MKRN3


Summary: The protein encoded by this gene contains a RING (C3HC4) zinc finger motif and several C3H zinc finger motifs. This gene is intronless and imprinted, with expression only from the paternal allele. Disruption of the imprinting at this locus may contribute to Prader-Willi syndrome. An antisense RNA of unknown function has been found overlapping this gene. [provided by RefSeq, Jul 2008].

Loading, please wait...
Name
OMIM ID
Ensembl ID
HGNC ID
PHARMGKB ID
Map Location

GO terms in MKRN3


Loading, please wait...
Term Type
Evidence Type
GO Term ID
GO Des.
CC TAS GO:1990904 ribonucleoprotein complex
BP IEA GO:0016567 protein ubiquitination
MF IPI GO:0005515 protein binding
MF IEA GO:0016740 transferase activity
MF IPI GO:0042802 identical protein binding
MF IEA GO:0046872 metal ion binding
Showing 1 to 6 of 6 rows

Gene expression in normal tissue: MKRN3

Gene-model tissue-cancer distribution: Bubble Plot

Gene-drug pathway distribution

undefined21Protein stability and degradation2Cell cycle1PI3K/MTOR signaling1Other, kinases1Apoptosis regulation1

Pathways in MKRN3


Loading, please wait...
Database
Pathway ID
Pathway Des.
wikipathways WP3998 Prader-Willi and Angelman Syndrome
Showing 1 to 1 of 1 rows

Gene-Drug: Aster Plot


Loading, please wait...
Drug ID
Drug Name
Model Num.
iGMDRD505 Pevonedistat 4
iGMDRD886 Compound 1541A 3
iGMDRD882 CIL41 2
iGMDRD577 BIX01294 3
Showing 1 to 4 of 27 rows rows per page

Gene in drug-gene network: Network Plot

Gene-drug targets distribution

Gene Structure: PDB

Models in MKRN3

Loading, please wait...
Model
Level
Reference ID
Tissue
Cancer
Drug
Clinical Response
Source
No matching records found

​​​​