ZMP
iars2
Ensembl ID:
ZFIN ID:
Description:
isoleucyl-tRNA synthetase, mitochondrial [Source:RefSeq peptide;Acc:NP_001157270]
Human Orthologue:
IARS2
Human Description:
isoleucyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:29685]
Mouse Orthologue:
Iars2
Mouse Description:
isoleucine-tRNA synthetase 2, mitochondrial Gene [Source:MGI Symbol;Acc:MGI:1919586]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa28862 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14246 | Nonsense | Available for shipment | Available now |
sa2910 | Essential Splice Site | Available for shipment | Available now |
sa17843 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa28862
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064803 | Nonsense | 75 | 983 | 2 | 23 |
ENSDART00000138853 | Nonsense | 75 | 886 | 2 | 21 |
Genomic Location (Zv9):
Chromosome 17 (position 25433162)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 25573081 |
GRCz11 | 17 | 25591472 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTGTAGAAATGTGGTTTTGACCAGCTGTACAAATGGCAGAGAGAGAAA[A/T]AGGCTAAGAAGGAGTACTGTCTTCATGATGGACCACCGTATGCCAATGGG
Long Flanking Sequence:
ACATGTTCTTGCATATATTTTCTAAATGGGTCTCACATTTTCTTAAACTGGTTAGATTTTTTCAGCTTTAGAAAGAAGAGAACATCACGAATCCACTGTGTTGGGTTTGTAGGTTCCTGATAAGTTTCCATTTAAAAAATATTAGCTGTTTGACCAGGAGCACAATAAAAGCTATGCAATCAGATTGTATTTTTTAAGATTATACGAGATGGAAAAAATCACAACAATGGCAATCAGTGAGCAAAGGGAGATACATATACCCAAAAAACTGAAGTGATATTTTTAAGGAGAAGGTTAGAATGTGTGAATATAAAACCAAACGTTTACTGATGCTGCTAAAGAACATAACAGCAACAATAAGGTGATGTCTGCTGTTGTAACTCTTTAAAGCCACACACTTTGAGACTTGACTGACTTGTCTTGTGTTGGAGTTTGAGTTTTCTTGTGTTTTTCTGTAGAAATGTGGTTTTGACCAGCTGTACAAATGGCAGAGAGAGAAA[A/T]AGGCTAAGAAGGAGTACTGTCTTCATGATGGACCACCGTATGCCAATGGGGACCCTCATGTTGGGCATGCACTCAATAAGGTACCTCCTGTCACTTCGTCATCACACACATATGTAGATGTTCCTGGATCTACATCATCTAATTTTCTTCTCATACATTTTTGTCATTGTTATTTCAGTTAGCCTAAATGTAAACACAGAGATATGGGATTTTTCAAAAATATGCCATCAGCATCTACTGTTAATCTTTCCTGTAGATTCTCAAAGACATACGAAACCGTTTCGAGGTGCTGAGAGGCAGGCAGGTGCACTATGTGCCCGGCTGGGACTGTCATGGTCTGCCCATTGAACTCAAAGCGCTGGGAGACCTGGGAACCAATGAGCTGACTCCTGTCCAGATCAGACAGAAAGGTCAGGAGGTTGTGTATAAGCCATGTCCATCCAGAGCCTCATCCTTCTTTTTCATCCCTTCAATTTATGCTGAAAAGTTATTTAGTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14246
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064803 | Nonsense | 181 | 983 | 4 | 23 |
