ATRAID all-trans retinoic acid induced differentiation factor
Information
- Symbol
- ATRAID
- Type
- protein-coding
- Description
- all-trans retinoic acid induced differentiation factor
- Entrez Gene ID
- 51374
- Genome
- hg19
- Position
- chr2:27,434,909-27,440,025
- Genome
- hg38
- Position
- chr2:27,212,041-27,217,157
- MIM
- 619682 OMIM
- HGNC
- HGNC:24090 HGNC
- Ensembl
- ENSG00000138085 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 44 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
50 |
 |
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 | APR--3 |
| SYNONYM | APR-3 |
| SYNONYM | APR3 |
| SYNONYM | C2orf28 |
| SYNONYM | HSPC013 |
| SYNONYM | PRO240 |
| SYNONYM | p18 |
| MIM | 619682 OMIM |
| HGNC | HGNC:24090 HGNC |
| Ensembl | ENSG00000138085 Ensembl |
| AllianceGenome | HGNC:24090 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000405489.7 | hg38 | chr2 | 27,212,370 | 27,217,178 | 4,809 |
| ENST00000380171.9 | hg38 | chr2 | 27,212,041 | 27,217,157 | 5,117 |
| ENST00000380171.9 | hg19 | chr2 | 27,434,909 | 27,440,025 | 5,117 |
| ENST00000405489.7 | hg19 | chr2 | 27,435,238 | 27,440,046 | 4,809 |
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