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Symbol Name ID |
Mecp2
methyl CpG binding protein 2 MGI:99918 |
| Darker colors indicate more annotations |
| Human Phenotypes | Facial hypotonia |
Wrist flexion contracture |
Flexion contracture |
Rigidity |
Spasticity |
Lower limb spasticity |
Spastic paraplegia |
Spastic tetraplegia |
Progressive spasticity |
Spastic gait |
Hypotonia |
Axial hypotonia |
Generalized hypotonia |
Infantile muscular hypotonia |
Neonatal hypotonia |
Generalized neonatal hypotonia |
Skeletal muscle atrophy |
| Disease(s) Associated with MECP2 | |||||||||||||||||
| Rett syndrome | |||||||||||||||||
| severe congenital encephalopathy due to MECP2 mutation | |||||||||||||||||
| syndromic X-linked intellectual disability Lubs type | |||||||||||||||||
| X-linked intellectual disability-psychosis-macroorchidism syndrome |
| Mouse Phenotypes | increased muscle fatigability |
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| Availability | Mouse Genotype | |
| Mecp2tm1.1Bird/Y | ||
| Mecp2tm1Nlnd/Y | ||
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 08/27/2024 MGI 6.24 |
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