|
Symbol Name ID |
Lbr
lamin B receptor MGI:2138281 |
| Darker colors indicate more annotations |
| Human Phenotypes | Postaxial hand polydactyly |
Short phalanx of finger |
Postaxial foot polydactyly |
Sandal gap |
Polydactyly |
Brachydactyly |
Abnormal ossification involving the femoral head and neck |
Abnormality of the calcaneus |
Short 3rd metacarpal |
Short 4th metacarpal |
Short 5th metacarpal |
Abnormality of the metaphysis |
Metaphyseal cupping |
Flared metaphysis |
Bowing of the long bones |
Upper limb undergrowth |
Abnormal foot bone ossification |
Pes cavus |
Lower limb hypertonia |
Foot dorsiflexor weakness |
Broad palm |
Ulnar deviation of the hand |
Mesomelia |
Micromelia |
Rhizomelia |
| Disease(s) Associated with LBR | |||||||||||||||||||||||||
| Greenberg dysplasia | |||||||||||||||||||||||||
| Pelger-Huet anomaly |
| Mouse Phenotypes | tail necrosis |
syndactyly |
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| Availability | Mouse Genotype | ||
| Lbric-J/Lbric-J | |||
| Lbric/Lbric | |||
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 02/11/2020 MGI 6.14 |
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