MAP3K9-DT MAP3K9 divergent transcript
Information
- Symbol
- MAP3K9-DT
- Type
- ncRNA
- Description
- MAP3K9 divergent transcript
- Entrez Gene ID
- 100506411
- Genome
- hg19
- Position
- chr14:71,276,414-71,283,547
- Genome
- hg38
- Position
- chr14:70,809,697-70,816,830
- HGNC
- HGNC:53189 HGNC
- Ensembl
- ENSG00000259153 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
0 |
 |
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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| 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
|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | lincNMR |
| HGNC | HGNC:53189 HGNC |
| Ensembl | ENSG00000259153 Ensembl |
| AllianceGenome | HGNC:53189 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000685546.1 | hg38 | chr14 | 70,809,900 | 70,815,396 | 5,497 |
| ENST00000697756.1 | hg38 | chr14 | 70,809,192 | 70,815,991 | 6,800 |
| ENST00000697759.1 | hg38 | chr14 | 70,809,728 | 70,815,386 | 5,659 |
| ENST00000697757.1 | hg38 | chr14 | 70,809,697 | 70,816,830 | 7,134 |
| ENST00000697760.1 | hg38 | chr14 | 70,809,874 | 70,815,391 | 5,518 |
| ENST00000697765.1 | hg38 | chr14 | 70,809,960 | 70,815,216 | 5,257 |
| ENST00000557691.3 | hg38 | chr14 | 70,809,841 | 70,816,055 | 6,215 |
| ENST00000697756.1 | hg19 | chr14 | 71,275,909 | 71,282,708 | 6,800 |
| ENST00000557691.3 | hg19 | chr14 | 71,276,558 | 71,282,772 | 6,215 |
| ENST00000685546.1 | hg19 | chr14 | 71,276,617 | 71,282,113 | 5,497 |
| ENST00000697757.1 | hg19 | chr14 | 71,276,414 | 71,283,547 | 7,134 |
| ENST00000697759.1 | hg19 | chr14 | 71,276,445 | 71,282,103 | 5,659 |
| ENST00000697760.1 | hg19 | chr14 | 71,276,591 | 71,282,108 | 5,518 |
| ENST00000697765.1 | hg19 | chr14 | 71,276,677 | 71,281,933 | 5,257 |
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