Identity
HGNC
LOCATION
Xq13.1
LOCUSID
ALIAS
CFND,CFNS,EFB1,EFL3,EPLG2,Elk-L,LERK2
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: 1947
MIM: 300035
HGNC: 3226
Ensembl: ENSG00000090776
Variants:
dbSNP: 1947
ClinVar: 1947
TCGA: ENSG00000090776
COSMIC: EFNB1
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000090776 | ENST00000204961 | P98172 |
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 35603962 | 2022 | Construction of three-gene-based prognostic signature and analysis of immune cells infiltration in children and young adults with B-acute lymphoblastic leukemia. | 3 |
| 35603962 | 2022 | Construction of three-gene-based prognostic signature and analysis of immune cells infiltration in children and young adults with B-acute lymphoblastic leukemia. | 3 |
| 32022998 | 2020 | Extracranial midline defects in a patient with craniofrontonasal syndrome with a novel EFNB1 mutation. | 3 |
| 32240825 | 2020 | Severe craniofrontonasal syndrome in a male patient mosaic for a novel nonsense mutation in EFNB1. | 3 |
| 32337793 | 2020 | EPH receptor B2 stimulates human monocyte adhesion and migration independently of its EphrinB ligands. | 9 |
| 33356837 | 2020 | Peripheral EphrinB1/EphB1 signalling attenuates muscle hyperalgesia in MPS patients and a rat model of taut band-associated persistent muscle pain. | 2 |
| 32022998 | 2020 | Extracranial midline defects in a patient with craniofrontonasal syndrome with a novel EFNB1 mutation. | 3 |
| 32240825 | 2020 | Severe craniofrontonasal syndrome in a male patient mosaic for a novel nonsense mutation in EFNB1. | 3 |
| 32337793 | 2020 | EPH receptor B2 stimulates human monocyte adhesion and migration independently of its EphrinB ligands. | 9 |
| 33356837 | 2020 | Peripheral EphrinB1/EphB1 signalling attenuates muscle hyperalgesia in MPS patients and a rat model of taut band-associated persistent muscle pain. | 2 |
| 30326247 | 2019 | Loss of EfnB1 in the osteogenic lineage compromises their capacity to support hematopoietic stem/progenitor cell maintenance. | 10 |
| 31285555 | 2019 | Four novel mutations in EFNB1 in Indian patients with craniofrontonasal syndrome. | 1 |
| 30326247 | 2019 | Loss of EfnB1 in the osteogenic lineage compromises their capacity to support hematopoietic stem/progenitor cell maintenance. | 10 |
| 31285555 | 2019 | Four novel mutations in EFNB1 in Indian patients with craniofrontonasal syndrome. | 1 |
| 29215649 | 2018 | A craniosynostosis massively parallel sequencing panel study in 309 Australian and New Zealand patients: findings and recommendations. | 15 |
Citation
Dessen P
EFNB1 (ephrin B1)
Atlas Genet Cytogenet Oncol Haematol. 2003-11-01
Online version: http://atlasgeneticsoncology.org/gene/40415/efnb1
