|
Symbol Name ID |
Alg9
ALG9 alpha-1,2-mannosyltransferase MGI:1924753 |
| Darker colors indicate more annotations |
| Human Phenotypes | Low posterior hairline |
Frontal bossing |
Brachycephaly |
Micrognathia |
Microretrognathia |
Shallow orbits |
Microcephaly |
Progressive microcephaly |
Prominent metopic ridge |
Delayed cranial suture closure |
Wide anterior fontanel |
Abnormal facial shape |
Long philtrum |
Smooth philtrum |
Thin upper lip vermilion |
Bifid uvula |
Wide mouth |
Low insertion of columella |
Underdeveloped nasal alae |
Convex nasal ridge |
Depressed nasal bridge |
Short nose |
Telecanthus |
| Disease(s) Associated with ALG9 | |||||||||||||||||||||||
| congenital disorder of glycosylation Il |
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 04/09/2024 MGI 6.23 |
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