ASRGL1 asparaginase and isoaspartyl peptidase 1
Information
- Symbol
- ASRGL1
- Type
- protein-coding
- Description
- asparaginase and isoaspartyl peptidase 1
- Entrez Gene ID
- 80150
- Genome
- hg19
- Position
- chr11:62,104,920-62,160,884
- Genome
- hg38
- Position
- chr11:62,337,448-62,393,412
- MIM
- 609212 OMIM
- HGNC
- HGNC:16448 HGNC
- Ensembl
- ENSG00000162174 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 24 |
| Likely benign | 0 | 190 |
| Conflicting classifications of pathogenicity | 0 | 4 |
| Uncertain significance | 0 | 278 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
58 |
 |
432 |
 |
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 | ALP |
| SYNONYM | ALP1 |
| SYNONYM | CRASH |
| MIM | 609212 OMIM |
| HGNC | HGNC:16448 HGNC |
| Ensembl | ENSG00000162174 Ensembl |
| AllianceGenome | HGNC:16448 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000415229.6 | hg38 | chr11 | 62,337,448 | 62,393,412 | 55,965 |
| ENST00000628829.2 | hg38 | chr11 | 62,337,493 | 62,392,568 | 55,076 |
| ENST00000534571.5 | hg38 | chr11 | 62,337,495 | 62,357,201 | 19,707 |
| ENST00000301776.9 | hg38 | chr11 | 62,337,453 | 62,393,406 | 55,954 |
| ENST00000415229.6 | hg19 | chr11 | 62,104,920 | 62,160,884 | 55,965 |
| ENST00000301776.9 | hg19 | chr11 | 62,104,925 | 62,160,878 | 55,954 |
| ENST00000628829.2 | hg19 | chr11 | 62,104,965 | 62,160,040 | 55,076 |
| ENST00000534571.5 | hg19 | chr11 | 62,104,967 | 62,124,673 | 19,707 |
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