ZMP
kars
Ensembl ID:
ZFIN IDs:
Description:
lysyl-tRNA synthetase [Source:RefSeq peptide;Acc:NP_001002386]
Human Orthologue:
KARS
Human Description:
lysyl-tRNA synthetase [Source:HGNC Symbol;Acc:6215]
Mouse Orthologue:
Kars
Mouse Description:
lysyl-tRNA synthetase Gene [Source:MGI Symbol;Acc:MGI:1934754]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa694 | Essential Splice Site | Available for shipment | Available now |
| sa21133 | Essential Splice Site | Available for shipment | Available now |
| sa21134 | Splice Site, Nonsense | Available for shipment | Available now |
| sa15144 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa694
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 |
|---|---|---|---|---|---|
| ENSDART00000064924 | Essential Splice Site | 15 | 577 | 1 | 15 |
| ENSDART00000064926 | Essential Splice Site | None | 602 | 1 | 15 |
Genomic Location (Zv9):
Chromosome 7 (position 69483470)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 67206230 |
| GRCz11 | 7 | 67429592 |
KASP Assay ID:
554-0602.1 (used for ordering genotyping assays)
KASP Sequence:
GAGAAGATGGCAGACGGAGCTGTGGTGGATGGAGACAAACTCAGCAAAAA[G/A]TATAGACATTTACACAATTATAGCGCTTAGGCTGCTTTTGTGCGAACTAA
Long Flanking Sequence:
NNNNTATATATATATATATATATATATATATATACCAAGCTTATGAAATTGTCTGTTGTGTTGCATTAGTAGGCTTTAATATAATTATATAAAAATCATTTAAGAATCAAGCACTAGGTTTATTAATATAGACATAAATGACCAATAATTTAGGAATAATCATTCTTGGTAACGTTAAATATACAGTTTATGGCTTCTTTTTAACATGTTTGTGTATATTTTACGGTTTCATCATATTTTAATCTGTTTTATTGTTAATCAATGACATTTTTATTGGTGTTGTTTATCTTAATATGCAAATATTTATTCAAAAAACAAACCACTTACGAGAAAAGGAAGTGATGCAACTTTAAGCAACGGAACTTTTACAGTGAAGCGTGGTCGAACATTAGCCGGTTTTATTGCTGCAGTGTTGTTTATATCTGGCTTCACTGTCCTGCTGCGAGCGTGGAGAAGATGGCAGACGGAGCTGTGGTGGATGGAGACAAACTCAGCAAAAA[G/A]TATAGACATTTACACAATTATAGCGCTTAGGCTGCTTTTGTGCGAACTAAAACCTAAGATAAGTTGGACTGTGTGCGTTGCGCGACGTTCATACTCTCTGTTGTCCTGTAAGATCCGTTGTGATGAAGTGCAACGTGGTTTGTTCTGCGTGAACGCGACTGAATGATAGCTTGTTTTGATTACGATTTATTGCGTGTAAATGGTTCTCCCTTGTCGGCATATTTCAGGATCAGTCAAAAATCTGTTTTACCTAAATTAATCTTAAAATGACACTCACGTTCTCATTTCATCCTCCATAGCGCGCCGAGAAAGCTAATGGCGTGTTCGCTTGAGACTCATTTCCGTGACCGTTAAAAATAATATTCGGCGACTATTTTACGCTGAGAATTCGTCAAATATTTGTTATCTTACCTTAAATGCGTTAAGTATGTTAATATAATCTTTTCTGCGCTTCTGTCAGTTAACGGAACTAAAGTACTTTCGATTCTGGGGGTCAGTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21133
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 |
|---|---|---|---|---|---|
