ZMP
asl
Ensembl ID:
ZFIN ID:
Description:
argininosuccinate lyase [Source:RefSeq peptide;Acc:NP_956745]
Human Orthologues:
AC068533.7, ASL
Human Description:
argininosuccinate lyase [Source:HGNC Symbol;Acc:746]
Mouse Orthologue:
Asl
Mouse Description:
argininosuccinate lyase Gene [Source:MGI Symbol;Acc:MGI:88084]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa12812 | Essential Splice Site | Available for shipment | Available now |
| sa13022 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12812
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000040190 | Essential Splice Site | 117 | 465 | 4 | 16 |
| ENSDART00000132317 | Essential Splice Site | 117 | 240 | 5 | 10 |
| ENSDART00000040190 | Essential Splice Site | 117 | 465 | 4 | 16 |
| ENSDART00000132317 | Essential Splice Site | 117 | 240 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 21 (position 30020980)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 31221231 |
| GRCz11 | 21 | 31257926 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGTGATGCTGCTGGAAAGCTTCATACTGGCAGGAGCAGAAATGATCAGG[T/G]TCCTCCAATTGTAATTTCAGTTTTGCTGTTATWTCGCATGACAYTTAATT
Long Flanking Sequence:
AGACTTATCTTTTTTTACAGATGAATTTACCACCAGTTGACCTGAAACCGATTGAAAGTGTTTGAGTTGTCCTGTGAAGTAGACCCTGGACACCACAGGGTCTGATAATGGGAATGCTCAACTTCTCATTACAAGCCATGAGTGAAAAAATACATGCAACCCTAGATGGAAATACAATGTGTGAAATTGCATAAAAGATCTTCATTATCTGACCCTGAGGAGATCCACTCTGTGAAGTCTGTTCCAGCACGTCACAAAGACTTTCGATGGTGTTCAGATCAATTGATAATCAATTCATGTGTCAAAATGAAACCTCTTTTCATAGTTTGAGTCTAATTTGCATTGCCATCTTAGAGTCTTCTAAAGAAATAAAAGCTCCACACAGCCTCATTTAGAGTTGCTTAAAATGAGTCAATGTTAATCTCATCTCTCTTTTTTAAAGGAATTGATTGGTGATGCTGCTGGAAAGCTTCATACTGGCAGGAGCAGAAATGATCAGG[T/G]TCCTCCAATTGTAATTTCAGTTTTGCTGTTATATCGCATGACATTTAATTAACTTGCATATTATTTGGCTCACTTGTCGGATAGGTTGCAACTGATATGCGACTCTGGTTACGGGATGGTATTGCCACGCTTAAAGAACTGGCTTTGCAACTCATCAACACTATGGTGGAAAGAGCTGCAGCGTAAGAATATGCACAGTAATCTTAATACATTTATTAATAAGAGTAATGTACTATTGCCAAATACATAGCTATTTTTTTTAATCCTTTTAGAGAGATTGAAATCCTGTGCCCAGGATACACTCACATGCAGAGAGCCCAGCCAATCAGATGGAGTCACTGGCTTCTCAGGTGTATTTCTATTTTAGATTTAAAGTGACTTTTCACACAGAAATGAACTTTTAATCACACTCAAGTGGTTCTAAAAAAATTACGAATTTCTTTTTTCACTTGTAAAGCATAAAAAAATATAAATTCTGAAGAATGTTGAAAACTAGCTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13022
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000040190 | Essential Splice Site | 117 | 465 | 4 | 16 |
| ENSDART00000132317 | Essential Splice Site | 117 | 240 | 5 | 10 |
| ENSDART00000040190 | Essential Splice Site | 117 | 465 | 4 | 16 |
| ENSDART00000132317 | Essential Splice Site | 117 | 240 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 21 (position 30020980)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 31221231 |
| GRCz11 | 21 | 31257926 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGTGATGCTGCTGGAAAGCTTCATACTGGCAGGAGCAGAAATGATCAGG[T/G]TCCTCCAATTGTAATTTCAGTTTTGCTGTTATWTCGCATGACAYTTAATT
Long Flanking Sequence:
AGACTTATCTTTTTTTACAGATGAATTTACCACCAGTTGACCTGAAACCGATTGAAAGTGTTTGAGTTGTCCTGTGAAGTAGACCCTGGACACCACAGGGTCTGATAATGGGAATGCTCAACTTCTCATTACAAGCCATGAGTGAAAAAATACATGCAACCCTAGATGGAAATACAATGTGTGAAATTGCATAAAAGATCTTCATTATCTGACCCTGAGGAGATCCACTCTGTGAAGTCTGTTCCAGCACGTCACAAAGACTTTCGATGGTGTTCAGATCAATTGATAATCAATTCATGTGTCAAAATGAAACCTCTTTTCATAGTTTGAGTCTAATTTGCATTGCCATCTTAGAGTCTTCTAAAGAAATAAAAGCTCCACACAGCCTCATTTAGAGTTGCTTAAAATGAGTCAATGTTAATCTCATCTCTCTTTTTTAAAGGAATTGATTGGTGATGCTGCTGGAAAGCTTCATACTGGCAGGAGCAGAAATGATCAGG[T/G]TCCTCCAATTGTAATTTCAGTTTTGCTGTTATATCGCATGACATTTAATTAACTTGCATATTATTTGGCTCACTTGTCGGATAGGTTGCAACTGATATGCGACTCTGGTTACGGGATGGTATTGCCACGCTTAAAGAACTGGCTTTGCAACTCATCAACACTATGGTGGAAAGAGCTGCAGCGTAAGAATATGCACAGTAATCTTAATACATTTATTAATAAGAGTAATGTACTATTGCCAAATACATAGCTATTTTTTTTAATCCTTTTAGAGAGATTGAAATCCTGTGCCCAGGATACACTCACATGCAGAGAGCCCAGCCAATCAGATGGAGTCACTGGCTTCTCAGGTGTATTTCTATTTTAGATTTAAAGTGACTTTTCACACAGAAATGAACTTTTAATCACACTCAAGTGGTTCTAAAAAAATTACGAATTTCTTTTTTCACTTGTAAAGCATAAAAAAATATAAATTCTGAAGAATGTTGAAAACTAGCTGC
Associated Phenotype:
Not determined