Symbol Name ID |
Mbd5
methyl-CpG binding domain protein 5 MGI:2138934 |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Secondary microcephaly |
Hypoplasia of the frontal lobes |
Cerebellar vermis hypoplasia |
Ataxia |
Aggressive behavior |
Inappropriate laughter |
Reduced eye contact |
Language impairment |
Anxiety |
Reduced social responsiveness |
Autistic behavior |
Polyphagia |
Bruxism |
Recurrent hand flapping |
Self-injurious behavior |
Short attention span |
Intellectual disability |
Intellectual disability, severe |
Global developmental delay |
Motor delay |
Delayed ability to sit |
Seizure |
Febrile seizure (within the age range of 3 months to 6 years) |
Disease(s) Associated with MBD5 | ||||||||||||||||||||||||
autosomal dominant intellectual developmental disorder 1 |
Mouse Phenotypes | small pituitary gland |
increased brain weight |
abnormal neurite morphology |
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Availability | Mouse Genotype | |||
Mbd5tm1.2Gxu/Mbd5tm1.2Gxu | ||||
Mbd5Gt(Ayu21-B205)Imeg/Mbd5+ |
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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