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Repository for lectin-assisted multimodality data
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MIRAGE
microcephaly
Summary
- Synonym
-
- Microcephalus
- microencephaly
- Definition
- A congenital nervous system abnormality that is characterized by a significantly smaller than normal head in infants.
- Super Class
- congenital nervous system abnormality
External Links
- Disease Ontology
- DOID:10907
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- GARD
- MGI genotype (from TogoID)
- WikiPathways (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 7846 | TUBA1A | tubulin alpha 1a | |
| 9343 | EFTUD2 | elongation factor Tu GTP binding domain containing 2 | |
| 55755 | CDK5RAP2 | CDK5 regulatory subunit associated protein 2 | |
| 60386 | SLC25A19 | solute carrier family 25 member 19 | |
| 64324 | NSD1 | nuclear receptor binding SET domain protein 1 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q15029 | 116 kDa U5 small nuclear ribonucleoprotein component | |
| Q71U36 | Tubulin alpha-1A chain | |
| Q96L73 | Histone-lysine N-methyltransferase, H3 lysine-36 specific | |
| Q96SN8 | CDK5 regulatory subunit-associated protein 2 | |
| Q9HC21 | Mitochondrial thiamine pyrophosphate carrier |
| UniProt ID | Protein Name | Source |
|---|---|---|
| P99024 | Tubulin beta-5 chain |
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9VI72 | Spindle assembly abnormal 4 |
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q5U3U7 | Sodium-dependent lysophosphatidylcholine symporter 1-A |
