VPS29 VPS29 retromer complex component

Information
Symbol
VPS29
Type
protein-coding
Description
VPS29 retromer complex component
Entrez Gene ID
51699
Genome
hg19
Position
chr12:110,929,496-110,939,897
Genome
hg38
Position
chr12:110,491,691-110,502,092
MIM
606932 OMIM
HGNC
HGNC:14340 HGNC
Ensembl
ENSG00000111237 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 10
Ranking
ClinVar
0
0
0
10
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 :
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 DC15
SYNONYM DC7
SYNONYM PEP11
MIM 606932 OMIM
HGNC HGNC:14340 HGNC
Ensembl ENSG00000111237 Ensembl
AllianceGenome HGNC:14340
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000549970.5 hg38 chr12 110,491,886 110,502,111 10,226
ENST00000621131.4 hg38 chr12 110,491,526 110,501,503 9,978
ENST00000549578.6 hg38 chr12 110,491,083 110,502,111 11,029
ENST00000447578.6 hg38 chr12 110,491,625 110,502,078 10,454
ENST00000552130.6 hg38 chr12 110,491,624 110,499,546 7,923
ENST00000546588.1 hg38 chr12 110,491,691 110,502,092 10,402
ENST00000360579.11 hg38 chr12 110,491,523 110,502,099 10,577
ENST00000549578.6 hg19 chr12 110,928,888 110,939,916 11,029
ENST00000360579.11 hg19 chr12 110,929,328 110,939,904 10,577
ENST00000621131.4 hg19 chr12 110,929,331 110,939,308 9,978
ENST00000552130.6 hg19 chr12 110,929,429 110,937,351 7,923
ENST00000447578.6 hg19 chr12 110,929,430 110,939,883 10,454
ENST00000546588.1 hg19 chr12 110,929,496 110,939,897 10,402
ENST00000549970.5 hg19 chr12 110,929,691 110,939,916 10,226
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