ZMP
si:dkey-261h15.1
Ensembl ID:
ZFIN ID:
Description:
homeodomain interacting protein kinase 3-like [Source:RefSeq peptide;Acc:NP_001073628]
Human Orthologue:
HIPK3
Human Description:
homeodomain interacting protein kinase 3 [Source:HGNC Symbol;Acc:4915]
Mouse Orthologue:
Hipk3
Mouse Description:
homeodomain interacting protein kinase 3 Gene [Source:MGI Symbol;Acc:MGI:1314882]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10340 | Nonsense | Available for shipment | Available now |
sa23319 | Essential Splice Site | Available for shipment | Available now |
sa14412 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10340
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 |
---|---|---|---|---|---|
ENSDART00000089303 | Nonsense | 294 | 1261 | 1 | 16 |
ENSDART00000124046 | Nonsense | 294 | 341 | 2 | 2 |
ENSDART00000126500 | Nonsense | 294 | 348 | 1 | 2 |
ENSDART00000142336 | Nonsense | 294 | 1261 | 2 | 16 |
Genomic Location (Zv9):
Chromosome 18 (position 27876626)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 27949478 |
GRCz11 | 18 | 27927718 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGTGGCAGTGAAGATCCTGAAGAATCATCCATCATATGCACGGCAGGGG[C/T]AGATTGAGGTGGGCATCCTGGCCCGCCTGAGCAATGAGAATGCCGATGAG
Long Flanking Sequence:
CTGGAAGGGGAAGGGGAGTGGGAAGCGACAGTCAAGAAGAAGGAGGTGGAGGACAGGGTGGAGTTGACGAAGGAGGTGGAGGAGAGGACGAGGGTGACCAGGAAGACTGTGGAGGTTTTGACTTGAATGACAGCTCCCACAGATGTGGGCTGAAACGTAAGAGCGGGGAGCTTGAGAACTTGGGGAGCACCATGCAGATTGTTGAGGACCTGTCAATGTTACCCGCAATGTTGCAATCAAATGTGGGAAATCCACCTGTTGCGGTTCCACAGGCAGTTGGCGGAGGGCCTGCAAAGCAAGGTGGAGGTTCAGGAAATGGGGATGGAGATTACCAGTTGGTGCAGCATGAGATGCTTTGCTCGTTGAAGAACACCTATGAGGTATTAGACTTCCTTGGTCGTGGTACTTTCGGCCAGGTTGTAAAATGCTGGAAACGAGGCACCAAAGACATTGTGGCAGTGAAGATCCTGAAGAATCATCCATCATATGCACGGCAGGGG[C/T]AGATTGAGGTGGGCATCCTGGCCCGCCTGAGCAATGAGAATGCCGATGAGCATAATTTAGTGCGGGCTTTTGAGTGTTTCCAGCACCGGAGCCACACCTGCCTCGTGTTTGAGATGCTGGAGCAGAACTTGTATGACTTCCTCAAGCAAAATAAATTCAGCCCATTACCTCTGAAGGTGATTCGTCCCATTCTTCAGCAGGTGGCCACGGCACTAAAAAAGTTGAAGGGAATGGGACTGATCCACGCAGACCTGAAGCCTGAGAACATCATGCTGGTGGACCCTGTACGGCAGCCCTACCGTGTGAAAGTCATAGACTTTGGCTCAGCAAGTCACGTGTCCAAAGCAGTCTGCTCAACGTACCTCCAGTCACGGTACTACAGGTATGTACAAACCCCATGACGGCTGAAATGCAAAAGTGAAATTATGGAATTCAACAATGTCCATTGTTCAGTTATTTGCACTTTTTAATATTTTTGTCCAGTAGATACAACCAAGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23319
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089303 | None | 344 | 1261 | 1 | 16 |
ENSDART00000124046 | None | None | 341 | None | 2 |
ENSDART00000126500 | Essential Splice Site | 344 | 348 | None | 2 |
ENSDART00000142336 | None | 344 | 1261 | 2 | 16 |
Genomic Location (Zv9):
Chromosome 18 (position 27876778)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 27949630 |
GRCz11 | 18 | 27927870 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCGTGTTTGAGATGCTGGAGCAGAACTTGTATGACTTCCTCAAGCAAAA[T/C]AAATTCAGCCCATTACCTCTGAAGGTGATTCGTCCCATTCTTCAGCAGGT
