Symbol Name ID |
Arid1a
AT-rich interaction domain 1A MGI:1935147 |
Darker colors indicate more annotations |
Human Phenotypes | Dandy-Walker malformation |
Microcephaly |
Short distal phalanx of finger |
Sandal gap |
Brachydactyly |
Delayed skeletal maturation |
Bone pain |
Pathologic fracture |
Disease(s) Associated with ARID1A | ||||||||
Coffin-Siris syndrome 2 | ||||||||
neuroblastoma |
Mouse Phenotypes | abnormal cranium morphology |
abnormal neurocranium morphology |
small temporal bone squamous part |
short premaxilla |
abnormal palatine bone morphology |
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Availability | Mouse Genotype | |||||
Arid1atm1.1Mag/Arid1atm1.1Mag H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
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Arid1atm1.1Mag/Arid1a+ H2az2Tg(Wnt1-cre)11Rth/H2az2+ (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 04/30/2024 MGI 6.23 |
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