ZMP
si:ch211-194e15.1
Ensembl ID:
ZFIN ID:
Description:
tRNA dimethylallyltransferase, mitochondrial [Source:RefSeq peptide;Acc:NP_001038239]
Human Orthologue:
TRIT1
Human Description:
tRNA isopentenyltransferase 1 [Source:HGNC Symbol;Acc:20286]
Mouse Orthologue:
Trit1
Mouse Description:
tRNA isopentenyltransferase 1 Gene [Source:MGI Symbol;Acc:MGI:1914216]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36863 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14214 | Nonsense | Available for shipment | Available now |
sa23552 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36863
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045504 | Nonsense | 373 | 455 | 9 | 11 |
ENSDART00000125893 | None | None | 330 | None | 9 |
ENSDART00000128560 | Nonsense | 365 | 447 | 9 | 11 |
The following transcripts of ENSDARG00000032876 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 31969583)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 31136872 |
GRCz11 | 19 | 30724185 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGGGAGACTACTGTACTTACTCCTGCTCTAGAGATCCTGGACTGCCTC[C/T]AAAAGGTTTGACTTGTTTCCATTTACTTTTAATGTCTTCCTTACACATCA
Long Flanking Sequence:
TATGTACATTTTTGTTCTATCAGCCTGACATTTTATCCTCCTCAGTAGTGCAGATTTTTGCAAAACTTTCTTTATGCAAATTCTTTTTTAAAATCTTAAATTTTTTCCCAAAATGCGTAAGTGGATGGAAACAGCTACTATCTGATTTGGTTGGTTTGTCGTCTGAGGTTAAACCTACTCCCTGTGACCAATCAGCAAATCATGATCATTGTTTTTCCCCGAGCTGAAAGTTTAACATGATGTAACCATTAGGTGAAACCATTGTCTTTTCTCAATTAGATTTAGTCTGAAAACAAAAGTATACCATGTTCACTCCGTTGCCTTGCACCACAATTGTTCTGCAAGATGCTATTTCATCAGTGTCATCTTTAATCAATTTATCATCTCAATCTTTAGGACCTGCTAGCAATGTGCCACCTGTTTATGGTCTGGATGTGACTGATGTGACCAATTGGGAGACTACTGTACTTACTCCTGCTCTAGAGATCCTGGACTGCCTC[C/T]AAAAGGTTTGACTTGTTTCCATTTACTTTTAATGTCTTCCTTACACATCACTGATTAAGAATGTGCTGCTAATACCCAGTCAGTGATTTTGATGTAATTTGATTGCTTGACTGTTTATTTTCTTTAATAGGCGACCTAGAAAGTTGAATTTTAGGCTGGTTATAAGCTTCAGTAACCTCTAATATCACCTGTCTTTTTAAACAATTTCAGGGAGAGCAACCATCTGCACAGCCAATTAAAGCAGAGGGGGTGGAGTCTCGCAATAAGCGGAGTCATCACATGTGCGATCTGTGCGAAAAGGTAATCATTGGAGACTTGGAATGGACAGGTGAGTTTTTAATCTAGTAAAACCAGTGCGTTCTCAAATGTCTTTAAAGAAGAAATAAGATACTAATACTTCACCTGTCTTGACTTTTAGCTCACCAGAAGTCCAAAAACCATCTTTATCAAGTCCGTAAGAAGAGGAAATCAGAGCAGGCCACAGATCTGGATACAAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14214
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045504 | Nonsense | 410 | 455 | 10 | 11 |
ENSDART00000125893 | None | None | 330 | None | 9 |
ENSDART00000128560 | Nonsense | 402 | 447 | 10 | 11 |
The following transcripts of ENSDARG00000032876 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 31969266)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 31136555 |
GRCz11 | 19 | 30723868 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCGGAGTCATCACATGTGCGATCTGTGCGAAAAGGTAATCATTGGAGACT[T/A]GGAATGGACRGGTGAGTTTTTAATYTAGTAAAACYAGTGCGTTCTCAAAT
