ZMP
wu:fb23g02
Ensembl ID:
Description:
RNA (guanine-9-) methyltransferase domain containing 1 [Source:RefSeq peptide;Acc:NP_001007333]
Human Orthologue:
RG9MTD1
Human Description:
RNA (guanine-9-) methyltransferase domain containing 1 [Source:HGNC Symbol;Acc:26022]
Mouse Orthologue:
Rg9mtd1
Mouse Description:
RNA (guanine-9-) methyltransferase domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:1196261]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1936 | Nonsense | Available for shipment | Available now |
sa5931 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa1936
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000060954 | Nonsense | 124 | 403 | 2 | 4 |
ENSDART00000112581 | None | None | 292 | None | 5 |
ENSDART00000144606 | Nonsense | 124 | 403 | 3 | 5 |
ENSDART00000148162 | None | None | 292 | None | 5 |
The following transcripts of ENSDARG00000041575 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 386371)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 516495 |
GRCz11 | 1 | 511674 |
KASP Assay ID:
554-1924.1 (used for ordering genotyping assays)
KASP Sequence:
CTAAATCCTCCAAGAAGAAATACCTCAAATTCCTGGCCATCAAGGAGGCG[C/T]AGAAGAACAACGACAAGAGGAAGCAGGAGAAGAAGAGAGCTGAGAGAGAA
Long Flanking Sequence:
TTTCTGCGCTGGTGTTTCCCGCCGGTCAGACGGATGTGTGTGTGTCAGCAGATCTCCGTCAGGTCCTTCAGCAGCAGCCGGACGCTCCTCAAAGATGACCCACAGCATGAGGAGAAGCTGGATCTGGACATCTGGAAGTCTGTGATGAGAGCTCAAGCTCTGCCGGAAGATCCTCCGCATCTCCAGGACTCGACATCGGCTGCGTCTGTGCTGGAGGCGCACCGAGAGCTGGTGGAGACCTGGCATCAAGCTGGAAAGGTGATGCTACACTTATTATAACCCTTAAATCCCCCTCAGATTGACTCCTCTTTGGTGATGTTGGTGCTGTTTTTGCCCCATTGACACACACATGCATGTATGTATGTATTTCTACACGTATACCTCCACGTGTGCAGCTGGTGCCGAAGGTGATCACGGATCAGCAGCTGCAGGAACTCTCCATTCTCACCACTAAATCCTCCAAGAAGAAATACCTCAAATTCCTGGCCATCAAGGAGGCG[C/T]AGAAGAACAACGACAAGAGGAAGCAGGAGAAGAAGAGAGCTGAGAGAGAAGCGGGAAAACTCCAGAACAATAATGGAGAGGAGGAGGAGGAGGAGCGAGCCGCAGGCCCCGAGAACACCTTCATGCTGAGGCTCCGCAACAACTCCATCGAGAGCGCACACAACTGGAGGACGGTGAGTGTGTGCTGATGCATATTCTTTATCTGAGTGTGCGTGTATGTGTAGGGTTTGAGTGTGTGTGTTACTTTCTGTGTGTGTGCAGTGTCTTGTGTGTGTGTGTGTGTGTTTGTGTCTGAGTGTAAATGTAGTTCTGAGTGTCTAGTGCAGGGGTGTCAAACTCAATTCCTGGAGGGCCGCAGCCCTGCACAGTTTAGTTCCAACCCTGCTCCAACACACTTACCTGTAGGATTCAAACAAGCCTGAAGAACTCAATTAGTTTGATCAGGTGTGTTTAATTAGGGTTGGAACTAAACGGTGCAGAGCTGCGGCCCTCCAGGAACT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa5931
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000060954 | Nonsense | 276 | 403 | 3 | 4 |
ENSDART00000112581 | Nonsense | 165 | 292 | 4 | 5 |
ENSDART00000144606 | Nonsense | 276 | 403 | 4 | 5 |
ENSDART00000148162 | Nonsense | 165 | 292 | 4 | 5 |
The following transcripts of ENSDARG00000041575 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 384421)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 514545 |
GRCz11 | 1 | 509724 |
KASP Assay ID:
554-3683.1 (used for ordering genotyping assays)
KASP Sequence:
CACACVGAGCGCTCGCCGCTGGAGCTGTTCCCGCATCAGGACCTGGTGTA[C/A]CTCACWGCAGACTCGCGCTCCGTCCTGCGCACGTTCGACCACACCAAGGT
Long Flanking Sequence:
TTATGTGTATGTCTAGTGTTTAAGTGTGGTGTGTAGTGTTTGGGTGAGTGTGTGTGTGTGTTTTTGAGTGTGTTTATGTGTCTATGTCTAGTGTTTAAGTGTGGTGTGTAGTGTTTGGCTGTGTGTGTGTTTGGTATTCATCACCTCTACTGGTGCTGTAGTTTGTCTTGTGAGATGACTGCAGCTGGTTAATGATCTCCTGTCCTTCATCTCCAGGCGCAGGCGATGCGCTTCGACCAGCCGCTGGTCTTCGACATGAGCTACGATCAGCAGATGAGCCGGCATGAGCTGGAGAATACGGTCAGTCAGCTGCTGGAGAGCGAAGGCTTCAACCGGCGGGTTCAGGAGCCGTTTCACCTGCACTTCTGCAACCTGCAGCCGGGGGGAGCGTACCACCGCGAGCTGCTGCGGAGATACGGGGACGAGACGTGGAGACGGCTGCTGATCACACACACCGAGCGCTCGCCGCTGGAGCTGTTCCCGCATCAGGACCTGGTGTA[C/A]CTCACAGCAGACTCGCGCTCCGTCCTGCGCACGTTCGACCACACCAAGGTGAACAACAAGCAGCCTTTCCACACGTGTGTGTTTCTCCACAGCAGCCATAGTGTCCTGACCCTCCCCATATCATCATTGGCTTCATCACTCTGTCTCCTAAATTCTGCAATGTCAGATTTCTGCAACATCGTGCAGCTCTGATGTTCATATATGTGTGTGTGTGTGTGTGTGCTGACAGGTGTATATAGTGGGAGCTATGGTGGACCGCAGCATCCGCGTAGGAGCATCGCTTGCTATTGCCAAACGCTTCAGACTGGCCACGGCGCGGCTCCCGCTGGACGAGTATCTGGACTGGGATTGTGGAGCTAAAAATCTGACTCTGGATCAGATGATCCGCATTCTGACCACGGTGAAGCAGACGGGCTGCTGGCAGAAAGCGCTGGAGTTCGTGCCCAAGAGGAAACACAAAGGTTTCCATCAACAAAGCGGCGACAAGAGGAGCCAGAAAA
Associated Phenotype:
Not determined