Long Flanking Sequence:
AAACGTAAGAGCGGGGAGCTTGAGAACTTGGGGAGCACCATGCAGATTGTTGAGGACCTGTCAATGTTACCCGCAATGTTGCAATCAAATGTGGGAAATCCACCTGTTGCGGTTCCACAGGCAGTTGGCGGAGGGCCTGCAAAGCAAGGTGGAGGTTCAGGAAATGGGGATGGAGATTACCAGTTGGTGCAGCATGAGATGCTTTGCTCGTTGAAGAACACCTATGAGGTATTAGACTTCCTTGGTCGTGGTACTTTCGGCCAGGTTGTAAAATGCTGGAAACGAGGCACCAAAGACATTGTGGCAGTGAAGATCCTGAAGAATCATCCATCATATGCACGGCAGGGGCAGATTGAGGTGGGCATCCTGGCCCGCCTGAGCAATGAGAATGCCGATGAGCATAATTTAGTGCGGGCTTTTGAGTGTTTCCAGCACCGGAGCCACACCTGCCTCGTGTTTGAGATGCTGGAGCAGAACTTGTATGACTTCCTCAAGCAAAA[T/C]AAATTCAGCCCATTACCTCTGAAGGTGATTCGTCCCATTCTTCAGCAGGTGGCCACGGCACTAAAAAAGTTGAAGGGAATGGGACTGATCCACGCAGACCTGAAGCCTGAGAACATCATGCTGGTGGACCCTGTACGGCAGCCCTACCGTGTGAAAGTCATAGACTTTGGCTCAGCAAGTCACGTGTCCAAAGCAGTCTGCTCAACGTACCTCCAGTCACGGTACTACAGGTATGTACAAACCCCATGACGGCTGAAATGCAAAAGTGAAATTATGGAATTCAACAATGTCCATTGTTCAGTTATTTGCACTTTTTAATATTTTTGTCCAGTAGATACAACCAAGTTTAACAGAATTGTTTTATTTGTGTGGAAATTTCTGCAAAAAGTACTCTAAAGCACATTATTCTTTCTTACCATCAGATCGCTGAAAACATTCTAGAATTTTCCCTCTCTGTGTATGTTATACAACTAAAGTCCTTACGGAATTAGCAGTCAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14412
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
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089303 | Essential Splice Site | 532 | 1261 | 5 | 16 |
ENSDART00000124046 | None | None | 341 | None | 2 |
ENSDART00000126500 | None | None | 348 | None | 2 |
ENSDART00000142336 | Essential Splice Site | 532 | 1261 | 6 | 16 |
Genomic Location (Zv9):
Chromosome 18 (position 27919029)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 27991881 |
GRCz11 | 18 | 27970121 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACATTGGAGGMCTCCATATGAATAATTAAAGTAGCTTATTTCTGTTTTC[A/T]GGTGAAWCTAGTGATGAATCTGGAAKGCTGTGATTTGTTGGCAGAGAAGG
Long Flanking Sequence:
TGAGAATTGTGGCGATGTCCAAATACTTATGGACCTAACGGTTTCAAATATCGCAAAGCTCTAAAGTAAATGTCTATATAACTTTGATCAATTCTCTTATCTTTAAAAAGAGACGAACAACTAATTCTTACTGACACCTAAACTTTTGAATCGTGCATATTATATTGACAGTTCTTTACAATTTAAAAACCTTCACTATACAAAAAATGTGGTATTAAACAATGCATTATAAATAAAAAAGCAGATAAGTAAAACATAATAATTGCACTACACCTTAAATGATTAATCCAGTGAAACATAATTGTAAGGAATGTTCAGAAATGGTAACACTTTAGTATGCAGACCAGAAGTCATAGATAATAAAAGATGTAGTCAATAATGAATGTGTTCTCTATACTGAAGTGTTGTTTAACTTTATTTGTTGTCTCCTTTTCTTTCTGTGTGTGCAGACACATTGGAGGACTCCATATGAATAATTAAAGTAGCTTATTTCTGTTTTC[A/T]GGTGAATCTAGTGATGAATCTGGAAGGCTGTGATTTGTTGGCAGAGAAGGTTGATCGTGCAGAGTTTGTGGCTTTGCTGAAGAAGATGTTGTTAATAGATGCAGAGGAAAGAATCGCCCCGAGTGATGCTCTTAGCCATCCTTTCGTTACCATGCAGCACCTGCTAGACTTTCCACACAGCAACCAGTGAGCGACTCATGTTTCTTCAACTTCAATTCATTCATGCTGATTCTTAGCACTTTGACAAACAGAGGTTTTATGTTCTAAACTCTCTCTCTTCACAGTGTCAAATCATGTTTTCACATCATGGATGTTTGCTGCTCACGACCAGGCAGTTATGAGTCTCACAGTCGGACCAAGGCTCAGTTTGTCAGGACAGTCCCGAGCACTGGTGCTGCATCCAACCTCACCCTGCCCTTCTGCAAGGTGACTGGCATTCACACTCAGGTACTGAAAGCTTCTGCATTAGGTGTGTAGCAATACAACATAATATCAGAAGT
Associated Phenotype:
Not determined