ZMP
zgc:158628
Ensembl ID:
ZFIN ID:
Description:
Poly(U)-specific endoribonuclease-A [Source:UniProtKB/Swiss-Prot;Acc:A1L237]
Human Orthologue:
ENDOU
Human Description:
endonuclease, polyU-specific [Source:HGNC Symbol;Acc:14369]
Mouse Orthologue:
Endou
Mouse Description:
endonuclease, polyU-specific Gene [Source:MGI Symbol;Acc:MGI:97746]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa33918 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa33919 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa9974 | Essential Splice Site | Available for shipment | Available now |
| sa17233 | Essential Splice Site, Missense | Available for shipment | Available now |
| sa40753 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33918
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 |
|---|---|---|---|---|---|
| ENSDART00000064904 | Nonsense | 8 | 303 | 1 | 8 |
| ENSDART00000114115 | Nonsense | 8 | 305 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 6 (position 39836278)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 39907878 |
| GRCz11 | 6 | 39905414 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGTGTGTTTAACGGATCGTCTAACAATGAAGATCATCCTCATACTTTG[T/A]CTCAGCATCACCCTGATCTCTCAGGGCCACTTTGGTAAGTTCATGCAATT
Long Flanking Sequence:
CACCTGCTCTTGCTGACTGTTTGCCCACGCAACAGCTCATGGAAACACACGAGGGAACGTGTTATTGGCAAGAAGACTTTCATGCCAAACACATACTGCAGACCATCATTTCAAGATAATCCTATATATTCTATATAAATGCCATAGTCATCTACAGAACCTGAACCCTGAAAGCTGATATTTCACATTTATTTGGGACATACAAACCAAAAAAAAGAGAGTAATTTACCTTTTTTATTATTGTGTATTTATTTATTAGTTTATTTATAAATCATTATTCGTCCTATTTTTATCATCTCACCACTTACAGTCTCATCTTTTTGCTCATAATTGAGTTATTTGGTCTTTGTTGCCCAATAATTATCACAACAAAGTGTTTGGGGGCATGGGAGGAGTTCCTAATAATTTCTTGATTTAAGAAGGTATAAAATCCAAAGTGGGTCTTACTCTGCAGTGTGTTTAACGGATCGTCTAACAATGAAGATCATCCTCATACTTTG[T/A]CTCAGCATCACCCTGATCTCTCAGGGCCACTTTGGTAAGTTCATGCAATTTATATCAACAGTATATGCATTAGTTATTATCATTGTCTTTTTACAATCACTAGGACACATTTCTCAATACTTTGGTGACTTGCAAAACTCTTTACAGTTCTAACCGACTTTTGTCTGTGCACTGCTGTTCATTCCATATTCAAAGGGCACTACATTTATCAAAATGCATAATGCATATCTCAGATTCATACATTCTTTCCTATTCAAAGCTTGTAATTCAGCAAACACACTTGGTCATCTATTTAAAAAGACCAAACAACACTAATTAGCAGGTGGATTTTTTTTTTTACAATATTGTTTACATTCAAAGTGTTTTTAGAAATCAGACATGATGCTGTAGGTTTAAGTAGATATTTGAAAAGTTCGAATGCAAAAGCTTCTAAGTGCTGTCTAAAATTTTCTTCTAAAATGAGCATTTTCCCTGTGATTATGTTCAGTAATTTGATTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33919
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 |
|---|---|---|---|---|---|
| ENSDART00000064904 | None | None | 303 | None | 8 |
| ENSDART00000114115 | Essential Splice Site | 20 | 305 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 6 (position 39839300)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 39910900 |
| GRCz11 | 6 | 39908436 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATTTTAATTCTTTTTAAGTGCTTCTTTGCTCTTTGGGTATTAATGTTT[T/A]CTTTATGTGCACGTTTTTCAAGCATTGGCCAATGTGTCAGATGCAGAGAT
Long Flanking Sequence:
