ZMP
qars
Ensembl ID:
ZFIN ID:
Description:
glutaminyl-tRNA synthetase [Source:RefSeq peptide;Acc:NP_957507]
Human Orthologue:
QARS
Human Description:
glutaminyl-tRNA synthetase [Source:HGNC Symbol;Acc:9751]
Mouse Orthologue:
Qars
Mouse Description:
glutaminyl-tRNA synthetase Gene [Source:MGI Symbol;Acc:MGI:1915851]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41293 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa17949 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41293
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000023780 | Essential Splice Site | 233 | 437 | 8 | 14 |
| ENSDART00000060919 | Essential Splice Site | 233 | 774 | 8 | 23 |
| ENSDART00000115253 | Essential Splice Site | 256 | 797 | 8 | 23 |
| ENSDART00000136602 | None | None | 224 | None | 7 |
| ENSDART00000137472 | Essential Splice Site | 233 | 457 | 8 | 14 |
Genomic Location (Zv9):
Chromosome 8 (position 48530440)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 46368698 |
| GRCz11 | 8 | 46376577 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCATTGATGGAGCAGCTGAGAGGAGAAGCTCTTAAGTTCCATAAGCCAG[G/A]TAAGTGTCCTTAACGACTATGTGTCCAGATAGCTACAATGTCATTCAATC
Long Flanking Sequence:
GTGATATGATAAGTGAAAAGCTTAGGTGGTAGCTCCAGACAACATAATCCACAACAATATTATAATAACAGTTAAGTACAAAAAACAATAAATATGTTTTAAAAATTTTTTTATTTGTTATAATGTTGTATTGTATAAATTTAGTATTTGGTATAATGCCAAACCAACAATAATTTAAGCGTCATTATTTTTGTGAAAATTATATGCTGCATCAGAGATGCTAGTAATGGCTAGGGTTTGGCAGTATGATGATATATCTTTTGGCGGCAACAATATAAAGTTTCTTTTGATAGGTCATTTGCTGTATTGTAAATATATTGAACATCTGGTTCTAGAACTATACTTTAAAAGGAGATTCTTGAACCATCTAACATGATTTCTTCATAAAATTGTAAAAGTCTGTTTTACTAATGCATCTTTCTCTCAAGGTGATGGGAACATTGAGAATAAGTCATTGATGGAGCAGCTGAGAGGAGAAGCTCTTAAGTTCCATAAGCCAG[G/A]TAAGTGTCCTTAACGACTATGTGTCCAGATAGCTACAATGTCATTCAATCTTCTTATTTTTCCTTTTATCTTCTCGGCACAGGGGAGAATTACAAAACGGAGGGTTATGTTGTAACACCTAACACCATGAACTTGCTGAAGAAGCACTTGGAAGAAACTGGAGGACAGGTATGACTACAACTGCAACTACAAGGGAGCTAGCTGGAGCTCGTCTACCCCAATAAAGACATGGGCTCTCCTAAAAACATGATTTGTGAAATTTCTGGGGATCTCAAAAAATATTAACAATGTGTTACTGTATTGTGCAATTTCAGTTTCATATTATTCGTTCAGCGATTCATTTGTTCCCAAGTCCCTTCTTAGCGCGATGCTAATCTGCGCTGATTGGTCCAATGACCCAGTCTGTGATTGTACGACTGCGTTAAGCGCGAGACAGAAAAAAAGATCAACAATTTGTAATCAGAGTGCAGAGAGTATGTGTAAGCATACCTGCCAGAGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17949
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000023780 | None | None | 437 | None | 14 |
| ENSDART00000060919 | Essential Splice Site | 759 | 774 | 23 | 23 |
| ENSDART00000115253 | Essential Splice Site | 782 | 797 | 23 | 23 |
| ENSDART00000136602 | None | None | 224 | None | 7 |
| ENSDART00000137472 | None | None | 457 | None | 14 |
Genomic Location (Zv9):
Chromosome 8 (position 48507330)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 46345588 |
| GRCz11 | 8 | 46353467 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNGACATTGAGTTTAACTTGTAWACTGTTTTTGYTTTGTTTTGTTCTYCA[G/A]CTGGTGTTCAACAGGACTGTTACACTCAAGGAGGATCCAGGAAAGATATG
Long Flanking Sequence:
ATGCTTTTATCCGATTAATTGGCCATCAAAATAATCGTTAGTTGAAACCCTGCTTGAATTGTTTACTTGCTACGTCACGCTCCGATTCGTTGTTGAATGAAGACCAATGCTTATAATATCCCAGCTTATTGACCTTATTCTAAAATGTGGAAGTGCGACTGTTTTCGCGATTGTCTTAGAACTTCCGATTCAGTCGCCTATGGGAGAAATGACTAGGGATAATAAACGGCAGAAAACGGTCAAACTACTTGCTCTACAAACAAATTTTTGCATGACTACACAGACCAAGTAGAATAATATAATAATAAAATATCAAATTGCAACATCAAGCAGCGTAACGAGCAGTTTTTAACGTCAAAAAATGAATGGAAGTGAATGAGACCAGAAGTCTCGAGCCAAAAAGATTCAAATGGCAGCGCCCGCTCATCGGCGGTGAATAAACAAATGAACATGACATTGAGTTTAACTTGTATACTGTTTTTGTTTTGTTTTGTTCTCCA[G/A]CTGGTGTTCAACAGGACTGTTACACTCAAGGAGGATCCAGGAAAGATATGATCAGACTTCAGGACAGAGACCGTACTTTGACTACATTTATGCATCACAAACCTGTCAATAAAATCTAATTAACCAGGGAATTCAGTATGTTTGTATTCAAACTCTCATTGTTATGACTGTCACATCCTGAGCTTACCTATGTGTAACCCATTCACTCTGCTGGGGTTTTGAAGTCCAATATTTAATTAAAATATTTTTACACTTGAAGTTCAAATGAGTGGAAACGATTTTTGGCCAGTTTCTAAAAGGGAAAATACATTCATATTTAAATGAATCTTTCTTGGATAATATAAAAACCTGTGGATAACCAGAGATTCACTTTAGTTTTCTACAGGTGAGTATGAAACAAAAATTGTGCAGGATGCGGGGGAAAGGACAGCTCGCCTCAAAGTAGATTCAGTCCTCATTTACATGGATTAAAGTTCTCCGTTGCTATAATAGACTGGAAA
Associated Phenotype:
Not determined