ZMP
dnmt3
Ensembl ID:
ZFIN ID:
Description:
DNA (cytosine-5-)-methyltransferase 3 [Source:RefSeq peptide;Acc:NP_571461]
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 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24284 | Nonsense | Available for shipment | Available now |
sa14072 | Nonsense | Available for shipment | Available now |
sa9741 | Nonsense | Available for shipment | Available now |
sa24283 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24284
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 |
---|---|---|---|---|---|
ENSDART00000080545 | Nonsense | 153 | 1448 | 4 | 24 |
ENSDART00000126841 | Nonsense | 153 | 1448 | 5 | 25 |
The following transcripts of ENSDARG00000057830 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 17169993)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 17072932 |
GRCz11 | 23 | 16999275 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCTATTTTCTTTATTCATAGTTGAAAAGGAAAATGTGTCAAGCCTCTA[C/A]AATACTGAAGAAACCAGTTCAAACCAGAAAACGCAACATGTTGAGAAGAC
Long Flanking Sequence:
ACGTAACTAAAGTGAATTTCACAGCAGAGGAGAACCTAGACATCTTGAATAATTATAATCTGCTACAGGAAGCTTTCAGCAAAGCACAGATTCAAAAAGTGAGTACACAATAGAATTCCACTGTAGAATGGAAAGTTTATGATGTACAATTTCAGTTAAATGAATGAATTATAGTGGTCAACACAGGCAACAGGCATCTTTTTTCGTCTTTATAGGAGCTGGAGCTGACATTGCTGGTGAATGGAGATATTATGACAACGTGTGATTTGCTTACATGGTTCAAAGACATGTATGATCACAATTTTGCAAAGCAGAAATGTAACCCACAGGTGGCCTTCATTAAACCTGAAGTAGTTTCATTGAAATCAAGCAGAGAGTTTGAAACAAGTAGGTGTTTACTTTTTGTGTTTGTAATAATTCTGTAAAATTGATATTTAAGTTTAATGATGTCATCTATTTTCTTTATTCATAGTTGAAAAGGAAAATGTGTCAAGCCTCTA[C/A]AATACTGAAGAAACCAGTTCAAACCAGAAAACGCAACATGTTGAGAAGACGTCACAAGAGTCAGTCTCCTGGAGTCCACTCACATCTTTCATAAGAAAGTATGGCTCATCCACCTTAACTGATGATGAATCAAACAATGTGAATAGTAAGGATTGTCCAGGCCAGAAATCTTTTGGAGACATTACACCATTCTGGAGACAGACTCCATACTGCCTTTATCTTTTACATGGAGTGGAGCTCGAGGATGACAAGAAGGCCAGTGTGCTCTTGTTGGGCTTTTTTGACAAAGAAACTGGGGAAAACAAAATCAGACTACTGGATGTTGTCTATCCAACAAAAGAGTCCACTGAAGACATCTGCAACTACATCTTGGACACTCTGAGGAAGATCGGAATACCTTTATTCAACATGGCCATATTATATTCAGATTTTCCAGATCACGAACATCTTGTAGCTGGTCTACAGTTAATGAAAGCTGAGATTGTGTCTTTATGTGGACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14072
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 |
---|---|---|---|---|---|
ENSDART00000080545 | Nonsense | 770 | 1448 | 7 | 24 |
ENSDART00000126841 | Nonsense | 770 | 1448 | 8 | 25 |
The following transcripts of ENSDARG00000057830 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 17167812)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 17070751 |
GRCz11 | 23 | 16997094 |
KASP Assay ID:
2261-7500.1 (used for ordering genotyping assays)
KASP Sequence:
GATGATGATGACGATTATGGCTGTGAAGCTGGCGAAGTCATGTGGAAGTA[T/A]TCGGTAAATATTTTCCCATTGGTTTTATGTTTTAAGTTTATTTCTGGGTG
Long Flanking Sequence:
GATGTTACGGACAGCAGCTCATATAAAAGCGCTCCATCACATCTCAGCCCAGAGACGCAGGGAAGCAGCATATCCGGTAAAAATACAAACTCCACAAAGATCAAAACATGCCAAGAAGCCAATCTGTACTACTGACTTTGGATCACAAATGAATTTTTATTTCAGATGTCATTGACCTTACTGAAATGGATGAGATAGGTCCAGTGGAAATAGAGGACATTGCACCAATGGATGTGGATGATATTGTGTCAATTTCTTCTGATTCCGAAACAGAAAACCAGAAAGGTCTCAGGCGCTCTTCAGATATACCAAAATAGGGGTATTTTGTCCGGCAGTTTTGCAGCAGTGAGACAGGTCTAAGTAACTTACCTTTCCCTTCTTTTTACAGTCAATGTTCCACATGTATCTATAGTCTTAGATGATGATGATGATGATGATGATGAAATGACAGATGATGATGACGATTATGGCTGTGAAGCTGGCGAAGTCATGTGGAAGTA[T/A]TCGGTAAATATTTTCCCATTGGTTTTATGTTTTAAGTTTATTTCTGGGTGTCTTGATTAAACTTTTTGTTTTTCTCCTAGAAAAATAAAGGAAATACACAAAATGAGATGACAGATAATACATACCAGGTAAATTCTTTAATATTTATATATAAAAAAATTATGACCCAATTTCAGCATTTATAACAGGGCATCTGTGGGGTCTTAAAAGTATTTAAAATTGATAAATCAATTTAGAGAAATTTAAGGCCCTTAAAAAGTATTGAAAAGTCTTAAATGCTATTTTACAAGGTTTTTAATTCGATATCAGTATGTTAAAGTTTACCTGAATTAATTTTTTATATTTTTTATGAATGCTGTGTAGTTTATGAAATAAAAAATATCCAGCTAGATTTGACACCACACTGCTTTGTTTACTTCAGTAAGCAGAGAAAACACTGTTAATCCTGCTGTTGTAAAGGCAGTACGTGCTGGATTACCAGTTTTTTGAGTATATAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9741