ENSDART00000138853 | Nonsense | 181 | 886 | 4 | 21 |
Genomic Location (Zv9):
Chromosome 17 (position 25434762)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 25574681 |
GRCz11 | 17 | 25593072 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGGCTGCTTTCCAGCGCTGGGGTGTGATGGCTGACTGGGACAACTGTTA[T/G]TACACTTTTGATGGGAAATATGAAGCAGCCCAGCTCAAGGTCTTCCAGGA
Long Flanking Sequence:
ACCTTGCCTGGCACTACTGTAAATTTATGAATTTTTACTAAAGTTTTTTTTGTCTTCAAATATTTCCGTTCCTCTGGCATTCGCTTACAATAAAAAAGAATCAGTTTAGCCTATGGGGGGTTGTTCTCAGCTTGCAACTTTTTTTGAAAGTGATCCTTGTCTAAAAACAAAAGAGGATTCACAGCTTGTAAAAAATTATGTTCTTTACAACAGCATCTGAAAAAGTTTATCTTTGAACCACTGTTTTGTTGCATTGTTAGATACTATTGACCTTTACTCCAAAATGATACTTGTTTTTAAAAGTGTAATCTGGCATTTTTGTTAACAAAAAGCTTAATCATACAAGTTTATTTAAAGTATGTGCTCCATATCTGATCTGACCAGTGATGAACTGTCTGTGTCTTTCTCCGTTCAGCTCGTGAGTTTGCAGAGAAGGCCATATCTCGACAGCGGGCTGCTTTCCAGCGCTGGGGTGTGATGGCTGACTGGGACAACTGTTA[T/G]TACACTTTTGATGGGAAATATGAAGCAGCCCAGCTCAAGGTCTTCCAGGAGATGCACAACAAGGTATTCATAAATGTTTCCTGTGCAACACAGCTTAGTATTAAAGGACTAAAGGAATTGTTCACAAAAGGATGAAAGTAAAAAAACGTTTTACATTTAGAAGCATGATACATTCCAGAATTCTTTGATAAAGAGAAACTTGATTTGAACGTTTTTTTCTTTAAAATGTAAATCTTTTTGTAACATTAAAGTCTCATCTATCAGTAAAAGTCATTTCAATTTAAATAAAGTAATAATTTAAAAACATTTAATAAGTTTAATAATAAAGTAATTCAATTAAATGTTAAAAAATATTTTAAAAATGTGATGTAAGTAATTTTTTTACCCTTTCTCATCTTAACATGTTGAAATGTGGTGCAAATGTCCTGATGTCCTTAAAAAGTTTCTCACTTTAGCTGTGTCTCTCTCTTTGAGTACAGGGTTTGATTTATCAAGACTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2910
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064803 | Essential Splice Site | 381 | 983 | 9 | 23 |
ENSDART00000138853 | Essential Splice Site | 381 | 886 | 9 | 21 |
Genomic Location (Zv9):
Chromosome 17 (position 25436412)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 25576331 |
GRCz11 | 17 | 25594722 |
KASP Assay ID:
554-2884.1 (used for ordering genotyping assays)
KASP Sequence:
CCCATGGCATGGATGACTACAGTGTCGCCACACACTTCAATCTACCAGTA[G/T]TATGTGACCCATACCTGTATATAACAACTAGGGATGCCAGATCGATTAAC
Long Flanking Sequence:
