Symbol Name ID |
Pomgnt1
protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase MGI:1915523 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Cardiomyopathy |
Abnormal EKG |
Abnormal retinal vascular morphology |
Attenuation of retinal blood vessels |
Disease(s) Associated with POMGNT1 | ||||
muscular dystrophy | ||||
retinitis pigmentosa |
Mouse Phenotypes | cardiovascular system phenotype |
abnormal retina blood vessel pattern |
retina microaneurysm |
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Availability | Mouse Genotype | |||
Pomgnt1Gt(OST179231)Lex/Pomgnt1Gt(OST179231)Lex | * | |||
Pomgnt1tm1Lex/Pomgnt1tm1Lex |
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 04/23/2024 MGI 6.23 |
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