SNX15 sorting nexin 15

Information
Symbol
SNX15
Type
protein-coding
Description
sorting nexin 15
Entrez Gene ID
29907
Genome
hg19
Position
chr11:64,794,911-64,808,044
Genome
hg38
Position
chr11:65,027,439-65,040,572
MIM
605964 OMIM
HGNC
HGNC:14978 HGNC
Ensembl
ENSG00000110025 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely 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 HSAF001435
MIM 605964 OMIM
HGNC HGNC:14978 HGNC
Ensembl ENSG00000110025 Ensembl
AllianceGenome HGNC:14978
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000352068.5 hg38 chr11 65,027,538 65,039,792 12,255
ENST00000377244.8 hg38 chr11 65,027,439 65,040,572 13,134
ENST00000377244.8 hg19 chr11 64,794,911 64,808,044 13,134
ENST00000352068.5 hg19 chr11 64,795,010 64,807,264 12,255
Genome browser