ZMP
iars
Ensembl ID:
ZFIN ID:
Description:
isoleucyl-tRNA synthetase, cytoplasmic [Source:RefSeq peptide;Acc:NP_956190]
Human Orthologue:
IARS
Human Description:
isoleucyl-tRNA synthetase [Source:HGNC Symbol;Acc:5330]
Mouse Orthologue:
Iars
Mouse Description:
isoleucine-tRNA synthetase Gene [Source:MGI Symbol;Acc:MGI:2145219]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa27708 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa21826 | Nonsense | Available for shipment | Available now |
sa41755 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa27708
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004423 | Essential Splice Site | None | 1270 | 1 | 35 |
Genomic Location (Zv9):
Chromosome 11 (position 1357459)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 1365832 |
GRCz11 | 11 | 1392420 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCAGTTGCATCATTTCCGCTGTCTCTGTTCACCGGCGACGGCCAGCATG[T/C]GAGTGTGATCTGACACTTCATCTTAATATAAAACTTTCTCAAACACACAC
Long Flanking Sequence:
ATCTGTTATCACATGCCTGACAGGACTTTTATTTTTATTTCATTTTAATAACGTCATCATTACCAGTTAAAGGGACAGTACACCCCAAAATAAAATAAAACGCATCATTATTTACTGAACTATTATGTGTTTCTTTCTCCTGTTAAAAGCAAAACAATATTCTAAATAATGCTGGGGAAATCCGTAATTGATATACACATTAGAAACAAAATACTATAAGAGTCATAAGCTCTTTTTCCAGCATTTTTCAATATAACTTGTTTTGTGTTCAACAGAATTAAGAAACTCATAAATATTTACAACCACTCGAGTGTGAGTAAATAATGAGGACATTTTATTTTTTGGATGAACTGTCCCATCATCACTGAAACTAAAATTAAAGAGCGTTCCCCTGTGGCTTTTATTATGTAAACTTTGGCTTGTATTTTGTCCAGTAGCTCAGGCGTTTCAGTCAGTTGCATCATTTCCGCTGTCTCTGTTCACCGGCGACGGCCAGCATG[T/C]GAGTGTGATCTGACACTTCATCTTAATATAAAACTTTCTCAAACACACACATATATAACTTACAGACACACACACATATACACAAACACACACTGCCTGCTCCGTGTCTATAGACTCGCTCATATATAGGCGAACTCGGTGATTAGCGGCTAGCTGAGACTGTAGCTGCTGCTCTATTACTGTAGTCTGATACTGTCTAATAATAAACAGTTATTAATCAGCATATGAGCGTGTATGATTGACACACATCAGTCAGTTTGAGTCTATTAGCCAGTTTGTATTCTGTTTATGCAGCAGAACACAGATATGACAGCACTATGATGTTAGTTCAGTGCTCCAAATATATATATNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNTATATATATATATATATATATATATATATATATACATCCATATATATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21826
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004423 | Nonsense | 409 | 1270 | 13 | 35 |
Genomic Location (Zv9):
Chromosome 11 (position 1335417)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 1343790 |
GRCz11 | 11 | 1370378 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAATATTGAACAACTCGTTGGTTTGCAGGTCGGACACGCCGCTGATCTA[C/A]AAAGCAGTGCCCAGCTGGTTTATAAGGGTGGAGCACATGGTGGAGAAACT
Long Flanking Sequence:
CAATCATCCAGTCGGAGTGTTAGTCTTCAGTTAATGACTCACTGATTCAATCATCCTGTCGGAGTGTGAGTCTTCAGTTAATGACTCACTGATTCAAATGATCCAGTCAAGGTGCGAATCTTCAGTTAATGACTCACTGATTTAATCATCCAGTCGGAGTGCGAGTCTTCAGTTAATGACTCACTGATTCAATCATCCAGTCGGAGTGTGAGTCTTCAGTTAATGACTCACTGATTTAATCATCCAGTCGGAGTGTGAATCTTCAGTTAATGACTCACTGATTCAAATGTTCCAGTCGGAATGTGAATCTTCAGGTAATGACTCACTGATTCAAATGGTCACTAGGGGTCGGCATACTAGAGGTTTCCATGACAATCTTACATTTTGTCATCTGGCACAGTTAGTCCTGCCATGTGATGATATCATAAGTAATTTAATGTTTCAGATGTTTAAATATTGAACAACTCGTTGGTTTGCAGGTCGGACACGCCGCTGATCTA[C/A]AAAGCAGTGCCCAGCTGGTTTATAAGGGTGGAGCACATGGTGGAGAAACTTCTGGACAACAACAGCAAGTGCTACTGGTACTGAGAATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGCTGCATGTTGATCAGATGCACATGCTTACAGCTCCTCTATAATCCGTCATCAGATTTGGGTTGGTCTTTTGTCATACATTGTAAAAGGCTATTCAGACTCTTGATGAAGTGTGATATGGTGATCTGCAAAGTAAGAGCTCGTCTTCGTTTCTCAGATGTGGTTTTAAAGTCTGTTGTGTTGGTTCTTAATGGTGCAGTAGGTAAGTTTGACACCCAGTGGTTGAACTAGGTATTGCACTTATGGATCAAAACAAAGGCAATCGCAGGTTGCCAGATTGAGGGCAGAATCAAATGATTTAAACCATGTTCTAAATAAGCTGCTTTTATTAAGAACACGGTTTAAATCATTCGCTCCTGCCCTCAATCTGGCAACCTGCGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41755
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 |
---|---|---|---|---|---|
ENSDART00000004423 | Essential Splice Site | 1143 | 1270 | 32 | 35 |
Genomic Location (Zv9):
Chromosome 11 (position 1306398)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 1314771 |
GRCz11 | 11 | 1341359 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTTCGGCCTCAACGGAGCTCCAGTCTCCATATTCAACGGCAAGACAG[G/A]TGAGAGCTCCAAATATAACAGTGGAGCCTGTTCACATGTGTGTGTGTGTG
Long Flanking Sequence:
GCACATGCATGCGCCTGTATGTTTGTGTATATGTGTGTGTAGATATGTGCATGTGTGTGTTCGTGCATTCATTCATTCATTCATGCGTGCGTTGTCGTGTGTGTGTGTTTCAGCTGAAGGGCTCAGATCTGGAGTTGACTATCGTGCGAGGCTCCTCCTCTTCCTCCGTCTGCAGGGCTCCTGTGAGCGGCTCGGCGTGTGCGTTTGTGAACCTCAGAGTGTCGCTCAAAGATAAACAGCAGGGTACGAGACGCTACACACACACACACACACACACACACACACACACACACACACACACACAAACACACACACACACAAACACACCTGCAGGATCTGATCTGCAGCTCATCTTCTGTGTGTTCTGCTGTCAGACGGTGTGGTTCTGCTGGAGAACCCCAAGGGAGACAACAGACTGGACCTGGAGCAGCTGAAGAGGATCTGCTGCAGTGTGTTCGGCCTCAACGGAGCTCCAGTCTCCATATTCAACGGCAAGACAG[G/A]TGAGAGCTCCAAATATAACAGTGGAGCCTGTTCACATGTGTGTGTGTGTGTTTCTCCGCAGCAGAAGTTGTCATAGTTGGTGGGAGAGCACAACAGATCATTCATTTACAATCCTATTGCTGAAATAATGACAGAAAAATTTCACAAGGGTCTTATGAAGACTTTCAGAAAGAGGAAAACAATGGTGTAAGACCGATAACTAGGGGTGTAACGGATCACGGTTGATCTGTGATTCATATGATTAATACATATTTTTACTTGTAGATTAATCCTAAACTTGTAATGATTGCAGAGAGATCGCCTCCTCTTTTTTTTAAAAGCAGCCAATAGCTGTTTATTTCATCATCGCTCAGCCAGTAAGAGTGCTTGAGCTCAGGTGAATCAAATGTCTTGAAGGGGGCGGGGCATGTCAGACACTAGAGAGCATTTGATTGGTCAGAAGATTTGATGAGACACTAAAGTATGACGTGACATAAATAAAAACCATAGATATATACATT
Associated Phenotype:
Not determined