SLC35B3 solute carrier family 35 member B3

Information
Symbol
SLC35B3
Type
protein-coding
Description
solute carrier family 35 member B3
Entrez Gene ID
51000
Genome
hg19
Position
chr6:8,411,668-8,435,778
Genome
hg38
Position
chr6:8,411,435-8,435,545
MIM
610845 OMIM
HGNC
HGNC:21601 HGNC
Ensembl
ENSG00000124786 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 34
Ranking
ClinVar
0
0
0
38
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 C6orf196
SYNONYM CGI-19
SYNONYM PAPST2
MIM 610845 OMIM
HGNC HGNC:21601 HGNC
Ensembl ENSG00000124786 Ensembl
AllianceGenome HGNC:21601
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000710437.1 hg38 chr6 8,411,435 8,435,545 24,111
ENST00000648987.1 hg38 chr6 8,412,885 8,435,271 22,387
ENST00000379660.4 hg38 chr6 8,413,068 8,435,483 22,416
ENST00000644923.2 hg38 chr6 8,411,435 8,435,545 24,111
ENST00000644923.2 hg19 chr6 8,411,668 8,435,778 24,111
ENST00000710437.1 hg19 chr6 8,411,668 8,435,778 24,111
ENST00000648987.1 hg19 chr6 8,413,118 8,435,504 22,387
ENST00000379660.4 hg19 chr6 8,413,301 8,435,716 22,416
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