ST13 ST13 Hsp70 interacting protein

Information
Symbol
ST13
Type
protein-coding
Description
ST13 Hsp70 interacting protein
Entrez Gene ID
6767
Genome
hg19
Position
chr22:41,220,539-41,252,643
Genome
hg38
Position
chr22:40,824,535-40,856,639
MIM
606796 OMIM
HGNC
HGNC:11343 HGNC
Ensembl
ENSG00000100380 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Uncertain significance 0 44
Ranking
ClinVar
0
0
0
46
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
SYNONYM AAG2
SYNONYM FAM10A1
SYNONYM FAM10A4
SYNONYM HIP
SYNONYM HOP
SYNONYM HSPABP
SYNONYM HSPABP1
SYNONYM P48
SYNONYM PRO0786
SYNONYM SNC6
MIM 606796 OMIM
HGNC HGNC:11343 HGNC
Ensembl ENSG00000100380 Ensembl
AllianceGenome HGNC:11343
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000216218.8 hg38 chr22 40,824,535 40,856,639 32,105
ENST00000216218.8 hg19 chr22 41,220,539 41,252,643 32,105
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