EFNB1, ephrin B1, 1947

N. diseases: 134; N. variants: 19
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0220767
Disease: Craniofrontonasal dysplasia
Craniofrontonasal dysplasia
1.000 GermlineCausalMutation disease ORPHANET Although EFNB1 is X-inactivated, we did not observe markedly skewed X-inactivation in either blood or cranial periosteum from females with CFNS, indicating that lack of ephrin-B1 does not compromise cell viability in these tissues. 15166289 2004
CUI: C0220767
Disease: Craniofrontonasal dysplasia
Craniofrontonasal dysplasia
1.000 GeneticVariation disease UNIPROT Although EFNB1 is X-inactivated, we did not observe markedly skewed X-inactivation in either blood or cranial periosteum from females with CFNS, indicating that lack of ephrin-B1 does not compromise cell viability in these tissues. 15166289 2004
CUI: C0220767
Disease: Craniofrontonasal dysplasia
Craniofrontonasal dysplasia
1.000 Biomarker disease CTD_human Although EFNB1 is X-inactivated, we did not observe markedly skewed X-inactivation in either blood or cranial periosteum from females with CFNS, indicating that lack of ephrin-B1 does not compromise cell viability in these tissues. 15166289 2004
CUI: C0220767
Disease: Craniofrontonasal dysplasia
Craniofrontonasal dysplasia
1.000 GeneticVariation disease BEFREE A novel mutation in EFNB1, probably with a dominant negative effect, underlying craniofrontonasal syndrome. 16526919 2006
CUI: C0220767
Disease: Craniofrontonasal dysplasia
Craniofrontonasal dysplasia
1.000 GeneticVariation disease BEFREE A novel EFNB1 mutation in a patient with craniofrontonasal syndrome and right hallux duplication. 23845783 2013
CUI: C0220767
Disease: Craniofrontonasal dysplasia
Craniofrontonasal dysplasia
1.000 GeneticVariation disease BEFREE A novel EFNB1 mutation (c.712delG) in a family with craniofrontonasal syndrome and diaphragmatic hernia. 20734337 2010
CUI: C0220767
Disease: Craniofrontonasal dysplasia
Craniofrontonasal dysplasia
1.000 GeneticVariation disease BEFREE CFNS is caused by mutations in the Ephrin 1 gene (EFNB1) located at Xq13.1, which encodes the transmembrane protein Ephrin B1. 31285555 2019
CUI: C0220767
Disease: Craniofrontonasal dysplasia
Craniofrontonasal dysplasia
1.000 GeneticVariation disease BEFREE Craniofrontonasal syndrome in a male due to chromosomal mosaicism involving EFNB1: further insights into a genetic paradox. 23614707 2014
CUI: C0220767
Disease: Craniofrontonasal dysplasia
Craniofrontonasal dysplasia
1.000 Biomarker disease BEFREE Craniofrontonasal syndrome (CFNS [MIM 304110]) is an X-linked malformation syndrome characterized by craniofrontonasal dysplasia and extracranial manifestations in heterozygous females. 17941886 2007
CUI: C0220767
Disease: Craniofrontonasal dysplasia
Craniofrontonasal dysplasia
1.000 GeneticVariation disease CLINVAR
CUI: C0220767
Disease: Craniofrontonasal dysplasia
Craniofrontonasal dysplasia
1.000 Biomarker disease GENOMICS_ENGLAND
CUI: C0220767
Disease: Craniofrontonasal dysplasia
Craniofrontonasal dysplasia
1.000 CausalMutation disease CLINVAR