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

TCTN3
Identifiers
AliasesTCTN3, C10orf61, JBTS18, OFD4, TECT3, tectonic family member 3
External IDsOMIM: 613847; MGI: 1914840; HomoloGene: 9221; GeneCards: TCTN3; OMA:TCTN3 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
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: 40.58 – 40.6 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

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 Oral-facial-digital syndrome IV and Joubert syndrome 18. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2012].

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000119977Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000025008Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: Tectonic family member 3". Retrieved 2012-12-22.

Further reading

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