FXYD6-FXYD2 FXYD6-FXYD2 readthrough

Information
Symbol
FXYD6-FXYD2
Type
protein-coding
Description
FXYD6-FXYD2 readthrough
Entrez Gene ID
100533181
Genome
hg19
Position
chr11:117,690,937-117,747,343
Genome
hg38
Position
chr11:117,820,222-117,876,628
HGNC
HGNC:39978 HGNC
Ensembl
ENSG00000255245 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Benign 0 64
Likely benign 0 58
Conflicting classifications of pathogenicity 0 4
Uncertain significance 0 46
Ranking
ClinVar
0
0
36
120
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
SYNONYM FXYD6
HGNC HGNC:39978 HGNC
Ensembl ENSG00000255245 Ensembl
AllianceGenome HGNC:39978
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000532984.1 hg38 chr11 117,820,163 117,876,667 56,505
ENST00000614497.5 hg38 chr11 117,820,222 117,876,628 56,407
ENST00000532984.1 hg19 chr11 117,690,878 117,747,382 56,505
ENST00000614497.5 hg19 chr11 117,690,937 117,747,343 56,407
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