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Symbol
Name
ID
Smarca4
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4
MGI:88192
Phenotype annotations related to craniofacial
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

Contributing Projects:
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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Funding Information
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory