ZMP
hipk2
Ensembl ID:
ZFIN ID:
Description:
homeodomain-interacting protein kinase 2 isoform 2 [Source:RefSeq peptide;Acc:NP_001093455]
Human Orthologue:
HIPK2
Human Description:
homeodomain interacting protein kinase 2 [Source:HGNC Symbol;Acc:14402]
Mouse Orthologue:
Hipk2
Mouse Description:
homeodomain interacting protein kinase 2 Gene [Source:MGI Symbol;Acc:MGI:1314872]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23245 | Nonsense | Available for shipment | Available now |
sa36590 | Nonsense | Available for shipment | Available now |
sa39193 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa23244 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23245
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 |
---|---|---|---|---|---|
ENSDART00000062343 | Nonsense | 81 | 1228 | 2 | 15 |
ENSDART00000090335 | Nonsense | 74 | 1220 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 18 (position 12061033)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 12643762 |
GRCz11 | 18 | 12612480 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGCATCAACGGCGCCAGTCTCCAGGTTTCCAACTCTTCCCTGTCATAC[G/T]AACAGGCCCTACTCTTCCCGGCCGGCTCGGGGCACATTGTTGTGGCCTCA
Long Flanking Sequence:
GTAGAAATGTTCATAAATATATATGCGTATATATGTGGTGAAATCAGTCCAGGTGCTGCCCTGAAGCTGACTCCTTCAACTTTGGTTTCAAGTCTCAACACTGCTGAGCAATCAAATCAAAAGTGTGCAAGGTATTTGTACAGCGGCTATTTTATAAGTTAGCATCTGGACTCTGACTCTATTAAACTGGCCTGCCATGACCTGTAGGATTTTTATTTAAAGCTTATACTCGAGTTTCAATCCAAGTCTCACATTCCCTCTCCCTCTCTCTTCCTTCAGGTATGGCCTCGCAAGTGCAAGTCTTCTCCCCTCACACTCTCCAGTCAAGTGCCTTCTTTAGCGTGAAGAAACTGAAGGTGGAGCAGAGTTGCAACTGGGATATGACAGGGTACGGCACGCACAGCAAGGTCTACAGTCAGAACAGCAAGCAGAGTGTGTCAGTCGCCCCTGTGGGCATCAACGGCGCCAGTCTCCAGGTTTCCAACTCTTCCCTGTCATAC[G/T]AACAGGCCCTACTCTTCCCGGCCGGCTCGGGGCACATTGTTGTGGCCTCAGCCAGCAGCACGTCTGGGGCAGCTGGTCAACTGTTGGGCAGCACTGGTAGCAGCGGAAGCGGCAGCGGAGGCCATAACCTGACGCGCCGCAGCACCGTCAGTCTGCTGGACACCTACCAGCGATGCGGGCTTAAGCGCAAAAGTGAGGAACTTGACAACAACAACGGCAGTGGTAGTGGGAGTAGTGTGCATGTGGTTGAGGAGCAGCAGCCGCCGGCACCCATGATCCAGAACAACGTGCAGAGCGGGGCCACCGTCGCGACCGCGACTGCCTCCACCACGGCCACATCCAAGAACAGTGGAGCCAACAGCGAGGGCGACTATCAGCTCCTACAACATGAAGTGCTGTGCTCCATGACCAACACCTACGAGGTGCTGGAGTTCCTGGGTCGAGGGACGTTCGGGCAAGTGGTGAAGTGCTGGAAACGGGGCACCAGTGAGATCGTGGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36590
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062343 | Nonsense | 279 | 1228 | 2 | 15 |
ENSDART00000090335 | Nonsense | 272 | 1220 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 18 (position 12060437)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 12643166 |
GRCz11 | 18 | 12611884 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGAGGTGAGCATACTGGCACGGCTGAGCACGGAGAGTGCGGACGACTA[C/A]AACTTTGTTCGAGCGTACGAGTGCTTCCAGCACAAGAACCACACGTGCCT
Long Flanking Sequence:
