SNX21 sorting nexin family member 21

Information
Symbol
SNX21
Type
protein-coding
Description
sorting nexin family member 21
Entrez Gene ID
90203
Genome
hg19
Position
chr20:44,462,438-44,471,915
Genome
hg38
Position
chr20:45,833,799-45,843,276
MIM
619200 OMIM
HGNC
HGNC:16154 HGNC
Ensembl
ENSG00000124104 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
not provided 1 0
Uncertain significance 0 52
Ranking
ClinVar
0
0
0
54
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
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 C20orf161
SYNONYM PP3993
SYNONYM SNX-L
SYNONYM SNXL
SYNONYM dJ337O18.4
MIM 619200 OMIM
HGNC HGNC:16154 HGNC
Ensembl ENSG00000124104 Ensembl
AllianceGenome HGNC:16154
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000342644.9 hg38 chr20 45,833,852 45,842,881 9,030
ENST00000614929.4 hg38 chr20 45,833,831 45,838,318 4,488
ENST00000372541.1 hg38 chr20 45,834,136 45,840,907 6,772
ENST00000372542.5 hg38 chr20 45,833,895 45,841,730 7,836
ENST00000462307.5 hg38 chr20 45,833,831 45,841,134 7,304
ENST00000491381.6 hg38 chr20 45,833,799 45,843,276 9,478
ENST00000491381.6 hg19 chr20 44,462,438 44,471,915 9,478
ENST00000614929.4 hg19 chr20 44,462,470 44,466,957 4,488
ENST00000462307.5 hg19 chr20 44,462,470 44,469,773 7,304
ENST00000342644.9 hg19 chr20 44,462,491 44,471,520 9,030
ENST00000372542.5 hg19 chr20 44,462,534 44,470,369 7,836
ENST00000372541.1 hg19 chr20 44,462,775 44,469,546 6,772
Genome browser