Entity Details
Primary name |
IL11RA |
Entity type |
gene |
Source |
Source Link |
Details
PrimaryID | 3590 |
RefseqGene | NG_028966 |
Symbol | IL11RA |
Name | interleukin 11 receptor subunit alpha |
Chromosome | 9 |
Location | 9p13.3 |
TaxID | 9606 |
Status | live |
SourceGenome | genomic |
SourceOrigin | natural |
CreationDate | 1996-06-19 |
ModificationDate | 2021-06-20 |
Diseases
Show/Hide Table
Disease ID | Source | Name | Description |
614188 | OMIM | Craniosynostosis and dental anomalies (CRSDA) | A disorder characterized by craniosynostosis, maxillary hypoplasia, and dental anomalies, including malocclusion, delayed and ectopic tooth eruption, and/or supernumerary teeth. Some patients also display minor digit anomalies, such as syndactyly and/or clinodactyly. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
2 interactions