Identity
HGNC
LOCATION
19q13.2
LOCUSID
ALIAS
C19orf49,CRPT2,EGFL4,SBP1
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: 1954
MIM: 604267
HGNC: 3233
Ensembl: ENSG00000105429
Variants:
dbSNP: 1954
ClinVar: 1954
TCGA: ENSG00000105429
COSMIC: MEGF8
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38039718 | 2024 | Role and mechanism of miR-871-3p/Megf8 in regulating formaldehyde-induced cardiomyocyte inflammation and congenital heart disease. | 0 |
| 38760421 | 2024 | The phenotype of MEGF8-related Carpenter syndrome (CRPT2) is refined through the identification of eight new patients. | 1 |
| 38039718 | 2024 | Role and mechanism of miR-871-3p/Megf8 in regulating formaldehyde-induced cardiomyocyte inflammation and congenital heart disease. | 0 |
| 38760421 | 2024 | The phenotype of MEGF8-related Carpenter syndrome (CRPT2) is refined through the identification of eight new patients. | 1 |
| 23063620 | 2012 | Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization. | 38 |
| 23063620 | 2012 | Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization. | 38 |
Citation
Dessen P
MEGF8 (multiple EGF like domains 8)
Atlas Genet Cytogenet Oncol Haematol. 2010-10-01
Online version: http://atlasgeneticsoncology.org/gene/51685/megf8
