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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 |
4-5 toe syndactyly |
Achilles tendon contracture |
| 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 humerus morphology |
abnormal deltoid tuberosity morphology |
decreased length of long bones |
abnormal rib morphology |
abnormal spine curvature |
kyphosis |
lordosis |
fusion of vertebral arches |
decreased bone mineral content |
decreased bone mineral density |
abnormal joint 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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