SOX11 SRY-box transcription factor 11

Information
Symbol
SOX11
Type
protein-coding
Description
SRY-box transcription factor 11
Entrez Gene ID
6664
Genome
hg19
Position
chr2:5,832,516-5,841,517
Genome
hg38
Position
chr2:5,692,384-5,701,385
MIM
600898 OMIM
HGNC
HGNC:11191 HGNC
Ensembl
ENSG00000176887 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 18 36
Likely pathogenic 0 98
Benign 0 28
Likely benign 0 154
Conflicting classifications of pathogenicity 0 24
not provided 1 0
Uncertain significance 0 224
Ranking
ClinVar
0
0
60
456
10
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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 CSS9
SYNONYM IDDMOH
SYNONYM MRD27
MIM 600898 OMIM
HGNC HGNC:11191 HGNC
Ensembl ENSG00000176887 Ensembl
AllianceGenome HGNC:11191
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000322002.5 hg38 chr2 5,692,384 5,701,385 9,002
ENST00000322002.5 hg19 chr2 5,832,516 5,841,517 9,002
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