ATF4 activating transcription factor 4

Information
Symbol
ATF4
Type
protein-coding
Description
activating transcription factor 4
Entrez Gene ID
468
Genome
hg19
Position
chr22:39,916,569-39,918,688
Genome
hg38
Position
chr22:39,520,564-39,522,683
MIM
604064 OMIM
HGNC
HGNC:786 HGNC
Ensembl
ENSG00000128272 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 20
Likely benign 0 8
Uncertain significance 0 52
Ranking
ClinVar
0
0
0
80
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
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Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM CREB-2
SYNONYM CREB2
SYNONYM TAXREB67
SYNONYM TXREB
MIM 604064 OMIM
HGNC HGNC:786 HGNC
Ensembl ENSG00000128272 Ensembl
AllianceGenome HGNC:786
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000679776.1 hg38 chr22 39,520,563 39,522,602 2,040
ENST00000674835.2 hg38 chr22 39,520,604 39,522,602 1,999
ENST00000676346.2 hg38 chr22 39,520,576 39,522,602 2,027
ENST00000680748.1 hg38 chr22 39,520,589 39,521,953 1,365
ENST00000675582.2 hg38 chr22 39,520,564 39,522,602 2,039
ENST00000396680.3 hg38 chr22 39,520,576 39,522,668 2,093
ENST00000337304.2 hg38 chr22 39,520,564 39,522,683 2,120
ENST00000404241.6 hg38 chr22 39,519,695 39,522,683 2,989
ENST00000674920.3 hg38 chr22 39,520,562 39,522,683 2,122
ENST00000674568.2 hg38 chr22 39,520,579 39,522,602 2,024
ENST00000680446.1 hg38 chr22 39,520,578 39,522,602 2,025
ENST00000404241.6 hg19 chr22 39,915,700 39,918,688 2,989
ENST00000674920.3 hg19 chr22 39,916,567 39,918,688 2,122
ENST00000679776.1 hg19 chr22 39,916,568 39,918,607 2,040
ENST00000675582.2 hg19 chr22 39,916,569 39,918,607 2,039
ENST00000337304.2 hg19 chr22 39,916,569 39,918,688 2,120
ENST00000676346.2 hg19 chr22 39,916,581 39,918,607 2,027
ENST00000396680.3 hg19 chr22 39,916,581 39,918,673 2,093
ENST00000680446.1 hg19 chr22 39,916,583 39,918,607 2,025
ENST00000674568.2 hg19 chr22 39,916,584 39,918,607 2,024
ENST00000680748.1 hg19 chr22 39,916,594 39,917,958 1,365
ENST00000674835.2 hg19 chr22 39,916,609 39,918,607 1,999
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