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Symbol Name ID |
Alg8
ALG8 alpha-1,3-glucosyltransferase MGI:2141959 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hydrops fetalis |
Oligohydramnios |
Decreased fetal movement |
| Disease(s) Associated with ALG8 | |||
| congenital disorder of glycosylation Ih |
| Mouse Phenotypes | abnormal embryo turning |
embryonic growth retardation |
abnormal embryo size |
abnormal chorioallantoic fusion |
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| Availability | Mouse Genotype | ||||
| Alg8em1(IMPC)J/Alg8em1(IMPC)J | |||||
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 04/30/2024 MGI 6.23 |
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