SERPINA2 serpin family A member 2 (gene/pseudogene)
Information
- Symbol
- SERPINA2
- Type
- protein-coding
- Description
- serpin family A member 2 (gene/pseudogene)
- Entrez Gene ID
- 390502
- Genome
- hg19
- Position
- chr14:94,830,653-94,833,035
- Genome
- hg38
- Position
- chr14:94,364,316-94,366,698
- MIM
- 107410 OMIM
- HGNC
- HGNC:8985 HGNC
- Ensembl
- ENSG00000258597 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 | ARGS |
| SYNONYM | ATR |
| SYNONYM | PIL |
| SYNONYM | SERPINA2P |
| SYNONYM | psiATR |
| MIM | 107410 OMIM |
| HGNC | HGNC:8985 HGNC |
| Ensembl | ENSG00000258597 Ensembl |
| AllianceGenome | HGNC:8985 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000553483.4 | hg38 | chr14 | 94,364,316 | 94,366,698 | 2,383 |
| ENST00000553483.4 | hg19 | chr14 | 94,830,653 | 94,833,035 | 2,383 |
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