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080545 | Nonsense | 984 | 1448 | 12 | 24 |
ENSDART00000126841 | Nonsense | 984 | 1448 | 13 | 25 |
The following transcripts of ENSDARG00000057830 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 17160480)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 17063419 |
GRCz11 | 23 | 16989762 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAAAATGGAATGGCAGATCAATGCAGACMGTTAAGATCCGTAGAAAATA[T/G]AAACAGCGGAATAAGAATATCATCCCAACTGTACAGATCGAGTCCAGGCA
Long Flanking Sequence:
TAAGCACACAAATGTCTTTGATTCTAGGTGGCTTCCAGACGCAGTAGAATGTTTTTTTCTCCTGAGAGTGAATCTAAGGATGAACTCCTTAGAGTCATGTTGAACTGGGCCTTTGGAGGCTTTGAACCACTGGGTGCAGATGGACTCCAGCCTCAAGCAGAATACAGTGGTATGCAACAACAACTGAATGACTTTCTTTGACCTCAGTGTTTTACTTCAGTATGCGGCATATTGTTTTCAATGCAGTATTCATATAATTTATTCTATTCTCTTTCTTTCTTATACACTTTCTTATATACAATAGTGAAAGTGAAAAAGGGAAAGCGCAAGAACCCTACAGGAAAGTTGTTTAATTTAACTGTGCCCCTCAATAAAATCCCTGAATCTCTGGACCTGAACAATGGCTCAGTAGATCTCGGGACAACAGACGCCGACAAGAAACGCTTGTATTCAAAATGGAATGGCAGATCAATGCAGACCGTTAAGATCCGTAGAAAATA[T/G]AAACAGCGGAATAAGAATATCATCCCAACTGTACAGATCGAGTCCAGGCAAAACAGCCAAAAAAGACGTATGTGCATGCTTTATATTCATTGCTGCTATTAAAACTGTGATGACAAATAAACAAAGAAACCTGATGTTTACTGAACTTTTTCCACAGATCAAATGGTGCATGAATTTCTTAAAAACAAGAGAAAGATTGAAGGTGGGACACTCTTTTATAAGTATTGTGTTAATTTAGGTTGATAATGAGGAAAGTTTAACCGTATGTCATATCCTTTTCCTCAGATTTCTGCTTATCATGTGGCAGTATGTCCGTTGACATCATTCATCCACTCTTCGAAGGAAAGCTGTGTACAAACTGCAAGGTATTACATGTAGTTTAACAGCTTTAGTTCTCAACACACATGGATTTAGTTATTTCAGCTACACCTGTAACTAAATGTTACAAATATAAAACATCCTCATGCTGGGTTCACATTGCTTCATGTCCTCTAAATTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24283
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 |
---|---|---|---|---|---|
ENSDART00000080545 | Essential Splice Site | 1255 | 1448 | 19 | 24 |
ENSDART00000126841 | Essential Splice Site | 1255 | 1448 | 20 | 25 |
The following transcripts of ENSDARG00000057830 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 17157459)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 17060398 |
GRCz11 | 23 | 16986741 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATGTAATGACTTGTCCATAGTCAATCCTGCTCGGAAAGGCTTGTATGG[T/G]AAGACAAAAGTACTGAAAGACAAAGTTCAAGCATTAAATCATAAAATATT
Long Flanking Sequence:
ATGTAAAGGCAGGAAACGCTGTTTGTCAATCATGTAAATAAAAATATATATATAATCTGTAAATAAAAAAGACCTGTTCAGGTAAAGGGATTTGTCTCTTTAGAAGACATGGATTAAACCTTTCTATATACTTATGTGTTATATTTAGTCTTGTTTATGTTTTATACCATCAGATTTACTTAGTGAACTGACTTTCAATGAAGGAACAGAAATAACTCAGATTTAAATGTCTTATTTTTTTGTTTTGTCAATAAATAAATATTCTATAGGTTTGGAATATAAGGGAGGGTAAATTATGAGATGCATTTTGAGTTCAAACATCTCTTCGTACTTTTTGGGACTTTAGTCACGCATATCAAAAAGACTCCTCGGCAGTCTGCTTATTGATTGTATTCTTCATTTTTTTAGATAGAGCAGTGGGGTCCATTTGATCTTCTCATTGGTGGAAGTCCATGTAATGACTTGTCCATAGTCAATCCTGCTCGGAAAGGCTTGTATGG[T/G]AAGACAAAAGTACTGAAAGACAAAGTTCAAGCATTAAATCATAAAATATTCATTTGCCAGGGCGTGACATTAACTTTTTTGATCACCAGCCACTAATGCCAGTAGTTTTATAATGTTACTAGCCACTCGCCATTTTCACTAGCCAATTTTATTGTTGGGAAAATGTATTTTATATGCATAAATGTTACTTTGGCATGCTAAAAAATTGACATTTCTTGTTATATCCACGTCTCCTTATTAATTTAACTTTTTTGACTTTTCATGACTTTTTAGGGCCCAACACTGGATTTACCGATTTTTCTCTGCACATCAAACTAAATATTTCCTTGCCACAATTTTTTTTAAATAATGTGGCAAAACAAGCTAAATGTAGCAGTATATATACAATTTTTATTCTATAATTTAAAAAAGAAAACAATTGACAATTTAAAAAATTATTATCATTTATCTAAAACTATACACAGTAGTTTGTCTGGGCTAAAGGTCCCAGATCATCAGTT
Associated Phenotype:
Not determined