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Query results
Results for
MEF2C
Expand for information on MEF2C
MEF2C
Description
myocyte enhancer factor 2C
Aliases
C5DELq14.3, DEL5q14.3
Gene Identifiers
mRNA Identifiers
RefSeq (mRNA)
NM_001131005.2; NM_001193347.1; NM_001193348.1; NM_001193349.2; NM_001193350.2; NM_001308002.3; NM_001363581.1; NM_001364329.2; NM_001364330.2; NM_001364331.2; NM_001364332.1; NM_001364333.2; NM_001364334.1; NM_001364335.1; NM_001364336.1; NM_001364337.1; NM_001364338.1; NM_001364339.2; NM_001364340.1; NM_001364341.1; NM_001364342.1; NM_001364343.1; NM_001364344.2; NM_001364345.2; NM_001364346.2; NM_001364347.2; NM_001364348.2; NM_001364349.2; NM_001364350.1; NM_001364352.2; NM_001364353.2; NM_001364354.2; NM_001364355.2; NM_001364356.1; NM_001364357.1; NM_002397.5; XM_005248511.3; XM_006714625.4; XM_011543396.3; XM_011543397.3; XM_017009475.2; XM_017009478.2; XM_024446055.1; XM_024446056.1; XM_024446057.1; XM_024446058.1; XM_024446059.1
Protein Identifiers
RefSeq (protein)
NP_001124477.1; NP_001180276.1; NP_001180277.1; NP_001180278.1; NP_001180279.1; NP_001294931.1; NP_001350510.1; NP_001351258.1; NP_001351259.1; NP_001351260.1; NP_001351261.1; NP_001351262.1; NP_001351263.1; NP_001351264.1; NP_001351265.1; NP_001351266.1; NP_001351267.1; NP_001351268.1; NP_001351269.1; NP_001351270.1; NP_001351271.1; NP_001351272.1; NP_001351273.1; NP_001351274.1; NP_001351275.1; NP_001351276.1; NP_001351277.1; NP_001351278.1; NP_001351279.1; NP_001351281.1; NP_001351282.1; NP_001351283.1; NP_001351284.1; NP_001351285.1; NP_001351286.1; NP_002388.2; XP_005248568.1; XP_006714688.1; XP_011541698.1; XP_011541699.1; XP_016864964.1; XP_016864967.1; XP_024301823.1; XP_024301824.1; XP_024301825.1; XP_024301826.1; XP_024301827.1
Uniprot ID
Q06413; Q06413; Q06413; Q06413; D8L7E9; Q06413; A0A024RAL7; Q06413; A0A024RAL6; A0A024RAL7; Q06413; A0A024RAL7; Q06413; Q06413; A0A024RAL7; Q06413; A0A0D9SGI5; A0A0D9SGI5; Q06413
Ensembl protein ID
ENSP00000389610.2; ENSP00000340874.5; ENSP00000487311.1; ENSP00000396219.2; ENSP00000423597.2; ENSP00000487184.1; ENSP00000486554.1; ENSP00000426665.2; ENSP00000424606.1; ENSP00000490630.1; ENSP00000422390.2; ENSP00000486490.1; ENSP00000425636.1; ENSP00000487437.2; ENSP00000421925.4; ENSP00000490473.1; ENSP00000487538.1
Protein Architecture
SMART
Disease Mapping
Druggability
- Candidate cancer driver
- Damaged in 47/7921 TCGA samples
- Damaged in 13/1291 cell lines
- Fewer loss of function mutations
- Equal damaging SNVs/indels
- Fewer structural variants