ZMP
si:ch211-254o18.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate polymerase (DNA directed) kappa (POLK) [Source:UniProtKB/TrEMBL;
Human Orthologue:
POLK
Human Description:
polymerase (DNA directed) kappa [Source:HGNC Symbol;Acc:9183]
Mouse Orthologue:
Polk
Mouse Description:
polymerase (DNA directed), kappa Gene [Source:MGI Symbol;Acc:MGI:1349767]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa40543 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa26563 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa40544 | Essential Splice Site, Missense | Mutation detected in F1 DNA | Not yet available |
| sa10869 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa40543
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000083937 | Nonsense | 53 | 846 | 2 | 17 |
| ENSDART00000141039 | Nonsense | 53 | 875 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 5 (position 47508589)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 45297329 |
| GRCz11 | 5 | 45897482 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATATAATTAATTTTTTTCTAATTTATAGGGATCTAGATTTTATGAGAAT[G/T]AATTGAAGAAAGAGCGGCAGGTGAATCAGCGCATTGAAAAGATGATGGAG
Long Flanking Sequence:
ACTATATAGACTACTTCCTAAAAATAATTACAAAAATTGGCCAATAATAACTACAGTACGTACTAACTCTGAAGCCGTTACCTTATTTTGTTTTGCCTTGCTCTTTCGAAACTATGTACACTGTAAGGGCACAAGTGCATCACTCTAAAGCAATGTGCAGCAAGTTACATTAGAAATATTACAGTATTTATTACATTTCTTATTCATTTGTTAATTTAAATAATTTTTGTGCTGTGAATTTATTTTAGTCAAATTAAAATAATGTATTATATTAAATAATTATATATTGTTTATATATTTAATTTATTATTATTTTCAAAGTTTTTCCTGTTTAAAAAGACAAGTATACTATTGTCTGTCAGTGAATATATATAATAATTATAATTGCAATTTATTGAAATAGTTTCAGATGAAGTTTAACTAGGCACTCTGCCTGACAGTGTTGTGGATGATATAATTAATTTTTTTCTAATTTATAGGGATCTAGATTTTATGAGAAT[G/T]AATTGAAGAAAGAGCGGCAGGTGAATCAGCGCATTGAAAAGATGATGGAGCAAAAAGCAAAAATCACTAAGGAACAGATGAAACAAGCTCAAGCAGAGGTAATCAGCCCTGTAATCACTGCTATAAATGTTTGTATTGGATTTCACAGTGAGTGGACACACACACACACAAATTCACCTCTGACTTTGATTACTGTTAAATATTGCATTCTCAGTGTCTTATTAAAATAAATGTATATGTGTATGATTAATTATTATTATCATTGTGTCTCGACCAGATGACTCTTATTAATGTTTTACACAATTGTAGCAACTATTAAAACAAGGTAGTTTACCGTAGTTAAAAAGGGGAAGGTGTACTGTAAAATATGATTAGTTGACATTACTTAAAAAGGTGAGTAAACCTGCTGCTTTTAAATTAATTAGTTGTATTTACTAGGGCAGCATGATATAAAAAAAAATTGGTATTGTGATATTTTGTTCTACTGCAATAAAAATTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26563
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000083937 | Essential Splice Site | 137 | 846 | 4 | 17 |
| ENSDART00000141039 | Essential Splice Site | 137 | 875 | 4 | 13 |
Genomic Location (Zv9):
Chromosome 5 (position 47512903)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 45301643 |
| GRCz11 | 5 | 45901796 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACGATTAATCATGCTGCTCTAGTTGACGTTATAATCTTTTATTCTTTTC[A/T]GTCAACCTCCAATTATCATGCCAGAAGGTTTGGTGTCCGTGCTGCCATGC
Long Flanking Sequence:
CAATGCTCAGCTAATGTTTACACTCGTAATATTTATATTATTTGCTTATTAATAACCTCATGTGGAAAAAGCACGTTTTCAAAGCAGATTAATTGACTTCAGCATTGTTTTTCAGAAAAACAGCCATGTTCTCTTAGTGTGTTTCTTAAATTTCTGCAAACATATTATGGTGTTTTTATGCTTTAGGAGAGTCAAAACTTTCATACAGCACTTTTGATAATACAACAACTCACTTATAAAGACTTCATGTGCCATTACTAGAATCTTTTAAAGTAATTATTCAGTGACAAATTCATTTTTGATGGTCGCTTGTCGCCAGTTGAGCAGCCATCAATGGTCATTTTAATCTTCACCATGAACATCAGTGTTTACATCCCAAACAGAGATAAAGACATATATGGTAATGGTGACCATTTATTAAGATTAAGTGTGTTTGAATCAAGATATTGTAACGATTAATCATGCTGCTCTAGTTGACGTTATAATCTTTTATTCTTTTC[A/T]GTCAACCTCCAATTATCATGCCAGAAGGTTTGGTGTCCGTGCTGCCATGCCCGGATTCATTGCTAAGAAGCTCTGTCCGGATCTAGTCATTGTCCCAACTAACTTTGACAAATACAGAGCAGTGAGTGCCCAGGTATGTTGTATCCTAGTCAAGCATTACTCATTAGTCATAATAACTCCTGTGTTTGTCTAATGTGTGAATCTGTCTTAAAGGTACGGGAGATATTTTCAGAGTACGACCCTAATTTCATGCCTATGAGTCTGGATGAGGCTTATCTGGACATCACTGAGCACCTGGAGCAGCGCAAGCACTGGCCGGACACCATGCGAACACACAAAATCTGTGATGCTAAGACAGGTGCATTACTAAGATATATTAATTAATACGGGGGGTTTCAGACTGTCTCTGTAAGGGAGTTGTAAATCATATTTAACACATTCATATATTTATATATACACACATATAAACAATGTATGTGAACAGTGATTTAAAAAAGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40544
