DRAM1 DNA damage regulated autophagy modulator 1
Information
- Symbol
- DRAM1
- Type
- protein-coding
- Description
- DNA damage regulated autophagy modulator 1
- Entrez Gene ID
- 55332
- Genome
- hg19
- Position
- chr12:102,271,358-102,317,390
- Genome
- hg38
- Position
- chr12:101,877,580-101,923,612
- MIM
- 610776 OMIM
- HGNC
- HGNC:25645 HGNC
- Ensembl
- ENSG00000136048 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 26 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
26 |
 |
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
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MGeND data only
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| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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| 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 | DRAM |
| MIM | 610776 OMIM |
| HGNC | HGNC:25645 HGNC |
| Ensembl | ENSG00000136048 Ensembl |
| AllianceGenome | HGNC:25645 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000258534.13 | hg38 | chr12 | 101,877,580 | 101,923,612 | 46,033 |
| ENST00000544152.5 | hg38 | chr12 | 101,877,683 | 101,921,814 | 44,132 |
| ENST00000258534.13 | hg19 | chr12 | 102,271,358 | 102,317,390 | 46,033 |
| ENST00000544152.5 | hg19 | chr12 | 102,271,461 | 102,315,592 | 44,132 |
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