TCTN3

TCTN3
Identifiers
AliasesTCTN3, C10orf61, JBTS18, OFD4, TECT3, tectonic family member 3
External IDsMGI: 1914840 HomoloGene: 9221 GeneCards: TCTN3
Gene location (Human)
Chr.Chromosome 10 (human)[1]
Band10q24.1Start95,663,396 bp[1]
End95,694,143 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

26123

67590

Ensembl

ENSG00000119977

ENSMUSG00000025008

UniProt

Q6NUS6

Q8R2Q6

RefSeq (mRNA)

NM_001143973
NM_015631

NM_026260
NM_001365072

RefSeq (protein)

NP_001137445
NP_056446

NP_080536
NP_001352001

Location (UCSC)Chr 10: 95.66 – 95.69 MbChr 19: 40.6 – 40.61 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Tectonic family member 3 is a protein in humans that is encoded by the TCTN3 gene. [5]

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].

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000119977 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000025008 - Ensembl, May 2017
  3. "Human PubMed Reference:".
  4. "Mouse PubMed Reference:".
  5. "Entrez Gene: Tectonic family member 3". Retrieved 2012-12-22.

Further reading


This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.