ZMP
dicer1
Ensembl ID:
ZFIN ID:
Description:
Endoribonuclease Dicer [Source:UniProtKB/Swiss-Prot;Acc:Q6TV19]
Human Orthologue:
DICER1
Human Description:
dicer 1, ribonuclease type III [Source:HGNC Symbol;Acc:17098]
Mouse Orthologue:
Dicer1
Mouse Description:
Dicer1, Dcr-1 homolog (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2177178]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9205 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19169 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa11548 | Nonsense | Available for shipment | Available now |
hu715 | Nonsense | Confirmed mutation in F2 line | Not yet available |
hu894 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9205
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 |
---|---|---|---|---|---|
ENSDART00000045881 | Nonsense | 459 | 1865 | 9 | 27 |
ENSDART00000109826 | Nonsense | 459 | 1865 | 8 | 26 |
Genomic Location (Zv9):
Chromosome 17 (position 19282841)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 19432852 |
GRCz11 | 17 | 19452688 |
KASP Assay ID:
2261-0862.1 (used for ordering genotyping assays)
KASP Sequence:
KATTTCAGACTTATTAAGGAGGCAGGAAAGCAAGACCCAGAGCTGGCTTA[C/A]ATCAGTAGCAACTTCATCACAGGGCACAGCATCGGCAAGAACCAGCCTCG
Long Flanking Sequence:
TTATGTCTTACCTGCACCCTCACAATCCTTACATTATATAGAAGTGGTGAGGAATTTTTTTGCAGTTTGTGCAGTAAGTAAACAAGGATGAAGTGCGAGTGATTAACATGTGAAGTCATAGCAAAGATGCGATTAGATATCCTGTGGCGCAAATCGAGTGAATAACACCGCACAAATTGGGGGTTTTGTGCATTGATACACTAGACTGCAAAAAAAATGTATGGCTGGTATTATGATCGATAAAAATTGATAAATGATTTTGCTGAACTCTTTTCCTGCAATATAATGTTTTAAAAATATTATATATATGTTTTCTGTATTTTATAAATTTGTGTCCTTCCTGAAAATCAGTATTATTTTTTTCTTAACAGTATTAAACAATCTTGCTGACCTGGAACAGCAAAAGCTGTATTAAAAGCAACATTTTTATTATGATTGTATTTTTTGTTGGATTTCAGACTTATTAAGGAGGCAGGAAAGCAAGACCCAGAGCTGGCTTA[C/A]ATCAGTAGCAACTTCATCACAGGGCACAGCATCGGCAAGAACCAGCCTCGCAACAAGCAGATGGAGGTGGAGTTCAGAAAACAAGAGGAAGTGAGTAAATCTGGCAATCTTAGGCCTGGTTTCTACCTGAAATCTCATAAGATGTGTTTTCGTCAATCCATTAACAGGCTGATGACACTAAATACTGGAGTAAACGGGATCTAAAGTGTTAGAGCTTCCACTTACCTCACTTCCAGAGGTTGACAGCAATGCATTTTGTTGTGTAAATACTTGCGGTCAGAAGCTTCCAAAAAACCTCAAAAGACAACATATGTTCTTTAAAAAAAATTCAAATGTCTTGTCTGACACATCAGATCACTGAAAATACTTTTTATTACCAAAAAGGTCCATGTCCACTTTATTAGCTTGTATTTCTAACTCTTCTCTCTGATTCCCATTACTTACCAGGTCTTGAGGAAATTCAGAGCCCATGAAACCAACTTGCTCATTGCAACCAGCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19169
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045881 | Essential Splice Site | 1332 | 1865 | 21 | 27 |
ENSDART00000109826 | Essential Splice Site | 1332 | 1865 | 20 | 26 |
Genomic Location (Zv9):
Chromosome 17 (position 19270054)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 19420065 |
GRCz11 | 17 | 19439901 |
KASP Assay ID:
2261-0860.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTACCCTGACGCCCACGAGGGCAGACTGTCCTACATGAGAAGCAAGAAGG[T/G]GAGATTTTGTCAAGTTAAAGGAATAGTTTAGCCAGAAATGAAAAATAGTC
Long Flanking Sequence:
