ANAPC11 anaphase promoting complex subunit 11

Information
Symbol
ANAPC11
Type
protein-coding
Description
anaphase promoting complex subunit 11
Entrez Gene ID
51529
Genome
hg19
Position
chr17:79,849,615-79,858,130
Genome
hg38
Position
chr17:81,891,739-81,900,254
MIM
614534 OMIM
HGNC
HGNC:14452 HGNC
Ensembl
ENSG00000141552 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 12
Ranking
ClinVar
0
0
0
12
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 APC11
SYNONYM Apc11p
SYNONYM HSPC214
MIM 614534 OMIM
HGNC HGNC:14452 HGNC
Ensembl ENSG00000141552 Ensembl
AllianceGenome HGNC:14452
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000583839.1 hg38 chr17 81,892,063 81,900,254 8,192
ENST00000575195.2 hg38 chr17 81,894,298 81,900,991 6,694
ENST00000577747.5 hg38 chr17 81,891,760 81,900,254 8,495
ENST00000612413.4 hg38 chr17 81,891,713 81,900,533 8,821
ENST00000571570.5 hg38 chr17 81,890,790 81,900,255 9,466
ENST00000579133.5 hg38 chr17 81,891,772 81,900,254 8,483
ENST00000578544.1 hg38 chr17 81,893,555 81,900,104 6,550
ENST00000574924.6 hg38 chr17 81,891,732 81,900,356 8,625
ENST00000572639.5 hg38 chr17 81,891,647 81,900,255 8,609
ENST00000577425.5 hg38 chr17 81,891,723 81,900,253 8,531
ENST00000578550.5 hg38 chr17 81,891,750 81,900,159 8,410
ENST00000572851.6 hg38 chr17 81,891,735 81,900,356 8,622
ENST00000582222.5 hg38 chr17 81,891,723 81,894,807 3,085
ENST00000584314.5 hg38 chr17 81,891,741 81,894,839 3,099
ENST00000344877.10 hg38 chr17 81,891,723 81,900,255 8,533
ENST00000571874.6 hg38 chr17 81,891,746 81,900,254 8,509
ENST00000357385.7 hg38 chr17 81,891,739 81,900,254 8,516
ENST00000579978.5 hg38 chr17 81,891,720 81,900,252 8,533
ENST00000571024.6 hg38 chr17 81,891,723 81,900,356 8,634
ENST00000392376.7 hg38 chr17 81,891,938 81,900,254 8,317
ENST00000571570.5 hg19 chr17 79,848,666 79,858,131 9,466
ENST00000572639.5 hg19 chr17 79,849,523 79,858,131 8,609
ENST00000344877.10 hg19 chr17 79,849,599 79,858,131 8,533
ENST00000571024.6 hg19 chr17 79,849,599 79,858,232 8,634
ENST00000572851.6 hg19 chr17 79,849,611 79,858,232 8,622
ENST00000357385.7 hg19 chr17 79,849,615 79,858,130 8,516
ENST00000571874.6 hg19 chr17 79,849,622 79,858,130 8,509
ENST00000392376.7 hg19 chr17 79,849,814 79,858,130 8,317
ENST00000574924.6 hg19 chr17 79,849,608 79,858,232 8,625
ENST00000575195.2 hg19 chr17 79,852,174 79,858,867 6,694
ENST00000577425.5 hg19 chr17 79,849,599 79,858,129 8,531
ENST00000577747.5 hg19 chr17 79,849,636 79,858,130 8,495
ENST00000578544.1 hg19 chr17 79,851,431 79,857,980 6,550
ENST00000578550.5 hg19 chr17 79,849,626 79,858,035 8,410
ENST00000579133.5 hg19 chr17 79,849,648 79,858,130 8,483
ENST00000579978.5 hg19 chr17 79,849,596 79,858,128 8,533
ENST00000582222.5 hg19 chr17 79,849,599 79,852,683 3,085
ENST00000583839.1 hg19 chr17 79,849,939 79,858,130 8,192
ENST00000584314.5 hg19 chr17 79,849,617 79,852,715 3,099
ENST00000612413.4 hg19 chr17 79,849,589 79,858,409 8,821
Genome browser