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NM_001256662.2 - NP_001243591.1
NM_003598.2 - NP_003589.1
NM_001256659.2 - NP_001243588.1
NM_001256660.2 - NP_001243589.1 (MANE)
NM_001256658.2 - NP_001243587.1
NM_001256661.2 - NP_001243590.1
DNA
Protein
Gene Info.
Genome Build
GRCh38
Chromosome
19
Location
Chr19:49,340,095-49,362,916
LOEUF
0.796
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Pathogenic/ Likely pa...
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GnomAD
Common [>1%]
Rare [<1%]
ToMMo
Common [>1%]
Rare [<1%]
By consequences
Missense
Loss-of-function
Synonymous
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Gene region:
CDS
SpliceSite
UTR
Intron
Flanking
External resources
NCBI Gene
8463
Ensembl
ENSG00000074219
GeneCards
TEAD2
UniProt
Q15562
KEGG
hsa:8463
gnomAD
ENSG00000074219
ICGC
ENSG00000074219
RefDIC
8463
RefEx
8463
DTX
TEAD2
AS-ALPS
TEAD2
TEAD2
TEA domain transcription factor 2
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