Identity
HGNC
LOCATION
10q23.33
LOCUSID
ALIAS
C10orf4,F26C11.1-like,FRA10A
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: 118924
MIM: 608866
HGNC: 1162
Ensembl: ENSG00000148690
Variants:
dbSNP: 118924
ClinVar: 118924
TCGA: ENSG00000148690
COSMIC: FRA10AC1
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000148690 | ENST00000359204 | Q70Z53 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 34694367 | 2022 | Biallelic FRA10AC1 variants cause a neurodevelopmental disorder with growth retardation. | 5 |
| 34694367 | 2022 | Biallelic FRA10AC1 variants cause a neurodevelopmental disorder with growth retardation. | 5 |
| 26252872 | 2015 | Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. | 29 |
| 26252872 | 2015 | Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. | 29 |
| 16385451 | 2006 | A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease. | 83 |
| 16385451 | 2006 | A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease. | 83 |
Citation
Dessen P
FRA10AC1 (FRA10A associated CGG repeat 1)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/63582/submit-meetings/
