Collagen triple helix repeat containing 1: Difference between revisions

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==Function==
==Function==


This locus encodes a protein that may play a role in the cellular response to arterial injury through involvement in vascular remodeling. Mutations at this locus have been associated with Barrett esophagus and esophageal adenocarcinoma. Alternatively, spliced transcript variants have been described.
This [[Locus (genetics)|locus]] encodes a protein that may play a role in the cellular response to [[Artery|arterial]] injury through involvement in vascular remodeling. [[Mutation|Mutations]] at this locus have been associated with [[Barrett's esophagus|Barrett esophagus]] and [[esophageal adenocarcinoma]]. Alternatively, spliced [[Alternative splicing|transcript variants]] have been described.


== References ==
== References ==

Revision as of 18:24, 30 June 2018

VALUE_ERROR (nil)
Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

n/a

n/a

Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

Collagen triple helix repeat containing 1 is a protein that in humans is encoded by the CTHRC1 gene. [1]

Function

This locus encodes a protein that may play a role in the cellular response to arterial injury through involvement in vascular remodeling. Mutations at this locus have been associated with Barrett esophagus and esophageal adenocarcinoma. Alternatively, spliced transcript variants have been described.

References

  1. "Entrez Gene: Collagen triple helix repeat containing 1". Retrieved 2017-07-25.

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.