Long Flanking Sequence:
TTGCCTTGCACCACAATTGTTCTGCAAGATGCTATTTCATCAGTGTCATCTTTAATCAATTTATCATCTCAATCTTTAGGACCTGCTAGCAATGTGCCACCTGTTTATGGTCTGGATGTGACTGATGTGACCAATTGGGAGACTACTGTACTTACTCCTGCTCTAGAGATCCTGGACTGCCTCCAAAAGGTTTGACTTGTTTCCATTTACTTTTAATGTCTTCCTTACACATCACTGATTAAGAATGTGCTGCTAATACCCAGTCAGTGATTTTGATGTAATTTGATTGCTTGACTGTTTATTTTCTTTAATAGGCGACCTAGAAAGTTGAATTTTAGGCTGGTTATAAGCTTCAGTAACCTCTAATATCACCTGTCTTTTTAAACAATTTCAGGGAGAGCAACCATCTGCACAGCCAATTAAAGCAGAGGGGGTGGAGTCTCGCAATAAGCGGAGTCATCACATGTGCGATCTGTGCGAAAAGGTAATCATTGGAGACT[T/A]GGAATGGACAGGTGAGTTTTTAATCTAGTAAAACCAGTGCGTTCTCAAATGTCTTTAAAGAAGAAATAAGATACTAATACTTCACCTGTCTTGACTTTTAGCTCACCAGAAGTCCAAAAACCATCTTTATCAAGTCCGTAAGAAGAGGAAATCAGAGCAGGCCACAGATCTGGATACAAAACATGCCAAACATCAAAATGACTGTGACAAGCAGGTACCTGCACTATAACATCCCTCGCTGCCTCTACTGGGGTGTTTTGGGGTCAAGCTTGGAGATGGACCAAAGGAATAAAAGTACTCTTAATGTATTTTTGAGATCAATATGACAAGGTACTTTGAGATTGATTGGTTTACAGTGTGCAGCAGAGATATCTCCAGTGTCCCTGTGGAGTAGCAAAACTTTACTTCAGGCTCTGTGATGCTTGGACCCCTGGATTTGGTGGTTTTCCCCATCTGCCACAGGCCTGTGGTTACAGTTAATGTCTGGATTTGGATTCTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23552
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 |
---|---|---|---|---|---|
ENSDART00000045504 | Nonsense | 423 | 455 | 11 | 11 |
ENSDART00000125893 | None | None | 330 | None | 9 |
ENSDART00000128560 | Nonsense | 415 | 447 | 11 | 11 |
The following transcripts of ENSDARG00000032876 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 31969136)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 31136425 |
GRCz11 | 19 | 30723738 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCACCTGTCTTGACTTTTAGCTCACCAGAAGTCCAAAAACCATCTTTA[T/G]CAAGTCCGTAAGAAGAGGAAATCAGAGCAGGCCACAGATCTGGATACAAA
Long Flanking Sequence:
CCAATTGGGAGACTACTGTACTTACTCCTGCTCTAGAGATCCTGGACTGCCTCCAAAAGGTTTGACTTGTTTCCATTTACTTTTAATGTCTTCCTTACACATCACTGATTAAGAATGTGCTGCTAATACCCAGTCAGTGATTTTGATGTAATTTGATTGCTTGACTGTTTATTTTCTTTAATAGGCGACCTAGAAAGTTGAATTTTAGGCTGGTTATAAGCTTCAGTAACCTCTAATATCACCTGTCTTTTTAAACAATTTCAGGGAGAGCAACCATCTGCACAGCCAATTAAAGCAGAGGGGGTGGAGTCTCGCAATAAGCGGAGTCATCACATGTGCGATCTGTGCGAAAAGGTAATCATTGGAGACTTGGAATGGACAGGTGAGTTTTTAATCTAGTAAAACCAGTGCGTTCTCAAATGTCTTTAAAGAAGAAATAAGATACTAATACTTCACCTGTCTTGACTTTTAGCTCACCAGAAGTCCAAAAACCATCTTTA[T/G]CAAGTCCGTAAGAAGAGGAAATCAGAGCAGGCCACAGATCTGGATACAAAACATGCCAAACATCAAAATGACTGTGACAAGCAGGTACCTGCACTATAACATCCCTCGCTGCCTCTACTGGGGTGTTTTGGGGTCAAGCTTGGAGATGGACCAAAGGAATAAAAGTACTCTTAATGTATTTTTGAGATCAATATGACAAGGTACTTTGAGATTGATTGGTTTACAGTGTGCAGCAGAGATATCTCCAGTGTCCCTGTGGAGTAGCAAAACTTTACTTCAGGCTCTGTGATGCTTGGACCCCTGGATTTGGTGGTTTTCCCCATCTGCCACAGGCCTGTGGTTACAGTTAATGTCTGGATTTGGATTCTTGTGTTGGACAGATGTCTTCCCTGCTGCTGTTTTGTCTGAGCAGTGGTCTTTTTTAACCACATCTAGCCACCTCTGTTGCCCTCTTAAACCACACTGTGGTGAGCTGTTCTAACCTTTTTGGCTGCTCTAAC
Associated Phenotype:
Not determined