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NM_001199513.2 - NP_001186442.1
NM_021809.7 - NP_068581.1 (MANE)
NM_001199514.2 - NP_001186443.1
NM_001199515.2 - NP_001186444.1
DNA
Protein
Gene Info.
Genome Build
GRCh38
Chromosome
20
Location
Chr20:36,572,964-36,594,450
LOEUF
1.104
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Pathogenic/ Likely pa...
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VUS
Benign/Likely benign
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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
NCBI Gene
60436
Ensembl
ENSG00000118707
GeneCards
TGIF2
UniProt
Q9GZN2
KEGG
hsa:60436
gnomAD
ENSG00000118707
ICGC
ENSG00000118707
RefDIC
60436
RefEx
60436
DTX
TGIF2
AS-ALPS
TGIF2
TGIF2
TGFB induced factor homeobox 2
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