USF2 upstream transcription factor 2, c-fos interacting

Information
Symbol
USF2
Type
protein-coding
Description
upstream transcription factor 2, c-fos interacting
Entrez Gene ID
7392
Genome
hg19
Position
chr19:35,759,865-35,770,724
Genome
hg38
Position
chr19:35,268,962-35,279,821
MIM
600390 OMIM
HGNC
HGNC:12594 HGNC
Ensembl
ENSG00000105698 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 40
Ranking
ClinVar
0
0
0
38
2
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 :
Filtering :
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 FIP
SYNONYM bHLHb12
MIM 600390 OMIM
HGNC HGNC:12594 HGNC
Ensembl ENSG00000105698 Ensembl
AllianceGenome HGNC:12594
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000594064.5 hg38 chr19 35,269,108 35,279,308 10,201
ENST00000595068.5 hg38 chr19 35,269,065 35,279,814 10,750
ENST00000379134.7 hg38 chr19 35,269,102 35,279,256 10,155
ENST00000222305.8 hg38 chr19 35,268,962 35,279,821 10,860
ENST00000343550.9 hg38 chr19 35,268,978 35,279,815 10,838
ENST00000222305.8 hg19 chr19 35,759,865 35,770,724 10,860
ENST00000343550.9 hg19 chr19 35,759,881 35,770,718 10,838
ENST00000595068.5 hg19 chr19 35,759,968 35,770,717 10,750
ENST00000379134.7 hg19 chr19 35,760,005 35,770,159 10,155
ENST00000594064.5 hg19 chr19 35,760,011 35,770,211 10,201
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