Symbol Name ID |
Pomt1
protein-O-mannosyltransferase 1 MGI:2138994 |
Darker colors indicate more annotations |
Human Phenotypes | Abdominal pain |
Autistic behavior |
Disease(s) Associated with POMT1 | ||
autosomal recessive limb-girdle muscular dystrophy type 2K |
Mouse Phenotypes | abnormal optokinetic reflex |
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Availability | Mouse Genotype | |
Pomt1tm1c(EUCOMM)Hmgu/Pomt1tm1c(EUCOMM)Hmgu Tg(Crx-cre)1Tfur/0 (conditional) |
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 07/02/2024 MGI 6.13 |
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