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Gene : TCTN2 Homo sapiens

Name  ? tectonic family member 2 Cytological Location  12q24.31
Brief Description  tectonic family member 2
Description  This gene encodes a type I membrane protein that belongs to the tectonic family. Studies in mice suggest that this protein may be involved in hedgehog signaling, and essential for ciliogenesis. Mutations in this gene are associated with Meckel syndrome type 8. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]
  • synonyms:
  • MKS8,
  • Meckel syndrome, type 8,
  • OTTHUMG00000168700,
  • chromosome 12 open reading frame 38,
  • TECT2,
  • AK056924,
  • uc001ufp.3,
  • HGNC:25774,
  • JBTS24,
  • TECT2,
  • JBTS24,
  • FLJ12975,
  • MKS8,
  • NM_024809,
  • C12orf38,
  • C12orf38,
  • TCTN2
  • identifiers:
  • 79867,
  • ENSG00000168778,
  • TCTN2

Genome feature

Region: gene ? Length: 37298  
Location: 12:123671108-123708405 Cyto location: 12q24.31

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


2 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



3753 SN Ps

5 Cross References

18 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results