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Symbol
Name
ID

Efnb1
ephrin B1
MGI:102708

Phenotype annotations related to craniofacial

Darker colors indicate more annotations

Human Phenotypes

Widow's peak

Low posterior hairline

Frontal bossing

Brachycephaly

Craniosynostosis

Coronal craniosynostosis

Plagiocephaly

Microcephaly

Facial asymmetry

Cleft upper lip

Cleft palate

High palate

Abnormality of the dentition

Orofacial cleft

Depressed nasal ridge

Bifid nasal tip

Hypoplastic nasal tip

Wide nasal bridge

Midline defect of the nose

Downslanted palpebral fissures

Telecanthus

Disease(s) Associated with EFNB1

craniofrontonasal syndrome

Mouse Phenotypes		decreased cranium height	abnormal frontal bone morphology	frontal bone foramen	failure of palatal shelf elevation	absent palatal shelf	cleft secondary palate	cleft palate
Availability	Mouse Genotype	decreased cranium height	abnormal frontal bone morphology	frontal bone foramen	failure of palatal shelf elevation	absent palatal shelf	cleft secondary palate	cleft palate
	Efnb1^tm1.1Rha/Efnb1^tm1.1Rha
	Efnb1^tm1.1Sor/Efnb1^tm1.1Sor
	Efnb1^tm1Rha/Efnb1^tm1Rha
	Efnb1^tm1.1Sor/Efnb1⁺
	Efnb1^tm1.1Sor/Y
	Efnb1^tm1Rha/Y
	Efnb1^tm1Sor/Efnb1⁺ H2az2^{Tg(Wnt1-cre)11Rth}/H2az2⁺ (conditional)
	Efnb1^tm1Rha/Y Tg(Pgk1-cre)1Lni/? (conditional)

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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