Identity
HGNC
LOCATION
10q26.3
LOCUSID
ALIAS
COE3,EBF-3,HADDS,O/E-2,OE-2
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: 253738
MIM: 607407
HGNC: 19087
Ensembl: ENSG00000108001
Variants:
dbSNP: 253738
ClinVar: 253738
TCGA: ENSG00000108001
COSMIC: EBF3
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000108001 | ENST00000355311 | Q9H4W6 |
| ENSG00000108001 | ENST00000368648 | Q9H4W6 |
| ENSG00000108001 | ENST00000440978 | H0Y3W9 |
Expression (GTEx)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38479556 | 2024 | Early B Cell Factor 3 (EBF3) attenuates Parkinson's disease through directly regulating contactin-associated protein-like 4 (CNTNAP4) transcription: An experimental study. | 0 |
| 38479556 | 2024 | Early B Cell Factor 3 (EBF3) attenuates Parkinson's disease through directly regulating contactin-associated protein-like 4 (CNTNAP4) transcription: An experimental study. | 0 |
| 34999443 | 2022 | Duplication/triplication mosaicism of EBF3 and expansion of the EBF3 neurodevelopmental disorder phenotype. | 2 |
| 35340043 | 2022 | An Integrated Phenotypic and Genotypic Approach Reveals a High-Risk Subtype Association for EBF3 Missense Variants Affecting the Zinc Finger Domain. | 4 |
| 34999443 | 2022 | Duplication/triplication mosaicism of EBF3 and expansion of the EBF3 neurodevelopmental disorder phenotype. | 2 |
| 35340043 | 2022 | An Integrated Phenotypic and Genotypic Approach Reveals a High-Risk Subtype Association for EBF3 Missense Variants Affecting the Zinc Finger Domain. | 4 |
| 34050706 | 2021 | Clinical spectrum of individuals with de novo EBF3 variants or deletions. | 4 |
| 34256850 | 2021 | Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism. | 11 |
| 34050706 | 2021 | Clinical spectrum of individuals with de novo EBF3 variants or deletions. | 4 |
| 34256850 | 2021 | Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism. | 11 |
| 31383000 | 2019 | Characterisation of DNA methylation changes in EBF3 and TBC1D16 associated with tumour progression and metastasis in multiple cancer types. | 22 |
| 31383000 | 2019 | Characterisation of DNA methylation changes in EBF3 and TBC1D16 associated with tumour progression and metastasis in multiple cancer types. | 22 |
| 29750239 | 2018 | MiR-23b-3p induces the proliferation and metastasis of esophageal squamous cell carcinomas cells through the inhibition of EBF3. | 12 |
| 29913442 | 2018 | Associations of Pulmonary Fibrosis with Peripheral Blood Th1/Th2 Cell Imbalance and EBF3 Gene Methylation in Uygur Pigeon Breeder's Lung Patients. | 6 |
| 29750239 | 2018 | MiR-23b-3p induces the proliferation and metastasis of esophageal squamous cell carcinomas cells through the inhibition of EBF3. | 12 |
Citation
Dessen P
EBF3 (EBF transcription factor 3)
Atlas Genet Cytogenet Oncol Haematol. 2007-12-01
Online version: http://atlasgeneticsoncology.org/gene/49861/ebf3
