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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 |
Long face |
Narrow face |
Short chin |
Short philtrum |
Smooth philtrum |
Thick upper lip vermilion |
Underdeveloped nasal alae |
Prominent nasal bridge |
Wide nasal bridge |
Prominent nose |
Synophrys |
Thick eyebrow |
Blepharophimosis |
Telecanthus |
| Disease(s) Associated with NSUN2 | |||||||||||||||
| autosomal recessive intellectual developmental disorder 5 |
| Mouse Phenotypes | abnormal cranium morphology |
basisphenoid bone foramen |
absent hypoglossal canal |
abnormal tooth morphology |
abnormal snout 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 04/16/2024 MGI 6.23 |
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