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Symbol
Name
ID
Arid1b
AT-rich interaction domain 1B
MGI:1926129
Phenotype annotations related to craniofacial
Darker colors indicate more annotations
Human Phenotypes
Low anterior hairline
Sparse scalp hair
Frontal bossing
Brachycephaly
Plagiocephaly
Retrognathia
Dandy-Walker malformation
Microcephaly
Abnormal facial shape
Coarse facial features
Preauricular skin tag
Short chin
Thick lower lip vermilion
Broad philtrum
Long philtrum
Short philtrum
Thin upper lip vermilion
Cleft palate
High palate
Wide mouth
Conical tooth
Microdontia
Delayed eruption of teeth
Choanal atresia
Anteverted nares
Thick nasal alae
Broad nasal tip
Wide nasal base
Depressed nasal bridge
Short nose
Recurrent upper respiratory tract infections
Thick eyebrow
Long eyelashes
Prominent eyelashes
Downslanted palpebral fissures
Periorbital ecchymosis with tarsal plate sparing
Disease(s) Associated with ARID1B
Coffin-Siris syndrome
Coffin-Siris syndrome 1
neuroblastoma


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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory