Symbol Name ID |
Efnb1
ephrin B1 MGI:102708 |
! | Indicates phenotype varies with strain background. |
Darker colors indicate more annotations |
Human Phenotypes | Clinodactyly of the 5th finger |
Camptodactyly of finger |
Hand polydactyly |
Broad hallux phalanx |
Broad hallux |
Sandal gap |
Toe syndactyly |
Brachydactyly |
Finger syndactyly |
3-4 finger syndactyly |
Hemihypotrophy of lower limb |
Disease(s) Associated with EFNB1 | |||||||||||
craniofrontonasal syndrome |
Mouse Phenotypes | abnormal autopod morphology |
abnormal carpal bone morphology |
fused carpal bones |
polydactyly |
polysyndactyly |
preaxial polydactyly |
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Availability | Mouse Genotype | ||||||
Efnb1tm1.1Sor/Efnb1+ | |||||||
Efnb1tm1Rha/Efnb1+ | |||||||
Efnb1tm1Rha/Efnb1+ Tg(Pgk1-cre)1Lni/? (conditional) |
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Efnb1tm1Rha/Efnb1+ Tg(Prrx1-cre)1Cjt/? (conditional) |
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Efnb1tm1Sor/Efnb1+ Meox2tm1(cre)Sor/Meox2+ (conditional) |
! | ||||||
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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