JPX JPX transcript, XIST activator
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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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 | DCBALD06 |
SYNONYM | ENOX |
SYNONYM | LINC00183 |
SYNONYM | NCRNA00183 |
MIM | 300832 OMIM |
HGNC | HGNC:37191 HGNC |
Ensembl | ENSG00000225470 Ensembl |
AllianceGenome | HGNC:37191 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000654005.1 | hg38 | chrX | 73,944,342 | 74,007,534 | 63,193 |
ENST00000670506.1 | hg38 | chrX | 73,944,317 | 74,004,545 | 60,229 |
ENST00000639185.1 | hg38 | chrX | 73,944,184 | 74,012,945 | 68,762 |
ENST00000639185.1 | hg19 | chrX | 73,164,019 | 73,232,780 | 68,762 |
ENST00000654005.1 | hg19 | chrX | 73,164,177 | 73,227,369 | 63,193 |
ENST00000670506.1 | hg19 | chrX | 73,164,152 | 73,224,380 | 60,229 |
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