ZMP
dnmt7
Ensembl ID:
ZFIN ID:
Description:
DNA methyltransferase [Source:RefSeq peptide;Acc:NP_001018312]
Human Orthologue:
DNMT3B
Human Description:
DNA (cytosine-5-)-methyltransferase 3 beta [Source:HGNC Symbol;Acc:2979]
Mouse Orthologue:
Dnmt3b
Mouse Description:
DNA methyltransferase 3B Gene [Source:MGI Symbol;Acc:MGI:1261819]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa14480 | Nonsense | Available for shipment | Available now |
| sa31654 | Essential Splice Site | Available for shipment | Available now |
| sa45320 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa41193 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14480
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000046460 | Nonsense | 298 | 1433 | 5 | 25 |
| ENSDART00000085361 | Nonsense | 298 | 1456 | 5 | 26 |
| ENSDART00000125729 | Nonsense | 298 | 1500 | 4 | 25 |
| ENSDART00000145062 | Nonsense | 298 | 1433 | 5 | 24 |
Genomic Location (Zv9):
Chromosome 8 (position 24214485)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 23340303 |
| GRCz11 | 8 | 23361542 |
KASP Assay ID:
2260-0538.1 (used for ordering genotyping assays)
KASP Sequence:
WATCCAAACGACATTGTTTCTGCTTGTAAGCTGAAYCCGTACTGTATCTA[C/A]ATATATGGGCAGGTACCACTTGATGTGAAGACTGGAGACAAGACCMACTG
Long Flanking Sequence:
ACTATACATAGGTCTGGGAAATCAGCTTGGCAGTGAAATGCAAACTCTAATGCCATTTGTTTTTCTTTTTATACAGGCAGAGCAGGAGAAGAGTCTGACATGGAAATAAATGGAGGGAGGCGTTCTGCAACTTATGATCCTAAGTGGCAAAGAAACTTGAAATGGATCAGAGCTAGCGATATGGGAGACAACTATGCTTACTGCACAACATGTGATTACAATATCATCCTACTTGCAGGTTTTCATGATCTGAAGCGCCACCAGCTGACTCAAAATCATATGAAACATGAGACAGGGAGAACAAATTTACCTGGGAGAAAGCAGATTGAAGAGTCTATTTCATGTAGTGAAACCATGCTGCTCTTTATTCAATCGCATTGTCTTTCCAGTTTACCCTCAAGGATCAACAGGGTCTCCCAACGCACTGCAAGATGCATCCTTGGTCTAAAGTATCCAAACGACATTGTTTCTGCTTGTAAGCTGAACCCGTACTGTATCTA[C/A]ATATATGGGCAGGTACCACTTGATGTGAAGACTGGAGACAAGACCAACTGTCATGTGGTACTTGCTGGATTTTTTGAGGAAAAACAAGCAAGATATTGTATTCGTTTCCTTGATGTCTTTCAGCCTGAAGACTCCGCTAGCTCTGTATCGGGAGGATTATTTAGCATACTAAAAAAGTTTGAAATTCCTGCAAGCAACATGGTAGCTGTTTATATTAATGACCACGAACTGACCTCAGAAAGTGTAGTGTCTCAGATCCGGGAGCTCAATCCACAGGTGATTGACCTTGGTGGACTTTACAGCATACCTGACACTGCCTGCAGTGCTGGCCTACAGACTCACTCTGTTCAGGTTCAGGAGCTTATTGCCAACATCTACAGACACTTCTCTACTGGTTCCACCAGCAATGACAACCTCAAGATGCTGTTTGCAGGTATTGATGGACTAAAAGTCCACAGCAATCCCCTCTCAAACAGTGAGGAGTTTTGCGTGCTTGTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31654
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000046460 | Essential Splice Site | 808 | 1433 | 7 | 25 |
