ZMP
prkri
Ensembl ID:
ZFIN ID:
Description:
protein-kinase, interferon-inducible double stranded RNA dependent inhibitor [Source:RefSeq peptide
Human Orthologue:
DNAJC3
Human Description:
DnaJ (Hsp40) homolog, subfamily C, member 3 [Source:HGNC Symbol;Acc:9439]
Mouse Orthologue:
Dnajc3
Mouse Description:
DnaJ (Hsp40) homolog, subfamily C, member 3 Gene [Source:MGI Symbol;Acc:MGI:107373]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa20911 | Essential Splice Site | Available for shipment | Available now |
| sa20910 | Nonsense | Available for shipment | Available now |
| sa31565 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20911
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000026098 | Essential Splice Site | 111 | 500 | None | 12 |
The following transcripts of ENSDARG00000017874 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 21960153)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 20550589 |
| GRCz11 | 7 | 20790776 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGCCGGATCTGACCCAAGCCATACAGCTCAAGCCAGACTTTCTTGCTG[T/A]GAGTTCATTTTTGTTGTTGTAATACAAAATTGAGTTCTATGTGGCAAACA
Long Flanking Sequence:
ACATTTTTTATAAAATTACAAATTGACAACAGACAAGCATTATAAACAAAATGTAATGAAAAGTAAAAAAAAAAAAATTCTTTTTTGAGAAATTCTTAAGAATCTGTTATTATGTAAAAAGAACTCCCAAGAATAATAATTGATAATTGTTAATTTGCTAAATCATGCGTTTAATTTTTCCAACATAAACCAAATAGTACAAATGTGTACGAATTGAGCATAAGACAAAAAAAAATTCTCCAAAATTTCTAAAAGTACATTTATTTTTCCATTTCCTTTTTTTTTCCAGATCTGTTTTAGATGCATTTTTGTTTAGACATATTTAATATGCATAATTCAAAGTGAAAATTAGATGTCTAATGTGTCTTAAACAGAGGGCGACTCTAAGAACTATTTGACCTACTACAAACGGGCTACCGTTTTCCTGGCCATGGGCAAATCCAAGTCAGCCCTGCCGGATCTGACCCAAGCCATACAGCTCAAGCCAGACTTTCTTGCTG[T/A]GAGTTCATTTTTGTTGTTGTAATACAAAATTGAGTTCTATGTGGCAAACAGTATATACACATTTATAGTATGCATATGTTTTCAGGCCAGACTGCAGAGGGGTAATATTCTTCTGAAACAAGGAAGTACTCAAGAGGCCAGAGAGGACTTCCAAGCAGTTGTGAGTAAAACCATTCTCTTTTTTCCTAAAGGATAGTTCACACAGAAAGGAAAATTCATCATTTACTCTCCTGCATGTGGTTTTAAGCCTTTACGAGTTTGTCTTCTTTATTTTATTTTATTTTTTTGATAGTATGGACGTTGATCTGTGCCAGCAATCAGCATTCTTTAAAATAGCTTTCTTTAATATATTATTGAAAAAGAAATGATAATGTATGGACTCTTAGTTGGTTCTGAAGATTTACGAGTTTCAAAAGAAACACAAAAGAAGATATTTTAAAGAGTGTTGAGAAACTGATAATCATTGACATCCATAGTAGAAAAACAAATGCTGTGGAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20910
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 |
|---|---|---|---|---|---|
| ENSDART00000026098 | Nonsense | 123 | 500 | 4 | 12 |
The following transcripts of ENSDARG00000017874 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 21960034)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 20550470 |
| GRCz11 | 7 | 20790657 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATGCATATGTTTTCAGGCCAGACTGCAGAGGGGTAATATTCTTCTGAAA[C/T]AAGGAAGTACTCAAGAGGCCAGAGAGGACTTCCAAGCAGTTGTGAGTAAA
