Toggle navigation
Home
Browse
Tools
Mutation Finder
Variant Mapper
About
Display
NM_001400049.1 - NP_001386978.1
NM_001400057.1 - NP_001386986.1
NM_001400064.1 - NP_001386993.1
NM_001400061.1 - NP_001386990.1
NM_001352617.4 - NP_001339546.1
NM_001400036.1 - NP_001386965.1
NM_001400055.1 - NP_001386984.1
NM_001400039.1 - NP_001386968.1
NM_001400071.1 - NP_001387000.1
NM_001400031.1 - NP_001386960.1
NM_001400066.1 - NP_001386995.1
NM_001400053.1 - NP_001386982.1
NM_001400059.1 - NP_001386988.1
NM_001352615.4 - NP_001339544.1
NM_001400063.1 - NP_001386992.1
NM_001400032.1 - NP_001386961.1
NM_001400058.1 - NP_001386987.1
NM_001400050.1 - NP_001386979.1
NM_001400056.1 - NP_001386985.1
NM_001171894.5 - NP_001165365.1
NM_001400040.1 - NP_001386969.1
NM_001400038.1 - NP_001386967.1
NM_001400065.1 - NP_001386994.1
NM_001400035.1 - NP_001386964.1
NM_001352614.4 - NP_001339543.1
NM_001400028.1 - NP_001386957.1
NM_001319206.4 - NP_001306135.1 (MANE)
NM_001365208.3 - NP_001352137.1
NM_001393560.2 - NP_001380489.1
NM_001365201.3 - NP_001352130.1
NM_001352618.4 - NP_001339547.1
NM_001365203.3 - NP_001352132.1
NM_005587.6 - NP_005578.2
NM_001365209.3 - NP_001352138.1
NM_001393559.2 - NP_001380488.1
NM_001393558.2 - NP_001380487.1
NM_001400069.1 - NP_001386998.1
NM_001393561.3 - NP_001380490.1
NM_001400037.1 - NP_001386966.1
NM_001400033.1 - NP_001386962.1
NM_001400062.1 - NP_001386991.1
NM_001365205.3 - NP_001352134.1
NM_001130926.5 - NP_001124398.1
NM_001365202.3 - NP_001352131.1
NM_001365206.3 - NP_001352135.1
NM_001365204.3 - NP_001352133.1
NM_001365207.3 - NP_001352136.1
NM_001130927.5 - NP_001124399.1
NM_001130928.4 - NP_001124400.1
NM_001400067.1 - NP_001386996.1
NM_001400068.1 - NP_001386997.1
NM_001365211.2 - NP_001352140.1
NM_001365210.2 - NP_001352139.1
NM_001400070.1 - NP_001386999.1
NM_001400030.1 - NP_001386959.1
NM_001400034.1 - NP_001386963.1
NM_001400054.1 - NP_001386983.1
NM_001400029.1 - NP_001386958.1
NM_001400052.1 - NP_001386981.1
NM_001352616.4 - NP_001339545.1
NM_001400060.1 - NP_001386989.1
NM_001400051.1 - NP_001386980.1
DNA
Protein
Gene Info.
Genome Build
GRCh38
Chromosome
15
Location
Chr15:99,564,917-99,716,988
LOEUF
0.287
Variant filter
By data sources
ClinVar
Pathogenic/ Likely pa...
Risk factor
Drug response
Association
Affect
VUS
Benign/Likely benign
Others
GnomAD
Common [>1%]
Rare [<1%]
ToMMo
Common [>1%]
Rare [<1%]
By consequences
Missense
Loss-of-function
Synonymous
Others
Gene region:
CDS
SpliceSite
UTR
Intron
Flanking
External resources
MEF2A
myocyte enhancer factor 2A
×
Warning!!
Variant Map
DNA Sequence
Variant Map
Amino Acid Sequence
3D structure
Powered by
NGL
.
×
Available 3D structures for MEF2A
Region
PDB code
Experiment
Protein name
Oligomeric state
%Identity
×
Options for Viewing Structures
Target protein
Style
Cartoon
Cartoon + Ball & Stick side-chains
Cartoon + Wireframe side-chains
Spacefill
Surface (It might take a while to show)
Color by
Variant source
Allele Frequency (in GnomAD)
Sequence Conservation
Secondary Structure
B-factor (pLDDT for AF2 model)
Element
Hydrophobicity
Electrostatic (Only Surface style)
Rainbow
The other protein(s)
Style
Cartoon
Cartoon + Ball & Stick side-chains
Cartoon + Wireframe side-chains
Backbone
Spacefill
Surface (It might take a while to show)
Color by
Chain
Display
Nucleotides
Color by
Element
Rainbow
Display
Ligands & Ions
Color
By Element
Display
Contacts
Display
×
Viewing Sequences
Single/MSA
Window Height
Short
Tall
Grande
Venti
Variant Table
variants
CSV
Show All
×
variants
Variant
Consequence
dbSNP
Allele Frequency
Clinical Significance
Prediction