| ENSDART00000064924 | Essential Splice Site | 211 | 577 | 5 | 15 |
| ENSDART00000064926 | Essential Splice Site | 236 | 602 | 6 | 15 |
Genomic Location (Zv9):
Chromosome 7 (position 69490361)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 67213030 |
| GRCz11 | 7 | 67436382 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCATGTCTTCATATGCTTCCACATCTTCACTTTGGCCTGAAAGACAAG[G/A]TAAAGCTTTGTTTTTAAATCACTTTGGAAATAATATCTCTCTTTCAGACT
Long Flanking Sequence:
TCGTAGGCCAACAATTGAAAGGACCACATAATACAAATACAACATGCTAACTTCAGTGAACTTGTTTGTTTATTTGTGTTTTTTAGGCAAATTGTGCATGTGTTGTTAGGATTTGCAGTGTGTTTTCTACATGTGTTTGCCTTGTCAGGATTTGTCAAATCAGTGAAGATGTTTTCTTAATTAGCTTTTGTTTTCTGATTCTGACATTTCTGATGAAGTGTTTTTGTTGTTTTTTTAAGTTGCAGCACGTTACGTTTTCTCGGCCACCATAGTCTTTTCATGTTATATACTTACATGACCAGTCTTTTCTTAGAAACTACACATCAGAAGAAGCGTTTGTGCACATCAACAACAAACTGAGGCGTGGAGACATCATCGGGGTCCGGGGGAACCCTGGCAAGACAAAGAAGGGCGAGTTGAGCATCATCCCAGTGGAGATGACCCTGCTGTCTCCATGTCTTCATATGCTTCCACATCTTCACTTTGGCCTGAAAGACAAG[G/A]TAAAGCTTTGTTTTTAAATCACTTTGGAAATAATATCTCTCTTTCAGACTTCTTTTTCTTTGTCTGCAACCTTTTGGGGGTGGGAGAAGCACACTTGTGTATTTTATAATATGCTGTTTAATTGCAATTCAGTAAAAATTCTTTATAGTTGTCAGTGCTAATAGCCTAGTGGTTAAGTGCGCTGACATGGAGGTGCTCACGGTGACAAAAGTTTGATTTCTGGCTCCAGGTCCTAAAATGATCCTAGTATCTGCTCTCATTACCGTTCTTTCTGTAATCTCTACTGTTCTATCCTAATAAAGGTGAAAACCCTCTGAAAATAATTAAGAAAATAGGCAAAAAAATGCATTATAGTTTAAATTTATGTAAAATGCAAGTGATTGAGTTTTAGAATACAAAACATTTAATAAAATAACTGACCTATTTTCTGTAGAAGACACTTAGAGTGCTCACACTAGGTACAGTTGCCTTGGAACTGTGCTAAAGCATGATTGTCCCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21134
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 > T
Consequence:
Splice Site, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000064924 | Splice Site, Nonsense | 406 | 577 | 9 | 15 |
| ENSDART00000064926 | Splice Site, Nonsense | 431 | 602 | 10 | 15 |
Genomic Location (Zv9):
Chromosome 7 (position 69497597)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 67220266 |
| GRCz11 | 7 | 67443618 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAGGAGTTGGGTGTGAAGTTTCCACCTCCTGACACCTATGACAGTGAC[G/T]GTATAGAAATGTTTGAAAACATATGTTTGCCATCACAAAAGGTGTGGGAA
Long Flanking Sequence:
