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: 80144
MIM: 607830
HGNC: 19185
Ensembl: ENSG00000138759
Variants:
dbSNP: 80144
ClinVar: 80144
TCGA: ENSG00000138759
COSMIC: FRAS1
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 32643034 | 2021 | Novel loss of function variants in FRAS1 AND FREM2 underlie renal agenesis in consanguineous families. | 8 |
| 33956343 | 2021 | A polymorphism in the promoter of FRAS1 is a candidate SNP associated with metastatic prostate cancer. | 4 |
| 32643034 | 2021 | Novel loss of function variants in FRAS1 AND FREM2 underlie renal agenesis in consanguineous families. | 8 |
| 33956343 | 2021 | A polymorphism in the promoter of FRAS1 is a candidate SNP associated with metastatic prostate cancer. | 4 |
| 31597194 | 2020 | Fraser extracellular matrix complex subunit 1 promotes liver metastasis of gastric cancer. | 13 |
| 31999076 | 2020 | Two unrelated families with variable expression of Fraser syndrome due to the same pathogenic variant in the FRAS1 gene. | 2 |
| 31597194 | 2020 | Fraser extracellular matrix complex subunit 1 promotes liver metastasis of gastric cancer. | 13 |
| 31999076 | 2020 | Two unrelated families with variable expression of Fraser syndrome due to the same pathogenic variant in the FRAS1 gene. | 2 |
| 29618029 | 2018 | The role of FREM2 and FRAS1 in the development of congenital diaphragmatic hernia. | 10 |
| 29618029 | 2018 | The role of FREM2 and FRAS1 in the development of congenital diaphragmatic hernia. | 10 |
| 24700879 | 2014 | Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tract. | 47 |
| 24700879 | 2014 | Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tract. | 47 |
| 22283518 | 2013 | A puzzle over several decades: eye anomalies with FRAS1 and STRA6 mutations in the same family. | 5 |
| 23473829 | 2013 | Expanding the mutation spectrum for Fraser syndrome: identification of a novel heterozygous deletion in FRAS1. | 10 |
| 22283518 | 2013 | A puzzle over several decades: eye anomalies with FRAS1 and STRA6 mutations in the same family. | 5 |
Citation
Dessen P
FRAS1 (Fraser extracellular matrix complex subunit 1)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/63583/fras1-(fraser-extracellular-matrix-complex-subunit-1)
