FXYD3 FXYD domain containing ion transport regulator 3

Information
Symbol
FXYD3
Type
protein-coding
Description
FXYD domain containing ion transport regulator 3
Entrez Gene ID
5349
Genome
hg19
Position
chr19:35,607,166-35,614,559
Genome
hg38
Position
chr19:35,116,262-35,123,655
MIM
604996 OMIM
HGNC
HGNC:4027 HGNC
Ensembl
ENSG00000089356 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 10
Uncertain significance 0 18
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
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 MAT8
SYNONYM PLML
MIM 604996 OMIM
HGNC HGNC:4027 HGNC
Ensembl ENSG00000089356 Ensembl
AllianceGenome HGNC:4027
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000605552.5 hg38 chr19 35,116,320 35,121,847 5,528
ENST00000605550.5 hg38 chr19 35,116,319 35,123,280 6,962
ENST00000604621.5 hg38 chr19 35,118,530 35,123,657 5,128
ENST00000603449.5 hg38 chr19 35,116,318 35,121,665 5,348
ENST00000346446.9 hg38 chr19 35,116,262 35,124,323 8,062
ENST00000603524.5 hg38 chr19 35,118,027 35,123,652 5,626
ENST00000604255.5 hg38 chr19 35,116,262 35,123,655 7,394
ENST00000344013.10 hg38 chr19 35,116,262 35,124,323 8,062
ENST00000605677.1 hg38 chr19 35,119,363 35,123,286 3,924
ENST00000604804.5 hg38 chr19 35,116,319 35,123,615 7,297
ENST00000604404.6 hg38 chr19 35,115,823 35,124,324 8,502
ENST00000603181.5 hg38 chr19 35,115,941 35,123,657 7,717
ENST00000435734.6 hg38 chr19 35,115,895 35,124,323 8,429
ENST00000604404.6 hg19 chr19 35,606,727 35,615,228 8,502
ENST00000435734.6 hg19 chr19 35,606,799 35,615,227 8,429
ENST00000603181.5 hg19 chr19 35,606,845 35,614,561 7,717
ENST00000604255.5 hg19 chr19 35,607,166 35,614,559 7,394
ENST00000344013.10 hg19 chr19 35,607,166 35,615,227 8,062
ENST00000346446.9 hg19 chr19 35,607,166 35,615,227 8,062
ENST00000603449.5 hg19 chr19 35,607,222 35,612,569 5,348
ENST00000605550.5 hg19 chr19 35,607,223 35,614,184 6,962
ENST00000604804.5 hg19 chr19 35,607,223 35,614,519 7,297
ENST00000605552.5 hg19 chr19 35,607,224 35,612,751 5,528
ENST00000603524.5 hg19 chr19 35,608,931 35,614,556 5,626
ENST00000604621.5 hg19 chr19 35,609,434 35,614,561 5,128
ENST00000605677.1 hg19 chr19 35,610,267 35,614,190 3,924
Genome browser