TTGTTATGAAGAGCACTAGAAACAATGTTTGATGGTGCCATATGCTGCATTGATTCAATAAGTTAAGTTGTTCTCTGACATCTACATGGTAGGTATGTGGCTTAGGCAAGTTCAAACTATTTTCCAGAAATGGTTTATGCTCATTTTTTCCCATAAAATATCCCTAGAATCAGAAGGTCCATATTGACCATATTTAGAATGGTCGGGAATATTAATGAGCTCTCTGATTTTTGCCCTCTGTTCTCTCTTGTATTGTATTGTGGATAAAATATAGGCTAATCAAACTCCACAAAAAAAAAAAAAAAAAAGAATTACAGAGATTTTTAAAGCCATACTATAATCTTTTGTAGATTTTCCTGATTACAAGACAACAATTTCATAATTTCACTTTCATAATTGTCACAACAAAATCCTTTAATTCCAGATACCGTTATTTAATTGCAGTGCTTACTATTTTAATTCTTTTTAAGTGCTTCTTTGCTCTTTGGGTATTAATGTTT[T/A]CTTTATGTGCACGTTTTTCAAGCATTGGCCAATGTGTCAGATGCAGAGATCAAGTCTCTGTCAGAGACGCTGTATAAGTTAGACTCAAACAGAGCCACGACCTCTGAGCTGCTGATTGATCCTCAGACACTGATTCCTTCTTCTCAGACCGGCTCCGGAAATGATCTCTCACCACAGCCGTAAGACACACACTAAACCACCACAGCCATGATAAAAATGAGTGACCCCTTTGAAAAATGTGAGCAAAATACATTTATTTTACGTATCCTTTTAATCTTTCATCCAAAAAAAAAAAAAAAAAGATTTTGCCCAATTTTTATTTGTTTTATTTCAATAAACATTGTTGTGATAGTTAAAAAATAAAAAGACAATCAAAGCAGATTAAAGCTCATATTATTAGGGGTGTCAATAATTCTGACCATGACTGTGTACTGTATATACGGCATGCTTGAATGTTATTGTGCATTCTAATGCTCTGTTTCTCTTTAGATTGTTCAAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9974
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000064904 | None | None | 303 | None | 8 |
| ENSDART00000114115 | Essential Splice Site | 20 | 305 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 6 (position 39839301)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 39910901 |
| GRCz11 | 6 | 39908437 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATTTTAATTCTTTTTAAGTGCTTCTTTGCTCTTTGGGTATTAATGTTTT[C/T]TTTATGTGCACGTTTTTCAAGCATTGGCCAATGTGTCAGATGCAGAGATC
Long Flanking Sequence:
TGTTATGAAGAGCACTAGAAACAATGTTTGATGGTGCCATATGCTGCATTGATTCAATAAGTTAAGTTGTTCTCTGACATCTACATGGTAGGTATGTGGCTTAGGCAAGTTCAAACTATTTTCCAGAAATGGTTTATGCTCATTTTTTCCCATAAAATATCCCTAGAATCAGAAGGTCCATATTGACCATATTTAGAATGGTCGGGAATATTAATGAGCTCTCTGATTTTTGCCCTCTGTTCTCTCTTGTATTGTATTGTGGATAAAATATAGGCTAATCAAACTCCACAAAAAAAAAAAAAAAAAAGAATTACAGAGATTTTTAAAGCCATACTATAATCTTTTGTAGATTTTCCTGATTACAAGACAACAATTTCATAATTTCACTTTCATAATTGTCACAACAAAATCCTTTAATTCCAGATACCGTTATTTAATTGCAGTGCTTACTATTTTAATTCTTTTTAAGTGCTTCTTTGCTCTTTGGGTATTAATGTTTT[C/T]TTTATGTGCACGTTTTTCAAGCATTGGCCAATGTGTCAGATGCAGAGATCAAGTCTCTGTCAGAGACGCTGTATAAGTTAGACTCAAACAGAGCCACGACCTCTGAGCTGCTGATTGATCCTCAGACACTGATTCCTTCTTCTCAGACCGGCTCCGGAAATGATCTCTCACCACAGCCGTAAGACACACACTAAACCACCACAGCCATGATAAAAATGAGTGACCCCTTTGAAAAATGTGAGCAAAATACATTTATTTTACGTATCCTTTTAATCTTTCATCCAAAAAAAAAAAAAAAAAGATTTTGCCCAATTTTTATTTGTTTTATTTCAATAAACATTGTTGTGATAGTTAAAAAATAAAAAGACAATCAAAGCAGATTAAAGCTCATATTATTAGGGGTGTCAATAATTCTGACCATGACTGTGTACTGTATATACGGCATGCTTGAATGTTATTGTGCATTCTAATGCTCTGTTTCTCTTTAGATTGTTCAAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17233
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:
A > T
Consequence:
Essential Splice Site, Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000064904 | Essential Splice Site | 25 | 303 | None | 8 |
