|
Symbol Name ID |
Nsd2
nuclear receptor binding SET domain protein 2 MGI:1276574 |
| Darker colors indicate more annotations |
| Human Phenotypes | Micrognathia |
Craniofacial asymmetry |
Microcephaly |
Frontal bossing |
Calvarial skull defect |
Dolichocephaly |
High anterior hairline |
Prominent glabella |
High forehead |
Preauricular pit |
Preauricular skin tag |
Abnormality of the mouth |
Abnormal lip morphology |
Abnormality of the philtrum |
Short philtrum |
Cleft upper lip |
Short upper lip |
Cleft palate |
Downturned corners of mouth |
Hypodontia |
Oral cleft |
Convex nasal ridge |
Wide nasal bridge |
Highly arched eyebrow |
Downslanted palpebral fissures |
Epicanthus |
Low posterior hairline |
| Disease(s) Associated with NSD2 | |||||||||||||||||||||||||||
| Wolf-Hirschhorn syndrome |
| Mouse Phenotypes | malocclusion |
cleft palate |
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| Availability | Mouse Genotype | ||
| Nsd2tm1Ykan/Nsd2tm1Ykan | |||
| Nsd2tm1Ykan/Nsd2+ | |||
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 10/08/2019 MGI 6.14 |
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