Identity
HGNC
LOCATION
Xq13.1
LOCUSID
ALIAS
ARC240,CAGH45,FGS1,HOPA,Kto,MED12S,OHDOX,OKS,OPA1,TNRC11,TRAP230
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 9968
MIM: 300188
HGNC: 11957
Ensembl: ENSG00000184634
Variants:
dbSNP: 9968
ClinVar: 9968
TCGA: ENSG00000184634
COSMIC: MED12
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 36894399 | 2024 | MED12 variants associated with X-linked recessive partial epilepsy without intellectual disability. | 0 |
| 37516697 | 2024 | The Mediator Complex Subunit 12 (MED-12) Gene and Uterine Fibroids: a Systematic Review. | 0 |
| 38279317 | 2024 | The Effect of Race/Ethnicity and MED12 Mutation on the Expression of Long Non-Coding RNAs in Uterine Leiomyoma and Myometrium. | 2 |
| 38290796 | 2024 | Racial disparity in uterine leiomyoma: new insights of genetic and environmental burden in myometrial cells. | 1 |
| 36894399 | 2024 | MED12 variants associated with X-linked recessive partial epilepsy without intellectual disability. | 0 |
| 37516697 | 2024 | The Mediator Complex Subunit 12 (MED-12) Gene and Uterine Fibroids: a Systematic Review. | 0 |
| 38279317 | 2024 | The Effect of Race/Ethnicity and MED12 Mutation on the Expression of Long Non-Coding RNAs in Uterine Leiomyoma and Myometrium. | 2 |
| 38290796 | 2024 | Racial disparity in uterine leiomyoma: new insights of genetic and environmental burden in myometrial cells. | 1 |
| 36150519 | 2023 | MED12 mutations in uterine leiomyomas: prediction of volume reduction by gonadotropin-releasing hormone agonists. | 2 |
| 36271811 | 2023 | Missense MED12 variants in 22 males with intellectual disability: From nonspecific symptoms to complete syndromes. | 1 |
| 36835153 | 2023 | Differential Expression of MED12-Associated Coding RNA Transcripts in Uterine Leiomyomas. | 6 |
| 37668348 | 2023 | RISING STARS: Role of MED12 mutation in the pathogenesis of uterine fibroids. | 1 |
| 38129817 | 2023 | Novel pathogenic variant in MED12 causing non-syndromic dilated cardiomyopathy. | 0 |
| 36150519 | 2023 | MED12 mutations in uterine leiomyomas: prediction of volume reduction by gonadotropin-releasing hormone agonists. | 2 |
| 36271811 | 2023 | Missense MED12 variants in 22 males with intellectual disability: From nonspecific symptoms to complete syndromes. | 1 |
Citation
Dessen P
MED12 (mediator complex subunit 12)
Atlas Genet Cytogenet Oncol Haematol. 2011-11-01
Online version: http://atlasgeneticsoncology.org/gene/52444
