YY1 YY1 transcription factor

Information
Symbol
YY1
Type
protein-coding
Description
YY1 transcription factor
Entrez Gene ID
7528
Genome
hg19
Position
chr14:100,705,481-100,749,125
Genome
hg38
Position
chr14:100,239,144-100,282,788
MIM
600013 OMIM
HGNC
HGNC:12856 HGNC
Ensembl
ENSG00000100811 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 30
Likely pathogenic 0 32
Benign 0 4
Likely benign 0 28
Conflicting classifications of pathogenicity 0 6
Uncertain significance 0 76
Ranking
ClinVar
0
0
12
140
18
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 DELTA
SYNONYM GADEVS
SYNONYM INO80S
SYNONYM NF-E1
SYNONYM UCRBP
SYNONYM YIN-YANG-1
MIM 600013 OMIM
HGNC HGNC:12856 HGNC
Ensembl ENSG00000100811 Ensembl
AllianceGenome HGNC:12856
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000704485.1 hg38 chr14 100,240,639 100,278,586 37,948
ENST00000262238.10 hg38 chr14 100,239,144 100,282,788 43,645
ENST00000262238.10 hg19 chr14 100,705,481 100,749,125 43,645
ENST00000704485.1 hg19 chr14 100,706,976 100,744,923 37,948
Genome browser