ZMP
si:dkey-229p15.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
HIPK1
Human Description:
homeodomain interacting protein kinase 1 [Source:HGNC Symbol;Acc:19006]
Mouse Orthologue:
Hipk1
Mouse Description:
homeodomain interacting protein kinase 1 Gene [Source:MGI Symbol;Acc:MGI:1314873]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24388 | Nonsense | Available for shipment | Available now |
sa37769 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11661 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24388
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 |
---|---|---|---|---|---|
ENSDART00000093061 | Nonsense | 213 | 1124 | 1 | 16 |
ENSDART00000134061 | Nonsense | 213 | 700 | 1 | 9 |
ENSDART00000142305 | None | None | 89 | None | 2 |
Genomic Location (Zv9):
Chromosome 23 (position 36953057)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 36734867 |
GRCz11 | 23 | 36857328 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGTCTCCAACAGCTACGAGGTCCTGGAGTTCCTTGGCCGGGGAACTTTC[G/T]GACAGGTCGCCAAATGCTGGAAGCGGGGAACCAATGAGATCGTGGCCATT
Long Flanking Sequence:
GCCCCAGCCAAACCAACGGTTCCTCTCCTTCCACATCTGGATTCAACCCCAGCTACAACTCCTCCAGCCTGGTGTTTCCTCCACCCGGAGCATCGAGGGAGCAGACGGTGGTCCGCGCGGCGGACAGCACCGGCAGTGGCCCGGAGCCTTCATCATCCTCCTCATCATCATCCACATCCAGCCACCGCGGAAAAGATGCGAGATCTAATTCTCTGACTTGCGAGGGCTATCAGAAACGGGCCAGTCTGAAGCGGAAGAGCGAGGAGGTGGACAGTAGTGACAGCGTGCAGATTTTGGAAGAGCTTTCAGCGCCTGTGCTCCCCAACCGCGTAGCCGGAGGTGGAGGAAACGCCACGGCTCAGTCCATCGCTCATTCCACGTCCACCACCAAAAGCAGCAACTCCCACAGCGAGGGCGACTACCAGCTGGTGCAGCACGAGATCCTCTGCTCCGTCTCCAACAGCTACGAGGTCCTGGAGTTCCTTGGCCGGGGAACTTTC[G/T]GACAGGTCGCCAAATGCTGGAAGCGGGGAACCAATGAGATCGTGGCCATTAAGATCCTCAAGAATCATCCTTCGTATGCGCGCCAGGGTCAGATAGAGGTGAGCTGTTAACTAGTGTAGGAAATGTGTAATTTCAGATCAAGTCCACACGTACATTTTCCATGCCTTCGTATTTAAAAAACCTCTATTGACATGACAATGCAAAAGCTCACTAAGATGCATGTTATAGTTACGCTAAACCAACAGGTGGAGATGATAACACTTTTATACTAGGTTCACAACAAACTGGGAATTTAGTATTATTGTGGGTAAATTGCATACAAGTCAATGCAAAGTGCGAACAGATGCGCATTACTATTGCGTGAATGAACAATGAGGAACATGCCTTGCGTTTGGCATAAACATCAGAAATTTGCCTCATTTATTTCTTCTGTGTTTGATGTGAACCCAGCCATGTTGACCAGGTAACGAGAAAACAAAGCACAAAGGCAGAACATTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37769
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 |
---|---|---|---|---|---|
ENSDART00000093061 | Nonsense | 402 | 1124 | 3 | 16 |
ENSDART00000134061 | Nonsense | 402 | 700 | 3 | 9 |
ENSDART00000142305 | None | None | 89 | None | 2 |
Genomic Location (Zv9):
Chromosome 23 (position 36947597)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 36729407 |
GRCz11 | 23 | 36851868 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGTGGTCTCTGGGTTGTGTCATTGCTGAACTGTTCCTGGGCTGGCCTT[T/A]GTATCCAGGAGCTTCAGAATACGATCAGGTCAGTAATAAGATTTGGTTTG
