SLC35B4 solute carrier family 35 member B4

Information
Symbol
SLC35B4
Type
protein-coding
Description
solute carrier family 35 member B4
Entrez Gene ID
84912
Genome
hg19
Position
chr7:133,974,084-134,001,682
Genome
hg38
Position
chr7:134,289,332-134,316,930
MIM
610923 OMIM
HGNC
HGNC:20584 HGNC
Ensembl
ENSG00000205060 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 26
Ranking
ClinVar
0
0
0
28
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
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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 YEA
SYNONYM YEA4
MIM 610923 OMIM
HGNC HGNC:20584 HGNC
Ensembl ENSG00000205060 Ensembl
AllianceGenome HGNC:20584
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000378509.9 hg38 chr7 134,289,332 134,316,930 27,599
ENST00000470969.2 hg38 chr7 134,299,309 134,316,897 17,589
ENST00000378509.9 hg19 chr7 133,974,084 134,001,682 27,599
ENST00000470969.2 hg19 chr7 133,984,061 134,001,649 17,589
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