SLC35F6 solute carrier family 35 member F6

Information
Symbol
SLC35F6
Type
protein-coding
Description
solute carrier family 35 member F6
Entrez Gene ID
54978
Genome
hg19
Position
chr2:26,987,152-27,004,099
Genome
hg38
Position
chr2:26,764,284-26,781,231
MIM
619667 OMIM
HGNC
HGNC:26055 HGNC
Ensembl
ENSG00000213699 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 46
Ranking
ClinVar
0
0
0
48
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 :
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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 :
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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 ANT2BP
SYNONYM C2orf18
SYNONYM TANGO9
MIM 619667 OMIM
HGNC HGNC:26055 HGNC
Ensembl ENSG00000213699 Ensembl
AllianceGenome HGNC:26055
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000344420.10 hg38 chr2 26,764,284 26,781,231 16,948
ENST00000344420.10 hg19 chr2 26,987,152 27,004,099 16,948
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