Symbol Name ID |
Mcph1
microcephaly, primary autosomal recessive 1 MGI:2443308 |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Primary microcephaly |
Abnormal cortical bone morphology |
Disease(s) Associated with MCPH1 | |||
primary autosomal recessive microcephaly | |||
primary autosomal recessive microcephaly 1 |
Mouse Phenotypes | decreased bone mineral content |
decreased bone mineral density |
decreased trabecular bone volume |
decreased bone trabecula number |
decreased trabecular bone mass |
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Availability | Mouse Genotype | |||||
Mcph1tm1a(EUCOMM)Wtsi/Mcph1tm1a(EUCOMM)Wtsi |
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 03/12/2024 MGI 6.23 |
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