|
Symbol Name ID |
Nog
noggin MGI:104327 |
| Darker colors indicate more annotations |
| Human Phenotypes | Shallow orbits |
Astigmatism |
Optic nerve hypoplasia |
Hypertelorism |
Hypotelorism |
Proptosis |
Abnormality of eye movement |
Strabismus |
Hypermetropia |
Myopia |
Amblyopia |
Visual field defect |
Ptosis |
| Disease(s) Associated with NOG | |||||||||||||
| brachydactyly type B2 | |||||||||||||
| craniosynostosis | |||||||||||||
| Huntington's disease | |||||||||||||
| multiple synostoses syndrome 1 | |||||||||||||
| proximal symphalangism |
| Mouse Phenotypes | abnormal eye development |
abnormal optic vesicle formation |
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| Availability | Mouse Genotype | ||
| Nogem1(IMPC)Mbp/Nogem1(IMPC)Mbp | |||
| Nogtm1Amc/Nogtm1Amc | |||
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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