SLC35B1 solute carrier family 35 member B1

Information
Symbol
SLC35B1
Type
protein-coding
Description
solute carrier family 35 member B1
Entrez Gene ID
10237
Genome
hg19
Position
chr17:47,778,305-47,785,326
Genome
hg38
Position
chr17:49,700,943-49,707,964
MIM
610790 OMIM
HGNC
HGNC:20798 HGNC
Ensembl
ENSG00000121073 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 28
Ranking
ClinVar
0
0
0
32
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 AXER
SYNONYM UGTREL1
MIM 610790 OMIM
HGNC HGNC:20798 HGNC
Ensembl ENSG00000121073 Ensembl
AllianceGenome HGNC:20798
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000649906.1 hg38 chr17 49,700,934 49,707,951 7,018
ENST00000240333.12 hg38 chr17 49,700,943 49,707,964 7,022
ENST00000240333.12 hg19 chr17 47,778,305 47,785,326 7,022
ENST00000649906.1 hg19 chr17 47,778,296 47,785,313 7,018
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