|
Symbol Name ID |
Arid1b
AT-rich interaction domain 1B MGI:1926129 |
| Darker colors indicate more annotations |
| Human Phenotypes | Frontal bossing |
Brachycephaly |
Plagiocephaly |
Retrognathia |
Dandy-Walker malformation |
Microcephaly |
Short distal phalanx of the 5th finger |
Short 5th finger |
Clinodactyly of the 5th finger |
Prominent interphalangeal joints |
Prominent fingertip pads |
Short distal phalanx of the 5th toe |
Aplasia/Hypoplasia of the distal phalanges of the toes |
Sandal gap |
Clinodactyly |
Coxa valga |
Aplasia/Hypoplasia of the patella |
Dislocated radial head |
Sacral dimple |
Joint hypermobility |
Delayed skeletal maturation |
Bone pain |
Pathologic fracture |
Short sternum |
Kyphosis |
Scoliosis |
| Disease(s) Associated with ARID1B | ||||||||||||||||||||||||||
| Coffin-Siris syndrome | ||||||||||||||||||||||||||
| Coffin-Siris syndrome 1 | ||||||||||||||||||||||||||
| neuroblastoma |
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 |
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