Symbol Name ID |
Lrp5
low density lipoprotein receptor-related protein 5 MGI:1278315 |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Facial palsy |
Dilatation of the cerebral artery |
Pituitary growth hormone cell adenoma |
Arachnoid cyst |
Delayed speech and language development |
Intellectual disability, mild |
Loss of ambulation |
Waddling gait |
Headache |
Global developmental delay |
Delayed gross motor development |
Focal impaired awareness seizure |
Disease(s) Associated with LRP5 | |||||||||||||
autosomal dominant osteopetrosis 1 | |||||||||||||
autosomal dominant polycystic kidney disease | |||||||||||||
osteoporosis-pseudoglioma syndrome | |||||||||||||
polycystic liver disease | |||||||||||||
Worth syndrome |
Mouse Phenotypes | gliosis |
retina ganglion cell degeneration |
retina photoreceptor degeneration |
abnormal blood-retina barrier function |
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Availability | Mouse Genotype | ||||
Lrp5tm1Dgen/Lrp5tm1Dgen | |||||
Lrp5tvrm111B/Lrp5tvrm111B |
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 08/02/2024 MGI 6.24 |
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