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 > C
Consequence:
Essential Splice Site, Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000083937 | Essential Splice Site | 599 | 846 | None | 17 |
| ENSDART00000141039 | Missense | 594 | 875 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 5 (position 47521464)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 45310204 |
| GRCz11 | 5 | 45910357 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACTCTCAATCAGACACAACATCGGCTAACAAAATGAATACAGGATACA[T/C]AAGCAAACTTGCAAAGGCGTCATTTAAGATTTCGACCCAGGTGCTGCAGT
Long Flanking Sequence:
CTAAGTCCCTCCCCACTGCAGTATTTGACCTCAGACAAAACAATTAAACAATGGCTTTTTTTTTTTTTTAAACGACTTTAGAGATGTTTGTTATTCAACAGGCGTTCGAGTGTCTGGCTTTATCAGCACTGAAGATAAAAAGCCTCTTCAAAAGAGTATAATGGGCTTTCTGCAGAAAGGTGGACCCGATCCAGCCGGTTTCACACAGTGTCCTGGATCAGAACCCAAAGCTGAAGAGGCTAGTGATGGTGCCAGATTTCTCAAGCCACAGTCCACTGAGATGAAAGTACCCAAACCTCAAGCACCTCAGCAGCAGTCATTCTTTCAAAGAGCCCAGTCCAAAAGACTACAGCAGCAGCAGGAACAAACATCTGCCAGCACAGTCACAGACAAAACAAACAACACTCAATCAGACACAACAAACAACACAGCTGCTAAAACACACGTGAATCACTCTCAATCAGACACAACATCGGCTAACAAAATGAATACAGGATACA[T/C]AAGCAAACTTGCAAAGGCGTCATTTAAGATTTCGACCCAGGTGCTGCAGTGTCTCACCTGTCCTGTGTGCAATAAAGAAATGAAGGATGTAAACCTCACAGCCTTCAACCAGCATATCGATGAATGTCTGAAGGGCAGTGCGATGGATAGTAATGAACACACAGATTTAAGTGCAGCTGAGCGCCAAGAAGAGCTCAGTGGCGAACCATCAAGTTTAGAAAGCAAGACTCTCGTCCATTATTCATCATGTAATGAAGAGAAAGCGTCTACTAGCACCTCTGAGCCAATGGCAGATGGCGATGACGGCAATGACTTCAAGACTCCACAGTTTAGTCAAAGTATGATAAACAGAAACCATTCAGTTGTTCTTAAAAAGCAGACATCTCTTTCTGAATCTAAAGTAAGAAGTTATGAAGCTTCGCACTCAGCGCATAATCCTGTCCCGGAGATGTCGTGTGATTTGAAAGGCTCGTCTTTGGTGTGTCCTGTGTGCAATCAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10869
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 |
|---|---|---|---|---|---|
| ENSDART00000083937 | None | None | 846 | None | 17 |
| ENSDART00000141039 | Nonsense | 834 | 875 | 13 | 13 |
Genomic Location (Zv9):
Chromosome 5 (position 47525436)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 45314176 |
| GRCz11 | 5 | 45914329 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCGACAAATTCTTCAGAGGAAACACCAGACAGAACGTCTAATTCTGCTA[C/T]AAATCCACACAGACCATATCCAGAAAATAKGAAGAAGAGACATGATAATC
Long Flanking Sequence:
AGAAAAGGATGATAACAAAATAAATAAATAATATTAGCAGTTCTGTAAACATTTGTAAAAAGATATGTTTCTTGAGCAACAAATTTGCATATTTGACTGGTTTCATACATCAATCGCACTGAAGACTGCAGCAATAATGCACAAGTTTCAGCTTAACAATCAAATAAATAAGTTACATTCTGAAATATATGTTAGTAATTAACAGTTAAAAATTTGAATATTTGTAACCTATTCGAAGCTGTTATATTATTTTATAATATATTACTGTATTCTAAAGTCTGTAATGCTTTGTCAATGAACATTTGCAGATCTTAACTGCCTCAAACTGTTAAATTAGGTATTTACAAATATTTAGTGTCTCATCATTTCTGTGTTTGTTTTAATTACAGACGAGGATCATCTCCTCTTCCTCCCTCAAAGAAAACCAAAGTGTTGAGCACAAAACACACAATCGACAAATTCTTCAGAGGAAACACCAGACAGAACGTCTAATTCTGCTA[C/T]AAATCCACACAGACCATATCCAGAAAATAGGAAGAAGAGACATGATAATCCATGAGGACTTTGCTGGATTCACTTCAGGGAATAATGTTAATGCAAGTAAGAAATCTGCAGACTGCAGATTAATATAAGATGAAGAAAATGCCAATGGGGGGGTGGGGGGGGGGGGGGGTGTATTCCTGAAGATTAAGGTCTATTTTGATATTTTTTGTATTTATTATTGAATGTTTGTGTGGTGGGAAAAATGCATCATATTTATGTTTTCTCTTGCCTTTTTTAAGATCGTAACATAAGAAGTCGATACTTTATTTAATTAAGCATTTAATATATTTTTACTGTTATTTACATAAATGCAAATGATCGTTTAATGTTAGATGCTCGAAGCACTTTATAGACATGACAAAAAAAATTACCGAAAATAATGGAAGTACACAGAGTTATCAGTTATCATAACTGAATACATTCAGAATTGTATAAATGTATCATTTAGTTTGCATCGAATA
Associated Phenotype:
Not determined