Symbol Name ID |
Mbd5
methyl-CpG binding domain protein 5 MGI:2138934 |
Darker colors indicate more annotations |
Human Phenotypes | Low posterior hairline |
Short stature |
Postnatal growth retardation |
Disease(s) Associated with MBD5 | |||
autosomal dominant intellectual developmental disorder 1 |
Mouse Phenotypes | abnormal nasal bone morphology |
abnormal lip morphology |
decreased body weight |
cachexia |
decreased body size |
postnatal growth retardation |
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Availability | Mouse Genotype | ||||||
Mbd5tm1.2Gxu/Mbd5tm1.2Gxu | |||||||
Mbd5Gt(Ayu21-B205)Imeg/Mbd5+ | |||||||
Mbd5tm1b(EUCOMM)Wtsi/Mbd5+ | |||||||
Mbd5tm1.1Gxu/Mbd5tm1.1Gxu Tg(Nes-cre)1Kln/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 04/23/2024 MGI 6.23 |
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