| ENSDART00000085361 | Essential Splice Site | 831 | 1456 | 8 | 26 |
| ENSDART00000125729 | Essential Splice Site | 831 | 1500 | 7 | 25 |
| ENSDART00000145062 | Essential Splice Site | 808 | 1433 | 7 | 24 |
Genomic Location (Zv9):
Chromosome 8 (position 24217326)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 23343144 |
| GRCz11 | 8 | 23364383 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGATGGAGCCAAAAATGATGGCACCTTGACTAGTAACACATTAAAGGAGG[T/G]AATATTATTATTTTTTACAAAAAAAGTATTCAGACTTGTTTTTAAGCAAG
Long Flanking Sequence:
TCTGTCCAGTCAGATCCAGCAGAGGCTGGTTAGATTGATGGAAACAATGTGTTGTTTTCCAGAGACGGTTCAACACTCAAATGCAGTGAAGCCTTGTGTGGTGCGACTGGAGAAGATCACCAGTCAGAGAGGTGTGAATGAAATGCTTAAGACCAGTTAAGAGGTTCTAGAGCAGCTATCAAATAATGCTTTACAATCTCAACTGCTTCTCTTGGTGTCGAACATCTTTTGGTGTTAACCTTTTTACTTTGCCTCCGCTCAAGAAAATGATTTATTGCATTGAAAATACTATTTTTATTTATTTATTTATTTTTTTTGTGGGGGAAGGCAATTTTAATTGTTGCTTTTTGTGTAGACACCACAATATACAGTAGATACATTTATTCCTGACTGTTCTTATCAGTTTAACTGTTTTATTTGGTTATGCTCTGCAGAAGTGAACCTGAAGAACGATGGAGCCAAAAATGATGGCACCTTGACTAGTAACACATTAAAGGAGG[T/G]AATATTATTATTTTTTACAAAAAAAGTATTCAGACTTGTTTTTAAGCAAGGAATTAGTCGTATTGTTATTATTTTATAGACTGATGCTTACTAAAGACGTATTGTATTCTTGAGATGACAAAGCAAAGTATAACTGATTAAATCAGCTTCACAGAAGACAAAGCACTGGCACACACATGCAAAACAACCATATCATCACACTCATCTCACTTGATGTAATATCTTTATAGAGTTTTGAAGCATCAAAACAATTAAAGTATAATGCAGCTTTTTCATTACAAATGTTCAATAAATAGGGCTGGGTGATTAATCGAAGTGTAACAGTCAGAACCTATAATCGATAAAAAAAATGTCCAGGTCCGTTTTTTCAATTACTTTCCCTACCCCGTGTGGACAACGCATAGCACAAGCTCTATGATTGGTCGGCTTGATGGCTTTGTCGAGTCCGGGTTTATAAAATTAAAAATAAATAGATGAATAAAAGAATCGTTCATTAATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45320
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000046460 | Nonsense | 901 | 1433 | 10 | 25 |
| ENSDART00000085361 | Nonsense | 924 | 1456 | 11 | 26 |
| ENSDART00000125729 | Nonsense | 968 | 1500 | 11 | 25 |
| ENSDART00000145062 | Nonsense | 901 | 1433 | 10 | 24 |
Genomic Location (Zv9):
Chromosome 8 (position 24224143)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 23349961 |
| GRCz11 | 8 | 23371200 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACTTCTGCCCTTTGGTGCGTTTTCAAAGAATTTTTGTAGTAAATCCTA[T/A]GAAGGTTTGCCTACCTACAAGAATGCCATCTACCAAATCCTAGAGGTACA
Long Flanking Sequence:
CTGTGCAGGATGGAAAAGGTTTTGCCGTTGGAGAGCTGGTTTGGGGTAAAGTCAAGGACTTCTCTTTGTGGCCTGGACTGGTGGTGCCATGGAAGGGCAGGATAGTTCCTGTGTCTATGAGGCGTGTAGAGTGGTTTGGAGATGGAATGTTTTCAGAGGTTAAGAGTCACTTTTGTTCTCCAGATTCTCATATTATTTTCCCAACATTGTTTAGTTCAGTGGTCTCAAACTCAATTCCTGGAGGGCCAACCAGCTCCAACTCACATCTGCTTAATAGTCAATAGTAGTCTTGAACACCTTGATTAGTTGGATCAGCTGTGTTTGAATAGGGTTGGAGCAAAACTGTGCAGAGCTGTGGCCCTCCAGGCATCCAGTTTGAAACCAATGATTTAAAGAATCCAGTTTTTCATTAAAACATGTTTTCATTGTCAATCTTAGATTCATACAGATGGACTTCTGCCCTTTGGTGCGTTTTCAAAGAATTTTTGTAGTAAATCCTA[T/A]GAAGGTTTGCCTACCTACAAGAATGCCATCTACCAAATCCTAGAGGTACAGCGGAAATATTCTCTTTGAACCATTATTTTGCTAGGAATCAAGAACCTGTTCTAATTGTGTTGAGATTTTAATGTTTATGTGTAGCTGGCAGCAGAGCGCAGTGGTAAGTTGTTCCCCCCCTCTGAGAAGAAAGGCGAAGAGGTAAAAGCCATGATGGATTGGGCATTTGGAGGCTTCCAGCCCATGGGTGCTGATGGCTTTTTGCCTTCTGCAGGTACGTACAAAAGCTACAAATTATTTGTATTTAAAAAAAAATGTGAACAGTAGCATGTTGTCTGTCACAAAAATAGCATAATTGTCACATTGACCAAAGAATAAAGCCTATGCACAAAAAAACATCTGCATTTATGAACCTCTGTTTCCTCTGCTTTTCCATTTACAGATAGCTCTGCCAGTAATAAAACAGAGTCAGATTCCTCTGTGTCTGATTATCAGCCTCCAGCAAAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41193
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 |
|---|---|---|---|---|---|
| ENSDART00000046460 | Nonsense | 991 | 1433 | 12 | 25 |
| ENSDART00000085361 | Nonsense | 1014 | 1456 | 13 | 26 |
| ENSDART00000125729 | Nonsense | 1058 | 1500 | 13 | 25 |
| ENSDART00000145062 | Nonsense | 991 | 1433 | 12 | 24 |
Genomic Location (Zv9):
Chromosome 8 (position 24224670)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 23350488 |
| GRCz11 | 8 | 23371727 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATTATCAGCCTCCAGCAAAGAGAAAGTATGTCTTCAAGAACAGACCAT[C/A]AACTCAGGAGTGCAACAGAGGTCAGTTATATCAGGGGTTCCCAAACATTT
Long Flanking Sequence:
CATCTACCAAATCCTAGAGGTACAGCGGAAATATTCTCTTTGAACCATTATTTTGCTAGGAATCAAGAACCTGTTCTAATTGTGTTGAGATTTTAATGTTTATGTGTAGCTGGCAGCAGAGCGCAGTGGTAAGTTGTTCCCCCCCTCTGAGAAGAAAGGCGAAGAGGTAAAAGCCATGATGGATTGGGCATTTGGAGGCTTCCAGCCCATGGGTGCTGATGGCTTTTTGCCTTCTGCAGGTACGTACAAAAGCTACAAATTATTTGTATTTAAAAAAAAATGTGAACAGTAGCATGTTGTCTGTCACAAAAATAGCATAATTGTCACATTGACCAAAGAATAAAGCCTATGCACAAAAAAACATCTGCATTTATGAACCTCTGTTTCCTCTGCTTTTCCATTTACAGATAGCTCTGCCAGTAATAAAACAGAGTCAGATTCCTCTGTGTCTGATTATCAGCCTCCAGCAAAGAGAAAGTATGTCTTCAAGAACAGACCAT[C/A]AACTCAGGAGTGCAACAGAGGTCAGTTATATCAGGGGTTCCCAAACATTTCAGCCTACGACCCCCAAAATAACAATGCCAGTGACTTGCGACCCCACTATCTTATGTGTAATTATCTAAGCATTGGGTGCACAAGAATAGGCCTTTATAAACACGAGAATATTGACAACAGGTGTAACAATCTAACAACACTATAAATGTTTATAGTCATTTATTAATTAGTTCAATTTAATATTAGCTTCACGTAATGAGACTGGTGGGCACAATGTTTTCAGCTTAAGTCTATTTTTGGTTTATTTTGGAGACCGCCACTTGGAGATTATCCTCATTGTTCAGTTGTAGCCTGTGTTTTAGTGTTTGATTGCCATAAAGGTGTCAGAAAGTTTAACCTGGTGATATAAAATCAATCTGCTGCACTTGACGCTATTGCTGTGTTGTTAATCTAACGTTAACACACCAGTCCTATGAAAAAAAAATGAAAAGGCTGATTAGTGTTGTTCT
Associated Phenotype:
Not determined