MPND MPN domain containing
Information
- Symbol
- MPND
- Type
- protein-coding
- Description
- MPN domain containing
- Entrez Gene ID
- 84954
- Genome
- hg19
- Position
- chr19:4,343,559-4,360,075
- Genome
- hg38
- Position
- chr19:4,343,562-4,360,078
- HGNC
- HGNC:25934 HGNC
- Ensembl
- ENSG00000008382 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 6 |
| Uncertain significance | 0 | 84 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
90 |
 |
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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| Category | : |
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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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| Category | : |
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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
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000599840.6 | hg38 | chr19 | 4,343,562 | 4,360,078 | 16,517 |
| ENST00000262966.12 | hg38 | chr19 | 4,343,527 | 4,360,086 | 16,560 |
| ENST00000359935.8 | hg38 | chr19 | 4,343,554 | 4,360,081 | 16,528 |
| ENST00000262966.12 | hg19 | chr19 | 4,343,524 | 4,360,083 | 16,560 |
| ENST00000359935.8 | hg19 | chr19 | 4,343,551 | 4,360,078 | 16,528 |
| ENST00000599840.6 | hg19 | chr19 | 4,343,559 | 4,360,075 | 16,517 |
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