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Repository for lectin-assisted multimodality data
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MIRAGE
autosomal dominant intellectual developmental disorder
Summary
- Synonym
-
- autosomal dominant mental retardation
- autosomal dominant non-syndromic mental retardation
- Definition
- A intellectual disability characterized by an autosomal dominant inheritance pattern.
- Super Class
- autosomal dominant disease intellectual disability
External Links
- Disease Ontology
- DOID:0060307
- Mondo Disease Ontology
- ORDO
- GARD
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 23036 | ZNF292 | zinc finger protein 292 | |
| 23524 | SRRM2 | serine/arginine repetitive matrix 2 | |
| 29072 | SETD2 | SET domain containing 2, histone lysine methyltransferase | |
| 57609 | DIP2B | disco interacting protein 2 homolog B | |
| 64864 | RFX7 | regulatory factor X7 | |
| 81562 | LMAN2L | lectin, mannose binding 2 like |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9BYW2 | Histone-lysine N-methyltransferase SETD2 | |
| Q9H0V9 | VIP36-like protein | |
| Q9P265 | Disco-interacting protein 2 homolog B | |
| Q9UHV7 | Mediator of RNA polymerase II transcription subunit 13 | |
| Q9UMN6 | Histone-lysine N-methyltransferase 2B | |
| Q9UQ35 | Serine/arginine repetitive matrix protein 2 |
