MYADM myeloid associated differentiation marker
Information
- Symbol
- MYADM
- Type
- protein-coding
- Description
- myeloid associated differentiation marker
- Entrez Gene ID
- 91663
- Genome
- hg19
- Position
- chr19:54,372,660-54,379,689
- Genome
- hg38
- Position
- chr19:53,869,406-53,876,435
- MIM
- 609959 OMIM
- HGNC
- HGNC:7544 HGNC
- Ensembl
- ENSG00000179820 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 40 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
40 |
 |
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
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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 | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | SB135 |
| MIM | 609959 OMIM |
| HGNC | HGNC:7544 HGNC |
| Ensembl | ENSG00000179820 Ensembl |
| AllianceGenome | HGNC:7544 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000421337.6 | hg38 | chr19 | 53,866,153 | 53,874,756 | 8,604 |
| ENST00000391771.1 | hg38 | chr19 | 53,867,883 | 53,876,428 | 8,546 |
| ENST00000391770.9 | hg38 | chr19 | 53,867,883 | 53,876,435 | 8,553 |
| ENST00000391768.2 | hg38 | chr19 | 53,869,439 | 53,874,619 | 5,181 |
| ENST00000391769.2 | hg38 | chr19 | 53,869,406 | 53,876,435 | 7,030 |
| ENST00000421337.6 | hg19 | chr19 | 54,369,407 | 54,378,010 | 8,604 |
| ENST00000391771.1 | hg19 | chr19 | 54,371,137 | 54,379,682 | 8,546 |
| ENST00000391770.9 | hg19 | chr19 | 54,371,137 | 54,379,689 | 8,553 |
| ENST00000391769.2 | hg19 | chr19 | 54,372,660 | 54,379,689 | 7,030 |
| ENST00000391768.2 | hg19 | chr19 | 54,372,693 | 54,377,873 | 5,181 |
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