ZMP
dimt1l
Ensembl ID:
ZFIN ID:
Description:
probable dimethyladenosine transferase [Source:RefSeq peptide;Acc:NP_001003556]
Human Orthologue:
DIMT1L
Human Description:
DIM1 dimethyladenosine transferase 1-like (S. cerevisiae) [Source:HGNC Symbol;Acc:30217]
Mouse Orthologue:
Dimt1
Mouse Description:
DIM1 dimethyladenosine transferase 1-like (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:1913504]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa7126 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34362 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa7126
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000050228 | Splice Site, Nonsense | 44 | 306 | 2 | 12 |
ENSDART00000140531 | Splice Site, Nonsense | 44 | 306 | 2 | 12 |
Genomic Location (Zv9):
Chromosome 8 (position 17705892)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 17150780 |
GRCz11 | 8 | 17186492 |
KASP Assay ID:
554-5131.1 (used for ordering genotyping assays)
KASP Sequence:
TCGGTCAGCATATTTTGAAAAACCCTTTGGTTGTCAACGGCATCATAGAG[A/T]AGGTCAGTAATAGGGATTATGAGTTTTTCTGGATTGTTKGTCTATTTCCT
Long Flanking Sequence:
ACTCCTGGTTAGACCTAAACTGCATTTCGTTGCCTTGTACTTGTACATGTATAATGACAATAAAGTTGAATCTAGTCTCACATCGGGGTAAAGTTGGTTTTATATTCACACATTCATTCTTTTTTGAATAGTGACAGTTTGTGACATGCTAGTTGGAATATTCAGTGAGAAATTCCATGTAAGTGTGACTTTTAAAAAACATTAGTGTTATTTATTTAACTGTAAACAGTGTTGTATTTTGATAGTCACTGGCTGCTAATATGATTTTACTATTTAGAATTGGCAAAGAATACTTTACTGAAATTATAAAGTCTGAATGTGGGAATATAGACAACTTTACCTTAAGTAATCTCACTCACCCATTCAAAAAATACTTTTGACTTTTTTTGTTCAATATTGGATTACATTAACCCATGTTCCATATTTCAGGAATTATGTTTAATACTGGTATCGGTCAGCATATTTTGAAAAACCCTTTGGTTGTCAACGGCATCATAGAG[A/T]AGGTCAGTAATAGGGATTATGAGTTTTTCTGGATTGTTTGTCTATTTCCTTTTAAGGCTGAATGAGCTTTCTCAGTGCACGTCTATACTGTTACAGCACATCATAATCAGCATATTTATTTATTAACAAAATGTATTTTTCAGGCAGCGCTGCGACCAACAGACGTTGTTCTGGAAGTTGGTCCTGGAACAGGTAACATGACTGTCAAACTTCTGGAGAAAGCCAAGAAAGTAAGTAGCTTTTAATGGATGTTTTCTTTCTAATTTAAATATTATTGGAACTCAACCAACCGTTATTTCATTGTTTACTTTTTACTTAAAGGTGGTTGCGTGTGAGTTGGACACCAGGCTTGTTGCTGAGCTTCAAAAAAGAGTCCAGTGCACGTAAGTACTTTTCATACAACTTTATCATCACTACCCCAACAACAAACTTAGCACATGCTTAATCGAAAAATCCTTTTTATTGAACAGTCCAATGCAGAACAAACTTCAGATCCTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34362
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000050228 | Essential Splice Site | 293 | 306 | 11 | 12 |
ENSDART00000140531 | Essential Splice Site | 293 | 306 | 11 | 12 |
Genomic Location (Zv9):
Chromosome 8 (position 17711064)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 17155952 |
GRCz11 | 8 | 17191664 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTCAGTGATAAGAGGGCACGTTCCATGGATATAGATGATTTCATGGTG[T/C]AAGTATAACCCGCTTCACTTCATGTACATTTTGTGTTTTGGGGGTGTTTT
Long Flanking Sequence:
AGTACTGTTTTTGTAATAAATAAAAAGCAAATGACATGTCTTCTCCCTTTTTGACTGATCCGAAAAATGGTCCGATGCGTGACAAAAAAAAAACAATAACGTGATCCGAACCGTGAGATTTGTAATCCGTAACACCACTAGTATATACAAGCTTGATCATTGTTGGGTCAGTTGGTGGAGTGGGGGTGTCTTTTATAGCTATTTATGCTACAAAAGAAGTCTAATCAAAATCATTTTCAAACATCTCTAAATCTGGAAAGCTCAACTCTTTAGACCCCCTTCACACCTGTATTTAGCTTCATCAGCTTGTGCTATCAGATGTAAACTGCACTTTTTCACTGCACTTATCTGTAGATGCAAGTATATTTAAATATTTCCAAATTGAATTGCAGGAAATCCCTGAGGATTTCAACATTGCTCCGAAAATTGAAAGCATCCTTCAAGAGTCCAAGTTCAGTGATAAGAGGGCACGTTCCATGGATATAGATGATTTCATGGTG[T/C]AAGTATAACCCGCTTCACTTCATGTACATTTTGTGTTTTGGGGGTGTTTTGTAAAGCATTTTTTTCTGCATCCATATTTTACGCTAGGCTTCTTCATGCGTTCAACTCTGCTGGGATACACTTCTCTTAAAATTTAAGGAACGGGGAACGGCTACTAGCTTTACAGAAGTGATGTCACGGTCTTCTCGTATTCTGGTTGATGCTTTCGTACATGCGAAGAAATGATTGACATTTCTTTTCAATGGACAAGCAATGGAACACTTAATCACTCAGGCTGGGATGTTTTGTGCCTTTCCTGTATTGGGGAAAGAATTATGGACTTCTTTTGAGAGGTAATACTTTAGATGTACGAGTGTGTGGTAAGAGCTTTTACTCTATAAGATTGTCTTAACGGATAAGACAAGTTTTTCATTACCGTCAGTCTCAGCACTGAACATCATCGTGTGTTTACTTCTCATTACTGAACTGTCAAGGTGAGAAATGATTGCTGTTAACACTTT
Associated Phenotype:
Not determined