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Symbol Name ID |
Pign
phosphatidylinositol glycan anchor biosynthesis, class N MGI:1351629 |
| Darker colors indicate more annotations |
| Human Phenotypes | Frontal bossing |
Micrognathia |
Macrocephaly |
Short distal phalanx of finger |
Abnormal ilium morphology |
| Disease(s) Associated with PIGN | |||||
| multiple congenital anomalies-hypotonia-seizures syndrome 1 |
| Mouse Phenotypes | abnormal cranium morphology |
abnormal cranial cartilage morphology |
abnormal interparietal bone morphology |
small interparietal bone |
abnormal occipital bone morphology |
abnormal supraoccipital bone morphology |
short femur |
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| Availability | Mouse Genotype | |||||||
| Pignm1Nisw/Pignm1Nisw | ||||||||
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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