Symbol Name ID |
Lmx1b
LIM homeobox transcription factor 1 beta MGI:1100513 |
Darker colors indicate more annotations |
Human Phenotypes | Internal carotid artery hypoplasia |
High anterior hairline |
High forehead |
Cleft upper lip |
Cleft palate |
Enamel hypoplasia |
Disease(s) Associated with LMX1B | ||||||
nail-patella syndrome |
Mouse Phenotypes | abnormal cranial suture morphology |
abnormal fontanelle morphology |
abnormal interparietal bone morphology |
absent supraoccipital bone |
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Availability | Mouse Genotype | ||||
Lmx1btm1Rjo/Lmx1btm1Rjo |
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 05/28/2024 MGI 6.13 |
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