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Symbol Name ID |
Chtop
chromatin target of PRMT1 MGI:1913761 |
| Darker colors indicate more annotations |
| Mouse Phenotypes | myelocele |
abnormal adenohypophysis morphology |
abnormal neurohypophysis morphology |
abnormal pineal gland morphology |
small superior cervical ganglion |
reduced sympathetic cervical ganglion size |
holoprosencephaly |
abnormal brain interventricular foramen morphology |
abnormal choroid plexus morphology |
abnormal forebrain morphology |
abnormal olfactory bulb position |
absent olfactory bulb |
abnormal brachial plexus formation |
small nodose ganglion |
absent hypoglossal nerve |
thin hypoglossal nerve |
absent dorsal root ganglion |
fused dorsal root ganglion |
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| Availability | Mouse Genotype | ||||||||||||||||||
| Chtoptm1a(EUCOMM)Wtsi/Chtoptm1a(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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