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Symbol Name ID |
Cyp17a1
cytochrome P450, family 17, subfamily a, polypeptide 1 MGI:88586 |
| Darker colors indicate more annotations |
| Human Phenotypes | Accelerated skeletal maturation |
Abnormal thorax morphology |
Back pain |
Osteoporosis |
| Disease(s) Associated with CYP17A1 | ||||
| congenital adrenal hyperplasia | ||||
| osteoporosis | ||||
| pancreatic cancer |
| Mouse Phenotypes | abnormal bone structure |
decreased bone mineral content |
decreased bone mineral density |
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| Availability | Mouse Genotype | |||
| Cyp17a1tm1b(EUCOMM)Wtsi/Cyp17a1tm1b(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 04/23/2024 MGI 6.23 |
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