00000550703B4DIB9
ENSG00000204852ENST00000551590Q2MV58
ENSG00000204852ENST00000552318S4R2Y1
ENSG00000204852ENST00000614115A0A087X1J4

Expression (GTEx)

0
5
10
15
20
25
30
35
40

Pathways

PathwaySourceExternal ID
Organelle biogenesis and maintenanceREACTOMER-HSA-1852241
Cilium AssemblyREACTOMER-HSA-5617833
Anchoring of the basal body to the plasma membraneREACTOMER-HSA-5620912

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
217253072011A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition.274
253040312014Expression and prognostic significance of TCTN1 in human glioblastoma.6
268448472016Tectonic 1 Is a Key Regulator of Cell Proliferation in Pancreatic Cancer.5
263107862015Tectonic‑1 contributes to the growth and migration of prostate cancer cells in vitro.4
281231722017Knockdown of TCTN1 Strongly Decreases Growth of Human Colon Cancer Cells.4
257370232015Lentivirus-Mediated Knockdown of TCTN1 Inhibits Glioma Cell Proliferation.3
286318932017Expanding the allelic disorders linked to TCTN1 to include Varadi syndrome (Orofaciodigital syndrome type VI).1
313029112019[Diagnosis of two cases from one family with Joubert syndrome caused by novel mutations of TCTN1 gene by whole exome sequencing].0

Citation

Dessen P

TCTN1 (tectonic family member 1)

Atlas Genet Cytogenet Oncol Haematol. 2015-03-01

Online version: http://atlasgeneticsoncology.org/gene/55624/tctn1