TGGGAGCAGAATCATACAAATTACGAGAGTTTTTTGGGGGAAATAACAAAGCGGGAGATGGGTGTGAAATGCAGGAGACTTCTAGAAAAATGTGAGTGTTGGCAGCCTGAAGTTAATGGTCATGTTTTTTCTTCTTCTTCAGGTATTCTGTAGTGAAGCGAGCTGATACTGAGCAGCTCCTGCTAGTGGCCACAGAGCGAATAAACAGCCTCTCCTCTTTACTGAAGACAAATCTGGAGAGTTTGGTCACATTTGCAGGTAGATCCAGTTTTATTGTTTAGAAAATGTTTATTAATCTGGCCTAAACCTCTCTCTTTCACTCATCTCCAGGGACAGATCTTGAAGGCGGAGTCTGTCAGCATCCCACAATTCCTTCAAAAGAAGTACCTTTGCTGCCAGCTAGTCATGTCACCATGACTAAGGGAACAGGATTGGTCCATACAGCTCCAGCCCATGGCATGGATGACTACAGTGTCGCCACACACTTCAATCTACCAGTA[G/T]TATGTGACCCATACCTGTATATAACAACTAGGGATGCCAGATCGATTAACTGAAGACTGATCAATCGATAATCTATTAGGTCTACTGTACATATCTTTAATGTGTAGTGCTTTTTTATTTTGTGTTAAATCGAATCATTAATTATCCTAAATGGACTGAAATATCACCTAACTCAGCTAGTGTATGTCATGGACATTTATGAGCAAATGTTCTCCAGATGTTCATTAATATAGTATACACAATATCCTAATCACAGTTGGAAAAATAAATATAACACTTACAATAACAAAGACAATTTGCTCACATTTACTATTGCTATATTTACTTTTTTTATATACCCTTATTACTATATGAACTATATTGCTATTGACATGTCTGGGTGTTATTATTTATTATTACTCAAGTCATTATGTAAATATATGTCATTGCATTTAGTCATTAGGTGGTTCAATTAAATGATCAATCGTTTATGTTTGCAATTCAACTAGCATTTCATTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17843
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064803 | Nonsense | 524 | 983 | 13 | 23 |
ENSDART00000138853 | Nonsense | 524 | 886 | 13 | 21 |
Genomic Location (Zv9):
Chromosome 17 (position 25438738)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 25578657 |
GRCz11 | 17 | 25597048 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGCAAAACAARTCCCTGTTTCWCTYAGACATACAGTGACCCACATCGCT[A/T]AAGTTTTCTCTGAGAAGGGGAGCGACAGCTGGTGGACAGAGCCAGTGGAG
Long Flanking Sequence:
CAGGTCAAGGAGCAAGAAAGAGAGAGAGAGAGAGGGAGAGACAGAAAGAACACGTGCAAAAAATTGTGTTTGGTTCATAACTGGCATTTTCTTTTTCTTCTTTTAGTTAGTCATTCAAAAGTCTGGTACTTTGTGACTTTGTTCAATAAAACAGATTTTCTAATATGTTTCCAGTTAAATAAGAGCTTTTCTCCTCAAAATAATGTATGATTTTGTGTGTGTAGGATGCCCTGCAGAAAGTGCGTGTGATACCCGAATCTGCGAGGTCCAGTTTGTTGTCAATGTTGGACAGAAGAACATACTGGTGTATATCTCGACAGAGGAGCTGGGGCGTCCCTATCCCAGTGTTCTACCATAAAGAGACTGGAGAGCCACTCTTAAACAAGTAGATACACTTACACTGTTATTACATACACACTTAATCAACAGATTTAAAACATCTTAAAGTATAAGCAAAACAAGTCCCTGTTTCTCTCAGACATACAGTGACCCACATCGCT[A/T]AAGTTTTCTCTGAGAAGGGGAGCGACAGCTGGTGGACAGAGCCAGTGGAGACGTTTTTGACACCAGATGTTCTTCAGAAGGTACATTTTCATACACTACTTACAAACACAAAATAAAAACATCTTCTATTTCAATTTTCACTTTTGAATTTAAAAATGAAAAGCAAATAATGGCTTGTTTTTTGTATTTCAATATCCCTTTCTAAAAGAAAAATCCAATGACCAAAATATACACCGATGTATTATAAATAAAATTCTGGCTTCACACCAAACACAAAGAAAACAAGTGGATTGATTACTTACTCTAGATTACTCACAAAGAGTTTTTCATCTCACAAGAATTTTCTGCTCTGGTTGAACTTTTTTTGAAGATATGATTGAATCAAATTCTTTGTGTTTGCAGTAAACATTCCACACACATCATGTCATAGACTGTTGGAAATTCTCCTCTATTTGCACATTTGCATTGACTTTGGCCCAATCCCAATTCTATGCTTTAAC
Associated Phenotype:
Not determined