SLC35F5 solute carrier family 35 member F5

Information
Symbol
SLC35F5
Type
protein-coding
Description
solute carrier family 35 member F5
Entrez Gene ID
80255
Genome
hg19
Position
chr2:114,464,286-114,514,219
Genome
hg38
Position
chr2:113,706,709-113,756,642
MIM
619997 OMIM
HGNC
HGNC:23617 HGNC
Ensembl
ENSG00000115084 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
Uncertain significance 0 28
Ranking
ClinVar
0
0
0
34
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 :
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
MIM 619997 OMIM
HGNC HGNC:23617 HGNC
Ensembl ENSG00000115084 Ensembl
AllianceGenome HGNC:23617
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000409342.1 hg38 chr2 113,741,884 113,756,620 14,737
ENST00000245680.7 hg38 chr2 113,706,709 113,756,642 49,934
ENST00000245680.7 hg19 chr2 114,464,286 114,514,219 49,934
ENST00000409342.1 hg19 chr2 114,499,461 114,514,197 14,737
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