MID2 (midline 2)

2017-01-01  

Identity

HGNC
LOCATION
Xq22.3
LOCUSID
ALIAS
FXY2,MRX101,RNF60,TRIM1
FUSION GENES

Other Information

Locus ID:

NCBI: 11043
MIM: 300204
HGNC: 7096
Ensembl: ENSG00000080561

Variants:

dbSNP: 11043
ClinVar: 11043
TCGA: ENSG00000080561
COSMIC: MID2

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000080561ENST00000262843Q9UJV3
ENSG00000080561ENST00000443968Q9UJV3
ENSG00000080561ENST00000451923A6PVI4

Expression (GTEx)

0
5
10
15

References

Pubmed IDYearTitleCitations
118067522002MID1 and MID2 homo- and heterodimerise to tether the rapamycin-sensitive PP2A regulatory subunit, alpha 4, to microtubules: implications for the clinical variability of X-linked Opitz GBBB syndrome and other developmental disorders.28
241153872014Targeted deep resequencing identifies MID2 mutation for X-linked intellectual disability with varied disease severity in a large kindred from India.11
162836792005An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndrome.8
267486992016The X-Linked-Intellectual-Disability-Associated Ubiquitin Ligase Mid2 Interacts with Astrin and Regulates Astrin Levels to Promote Cell Division.7
267917552016Midline2 is overexpressed and a prognostic indicator in human breast cancer and promotes breast cancer cell proliferation in vitro and in vivo.5

Citation

Dessen P

MID2 (midline 2)

Atlas Genet Cytogenet Oncol Haematol. 2017-01-01

Online version: http://atlasgeneticsoncology.org/gene/56701/mid2