SP9 Sp9 transcription factor

Information
Symbol
SP9
Type
protein-coding
Description
Sp9 transcription factor
Entrez Gene ID
100131390
Genome
hg19
Position
chr2:175,199,682-175,203,228
Genome
hg38
Position
chr2:174,334,954-174,338,500
HGNC
HGNC:30690 HGNC
Ensembl
ENSG00000217236 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 6
Likely pathogenic 0 2
Likely benign 0 4
Uncertain significance 0 34
Ranking
ClinVar
0
0
2
38
6
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 ZNF990
HGNC HGNC:30690 HGNC
Ensembl ENSG00000217236 Ensembl
AllianceGenome HGNC:30690
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000394967.3 hg38 chr2 174,334,954 174,338,500 3,547
ENST00000394967.3 hg19 chr2 175,199,682 175,203,228 3,547
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