ZMP
zgc:153625
Ensembl ID:
ZFIN ID:
Description:
dimethyladenosine transferase 1, mitochondrial [Source:RefSeq peptide;Acc:NP_001070237]
Human Orthologue:
TFB1M
Human Description:
transcription factor B1, mitochondrial [Source:HGNC Symbol;Acc:17037]
Mouse Orthologue:
Tfb1m
Mouse Description:
transcription factor B1, mitochondrial Gene [Source:MGI Symbol;Acc:MGI:2146851]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa36527 | Nonsense | Available for shipment | Available now |
| sa45622 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36527
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 |
|---|---|---|---|---|---|
| ENSDART00000059658 | Nonsense | 81 | 269 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 49434556)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 49195640 |
| GRCz11 | 17 | 49278615 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGACCTGGGGGTCTCACCAGGTCTATTCTGAAAGCTGGAGCTGCAGATT[T/A]ATTAGTGGTGGAGAAAGACATGCGCTTTATTCCAGGATTACAGGTTTGCA
Long Flanking Sequence:
TTCTTGATATAAGAATTTTTAGATATTTAGAAGAAAAACAAGACAAAACATCTAAGCAAGAAAAGCATTTTTTGCAGTGTATATAAAAGCAGTTGTGATAAATGGACTGTATTCGCTTAATGTTTTTCAGATGGCAGCCACACAGAAACTCTCCGGTTGTCGGCTACCTCCTCTCCCTACCATAGGGGAGATCATCAAACTCTATAATCTGAAAGCACAGAAGCAGCTTTCTCAGAACTTTCTCCTAGACACGAGACTCACCGGTATGTCCTATCACCGTGTACATCTTTATTTGTTTATTTTACTTGATTTGATGGAAATCAGTGGAGTGGCACACTGTTTATGAATGTTGGCTGCCTTCTGTTAAGCTCTAAATCTTTGTGATTTTCCAGATAAGATTGTCCGGCAGGCGGGAAACCTCAACAATGCACATGTGTGTGAGGTGGGACCTGGACCTGGGGGTCTCACCAGGTCTATTCTGAAAGCTGGAGCTGCAGATT[T/A]ATTAGTGGTGGAGAAAGACATGCGCTTTATTCCAGGATTACAGGTTTGCAAATACAGTAAATCCATTGGTCATGCCGTTTAAGATTACACTCGCTGGCCACTTTATTAGGTATACCTTACTGGCACTGGGTTGGACCCCCTTTTGCCTTATGACTTAATCCTTCGTGGCATTGATTCAACAAGGTACTGGAAATATTCCTCAGAGATTTTGCTTCATATTGACATGATAGCATCACTTAGTTGCTGCAGATTTGTCGGCTGCACATCCATGAGGCCAATCTCCCATTCCATCCCATCCCAAAGGTGCACTATTGGATTGAGATCTGGTGACTGTGGAGGCCATTTGGGTACAGTCAACTCATTGTGATGTTAAGGAAACTAGTCCAAGATGATTCGCGCTTTATGACATGGTGCGTCATCCTGCTGGAAGTAGCCATCAGAAGATGGAGACACTGTGGTCATAAAAGGATGGACATGGTCAGCAACAACACTTAGGTTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45622
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000059658 | Essential Splice Site | 132 | 269 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 49431521)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 49192605 |
| GRCz11 | 17 | 49275580 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACTGGAAAGAAGGTTCCCAGCCAACATAACCAAGACATGGGAAGATGG[T/A]AAAGTTATCTACTTCATAATGTAATGTGTGTGTATTTATATAGCACATTT
Long Flanking Sequence:
ATTTATTTTATCTTTGACATGATGACAGTAAATAATATTTTACTTGATATTTTTTAAGACACTTCTATGCAGCTTAAAGTGATATTTAAAGGCTTAACTAGGTTAATAAGGTGAACTAGGCAGAAGAATAGCTTTAAGGGGCTAATAATTTTGTCCCAAAAATGTTTTTTTAAAAATTAATAACTGCTTTTAATATAGCCAAAATAAAACAAATAAGACTTTCTCCAGAGGAAAACATATTATCAGACATACTGTGAAAATCTCCTTGCTCTGTTAAACATCATTTGGGAAATATTTAAAAAATAAAAAATCAAATCAAAAGGAGGCTAATAATTCTGACTTCAACTGTATATGTGTAATGTGTGTGTATATATATATTTTTTCCTCCAGCTCTTGTCAGAGGCTGCTCCTGGAAGAATAAGGATAGCCCAGGGAGATATTCTCGCATACAAACTGGAAAGAAGGTTCCCAGCCAACATAACCAAGACATGGGAAGATGG[T/A]AAAGTTATCTACTTCATAATGTAATGTGTGTGTATTTATATAGCACATTTATTGTGTATGGTCATACAACCAAAGCGCTTCACAATCATTAGGGGGGTCTCTCCACACCACATCCAGTGTGCAGCATCCACTTCAATCAGTGGTTCTCCAACTTTTTCATCAAGTACCACCTCAGAAAAAGTAAATTGTCTCTCCAAGTACCACTATAATGACCAGTATTGAAATACTGTAGTGTAATAAGCCCAGTAAAGCAGCTACAGCTCTGGAAAGTTCAAAAACGTGTCAGATTAATTCCTATTATTAAGAATATTTTTTATTGTCAGCCACTTTAAACATTCTACATAGTTTGAACATTAACACTGTACTGTGCTTATATGTAAAAACTAAAATAAAAAAAGTCAACATTTAAATTAAAATGTGCTTTTAAAAGTTAAAAATGAGGCGAAGAAACCCTCCTGTACTTCAATGTAAAGTATTAACATAGATTAGACTATTTATCA
Associated Phenotype:
Not determined