FTX FTX transcript, XIST regulator

Information
Symbol
FTX
Type
ncRNA
Description
FTX transcript, XIST regulator
Entrez Gene ID
100302692
Genome
hg19
Position
chrX:73,166,390-73,232,780
Genome
hg38
Position
chrX:73,946,555-74,012,945
MIM
300936 OMIM
HGNC
HGNC:37190 HGNC
Ensembl
ENSG00000230590 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 6 0
Ranking
ClinVar
0
0
0
0
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
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 LINC00182
SYNONYM MIR374AHG
SYNONYM NCRNA00182
MIM 300936 OMIM
HGNC HGNC:37190 HGNC
Ensembl ENSG00000230590 Ensembl
AllianceGenome HGNC:37190
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000638681.1 hg38 chrX 73,998,242 74,292,583 294,342
ENST00000652609.1 hg38 chrX 74,028,140 74,112,334 84,195
ENST00000652013.2 hg38 chrX 74,202,647 74,292,079 89,433
ENST00000638437.1 hg38 chrX 73,946,555 74,012,945 66,391
ENST00000603037.2 hg38 chrX 74,196,351 74,293,574 97,224
ENST00000652319.1 hg38 chrX 74,004,513 74,293,459 288,947
ENST00000638985.1 hg38 chrX 74,130,309 74,292,594 162,286
ENST00000652527.1 hg38 chrX 74,067,493 74,292,075 224,583
ENST00000701585.1 hg38 chrX 74,069,027 74,292,351 223,325
ENST00000657327.1 hg38 chrX 74,245,130 74,292,293 47,164
ENST00000603037.2 hg19 chrX 73,416,186 73,513,409 97,224
ENST00000638681.1 hg19 chrX 73,218,077 73,512,418 294,342
ENST00000638985.1 hg19 chrX 73,350,144 73,512,429 162,286
ENST00000652013.2 hg19 chrX 73,422,482 73,511,914 89,433
ENST00000638437.1 hg19 chrX 73,166,390 73,232,780 66,391
ENST00000652319.1 hg19 chrX 73,224,348 73,513,294 288,947
ENST00000652609.1 hg19 chrX 73,247,975 73,332,169 84,195
ENST00000652527.1 hg19 chrX 73,287,328 73,511,910 224,583
ENST00000657327.1 hg19 chrX 73,464,965 73,512,128 47,164
ENST00000701585.1 hg19 chrX 73,288,862 73,512,186 223,325
Genome browser