Symbol Name ID |
Efnb1
ephrin B1 MGI:102708 |
Darker colors indicate more annotations |
Human Phenotypes | Low posterior hairline |
Thickened nuchal skin fold |
Short neck |
Webbed neck |
Hemihypotrophy of lower limb |
Umbilical hernia |
Congenital diaphragmatic hernia |
Short stature |
Disease(s) Associated with EFNB1 | ||||||||
craniofrontonasal syndrome |
Mouse Phenotypes | failure of palatal shelf elevation |
absent palatal shelf |
cleft secondary palate |
cleft palate |
omphalocele |
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Availability | Mouse Genotype | |||||
Efnb1tm1.1Rha/Efnb1tm1.1Rha | ||||||
Efnb1tm1.1Sor/Efnb1tm1.1Sor | ||||||
Efnb1tm1Rha/Efnb1tm1Rha | ||||||
Efnb1tm1.1Sor/Y | ||||||
Efnb1tm1Rha/Y | ||||||
Efnb1tm1Rha/Efnb1+ Tg(Pgk1-cre)1Lni/? (conditional) |
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Efnb1tm1Sor/Efnb1+ H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
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Efnb1tm1Rha/Y Tg(Pgk1-cre)1Lni/? (conditional) |
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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last database update 04/09/2024 MGI 6.23 |
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