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Gene Symbol:
MDM2
Entrez Gene ID
4193
Gene Name:
MDM2 proto-oncogene
Gene Aliases
ACTFS, HDMX, hdm2
Gene Chromosome Location
Chr.12: on Build GRCh38
UniGene
Hs.484551
Species:
Human
Primer Chromosome Location
Chr.12: 68828692-68828925 on Build GRCh38
Amplicon Length
234
Primer Sequences
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Ampliseq ID's
Primer ID Hs00761736_CE
Primer 5'-tail Option
Purification
Primer Pair /FWD/REV
Synthesis Scale 25 nmol
Availability Made To Order
Catalog #'s A15629,A15630
Price (USD) USD 16.46,USD 16.46

Genomic Map

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Assay Details

Gene Information


MDM2
Accession Protein COSMIC ID Mutation AA
RefSeq NM_001145337.2 NP_001138809.1 - - -
NM_001145339.2 NP_001138811.1 - - -
NM_001145340.2 NP_001138812.1 - - -
NM_001278462.1 NP_001265391.1 - - -
NM_002392.5 NP_002383.2 6908694 c.629A>T p.E210V
4044444 c.671C>T p.T224M
6935841 c.548G>A p.G183D
1639226 c.583A>G p.I195V
6931936 c.628G>A p.E210K
1257522 c.664A>T p.T222S
6968212 c.677C>G p.S226W
217034 c.614T>A p.L205Q
4501394 c.587C>T p.S196F
6913416 c.554G>C p.R185P
942905 c.678G>A p.S226S
6940116 c.628_639del12 p.I211_E214delICCE
1606548 c.566G>A p.R189H
7148804 c.658G>A p.E220K
1214768 c.565C>T p.R189C
6462865 c.545C>T p.S182F
368555 c.662C>G p.S221C
5020625 c.607C>T p.L203L
6357826 c.550G>A p.E184K
3356352 c.614T>C p.L205P
282733 c.630G>T p.E210D
6921608 c.677C>A p.S226*
6916631 c.535G>T p.D179Y
6023216 c.572A>G p.K191R
5792965 c.648C>T p.S216S
4554043 c.609G>A p.L203L
XM_005268872.4 XP_005268929.1 - - -
XM_006719399.3 XP_006719462.1 - - -
XM_006719400.3 XP_006719463.1 - - -
GenBank AF092843.1 AAL40178.1 - - -
AF092844.1 AAL40179.1 - - -
AF092845.1 AAL40180.1 - - -
AF201370.1 AAF42995.1 - - -
AF201371.1 - - -
AF385322.1 AAL13242.1 - - -
AF385323.1 AAL13243.1 - - -
AF385324.1 AAL13244.1 - - -
AF385325.1 AAL13245.1 - - -
AF385326.1 AAL13246.1 - - -
AF385327.1 AAL13247.1 - - -
AJ276888.1 - - -
AJ278975.1 CAC07809.1 - - -
AJ278976.1 CAC07810.1 - - -
AJ278977.1 CAC07811.1 - - -
AJ278978.1 CAC07812.1 - - -
AJ430612.1 CAD23251.1 - - -
AJ430613.1 - - -
AJ430614.1 CAD23252.1 - - -
AJ491698.1 CAD36959.1 - - -
AJ491699.1 CAD36960.1 - - -
AJ491700.1 CAD36961.1 - - -
AJ550516.1 CAD79455.1 - - -
AJ550517.1 CAD79456.1 - - -
AJ550518.1 CAD79457.1 - - -
AJ550519.1 CAD79458.1 - - -
AJ550520.1 CAD79459.1 - - -
AK290341.1 - - -
AM902641.1 - - -
AM902642.1 - - -
AM902643.1 - - -
AM902644.1 - - -
AM902645.1 - - -
AM902646.1 - - -
AM902647.1 - - -
AM902648.1 - - -
AM902649.1 - - -
AM902650.1 - - -
AM902651.1 - - -
AM902652.1 - - -
AM902653.1 - - -
AM902654.1 - - -
AM902655.1 - - -
AM902656.1 - - -
AM902657.1 - - -
AM902658.1 - - -
AM902659.1 - - -
AM902660.1 - - -
AM902661.1 - - -
AM902662.1 - - -
AM902663.1 - - -
AM902664.1 - - -
AM902665.1 - - -
AM902666.1 - - -
AM902667.1 - - -
AM902668.1 - - -
AM902669.1 - - -
AM902670.1 - - -
AM902671.1 - - -
AM902672.1 - - -
AM902673.1 - - -
AM902674.1 - - -
AM902675.1 - - -
AM902676.1 - - -
AM902677.1 - - -
AM902678.1 - - -
AM902679.1 - - -
AM902680.1 - - -
AM902681.1 - - -
BC152384.1 - - -
BC152390.1 - - -
BT007258.1 AAP35922.1 - - -
ENST00000258149.0 - - -
EU076746.1 - - -
EU076747.1 - - -
EU076748.1 - - -
EU076749.1 - - -
GQ848196.1 - - -
HM213901.1 - - -
HM213902.1 - - -
HM213903.1 - - -
HM213904.1 - - -
JX015379.1 - - -
JX015380.1 - - -
JX015381.1 - - -
JX015382.1 - - -
JX015383.1 - - -
JX015384.1 - - -
JX015385.1 - - -
JX015387.1 - - -
JX015388.1 - - -
JX015389.1 - - -
JX015390.1 - - -
JX015391.1 - - -
JX015392.1 - - -
M92424.1 AAA60568.1 - - -
U33199.1 AAA75514.1 - - -
U33200.1 AAA75515.1 - - -
U33201.1 AAA75516.1 - - -
U33202.1 AAA75517.1 - - -
U33203.1 AAA75518.1 - - -
Z12020.1 CAA78055.1 - - -


Phenotype

MIM: 164785

Literature Links:

MDM2 PubMed Links

SNP ID

rs752390412 rs576062594 rs779990530 rs778675786 rs1795480 rs763423670 rs369948638 rs758396646 rs750452466 rs764783109 rs766801308 rs377246600 rs372899015 rs561760184 rs373328180 rs776774609 rs748134261 rs757225399 rs138567205 rs370504060 rs764554024 rs961573654 rs756673959 rs774688124 rs373759829 rs375746507 rs375488359 rs955096885 rs758319082 rs745680967 rs763587937 rs780006768

Submission count

NA

Allele Nomenclature



Chromosome Location

Chr.12: 68828734-68828734 on Build GRCh38

Allele Frequency



1000Genome Applied Biosystems® HapMap
Global - Not Available Caucasian - Not Available CEPH (CEU) - Not Available
EAS - Not Available African American - Not Available YRI (Yoruba) - Not Available
SAS - Not Available Chinese - Not Available CHB (Han Chinese) - Not Available
AFR - Not Available Japanese - Not Available JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available


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More Information


Set Membership:

 Between 200-400 bp

Panther Classification:

Gene Ontology Categories:

Function(s) Process(es)

Format:

Each primer will be delivered in a single tube, dried-down

Quick Reference Guide

Primer Designer™ Tool Quick Reference




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