ZMP
yars
Ensembl ID:
ZFIN ID:
Description:
Tyrosyl-tRNA synthetase, cytoplasmic [Source:UniProtKB/Swiss-Prot;Acc:Q6TGS6]
Human Orthologue:
YARS
Human Description:
tyrosyl-tRNA synthetase [Source:HGNC Symbol;Acc:12840]
Mouse Orthologue:
Yars
Mouse Description:
tyrosyl-tRNA synthetase Gene [Source:MGI Symbol;Acc:MGI:2147627]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23553 | Essential Splice Site, Splice Site | Available for shipment | Available now |
sa15803 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23553
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, Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052126 | Splice Site | None | 529 | 2 | 14 |
ENSDART00000124491 | None | None | 529 | 1 | 13 |
ENSDART00000135484 | Splice Site | None | 286 | None | 9 |
ENSDART00000139599 | Essential Splice Site | None | 87 | 2 | 4 |
ENSDART00000140603 | Splice Site | None | 251 | 2 | 8 |
ENSDART00000143394 | None | None | 228 | 1 | 6 |
The following transcripts of ENSDARG00000035913 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 32130712)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 31298001 |
GRCz11 | 19 | 30885314 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATGTCTATTACTTGACATATACACTTATAATACCTTATTTTGCACAGAA[G/A]CAGCAGACATCATGGGAGAGCAGCTGAGTCCTGATGAGAAGTTCCAGCTC
Long Flanking Sequence:
TAAAAACTGTTATCTAATACGTATTTAAGTGCATTTATAAAATTATAAATAATTAGATATTTTTAAAAATGTGTCTATACAATTTTAACTGAAGTGTAATTAAACTTTTATATTAGATGTGGCTTTTATTATGATACACGTGATGAAATCTTGGTTCAACCGGAACAGCCTGTCACCGGCACACACGTTTCTCAGCGACCGCCGGTGAGATATAATGTATGTTATTATGAACATCAAAATTTTGTTATAGTTATTATCACTGACGATTTATAAACACAATATTCACATTTATACCGACACATTTTCCGCTCTGCAGTGTTTCTAGTAACGTTACTGTGTTTTAGACAGCTCAGCGATTCATTCATTACAGACGTCACTGATTCTGAATAATTGAGATCGTAAAAACGTCAATCGTGACACAAAGTTTCTACCGAAATGACAAGTTCTGTGTATGTCTATTACTTGACATATACACTTATAATACCTTATTTTGCACAGAA[G/A]CAGCAGACATCATGGGAGAGCAGCTGAGTCCTGATGAGAAGTTCCAGCTCATCACCAGAAACCTTCAGGTGACAAACGTGTTATTATTGTTTGCTATGAGCTAAAAACATAGTTAACATTTAAAGTATATTATCAAAAGAATATTCGGAAATACATTTAAAAAATAGTTTTTGTTTCATCTTCATTTGAGTACAAGAGCTGTCACACCCTGTTGTTTTCTCTATTGAGGTAAAGTTGGTTTCATTTTCTCACGTTCTCCTTAATAATATTCATTCATTCGTTCATTCATTTTCTTTTCGGCTTAGTTCCTTTATTAATCATAAGTCACCACAGCGGAATGAACTGCCAACTTGTTCAGCCAATGTTTTACGCAGCGGATTTCCTTCCAGCTGCAACCCAGCTCTGGGAAACACCCATACACACACCGCGGTCAATTTAGCTCATTCAATTCACCTACAGTGCATGTCTTTGGACTGTGGGGGAAACCGGAGCACCCAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15803
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052126 | Nonsense | 124 | 529 | 4 | 14 |
ENSDART00000124491 | Nonsense | 124 | 529 | 3 | 13 |
ENSDART00000135484 | Nonsense | 124 | 286 | 4 | 9 |
ENSDART00000139599 | None | None | 87 | None | 4 |
ENSDART00000140603 | Nonsense | 124 | 251 | 4 | 8 |
ENSDART00000143394 | Nonsense | 124 | 228 | 3 | 6 |
The following transcripts of ENSDARG00000035913 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 32132447)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 31299736 |
GRCz11 | 19 | 30887049 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCATTGGAGTTCCTCTTGACAAACTCAAATTTGTCAAAGGCACAGATTAT[C/T]AGCTCRGCAGGTAACCGGATGATGATTGACTGAAAATTTGTTTTACGGAT
Long Flanking Sequence:
CCTTCTATTTGTGGGTTGCTTTTTGGTTTTGCTCCTGCTGAATATGCAGAAAAATGTTTTAAAGAAAATTGGAAGCTGTATTTATTAACATTTACCGTAATAAAAAATTCAGTGGCTTTCAGTTTCCAAAGATATCGTCCTTTGTGTTTGAAACTCAAACAGACTTGGAATTATTGGTGGATGAGTAAATAATGACAGAATTTTAGTTTGTTTTTGAACTATACTTTTAAGATGCTTTCATGTGAAATTGTTTGTAAAGGTCACAAGAATAAGTTACAAAAATGTGATCTCACATCTTTGCCCCTCTCATACCTATTTGTCCATTTGTTCTCAAGGTGACCATCCTCTTTGCTGATCTCCATGCTTATCTGGATAACATGAAGGCTCCCTGGGAGCTGCTGGAGCTCCGGGTGAAGTATTATGAGCAGGTCATCAAGGCCATGTTGGAGAGCATTGGAGTTCCTCTTGACAAACTCAAATTTGTCAAAGGCACAGATTAT[C/T]AGCTCAGCAGGTAACCGGATGATGATTGACTGAAAATTTGTTTTACGGATATTTCAGGTTTATTCCATAGAATAAGAAATGTATTTTAACCATGCATGTATAAGGTTTGTCTGTGGTTGCTTTGTTAAAAAGAATAAATGAAAATGTCATGGTTGGTTTGTTATAGAGAATACACTCTGGATGTTTACCGACTGTCATCCATGGTCACTGAACACGATGCAAAGAAAGCAGGGGCAGAGGTGGTCAAACAGGTTGAGCATCCTCTTCTCAGTGGTCTGCTGTATCCTGGACTACAGGTATGCAGATTGGGTTTTTCCCATCTTTGTCACCTACTGAAGGATTAAAACAGCTTTTAAAAACATCTCTTCATTCTTTTTTCAGTTTTTTAAAATGATTGTTATTATTTTTAGAACTTGTATATATATTTTAACTTACTTTATTAAAATTGCCACACATTCTGTTCTGAGTCTATAAAATAATCACCAAAGTTTCCACAAAAC
Associated Phenotype:
Not determined