Identity
HGNC
LOCATION
3p26.1
LOCUSID
ALIAS
AAPA3037,FGE,UNQ3037
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: 285362
MIM: 607939
HGNC: 20376
Ensembl: ENSG00000144455
Variants:
dbSNP: 285362
ClinVar: 285362
TCGA: ENSG00000144455
COSMIC: SUMF1
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38460946 | 2024 | SUMF1 overexpression promotes tumorous cell growth and migration and is correlated with the immune status of patients with glioma. | 0 |
| 38460946 | 2024 | SUMF1 overexpression promotes tumorous cell growth and migration and is correlated with the immune status of patients with glioma. | 0 |
| 37344788 | 2023 | Association between SUMF1 polymorphisms and COVID-19 severity. | 1 |
| 37344788 | 2023 | Association between SUMF1 polymorphisms and COVID-19 severity. | 1 |
| 32048457 | 2020 | A homozygous missense variant of SUMF1 in the Bedouin population extends the clinical spectrum in ultrarare neonatal multiple sulfatase deficiency. | 2 |
| 32414121 | 2020 | Multiple Sulfatase Deficiency: A Disease Comprising Mucopolysaccharidosis, Sphingolipidosis, and More Caused by a Defect in Posttranslational Modification. | 19 |
| 32621519 | 2020 | A systematic review and meta-analysis of published cases reveals the natural disease history in multiple sulfatase deficiency. | 7 |
| 32749716 | 2020 | Natural history of multiple sulfatase deficiency: Retrospective phenotyping and functional variant analysis to characterize an ultra-rare disease. | 14 |
| 32048457 | 2020 | A homozygous missense variant of SUMF1 in the Bedouin population extends the clinical spectrum in ultrarare neonatal multiple sulfatase deficiency. | 2 |
| 32414121 | 2020 | Multiple Sulfatase Deficiency: A Disease Comprising Mucopolysaccharidosis, Sphingolipidosis, and More Caused by a Defect in Posttranslational Modification. | 19 |
| 32621519 | 2020 | A systematic review and meta-analysis of published cases reveals the natural disease history in multiple sulfatase deficiency. | 7 |
| 32749716 | 2020 | Natural history of multiple sulfatase deficiency: Retrospective phenotyping and functional variant analysis to characterize an ultra-rare disease. | 14 |
| 29479672 | 2018 | The report of two cases with multiple sulfatase deficiency resulting from a rare similar gene mutation. | 0 |
| 29972788 | 2018 | Recognition and ER Quality Control of Misfolded Formylglycine-Generating Enzyme by Protein Disulfide Isomerase. | 8 |
| 30124108 | 2018 | Multiple Sulfatase Deficiency: A Case Series With a Novel Mutation. | 7 |
Citation
Dessen P
SUMF1 (sulfatase modifying factor 1)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/74371/sumf1-(sulfatase-modifying-factor-1)
