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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
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Pathogenic/ Likely pa...
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ToMMo
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Gene region:
CDS
SpliceSite
UTR
Intron
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External resources
NCBI Gene
2305
Ensembl
ENSG00000111206
GeneCards
FOXM1
UniProt
Q08050
KEGG
hsa:2305
gnomAD
ENSG00000111206
ICGC
ENSG00000111206
RefDIC
2305
RefEx
2305
DTX
FOXM1
AS-ALPS
FOXM1
FOXM1
forkhead box M1
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