Long Flanking Sequence:
AGAACTCCCAAGAATAATAATTGATAATTGTTAATTTGCTAAATCATGCGTTTAATTTTTCCAACATAAACCAAATAGTACAAATGTGTACGAATTGAGCATAAGACAAAAAAAAATTCTCCAAAATTTCTAAAAGTACATTTATTTTTCCATTTCCTTTTTTTTTCCAGATCTGTTTTAGATGCATTTTTGTTTAGACATATTTAATATGCATAATTCAAAGTGAAAATTAGATGTCTAATGTGTCTTAAACAGAGGGCGACTCTAAGAACTATTTGACCTACTACAAACGGGCTACCGTTTTCCTGGCCATGGGCAAATCCAAGTCAGCCCTGCCGGATCTGACCCAAGCCATACAGCTCAAGCCAGACTTTCTTGCTGTGAGTTCATTTTTGTTGTTGTAATACAAAATTGAGTTCTATGTGGCAAACAGTATATACACATTTATAGTATGCATATGTTTTCAGGCCAGACTGCAGAGGGGTAATATTCTTCTGAAA[C/T]AAGGAAGTACTCAAGAGGCCAGAGAGGACTTCCAAGCAGTTGTGAGTAAAACCATTCTCTTTTTTCCTAAAGGATAGTTCACACAGAAAGGAAAATTCATCATTTACTCTCCTGCATGTGGTTTTAAGCCTTTACGAGTTTGTCTTCTTTATTTTATTTTATTTTTTTGATAGTATGGACGTTGATCTGTGCCAGCAATCAGCATTCTTTAAAATAGCTTTCTTTAATATATTATTGAAAAAGAAATGATAATGTATGGACTCTTAGTTGGTTCTGAAGATTTACGAGTTTCAAAAGAAACACAAAAGAAGATATTTTAAAGAGTGTTGAGAAACTGATAATCATTGACATCCATAGTAGAAAAACAAATGCTGTGGAAGTCAGTGGTCACTGGTTACCTTTTGCTTGTTTTCAACAGAAGAAAGAAATCCACACTTGTTTTAAAACATATTTATAGCATGCATTAAAAATTTTCTGTTGGATGTTATGAGCTTATTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31565
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 |
|---|---|---|---|---|---|
| ENSDART00000026098 | Nonsense | 168 | 500 | 5 | 12 |
The following transcripts of ENSDARG00000017874 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 21959336)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 20549772 |
| GRCz11 | 7 | 20789960 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGGCTGATAAGCTGGAGTCTCTCCAGGAAGAGGCGCATGAAGCTCAT[C/T]GACGTGGAGACTGCAGGATTGCTGTCCAGGTGCTGGAGCATGTCATAGAG
Long Flanking Sequence:
ATCAGCATTCTTTAAAATAGCTTTCTTTAATATATTATTGAAAAAGAAATGATAATGTATGGACTCTTAGTTGGTTCTGAAGATTTACGAGTTTCAAAAGAAACACAAAAGAAGATATTTTAAAGAGTGTTGAGAAACTGATAATCATTGACATCCATAGTAGAAAAACAAATGCTGTGGAAGTCAGTGGTCACTGGTTACCTTTTGCTTGTTTTCAACAGAAGAAAGAAATCCACACTTGTTTTAAAACATATTTATAGCATGCATTAAAAATTTTCTGTTGGATGTTATGAGCTTATTACAGTAGGTGCAGCTTCCACCTTCATCCTTAAACCAGATCAGGTTGTTGATGTACTCGGAGCTATCCTCTGATTCCTGCCTCATCTGTTAACCTCTCTATTGTGCAGCTGAATCATTCCCCAGATCATGAGGAGGCACATGATCAGCTCCTGAAGGCTGATAAGCTGGAGTCTCTCCAGGAAGAGGCGCATGAAGCTCAT[C/T]GACGTGGAGACTGCAGGATTGCTGTCCAGGTGCTGGAGCATGTCATAGAGGTGAGTTAGTCTGACATCATAATATATAGCAATAGGACTACAAATATTGCAGGAGAAAAGTCACAAAAAGGAGAAATGCATTTTCAAAAACACAGACAGTTGTCTACATTACAGAAATTGCCATAAAAGTGACCAAAAAGATCCAAATAATAACATTGTGAAGACATTCTAAATCCACGTAGTAACATGTAGAGCATCCAATCACATGCCTAATTACCCTAACTTGTCTAGTTACCCTAATTAATCTTAATAAGGCTTTAAATTGCAATTTAAGCTGTAAATCACAGGGTTTATACAGTCATGGAAAACCCGAAAAAGTCATAGACTTTTGACATGGCATTTTCCAGGCCTGGAAAAGTTTTGGGAAAACAGAAAACCCCACACAGTCTTGAAAAAGTCATGGAAATTAGTTTAACAAATGTCTGTATACTTAAAATTATGGCAGCGCAA
Associated Phenotype:
Not determined