SNX18 sorting nexin 18

Information
Symbol
SNX18
Type
protein-coding
Description
sorting nexin 18
Entrez Gene ID
112574
Genome
hg19
Position
chr5:53,813,695-53,816,834
Genome
hg38
Position
chr5:54,517,865-54,521,004
HGNC
HGNC:19245 HGNC
Ensembl
ENSG00000178996 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Uncertain significance 0 78
Ranking
ClinVar
0
0
0
84
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 SH3PX2
SYNONYM SH3PXD3B
SYNONYM SNAG1
HGNC HGNC:19245 HGNC
Ensembl ENSG00000178996 Ensembl
AllianceGenome HGNC:19245
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000326277.5 hg38 chr5 54,517,759 54,543,273 25,515
ENST00000343017.11 hg38 chr5 54,517,865 54,521,004 3,140
ENST00000381410.5 hg38 chr5 54,517,759 54,546,586 28,828
ENST00000326277.5 hg19 chr5 53,813,589 53,839,103 25,515
ENST00000381410.5 hg19 chr5 53,813,589 53,842,416 28,828
ENST00000343017.11 hg19 chr5 53,813,695 53,816,834 3,140
Genome browser