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Symbol Name ID |
Nsun2
NOL1/NOP2/Sun domain family member 2 MGI:107252 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Spasticity |
Delayed speech and language development |
Dysarthria |
Intellectual disability |
Intellectual disability, moderate |
Hyperreflexia |
Broad-based gait |
Global developmental delay |
Seizure |
| Disease(s) Associated with NSUN2 | ||||||||||
| autosomal recessive intellectual developmental disorder 5 |
| Mouse Phenotypes | absent segment of posterior cerebral artery |
increased trigeminal neuroma incidence |
small superior cervical ganglion |
reduced sympathetic cervical ganglion size |
abnormal forebrain morphology |
abnormal hypoglossal nerve topology |
absent hypoglossal nerve |
thin hypoglossal nerve |
abnormal optic chiasm morphology |
thin motoric part of trigeminal nerve |
abnormal dorsal root ganglion morphology |
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| Availability | Mouse Genotype | |||||||||||
| Nsun2tm1a(EUCOMM)Wtsi/Nsun2tm1a(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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