GGCCGACAGCGACGACCTCCCTCACAGAAGTGACGTTTGCCAATGCTCTCAGCTGGGCCCTCTGGAGAGAGACCTATCAACACAAACCACTACCTCAGTTTCAGTGCGGCCCTCTCCAGCTGGAGAACCACAGCCATGGCCCAGCGATGAATGTACAGGCAGGAGCTCGGATCTCTGCGACCCACATGTGAAGAAACCTACCTCAAAGCATTGCCCTAAATCGGAGACGGCGACTAGCACCCCAGCACCTTCAGAAACGTCATCAGAGGACTGTAGATCAGCCTGCGCTGGTCCAGCCTGGGATTCGCCCAAAACCCTGGGCCCGAACCCCGGGCTCATCCTGCAGGCCCTGACTCTCTCCAACGCCAGTGACGGCTTCAATCTGGAACGCCTGGAGATGCTGGGCGACTCCTTCCTGAAACACGCCATCACCACATACCTGTTCTGCACTTACCCTGACGCCCACGAGGGCAGACTGTCCTACATGAGAAGCAAGAAGG[T/G]GAGATTTTGTCAAGTTAAAGGAATAGTTTAGCCAGAAATGAAAAATAGTCCATAATTTACTCTCCCCCAAACCATTCTCTTTGTGTCGGTTTTGTCTAGTATTTTTCTGACACAGATATAGTAGTTTTAAATTTTACCCTGGATCTTCCATGCTACATAATGGTTTAAGATAGATACGTTTTATTTGAAACCTCCAAAAGCACATTTTGATCTGTATTTAAAACAAAAATATTACACATTTTTGAATTATAATTTCCAATCACTGACTTCAGGTGGAGGCCGAATGCATGTTATGTATCACTGACATATACTATGGGATTATATATAGAGTTTATACGGTCATGGAAAACCTGGAAAAATCGTGTAATTTTGACATGGCATTTTCCAGGCCTGGAAAAACCCACAAGGTTTTGGAAAAGTCATGGAAATTACATTTAGTCATTTAGTAGAAATTTTTGTCCAAAACGACTTAAGCTGCGGTCACACTAGAGCTTGTGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11548
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045881 | Nonsense | 1414 | 1865 | 23 | 27 |
ENSDART00000109826 | Nonsense | 1414 | 1865 | 22 | 26 |
Genomic Location (Zv9):
Chromosome 17 (position 19261891)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 19411902 |
GRCz11 | 17 | 19431738 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACGAGGATGACGATGATGAGCCGGAAGAAGCAGAGGTCGAGCCATCTAAA[G/T]AAGATGTAAATGTTGAAGAYGACCTGGAGTATTATTACGAACACATCCGC
Long Flanking Sequence:
TATAATTATTAATAAATGTTTAATTTTCTAAATATTATTGATTATATTTGAAAGAAAATTGCGATTGTGTAAAATTGTAATATATAACAGTTTATAATGTATTGTATTAACAGTATTGTTTTTTTACAAGTTATAAATATTATAAAATGTTTAATTTTATAAATATTATTAATTATTTTGGAAAACCAATGTTAGTTTCAATTATAAATATAGTAGTAGTATTGTATAGTTGTAAAATAATGGTTGTTTAAAAATTAATAAAAATAATGGATAGTCTTACATTAGATTATATAGCAATATATAATAACTAATGATTGTTTTGGTGATGATTGTAACATTTCCTTTCATAATTTAGTATCATTTTGTTTTTTCAGCTTTAACATAAGCCCAATTCTATTGTTGTTTTTCAGAATAAAGATTTAGCGAATGGAAAAGCCAGCGATGACGAAGACGAGGATGACGATGATGAGCCGGAAGAAGCAGAGGTCGAGCCATCTAAA[G/T]AAGATGTAAATGTTGAAGACGACCTGGAGTATTATTACGAACACATCCGCTTCATCGACAGCATGTTAATCGGCTCTGGCGCTTTCGGCAAGAAGATCTCCCTCCAGCCCACAGACCCCGGCTACGAATGGAAAGCTCCTAAAAAAGCCCACAACTCCCACTTCTCGCCAGACGGGGGTGCTGACGAGTTCGATTACAGCTCCTGGGACGCCATGTGTTACCTGGACCCCAGTAAAGCAGGTGAGGAGGACGATTTCGTGGTGGGCTTCTGGAATCCCTCTGAGGAAAACTGCGGCACGGACATCGGGAAACAGTCCATCTCTTATGACCTTCACACGGAGCAGTGCATCGCAGATAAGAGCATAGCGGACTGTGTGGAGGCTCTGCTGGGCTGCTATCTGACCAGCTGTGGTGAGCGAGCGGCTCAGCTGTTTCTCTGCTCTCTGGGCCTGAAGGTGCTACCACCGGAGAAGCAGAGTTCGGGAGGCTCTGCCGAGCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
hu715
Status:
Confirmed mutation in F2 line
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045881 | Nonsense | 1427 | 1865 | 23 | 27 |
ENSDART00000109826 | Nonsense | 1427 | 1865 | 22 | 26 |
Genomic Location (Zv9):