CTACATTGTAAAAGAGCTATACAAATAAAGCTGGATTGAATTGAATTATACAGAATAGAATTTGAATGAAGTATAAAAGAAATAATTTATATTGCCATTCCTTGTCATTTTTATCTAAATGACAAGACTAAAATAATGAAACGCGAATTTGAATTAATCAGTTTAAGGCATAATGTTGGTCTCTTGTTCATCAGAAATGTAAATGTTTCAATTGATTTAGAAAATATTGCTTGATTCTGAAGTGCACAGTAAAGATTGAATTTTGTATTTGAAGATGTGTCTGAAAACACCAAGTGATGTTTTTTGTTGATGTTGTTGTTTTTACAGGAATGGTGAAGCACATTACCGGAGCTTATAAAGTGACGTATCATCCTGATGGTCCAGAGGGACAGGCCTACGAAATAGACTTCACCCCTCCCTTCAGGCGAATCAGCATGACCCAAGAGCTGGAGAAGGAGTTGGGTGTGAAGTTTCCACCTCCTGACACCTATGACAGTGAC[G/T]GTATAGAAATGTTTGAAAACATATGTTTGCCATCACAAAAGGTGTGGGAAGGTGTTTTTTTTCTGTTGCTAAAATAGTTTTGTGTGTGTTTTTGACAGAAATGCGCAAGTTCTTAGACGACCTGTGTGTTCAGAAAGAAGTTGAATGTCCTCCTCCCAGGACAACTGCTCGACTTCTTGATAAGGTATGAAGTAGGGCTGCACGATATTGGGAAAAGAAAAAAAGCTGACATTGCGATATTTAGTTTTTCTGTGATTAAATTGCGATATAAATATAACTTCAAAAGATGACTGACTCGATTTGGCAATATTTTATAAGGTTGAAATAGTGAGTAGTGCAACATGATTTGTGGTACATTCTCCATGCACATTGTGGTAATATTATCCATACACATTGTGGTAATATATTCAAAAAGGCGGCAACACCATACAAAGCTAATTCATTAGATTAAAAAAGGCTGATAAAAAGTGTGTAACGTTTCGAGCACACCGACTCTTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15144
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000064924 | Essential Splice Site | 406 | 577 | 9 | 15 |
| ENSDART00000064926 | Essential Splice Site | 431 | 602 | 10 | 15 |
Genomic Location (Zv9):
Chromosome 7 (position 69497599)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 67220268 |
| GRCz11 | 7 | 67443620 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGGAGTTGGGTGTGAARTTTCCACCTCCTGACACCTATGACAGTGACGG[T/C]AWAGNAAATGTTTGAAAACATATGTTTGCCATCACAAAAGGTGTGGGAAGG
Long Flanking Sequence:
ACATTGTAAAAGAGCTATACAAATAAAGCTGGATTGAATTGAATTATACAGAATAGAATTTGAATGAAGTATAAAAGAAATAATTTATATTGCCATTCCTTGTCATTTTTATCTAAATGACAAGACTAAAATAATGAAACGCGAATTTGAATTAATCAGTTTAAGGCATAATGTTGGTCTCTTGTTCATCAGAAATGTAAATGTTTCAATTGATTTAGAAAATATTGCTTGATTCTGAAGTGCACAGTAAAGATTGAATTTTGTATTTGAAGATGTGTCTGAAAACACCAAGTGATGTTTTTTGTTGATGTTGTTGTTTTTACAGGAATGGTGAAGCACATTACCGGAGCTTATAAAGTGACGTATCATCCTGATGGTCCAGAGGGACAGGCCTACGAAATAGACTTCACCCCTCCCTTCAGGCGAATCAGCATGACCCAAGAGCTGGAGAAGGAGTTGGGTGTGAAGTTTCCACCTCCTGACACCTATGACAGTGACGG[T/C]ATAGAAATGTTTGAAAACATATGTTTGCCATCACAAAAGGTGTGGGAAGGTGTTTTTTTTCTGTTGCTAAAATAGTTTTGTGTGTGTTTTTGACAGAAATGCGCAAGTTCTTAGACGACCTGTGTGTTCAGAAAGAAGTTGAATGTCCTCCTCCCAGGACAACTGCTCGACTTCTTGATAAGGTATGAAGTAGGGCTGCACGATATTGGGAAAAGAAAAAAAGCTGACATTGCGATATTTAGTTTTTCTGTGATTAAATTGCGATATAAATATAACTTCAAAAGATGACTGACTCGATTTGGCAATATTTTATAAGGTTGAAATAGTGAGTAGTGCAACATGATTTGTGGTACATTCTCCATGCACATTGTGGTAATATTATCCATACACATTGTGGTAATATATTCAAAAAGGCGGCAACACCATACAAAGCTAATTCATTAGATTAAAAAAGGCTGATAAAAAGTGTGTAACGTTTCGAGCACACCGACTCTTCATCA
Associated Phenotype:
Not determined