Long Flanking Sequence:
TAAATGGCTTTTTTTTTTTGTCAATTTATGCAAAAAAAAAGGCCATATTTTTAATCAAAATTTTGAAGAATTGTCATGAATAGTTAAAAATGTAGAACTATAAAATGTGAATCCCGAGCAACTTACGTTGGTCTCTTAATTATTTTTTCCATGCCAATATATGGTATCAGATTTTTAGGCGTCAATATTAGATTTCAAAATAAATAAACCATCAAGTATATAAATACACACGAAATAAAGTTAGAAAATACTTTTATAAATTGTGTTTTCAAACTGAATTGAAAATATATAAGATAAATTACGAACAGACAAACTCGTGCATCATGTGCGTCTTTGTCTTTTATATTACGAAAGGAAATCTGCGGTATGAAATAATTGTATTATAATTCGTCTGTTGTGACGCAGAGCTCCAGAGATCATTCTGGGCCTTCCGTTCTGTGAGGCCATTGACATGTGGTCTCTGGGTTGTGTCATTGCTGAACTGTTCCTGGGCTGGCCTT[T/A]GTATCCAGGAGCTTCAGAATACGATCAGGTCAGTAATAAGATTTGGTTTGATTTAATTGAATCAGTCCTGTGCAAAGAATTGATTAGATTTGCATAATTCAATTGGGAAAGCTAGACGTGAAAAGTGACACAAGGGGGCGCCTACACTTCTGCTCTCTAAATGACAAATATTGGCTTATATTTTAGTGTATTAATAGAAAATACACTAGCAATCAAATGTTTAGGATCAGGAAGGCTTTTAAATTGTTTTAGCCTATTCTGCTCACCAAACCTGTATTTATTTGGTTTTATTTAAATCTGTGAAATTCTGAAATAATATTAAAATAACTTTCACTTAATAAAAAAAAAAAAATTAATGTTATTAAATTAAATGTAATTATTAAATGTAATTTATTCCTGCAATTTAAAACGTAATTTTCAGCAGCATTACTCCAGTCTTCAGTGTCACATGATCCTCCTGGCATAATTCTTACATGATGATCTGCTGCTCTAGAAACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11661
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 |
---|---|---|---|---|---|
ENSDART00000093061 | Essential Splice Site | 739 | 1124 | 10 | 16 |
ENSDART00000134061 | None | None | 700 | None | 9 |
ENSDART00000142305 | None | None | 89 | None | 2 |
Genomic Location (Zv9):
Chromosome 23 (position 36934001)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 36715811 |
GRCz11 | 23 | 36838272 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCGCTGACCCTCAGCTCTCGCCATCTGGAGCAGAGTGCCACAATGCTGG[T/C]AAACCTGTGTCCTGCCAACCAGATAAACCTGTTTCTCTTTCTTTCTGCCA
Long Flanking Sequence:
AGAAGATATTTTGAAGAATGACACCTGTAACCATTGACTTCCATAATAGGGAAAAAATGCTCTTCCATAGAGCATTTTCCCACCCAAAAAATGAAATCCCAAATGCCCAAAATATCAAAATTAACATGTGCATGACAAAAACAGTGTATTTGCCCACAGTGTTTCACCTTAATTGGTGACTCGGAAAGACTCTGAAAAGAAGAGGGTGGGATTTCAACAGAAGTCAGTAGGTTGGTGCCTCTACTGTCATATTGGTCTGTTTTTGTACTTGATGTTGCTTTTCTGCATTTACATCAATGATGGTGGGTCTTGGCGAGAAGTGTCTCCATCAGTTCAGCCGGCGTGTTGTTAACCGTGCCACCCTTTCCTCCATCCTCAGTTCCTCCACACATCCCTCTATCCCTTCCCCAACCAGAGCAACAGCAGCAGCACTCCTCTGACCCTGCGCCTCCCGCTGACCCTCAGCTCTCGCCATCTGGAGCAGAGTGCCACAATGCTGG[T/C]AAACCTGTGTCCTGCCAACCAGATAAACCTGTTTCTCTTTCTTTCTGCCACCTATTTGCCTTGCTGCATGCTGCAATTCTGGGTCAAATCCTGAACTGAAAGAGTTACGAACAAAAAATGAAGTGACTACAAAAGTGACTATGTAATCATCAGTAATCTACTAAGAATATCAGGACTACGGACATCAGTAATCAAATTATTTACCTTAATCTAAATAAGGCAATATCATGATTAAGATTGATTATGATTGCTTACATGAGTTGCTTTAAAAATGTTCCTTTCATGATTTTTAAATTTTTCGACTTTAACTGCAGTTTAGCAGTTTCACTTTTATTCAGCAACGTTTCATTCATGTCCCTGTGTCAAACTGAGGTGTTGGATACGAGTATGAAGTTAGAACTGGTAGGAAAGGGGTTGTTTTAATGGAAAAAACACTGTCTGTGGTCCTTTACTGACTGCAATGTAGGTGCAGAGAATAGTGTCAAACAGCGTTTGTGTGG
Associated Phenotype:
Not determined