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: 2235
MIM: 612386
HGNC: 3647
Ensembl: ENSG00000066926
Variants:
dbSNP: 2235
ClinVar: 2235
TCGA: ENSG00000066926
COSMIC: FECH
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 34581821 | 2021 | Cockayne syndrome group A and ferrochelatase finely tune ribosomal gene transcription and its response to UV irradiation. | 5 |
| 34686726 | 2021 | Nkx3-1 and Fech genes might be switch genes involved in pituitary non-functioning adenoma invasiveness. | 4 |
| 34581821 | 2021 | Cockayne syndrome group A and ferrochelatase finely tune ribosomal gene transcription and its response to UV irradiation. | 5 |
| 34686726 | 2021 | Nkx3-1 and Fech genes might be switch genes involved in pituitary non-functioning adenoma invasiveness. | 4 |
| 31273344 | 2020 | Targeted resequencing of FECH locus reveals that a novel deep intronic pathogenic variant and eQTLs may cause erythropoietic protoporphyria (EPP) through a methylation-dependent mechanism. | 7 |
| 32056258 | 2020 | Novel mutation of the ferrochelatase gene in a Japanese family with erythropoietic protoporphyria. | 1 |
| 31273344 | 2020 | Targeted resequencing of FECH locus reveals that a novel deep intronic pathogenic variant and eQTLs may cause erythropoietic protoporphyria (EPP) through a methylation-dependent mechanism. | 7 |
| 32056258 | 2020 | Novel mutation of the ferrochelatase gene in a Japanese family with erythropoietic protoporphyria. | 1 |
| 30391163 | 2019 | Strong correlation of ferrochelatase enzymatic activity with Mitoferrin-1 mRNA in lymphoblasts of patients with protoporphyria. | 5 |
| 30403821 | 2019 | Admixture mapping identifies novel loci for obstructive sleep apnea in Hispanic/Latino Americans. | 28 |
| 30454868 | 2019 | Congenital erythropoietic porphyria and erythropoietic protoporphyria: Identification of 7 uroporphyrinogen III synthase and 20 ferrochelatase novel mutations. | 4 |
| 30767226 | 2019 | Ferrochelatase Deficiency Abrogated the Enhancement of Aminolevulinic Acid-mediated Protoporphyrin IX by Iron Chelator Deferoxamine. | 13 |
| 30391163 | 2019 | Strong correlation of ferrochelatase enzymatic activity with Mitoferrin-1 mRNA in lymphoblasts of patients with protoporphyria. | 5 |
| 30403821 | 2019 | Admixture mapping identifies novel loci for obstructive sleep apnea in Hispanic/Latino Americans. | 28 |
| 30454868 | 2019 | Congenital erythropoietic porphyria and erythropoietic protoporphyria: Identification of 7 uroporphyrinogen III synthase and 20 ferrochelatase novel mutations. | 4 |
Citation
Dessen P
FECH (ferrochelatase)
Atlas Genet Cytogenet Oncol Haematol. 2016-10-01
Online version: http://atlasgeneticsoncology.org/gene/56011/fech-(ferrochelatase)
