XAGE1B X antigen family member 1B
Information
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
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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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| 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 | CT12.1 |
| SYNONYM | CT12.1C |
| SYNONYM | CT12.1D |
| SYNONYM | CT12.1E |
| SYNONYM | CT12.1b |
| SYNONYM | CTP9 |
| SYNONYM | GAGED2 |
| SYNONYM | XAGE-1 |
| SYNONYM | XAGE1 |
| SYNONYM | XAGE1C |
| SYNONYM | XAGE1D |
| SYNONYM | XAGE1E |
| MIM | 300289 OMIM |
| HGNC | HGNC:25400 HGNC |
| Ensembl | ENSG00000204382 Ensembl |
| AllianceGenome | HGNC:25400 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000375613.7 | hg38 | chrX | 52,512,077 | 52,517,057 | 4,981 |
| ENST00000375616.6 | hg38 | chrX | 52,512,077 | 52,517,063 | 4,987 |
| ENST00000518075.1 | hg38 | chrX | 52,512,080 | 52,520,803 | 8,724 |
| ENST00000518075.1 | hg19 | chrX | 52,235,228 | 52,243,951 | 8,724 |
| ENST00000437949.2 | hg19 | chrX | 52,238,810 | 52,243,954 | 5,145 |
| ENST00000375616.1 | hg19 | chrX | 52,238,818 | 52,243,954 | 5,137 |
| ENST00000375613.3 | hg19 | chrX | 52,238,974 | 52,243,954 | 4,981 |
| ENST00000375612.4 | hg19 | chrX | 52,239,019 | 52,243,954 | 4,936 |
| ENST00000399805.2 | hg19 | chrX | 52,240,504 | 52,243,954 | 3,451 |
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