Symbol Name ID |
Mettl23
methyltransferase like 23 MGI:1921569 |
Darker colors indicate more annotations |
Human Phenotypes | Intellectual disability |
Intellectual disability, mild |
Global developmental delay |
Bilateral tonic-clonic seizure |
Focal-onset seizure |
Disease(s) Associated with METTL23 | |||||
autosomal recessive intellectual developmental disorder 44 |
Mouse Phenotypes | retina ganglion cell degeneration |
abnormal optic disk morphology |
optic nerve atrophy |
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Availability | Mouse Genotype | |||
Mettl23em1(IMPC)Hmgu/Mettl23em1(IMPC)Hmgu | ||||
Mettl23em1Itwa/Mettl23em1Itwa | ||||
Mettl23em2Itwa/Mettl23em2Itwa | ||||
Mettl23em1Itwa/Mettl23+ | ||||
Mettl23em2Itwa/Mettl23+ |
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 09/03/2024 MGI 6.24 |
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