Symbol Name ID |
Gcm2
glial cells missing homolog 2 MGI:1861438 |
Darker colors indicate more annotations |
Human Phenotypes | Chondrocalcinosis |
Osteopenia |
Generalized osteoporosis |
Cerebral calcification |
Disease(s) Associated with GCM2 | ||||
familial isolated hypoparathyroidism | ||||
hyperparathyroidism |
Mouse Phenotypes | abnormal trabecular bone morphology |
increased bone mass |
abnormal bone ossification |
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Availability | Mouse Genotype | |||
Gcm2tm1Kry/Gcm2tm1Kry |
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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