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Details of MED23 gene in Homo sapiens
IDs |
|---|
| Link outs |
Gene Name |
Alias |
Uniprot ID |
SwissProt ID |
NCBI gene ID |
ENSEMBL ID |
Description |
Source |
|
| MED23 | ARC130,CRSP3,DRIP130,KIAA1216,SUR2 | Q9ULK4 | MED23_HUMAN | 9439
| ENSG00000112282
| Mediator of RNA polymerase II transcription subunit 23 | SPROT |
Disease |
|---|
| Disease |
OMIM id |
| Mental retardation, autosomal recessive 18 (MRT18) [MIM:614249]: A disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptative behavior and manifested during the developmental period. Note=The disease is caused by mutations affecting the gene represented in this entry. |
614249 |
Orthologs in other species |
|---|
| M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
|
