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Symbol Name ID |
Setd5
SET domain containing 5 MGI:1920145 |
| Darker colors indicate more annotations |
| Human Phenotypes | Delayed speech and language development |
Autistic behavior |
Compulsive behaviors |
Intellectual disability |
Global developmental delay |
Delayed ability to walk |
| Disease(s) Associated with SETD5 | ||||||
| autosomal dominant intellectual developmental disorder 23 |
| Mouse Phenotypes | anastomosis between internal carotid artery and basilar artery |
absent segment of posterior cerebral artery |
abnormal pineal gland morphology |
small superior cervical ganglion |
reduced sympathetic cervical ganglion size |
abnormal forebrain morphology |
abnormal olfactory bulb morphology |
abnormal hindbrain morphology |
abnormal hypoglossal nerve topology |
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| Availability | Mouse Genotype | |||||||||
| Setd5tm1a(EUCOMM)Wtsi/Setd5+ | ||||||||||
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 07/05/2024 MGI 6.24 |
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