SP2 Sp2 transcription factor

Information
Symbol
SP2
Type
protein-coding
Description
Sp2 transcription factor
Entrez Gene ID
6668
Genome
hg19
Position
chr17:45,973,602-46,006,323
Genome
hg38
Position
chr17:47,896,236-47,928,957
MIM
601801 OMIM
HGNC
HGNC:11207 HGNC
Ensembl
ENSG00000167182 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 54
Ranking
ClinVar
0
0
0
58
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 :
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
MIM 601801 OMIM
HGNC HGNC:11207 HGNC
Ensembl ENSG00000167182 Ensembl
AllianceGenome HGNC:11207
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000376741.5 hg38 chr17 47,896,236 47,928,957 32,722
ENST00000376741.5 hg19 chr17 45,973,602 46,006,323 32,722
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