MISP mitotic spindle positioning

Information
Symbol
MISP
Type
protein-coding
Description
mitotic spindle positioning
Entrez Gene ID
126353
Genome
hg19
Position
chr19:751,112-764,318
Genome
hg38
Position
chr19:751,112-764,318
MIM
615289 OMIM
HGNC
HGNC:27000 HGNC
Ensembl
ENSG00000099812 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 18
Likely benign 0 16
Uncertain significance 0 154
Ranking
ClinVar
0
0
0
188
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 :
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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 :
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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 C19orf21
SYNONYM MISP1
MIM 615289 OMIM
HGNC HGNC:27000 HGNC
Ensembl ENSG00000099812 Ensembl
AllianceGenome HGNC:27000
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000215582.8 hg38 chr19 751,112 764,318 13,207
ENST00000215582.8 hg19 chr19 751,112 764,318 13,207
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