Busch Lab

ZMP

trmt5

Ensembl ID:
ENSDARG00000069278
ZFIN ID:
ZDB-GENE-030131-5978
Description:
tRNA (guanine-N(1)-)-methyltransferase [Source:RefSeq peptide;Acc:NP_001139055]
Human Orthologue:
TRMT5
Human Description:
TRM5 tRNA methyltransferase 5 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:23141]
Mouse Orthologue:
Trmt5
Mouse Description:
TRM5 tRNA methyltransferase 5 homolog (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:1923607]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa2689 Nonsense F2 line generated Not yet available
sa42236 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa2689
Status:
F2 line generated
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
ENSDART00000085989 Nonsense 6 480 1 5
Genomic Location (Zv9):
Chromosome 13 (position 31911477)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 31557425
GRCz11 13 31687875
KASP Assay ID:
554-2768.1 (used for ordering genotyping assays)
KASP Sequence:
CGCATAGAAATGACGTAGGATAAACGCGTGTTCACATGGCAGCAGTGTGG[A/T]GAAGGTGAGCTGTGGCAGTTTGTTTTTAATATAAGGATTAGGGTANNNNN
Long Flanking Sequence:
CACAATAATCCTAAAGACTACTTCTAAATAGTTTGTTATTTAGAGGACGGCTTAACCTCGTTCTTTAGTCATCATTTAGACATGTTAGACATGGACACGGTTCTATTTGTTGTTCTACAATATTTATTTATGAATGTCAGTGTTATAGGGAAATGACAGGTTTGTGGTTTACCTGCGGTAACAGCGGTGTTCTCTCTTCATCTTCTCCGATGGGCTCATACTCGCTCACCGTCTGTATGCTGTGGTTTGCGCCGTTTCTCCCCATGTCCCACCGTGTAGTGTTTCTTTATTCCCTACTGAACCGACAAAAGGCGCAACGCTCGCGCTCAGGTACTACCGGAGCCGTCAGTACATTTCTCTGGTTCCCCAAACCACCGGCTCTAGCAAACGTAAACAGCCATTCACGTGATTCTCGACGGTCAATTTATATTTTCCGTCACAGACCCAGGTCGCATAGAAATGACGTAGGATAAACGCGTGTTCACATGGCAGCAGTGTGG[A/T]GAAGGTGAGCTGTGGCAGTTTGTTTTTAATATAAGGATTAGGGTAACGTTATATGTTTTTATGTGCGTTCGTTGAATAACGCAAATGAAGCTCTGAGGTTATAAGTCATTCTGTAGGATGTCACTAGGCGTAGAAAACAGATTGCTGTGCATCCATGTACACTAAATTTGGTAGGCGACGTTACTTCCAGGATTTCGCTGGACATTTTTAAATGGTTTTTACGAACTAACATTTATGATTCTGCGGCAATATTTGTGTGTAACTTATGTGTTGCTTAACAGCAAAGATAAACAAAAAACATTGTTAAGGAAAGTATATTACTTTTTTATCTAAAATAGAGTATTGGGCTTCACCTTTTACATAAAAGCAAGTAAAAGAAACGGTTGAAAACTCAACAAGTAGTGTACACTAGCAAATCAATTAGCATTAGAAAAGAAAATCTTGCTGAATTTTTTTAGCATGTGAGAGCACTGCATTGTGTTTCCCAATACTATTAAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42236
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000085989 Essential Splice Site 7 480 2 5
Genomic Location (Zv9):
Chromosome 13 (position 31909830)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 31555778
GRCz11 13 31686228
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAATTCTAGGTACACAGGCCATAACTCCATCTCTCTCTTTTTCACCAAC[A/C]GATCTGCCAGACTTTTCATCCTCCTGCAGAGACATCACAGTTGTACATTT
Long Flanking Sequence:
CAGTAGAAAAAATCTTTAACGCTGGATTTAGGGCAACTAATTATATACATTTTATGCAAGCTATGTGCTACACTTTTGTTAAAATAAAATAATTTATTTTTAGCATCATAAATGGCAAGATGGCTGTTTGTGCATCCAAGTAAAACTTTACTAATTCTTTTATATTCTCACTATATATCATTCGGTCCATGGACTGTTGTATGGGGGTTTCATGGTGTTTGGCTATTTGAACACAAAGGCTGTAGCATGTAAACAGACTGATGGTTTTCAGTGGTTCACTGACTGGGAGTGACAGATGCATAGATAAAGTAACTACGAGTTTAGCGATTGATTTAACGCACACAGCCTGGTGGACTTTGGCTAAATGTACAGGTAGCAATGCATCCACAGCTGCTTAAAATCTGCAGGACATCTAAGGCAATTTTAAAAATTCTGAACTTTTTTCCTCAATAAATTCTAGGTACACAGGCCATAACTCCATCTCTCTCTTTTTCACCAAC[A/C]GATCTGCCAGACTTTTCATCCTCCTGCAGAGACATCACAGTTGTACATTTACATCTCAGAATTTAAACCATTTTATGAGGTCTCAGAAAGTCATGACTGACCAATCACAGACCGATCTGGGCCTCTTCAAGCCCCCTTCCACTGTACGGGGCATGACAGAACTGGACCGCTCTGCTTTCAATCAGACAGTGAGCGTTCCCGCCATACGGTTACCAACCAACATTCTCAACAAAGCAGTGAAAAGTTTGAAGAAAGTGGCATTACAGAGGCCAGGACTCAAGCGTGTTGTGGAGGAACACAGTGAAGATGGAAATGCAGACTGTGGTAATATTGAACATCGGCTGCTGTTATTGGACCCAAACAGCATTACATCTTCAGACTCGTTTGGCAGTGATGAGGCAGAAGCTCTGAAAGCTTATAGCGTGCCTCAGGAGATCCAGAGCTATGAACTGAAACTCACCTATGAGAACTTTAAAAGCGAAGAGATTTTGCGAGCTGTT
Associated Phenotype:
Not determined