Symbol Name ID |
Smarca4
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 MGI:88192 |
Darker colors indicate more annotations |
Human Phenotypes | Sparse scalp hair |
Dandy-Walker malformation |
Microcephaly |
Coarse facial features |
Thick lower lip vermilion |
Long philtrum |
Short philtrum |
Everted upper lip vermilion |
Thin upper lip vermilion |
Cleft palate |
Macroglossia |
Wide mouth |
Anteverted nares |
Thick nasal alae |
Depressed nasal bridge |
Narrow nasal bridge |
Wide nasal bridge |
Wide nose |
Thick eyebrow |
Long eyelashes |
Disease(s) Associated with SMARCA4 | ||||||||||||||||||||
Coffin-Siris syndrome 4 |
Mouse Phenotypes | micrognathia |
|
Availability | Mouse Genotype | |
Smarca4b2b508.1Clo/Smarca4b2b508.1Clo |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/16/2024 MGI 6.23 |
|
|