TSIX TSIX transcript, XIST antisense RNA
Clinical Significance
MGeND | ClinVar | |
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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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | LINC00013 |
SYNONYM | NCRNA00013 |
SYNONYM | XIST-AS |
SYNONYM | XIST-AS1 |
SYNONYM | XISTAS |
MIM | 300181 OMIM |
HGNC | HGNC:12377 HGNC |
Ensembl | ENSG00000270641 Ensembl |
AllianceGenome | HGNC:12377 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000706914.1 | hg38 | chrX | 73,809,317 | 73,820,983 | 11,667 |
ENST00000604411.1 | hg38 | chrX | 73,792,205 | 73,829,231 | 37,027 |
ENST00000604411.1 | hg19 | chrX | 73,012,040 | 73,049,066 | 37,027 |
ENST00000706914.1 | hg19 | chrX | 73,029,152 | 73,040,818 | 11,667 |
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