Toggle navigation
Home
Browse
Tools
Mutation Finder
Variant Mapper
About
Display
NM_001413936.1 - NP_001400865.1
NM_001413935.1 - NP_001400864.1
NM_001413934.1 - NP_001400863.1
NM_001243089.2 - NP_001230018.1
NM_001413942.1 - NP_001400871.1
NM_001413928.1 - NP_001400857.1
NM_001243088.2 - NP_001230017.1
NM_001413931.1 - NP_001400860.1
NM_001413938.1 - NP_001400867.1
NM_001413926.1 - NP_001400855.1
NM_001413930.1 - NP_001400859.1
NM_001413940.1 - NP_001400869.1
NM_001413933.1 - NP_001400862.1
NM_202003.3 - NP_973732.1
NM_001413941.1 - NP_001400870.1
NM_001413927.1 - NP_001400856.1
NM_001413932.1 - NP_001400861.1
NM_021953.4 - NP_068772.2 (MANE)
NM_001413937.1 - NP_001400866.1
NM_202002.3 - NP_973731.1
NM_001413929.1 - NP_001400858.1
NM_001413925.1 - NP_001400854.1
NM_001413939.1 - NP_001400868.1
NM_001413943.1 - NP_001400872.1
DNA
Protein
Gene Info.
Genome Build
GRCh38
Chromosome
12
Location
Chr12:2,857,180-2,877,674
LOEUF
0.591
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
FOXM1
forkhead box M1
×
Warning!!
Variant Map
DNA Sequence
Variant Map
Amino Acid Sequence
3D structure
Powered by
NGL
.
×
Available 3D structures for FOXM1
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