|
Symbol Name ID |
Brd4
bromodomain containing 4 MGI:1888520 |
| Darker colors indicate more annotations |
| Human Phenotypes | Low posterior hairline |
Increased nuchal translucency |
Short neck |
Delayed puberty |
Congenital diaphragmatic hernia |
Short stature |
Failure to thrive |
Truncal obesity |
Intrauterine growth retardation |
Severe postnatal growth retardation |
| Disease(s) Associated with BRD4 | ||||||||||
| Cornelia de Lange syndrome |
| Mouse Phenotypes | short nasal bone |
embryonic growth retardation |
postnatal growth retardation |
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| Availability | Mouse Genotype | |||
| Brd4Gt(pGT1.8TM)ST132Nimr/Brd4+ | ||||
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 04/09/2024 MGI 6.23 |
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