Identity
HGNC
LOCATION
4q21.22
LOCUSID
ALIAS
ACOD4,DFNA79,FADS4,HSCD5,SCD2,SCD4
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 79966
MIM: 608370
HGNC: 21088
Ensembl: ENSG00000145284
Variants:
dbSNP: 79966
ClinVar: 79966
TCGA: ENSG00000145284
COSMIC: SCD5
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000145284 | ENST00000273908 | Q86SK9 |
| ENSG00000145284 | ENST00000319540 | Q86SK9 |
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 37047490 | 2023 | Molecular Basis of Unequal Alternative Splicing of Human SCD5 and Its Alteration by Natural Genetic Variations. | 0 |
| 37047490 | 2023 | Molecular Basis of Unequal Alternative Splicing of Human SCD5 and Its Alteration by Natural Genetic Variations. | 0 |
| 36059459 | 2022 | SCD2-mediated cooperative activation of IRF3-IRF9 regulatory circuit controls type I interferon transcriptome in CD4(+) T cells. | 0 |
| 36292669 | 2022 | A Single Nucleotide Polymorphism (rs3811792) Affecting Human SCD5 Promoter Activity Is Associated with Diabetes Mellitus. | 3 |
| 36059459 | 2022 | SCD2-mediated cooperative activation of IRF3-IRF9 regulatory circuit controls type I interferon transcriptome in CD4(+) T cells. | 0 |
| 36292669 | 2022 | A Single Nucleotide Polymorphism (rs3811792) Affecting Human SCD5 Promoter Activity Is Associated with Diabetes Mellitus. | 3 |
| 33049404 | 2021 | Stearoyl-CoA desaturase 5 (SCD5), a Δ-9 fatty acyl desaturase in search of a function. | 21 |
| 33903614 | 2021 | SCD5 expression correlates with prognosis and response to neoadjuvant chemotherapy in breast cancer. | 8 |
| 33049404 | 2021 | Stearoyl-CoA desaturase 5 (SCD5), a Δ-9 fatty acyl desaturase in search of a function. | 21 |
| 33903614 | 2021 | SCD5 expression correlates with prognosis and response to neoadjuvant chemotherapy in breast cancer. | 8 |
| 31972369 | 2020 | Whole exome sequencing identifies SCD5 as a novel causative gene for autosomal dominant nonsyndromic deafness. | 5 |
| 31972369 | 2020 | Whole exome sequencing identifies SCD5 as a novel causative gene for autosomal dominant nonsyndromic deafness. | 5 |
| 30168096 | 2018 | Polymorphisms in the 3'-UTR of SCD5 gene are associated with hepatocellular carcinoma in Korean population. | 2 |
| 30168096 | 2018 | Polymorphisms in the 3'-UTR of SCD5 gene are associated with hepatocellular carcinoma in Korean population. | 2 |
| 25802234 | 2015 | SCD5-induced oleic acid production reduces melanoma malignancy by intracellular retention of SPARC and cathepsin B. | 25 |
Citation
Dessen P
SCD5 (stearoyl-CoA desaturase 5)
Atlas Genet Cytogenet Oncol Haematol. 2015-09-01
Online version: http://atlasgeneticsoncology.org/gene/55387/scd5-(stearoyl-coa-desaturase-5)
