CD9 CD9 molecule
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 6 |
| Uncertain significance | 0 | 6 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
12 |
 |
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
[No Data.]
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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| 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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| 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 | BTCC-1 |
| SYNONYM | DRAP-27 |
| SYNONYM | MIC3 |
| SYNONYM | MRP-1 |
| SYNONYM | TSPAN-29 |
| SYNONYM | TSPAN29 |
| MIM | 143030 OMIM |
| HGNC | HGNC:1709 HGNC |
| Ensembl | ENSG00000010278 Ensembl |
| AllianceGenome | HGNC:1709 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000538834.6 | hg38 | chr12 | 6,199,875 | 6,238,259 | 38,385 |
| ENST00000645565.1 | hg38 | chr12 | 6,200,759 | 6,236,738 | 35,980 |
| ENST00000676764.1 | hg38 | chr12 | 6,226,302 | 6,238,248 | 11,947 |
| ENST00000009180.10 | hg38 | chr12 | 6,200,400 | 6,238,266 | 37,867 |
| ENST00000646407.1 | hg38 | chr12 | 6,226,328 | 6,238,253 | 11,926 |
| ENST00000610354.5 | hg38 | chr12 | 6,200,327 | 6,238,247 | 37,921 |
| ENST00000642746.1 | hg38 | chr12 | 6,199,841 | 6,238,247 | 38,407 |
| ENST00000382519.9 | hg38 | chr12 | 6,200,385 | 6,238,139 | 37,755 |
| ENST00000679331.1 | hg38 | chr12 | 6,200,364 | 6,236,910 | 36,547 |
| ENST00000382518.6 | hg38 | chr12 | 6,199,715 | 6,238,271 | 38,557 |
| ENST00000382515.7 | hg38 | chr12 | 6,200,797 | 6,238,225 | 37,429 |
| ENST00000382518.6 | hg19 | chr12 | 6,308,881 | 6,347,437 | 38,557 |
| ENST00000642746.1 | hg19 | chr12 | 6,309,007 | 6,347,413 | 38,407 |
| ENST00000009180.10 | hg19 | chr12 | 6,309,566 | 6,347,432 | 37,867 |
| ENST00000382515.7 | hg19 | chr12 | 6,309,963 | 6,347,391 | 37,429 |
| ENST00000382519.9 | hg19 | chr12 | 6,309,551 | 6,347,305 | 37,755 |
| ENST00000538834.6 | hg19 | chr12 | 6,309,041 | 6,347,425 | 38,385 |
| ENST00000610354.5 | hg19 | chr12 | 6,309,493 | 6,347,413 | 37,921 |
| ENST00000679331.1 | hg19 | chr12 | 6,309,530 | 6,346,076 | 36,547 |
| ENST00000645565.1 | hg19 | chr12 | 6,309,925 | 6,345,904 | 35,980 |
| ENST00000676764.1 | hg19 | chr12 | 6,335,468 | 6,347,414 | 11,947 |
| ENST00000646407.1 | hg19 | chr12 | 6,335,494 | 6,347,419 | 11,926 |
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