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: 340665
MIM: 608428
HGNC: 20577
Ensembl: ENSG00000187553
Variants:
dbSNP: 340665
ClinVar: 340665
TCGA: ENSG00000187553
COSMIC: CYP26C1
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000187553 | ENST00000624358 | A0A096LNL5 |
| ENSG00000187553 | ENST00000651965 | Q6V0L0 |
Expression (GTEx)
Pathways
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 34681016 | 2021 | Association of CYP26C1 Promoter Hypomethylation with Small Vessel Occlusion in Korean Subjects. | 1 |
| 34681016 | 2021 | Association of CYP26C1 Promoter Hypomethylation with Small Vessel Occlusion in Korean Subjects. | 1 |
| 31419517 | 2019 | Biochemical and physiological importance of the CYP26 retinoic acid hydroxylases. | 47 |
| 31419517 | 2019 | Biochemical and physiological importance of the CYP26 retinoic acid hydroxylases. | 47 |
| 29476041 | 2018 | CYP26C1 Is a Hydroxylase of Multiple Active Retinoids and Interacts with Cellular Retinoic Acid Binding Proteins. | 25 |
| 29706635 | 2018 | Functional missense and splicing variants in the retinoic acid catabolizing enzyme CYP26C1 in idiopathic short stature. | 8 |
| 29476041 | 2018 | CYP26C1 Is a Hydroxylase of Multiple Active Retinoids and Interacts with Cellular Retinoic Acid Binding Proteins. | 25 |
| 29706635 | 2018 | Functional missense and splicing variants in the retinoic acid catabolizing enzyme CYP26C1 in idiopathic short stature. | 8 |
| 26009309 | 2016 | Elevated expression of the retinoic acid-metabolizing enzyme CYP26C1 in primary breast carcinomas. | 2 |
| 27861128 | 2016 | Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency. | 12 |
| 26009309 | 2016 | Elevated expression of the retinoic acid-metabolizing enzyme CYP26C1 in primary breast carcinomas. | 2 |
| 27861128 | 2016 | Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency. | 12 |
| 23161670 | 2013 | Focal facial dermal dysplasia, type IV, is caused by mutations in CYP26C1. | 19 |
| 23161670 | 2013 | Focal facial dermal dysplasia, type IV, is caused by mutations in CYP26C1. | 19 |
| 21850183 | 2011 | Nonsyndromic bilateral and unilateral optic nerve aplasia: first familial occurrence and potential implication of CYP26A1 and CYP26C1 genes. | 13 |
Citation
Dessen P
CYP26C1 (cytochrome P450 family 26 subfamily C member 1)
Atlas Genet Cytogenet Oncol Haematol. 2016-10-01
Online version: http://atlasgeneticsoncology.org/gene/56075/cyp26c1-(cytochrome-p450-family-26-subfamily-c-member-1)
