|
Symbol Name ID |
Arid1a
AT-rich interaction domain 1A MGI:1935147 |
| Darker colors indicate more annotations |
| Human Phenotypes | Dandy-Walker malformation |
Microcephaly |
Horner syndrome |
Abnormal corpus callosum morphology |
Cerebellar hypoplasia |
Spinal cord compression |
Neuroblastoma |
Neoplasm of the nervous system |
Ataxia |
Myoclonus |
Delayed speech and language development |
Irritability |
Hyperactivity |
Intellectual disability |
Antalgic gait |
Global developmental delay |
Seizure |
| Disease(s) Associated with ARID1A | |||||||||||||||||
| Coffin-Siris syndrome 2 | |||||||||||||||||
| neuroblastoma |
| Mouse Phenotypes | abnormal cardiac neural crest cell morphology |
open neural tube |
forebrain hypoplasia |
|
| Availability | Mouse Genotype | |||
| Arid1am1Mag/Arid1am1Mag | ||||
| Arid1atm1.1Mag/Arid1atm1.1Mag 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) |
||
|
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 05/14/2024 MGI 6.23 |
|
|
|
||
Analysis Tools