| ENSDART00000114115 | Missense | 26 | 305 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 6 (position 39839321)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 39910921 |
| GRCz11 | 6 | 39908457 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTTCTTTGCTCTTTGGGTATTAATGTTTTYTTTATGTGCACGTTTTTCA[A/T]GCATTGGCCAATGTGTCAGATGCAGAGATCAAGTCTCTGTCAGAGACGCT
Long Flanking Sequence:
ACAATGTTTGATGGTGCCATATGCTGCATTGATTCAATAAGTTAAGTTGTTCTCTGACATCTACATGGTAGGTATGTGGCTTAGGCAAGTTCAAACTATTTTCCAGAAATGGTTTATGCTCATTTTTTCCCATAAAATATCCCTAGAATCAGAAGGTCCATATTGACCATATTTAGAATGGTCGGGAATATTAATGAGCTCTCTGATTTTTGCCCTCTGTTCTCTCTTGTATTGTATTGTGGATAAAATATAGGCTAATCAAACTCCACAAAAAAAAAAAAAAAAAAGAATTACAGAGATTTTTAAAGCCATACTATAATCTTTTGTAGATTTTCCTGATTACAAGACAACAATTTCATAATTTCACTTTCATAATTGTCACAACAAAATCCTTTAATTCCAGATACCGTTATTTAATTGCAGTGCTTACTATTTTAATTCTTTTTAAGTGCTTCTTTGCTCTTTGGGTATTAATGTTTTCTTTATGTGCACGTTTTTCA[A/T]GCATTGGCCAATGTGTCAGATGCAGAGATCAAGTCTCTGTCAGAGACGCTGTATAAGTTAGACTCAAACAGAGCCACGACCTCTGAGCTGCTGATTGATCCTCAGACACTGATTCCTTCTTCTCAGACCGGCTCCGGAAATGATCTCTCACCACAGCCGTAAGACACACACTAAACCACCACAGCCATGATAAAAATGAGTGACCCCTTTGAAAAATGTGAGCAAAATACATTTATTTTACGTATCCTTTTAATCTTTCATCCAAAAAAAAAAAAAAAAAGATTTTGCCCAATTTTTATTTGTTTTATTTCAATAAACATTGTTGTGATAGTTAAAAAATAAAAAGACAATCAAAGCAGATTAAAGCTCATATTATTAGGGGTGTCAATAATTCTGACCATGACTGTGTACTGTATATACGGCATGCTTGAATGTTATTGTGCATTCTAATGCTCTGTTTCTCTTTAGATTGTTCAAGGTAGTGAGCAGTACATTGCTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40753
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000064904 | Nonsense | 237 | 303 | 7 | 8 |
| ENSDART00000114115 | Nonsense | 239 | 305 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 6 (position 39842461)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 39914061 |
| GRCz11 | 6 | 39911597 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACGTATCCTGATGTATTGGGAATGCAGTTTAACTGGGATGGATATTTC[A/T]AAGAGCTGGGTTCTGCCTTTATTGGCTGTAGTCCTGAGTTTGATCTGGCC
Long Flanking Sequence:
GGATTTCTCAGACTTGTTTCTTCTGCACTGAATCATAAACCTCTGTTTCAGCATCACTTACATCTTAAAAATTGAAACGTCAATTGAAAGTCAATTTAAGCATGAACTAATTCTTCTGGGAAAACCTTGGTGTGTGTATTTACTGCTGAAATGGAGATTTAGGATGGAGAAAATTCATGCATGAGAAAAAAAACAGCCTTTAAAAATATTTTTAATTTAAATCCATGGACAAAAATTAATAAAGGGTGACACAAAGTTAACTTTTTCAGTAATTTCTTTACATAAAATATCCATTAAATTTACAAAAAAAATCACTTTGAGACCACAAATTTACAGGTACATGAAAAAAAATGAGCTGTAGCTGCAGTGTTTCACCTTAAAAGTGTGAAAGTTTGCTAAAAGTGCAGTTTGTCCTCTCTTTCTCTCTCTCTCTCTCTCTCTCTCAGTGGACCACGTATCCTGATGTATTGGGAATGCAGTTTAACTGGGATGGATATTTC[A/T]AAGAGCTGGGTTCTGCCTTTATTGGCTGTAGTCCTGAGTTTGATCTGGCCATCTACAGCCTTTGCTACATCACCCGTCCTGGAAAGAAGTGAGTTGTCCTATTTTTATTTCTGTCTTTATACTCATTTATGCATGATTTCAGTAAAAACAAAAACAAGGAAAAACATTTTGACCTTGAAACTGTGGGTAAAATGATTCCACTAATGAGACCCAAAGGGCATCTGCTGCATAAAAAGCATATGCCAGAGTAATTGGTGGTTCATTCCACTGTGGTGACTAAGCCAAAGGACAATGAGTGATTCAACTAAAGTTAAGAATGCAAAAAATTATTATTTTTTTTAGTTTATTTATATTCCTACAAAAAAAATCCATGATCCATTCAAAGCTAGTCACTTGCTTGATTTCCTTTGATTTGAATTGAATTCAAATGATCTAACCATTTTGAGCAAAACATGTGAACGAATGCTTCAAGGAATCACCCAAGCAATAAACTGTGCAAA
Associated Phenotype:
Not determined