Homo sapiens Gene: TCTN3
Summary
InnateDB Gene IDBG-83525.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol TCTN3
Gene Name tectonic family member 3
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000119977
Encoded Proteins
tectonic family member 3
tectonic family member 3
tectonic family member 3
tectonic family member 3
tectonic family member 3
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a member of the tectonic gene family which functions in Hedgehog signal transduction and development of the neural tube. Mutations in this gene have been associated with Orofaciodigital Syndrome IV and Joubert Syndrom 18. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2012]
Gene Information
Type Protein coding
Genomic Location Chromosome 10:95663396-95694143
Strand Reverse strand
Band q24.1
Transcripts
ENST00000371217 ENSP00000360261
ENST00000265993 ENSP00000265993
ENST00000371209 ENSP00000360253
ENST00000430368 ENSP00000387567
ENST00000497399
ENST00000478245
ENST00000614499 ENSP00000483364
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
Biological Process
GO:0006915 apoptotic process
GO:0007224 smoothened signaling pathway
GO:0060271 cilium morphogenesis
Cellular Component
GO:0016021 integral component of membrane
GO:0070062 extracellular vesicular exosome
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.438991 Hs.596998
RefSeq NM_001143973 NM_015631
HUGO
OMIM
CCDS CCDS31258 CCDS44461
HPRD 12582
IMGT
EMBL
GenPept
RNA Seq Atlas