GSKIP GSK3B interacting protein

Information
Symbol
GSKIP
Type
protein-coding
Description
GSK3B interacting protein
Entrez Gene ID
51527
Genome
hg19
Position
chr14:96,829,894-96,853,623
Genome
hg38
Position
chr14:96,363,557-96,387,286
MIM
616605 OMIM
HGNC
HGNC:20343 HGNC
Ensembl
ENSG00000100744 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 12
Likely benign 0 2
Uncertain significance 0 18
Ranking
ClinVar
0
0
0
30
2
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 C14orf129
SYNONYM HSPC210
MIM 616605 OMIM
HGNC HGNC:20343 HGNC
Ensembl ENSG00000100744 Ensembl
AllianceGenome HGNC:20343
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000438650.5 hg38 chr14 96,363,452 96,387,286 23,835
ENST00000556095.5 hg38 chr14 96,363,557 96,387,286 23,730
ENST00000554182.5 hg38 chr14 96,363,526 96,385,912 22,387
ENST00000555181.6 hg38 chr14 96,363,526 96,387,288 23,763
ENST00000438650.5 hg19 chr14 96,829,789 96,853,623 23,835
ENST00000554182.5 hg19 chr14 96,829,863 96,852,249 22,387
ENST00000555181.6 hg19 chr14 96,829,863 96,853,625 23,763
ENST00000556095.5 hg19 chr14 96,829,894 96,853,623 23,730
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