Chromosome 17 (position 19261852)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 19411863 |
GRCz11 | 17 | 19431699 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCCATCTAAAGAAGATGTAAATGTTGAAGACGACCTGGAGTATTATTAC[G/T]AACACATCCGCTTCATCGACAGCATGTTAATCGGCTCTGGCGCTTTCGGC
Long Flanking Sequence:
GATTATATTTGAAAGAAAATTGCGATTGTGTAAAATTGTAATATATAACAGTTTATAATGTATTGTATTAACAGTATTGTTTTTTTACAAGTTATAAATATTATAAAATGTTTAATTTTATAAATATTATTAATTATTTTGGAAAACCAATGTTAGTTTCAATTATAAATATAGTAGTAGTATTGTATAGTTGTAAAATAATGGTTGTTTAAAAATTAATAAAAATAATGGATAGTCTTACATTAGATTATATAGCAATATATAATAACTAATGATTGTTTTGGTGATGATTGTAACATTTCCTTTCATAATTTAGTATCATTTTGTTTTTTCAGCTTTAACATAAGCCCAATTCTATTGTTGTTTTTCAGAATAAAGATTTAGCGAATGGAAAAGCCAGCGATGACGAAGACGAGGATGACGATGATGAGCCGGAAGAAGCAGAGGTCGAGCCATCTAAAGAAGATGTAAATGTTGAAGACGACCTGGAGTATTATTAC[G/T]AACACATCCGCTTCATCGACAGCATGTTAATCGGCTCTGGCGCTTTCGGCAAGAAGATCTCCCTCCAGCCCACAGACCCCGGCTACGAATGGAAAGCTCCTAAAAAAGCCCACAACTCCCACTTCTCGCCAGACGGGGGTGCTGACGAGTTCGATTACAGCTCCTGGGACGCCATGTGTTACCTGGACCCCAGTAAAGCAGGTGAGGAGGACGATTTCGTGGTGGGCTTCTGGAATCCCTCTGAGGAAAACTGCGGCACGGACATCGGGAAACAGTCCATCTCTTATGACCTTCACACGGAGCAGTGCATCGCAGATAAGAGCATAGCGGACTGTGTGGAGGCTCTGCTGGGCTGCTATCTGACCAGCTGTGGTGAGCGAGCGGCTCAGCTGTTTCTCTGCTCTCTGGGCCTGAAGGTGCTACCACCGGAGAAGCAGAGTTCGGGAGGCTCTGCCGAGCTCCAGTACGGCTGGCTGAAGATCCCACCACGCTGCATGTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
hu894
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045881 | Nonsense | 1457 | 1865 | 23 | 27 |
ENSDART00000109826 | Nonsense | 1457 | 1865 | 22 | 26 |
Genomic Location (Zv9):
Chromosome 17 (position 19261760)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 19411771 |
GRCz11 | 17 | 19431607 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTTCGGCAAGAAGATCTCCCTCCAGCCCACAGACCCCGGCTACGAATG[G/A]AAAGCTCCTAAAAAAGCCCACAACTCCCACTTCTCGCCAGACGGGGGTGC
Long Flanking Sequence:
TATAAATATTATAAAATGTTTAATTTTATAAATATTATTAATTATTTTGGAAAACCAATGTTAGTTTCAATTATAAATATAGTAGTAGTATTGTATAGTTGTAAAATAATGGTTGTTTAAAAATTAATAAAAATAATGGATAGTCTTACATTAGATTATATAGCAATATATAATAACTAATGATTGTTTTGGTGATGATTGTAACATTTCCTTTCATAATTTAGTATCATTTTGTTTTTTCAGCTTTAACATAAGCCCAATTCTATTGTTGTTTTTCAGAATAAAGATTTAGCGAATGGAAAAGCCAGCGATGACGAAGACGAGGATGACGATGATGAGCCGGAAGAAGCAGAGGTCGAGCCATCTAAAGAAGATGTAAATGTTGAAGACGACCTGGAGTATTATTACGAACACATCCGCTTCATCGACAGCATGTTAATCGGCTCTGGCGCTTTCGGCAAGAAGATCTCCCTCCAGCCCACAGACCCCGGCTACGAATG[G/A]AAAGCTCCTAAAAAAGCCCACAACTCCCACTTCTCGCCAGACGGGGGTGCTGACGAGTTCGATTACAGCTCCTGGGACGCCATGTGTTACCTGGACCCCAGTAAAGCAGGTGAGGAGGACGATTTCGTGGTGGGCTTCTGGAATCCCTCTGAGGAAAACTGCGGCACGGACATCGGGAAACAGTCCATCTCTTATGACCTTCACACGGAGCAGTGCATCGCAGATAAGAGCATAGCGGACTGTGTGGAGGCTCTGCTGGGCTGCTATCTGACCAGCTGTGGTGAGCGAGCGGCTCAGCTGTTTCTCTGCTCTCTGGGCCTGAAGGTGCTACCACCGGAGAAGCAGAGTTCGGGAGGCTCTGCCGAGCTCCAGTACGGCTGGCTGAAGATCCCACCACGCTGCATGTTCGAACATCCTGACGCTGAACGCACGCTCAACCACCTCATCTCTGGCTTCCTGAACTTCGAGAGCAAGATCAACTACACGTTTAAGAACAAGGC
Associated Phenotype:
Not determined