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TECR
Protein-coding gene in the species Homo sapiens

Trans-2,3-enoyl-CoA reductase is an enzyme that in humans is encoded by the TECR gene.

This gene encodes a multi-pass membrane protein that resides in the endoplasmic reticulum, and belongs to the steroid 5-alpha reductase family. The elongation of microsomal long and very long chain fatty acid consists of 4 sequential reactions. This protein catalyzes the final step, reducing trans-2,3-enoyl-CoA to saturated acyl-CoA. Alternatively spliced transcript variants have been found for this gene.

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Clinical relevance

Mutations in this gene have been shown to cause non-syndromic mental retardation.3

Further reading

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

References

  1. "Entrez Gene: Trans-2,3-enoyl-CoA reductase". Retrieved 2011-12-30. https://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=retrieve&list_uids=9524

  2. "Entrez Gene: Trans-2,3-enoyl-CoA reductase". Retrieved 2011-12-30. https://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=retrieve&list_uids=9524

  3. Çalışkan M, Chong JX, Uricchio L, Anderson R, Chen P, Sougnez C, Garimella K, Gabriel SB, dePristo MA, Shakir K, Matern D, Das S, Waggoner D, Nicolae DL, Ober C (April 2011). "Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13". Hum. Mol. Genet. 20 (7): 1285–9. doi:10.1093/hmg/ddq569. PMC 3115579. PMID 21212097. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3115579