SLC35C1 solute carrier family 35 member C1

Information
Symbol
SLC35C1
Type
protein-coding
Description
solute carrier family 35 member C1
Entrez Gene ID
55343
Genome
hg19
Position
chr11:45,826,700-45,834,567
Genome
hg38
Position
chr11:45,805,149-45,813,016
MIM
605881 OMIM
HGNC
HGNC:20197 HGNC
Ensembl
ENSG00000181830 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 12
Likely pathogenic 0 8
Benign 0 42
Likely benign 0 190
Conflicting classifications of pathogenicity 0 26
Uncertain significance 0 316
Ranking
ClinVar
0
0
58
500
6
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 :
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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 CDG2C
SYNONYM FUCT1
MIM 605881 OMIM
HGNC HGNC:20197 HGNC
Ensembl ENSG00000181830 Ensembl
AllianceGenome HGNC:20197
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000526817.2 hg38 chr11 45,804,086 45,813,007 8,922
ENST00000314134.4 hg38 chr11 45,805,149 45,813,016 7,868
ENST00000442528.2 hg38 chr11 45,804,072 45,811,558 7,487
ENST00000442528.2 hg19 chr11 45,825,623 45,833,109 7,487
ENST00000526817.2 hg19 chr11 45,825,637 45,834,558 8,922
ENST00000314134.4 hg19 chr11 45,826,700 45,834,567 7,868
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