FTX FTX transcript, XIST regulator
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| not provided | 6 | 0 |
Ranking
| ClinVar | |
|---|---|
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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
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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
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| 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
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| Category | : |
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| 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 | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | LINC00182 |
| SYNONYM | MIR374AHG |
| SYNONYM | NCRNA00182 |
| MIM | 300936 OMIM |
| HGNC | HGNC:37190 HGNC |
| Ensembl | ENSG00000230590 Ensembl |
| AllianceGenome | HGNC:37190 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| 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 |
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