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: 84466
MIM: 612453
HGNC: 29634
Ensembl: ENSG00000145794
Variants:
dbSNP: 84466
ClinVar: 84466
TCGA: ENSG00000145794
COSMIC: MEGF10
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000145794 | ENST00000274473 | Q96KG7 |
| ENSG00000145794 | ENST00000418761 | Q96KG7 |
| ENSG00000145794 | ENST00000503335 | Q96KG7 |
| ENSG00000145794 | ENST00000508365 | Q96KG7 |
Expression (GTEx)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 36849355 | 2023 | [A family with early onset myopathy caused by MEGF10 gene defect and literature review]. | 0 |
| 36849355 | 2023 | [A family with early onset myopathy caused by MEGF10 gene defect and literature review]. | 0 |
| 33512044 | 2021 | ZNF667-AS1, a positively regulating MEGF10, inhibits the progression of uveal melanoma by modulating cellular aggressiveness. | 8 |
| 34828389 | 2021 | Phenotypic Variability of MEGF10 Variants Causing Congenital Myopathy: Report of Two Unrelated Patients from a Highly Consanguineous Population. | 3 |
| 33512044 | 2021 | ZNF667-AS1, a positively regulating MEGF10, inhibits the progression of uveal melanoma by modulating cellular aggressiveness. | 8 |
| 34828389 | 2021 | Phenotypic Variability of MEGF10 Variants Causing Congenital Myopathy: Report of Two Unrelated Patients from a Highly Consanguineous Population. | 3 |
| 29887919 | 2018 | MEGF10, a Glioma Survival-Associated Molecular Signature, Predicts IDH Mutation Status. | 6 |
| 29887919 | 2018 | MEGF10, a Glioma Survival-Associated Molecular Signature, Predicts IDH Mutation Status. | 6 |
| 27862318 | 2017 | Genome-wide DNA methylation analysis identifies MEGF10 as a novel epigenetically repressed candidate tumor suppressor gene in neuroblastoma. | 13 |
| 28536440 | 2017 | Genetic variants in the transcription regulatory region of MEGF10 are associated with autism in Chinese Han population. | 4 |
| 27862318 | 2017 | Genome-wide DNA methylation analysis identifies MEGF10 as a novel epigenetically repressed candidate tumor suppressor gene in neuroblastoma. | 13 |
| 28536440 | 2017 | Genetic variants in the transcription regulatory region of MEGF10 are associated with autism in Chinese Han population. | 4 |
| 26802438 | 2016 | Adult-onset respiratory insufficiency, scoliosis, and distal joint hyperlaxity in patients with multiminicore disease due to novel Megf10 mutations. | 11 |
| 26802438 | 2016 | Adult-onset respiratory insufficiency, scoliosis, and distal joint hyperlaxity in patients with multiminicore disease due to novel Megf10 mutations. | 11 |
| 25044114 | 2014 | Myogenin is a positive regulator of MEGF10 expression in skeletal muscle. | 10 |
Citation
Dessen P
MEGF10 (multiple EGF like domains 10)
Atlas Genet Cytogenet Oncol Haematol. 2016-10-01
Online version: http://atlasgeneticsoncology.org/gene/56460/megf10-(multiple-egf-like-domains-10)