GGTAGCAGCGGAAGCGGCAGCGGAGGCCATAACCTGACGCGCCGCAGCACCGTCAGTCTGCTGGACACCTACCAGCGATGCGGGCTTAAGCGCAAAAGTGAGGAACTTGACAACAACAACGGCAGTGGTAGTGGGAGTAGTGTGCATGTGGTTGAGGAGCAGCAGCCGCCGGCACCCATGATCCAGAACAACGTGCAGAGCGGGGCCACCGTCGCGACCGCGACTGCCTCCACCACGGCCACATCCAAGAACAGTGGAGCCAACAGCGAGGGCGACTATCAGCTCCTACAACATGAAGTGCTGTGCTCCATGACCAACACCTACGAGGTGCTGGAGTTCCTGGGTCGAGGGACGTTCGGGCAAGTGGTGAAGTGCTGGAAACGGGGCACCAGTGAGATCGTGGCCATCAAGATCCTGAAGAACCACCCTTCCTATGCGAGGCAGGGCCAGATTGAGGTGAGCATACTGGCACGGCTGAGCACGGAGAGTGCGGACGACTA[C/A]AACTTTGTTCGAGCGTACGAGTGCTTCCAGCACAAGAACCACACGTGCCTGGTCTTCGAGATGTTGGAGCAGAACCTCTACGACTTCCTCAAACAGAACAAGTTCAGCCCGTTGCCGCTCAAGTACATCCGACCGATCCTGCAGCAGGTCGCCACTGCCCTGATGAAGCTCAAGAGCCTAGGACTGATCCACGCTGACTTGAAGCCTGAGAACATCATGCTTGTAGACCCAGCCCGCCAACCCTACAGGGTCAAGGTGATCGACTTCGGATCTGCTAGTCACGTCTCCAAAGCGGTGTGCTCCACCTACCTGCAATCTAGATACTATAGGTAAGGTGCTGATCTTGTCATCCCTTTATCAGAATCATTGCTTTGTTTTGGTTTCTGAATGGATATTTTGGCTGGATCAAGATTCTTGTGCCTCATAGATATTTACATTAGATGTCACCTACGCTATTGTTGCCTATTGGAAGGATTGCATTAGAGCTGCACAATTAATCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39193
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062343 | Essential Splice Site | 430 | 1228 | 3 | 15 |
ENSDART00000090335 | Essential Splice Site | 423 | 1220 | 2 | 14 |
Genomic Location (Zv9):
Chromosome 18 (position 11967240)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 12549969 |
GRCz11 | 18 | 12518687 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTGTTTTTGGGATGGCCTCTTTATCCCGGAGCATCAGAGTATGACCAG[G/A]TAACACACTCAGCTACTTCTTTAATGCATTATAATAAAGGCGCAAGTTGA
Long Flanking Sequence:
GGTAATTATTTATTTTTTATATTAGGTTTTATTTTATATTTTTTGTACTATTTAACTATTTTTTATTTTGTTTAAATGTACTATTATTTTTATTGTATTGTTTTCTTTAAATTTAATTTAATTTCTCTTCTTTTTTATTAATTTCATTATATTTTATTTTATTTTTTATACTTTATTACATTGTATTTTTATCTTTTTACTTAATTGAACTATTATTATCATTTTTATTTTACTAATTTTCTCAAATAATTTTTTAGATTTTATTTTACTTTACTTTATTCATTAATGCACCAAACTGATTCACTTTATCTGCATAATTCTTGACTTGTTTTTTGCTGTTGAAGCTTATCCTCTTCCTGTATATGTGTGTCTGCAGGGCTCCAGAGATCATCCTGGGTCTGCCGTTCTGCGAGGCCATAGACATGTGGTCTTTGGGTTGTGTGATCGCTGAACTGTTTTTGGGATGGCCTCTTTATCCCGGAGCATCAGAGTATGACCAG[G/A]TAACACACTCAGCTACTTCTTTAATGCATTATAATAAAGGCGCAAGTTGAGCTTTAAACATGCACCGGCATCTACCATACCTCTATTTTAGGGAATTTTGTTGTACTTTATCCTTGCTGTTCCCATGCGGCTGTTACCAGGGAATGGATCGGTACACCTGAGACACCAGCTTCTGCCCAAACATTCCCTTGATCCCCTGTGCAACATAAAAATAGAAACAAAACAAGATAGATATGACTTGTTACTGTATATACAGTACACTGTGGTTCAGAGGTTTCACATCAGGAGGTTGTTTGTAAGAATTGTGTGCCCTTATTGAGCAGGAATGCATTAATTTGATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTATATTTATTTATTTATTTATTTATTTATTTATTTATTTATTCATTTATTTACAGTACTAACAGAGCTTTTTCCCCAGGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23244
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 |
---|---|---|---|---|---|
ENSDART00000062343 | Nonsense | 768 | 1228 | 10 | 15 |
ENSDART00000090335 | Nonsense | 761 | 1220 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 18 (position 11924339)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 12507068 |
GRCz11 | 18 | 12475786 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACTTCAGTGCAACACGCCACCGTCATCCCAGACTCCATGACCAGCTCA[C/T]AGCCTCTGGCTAACTGGAGGTGAGACAGCACTACATCAATTTGACTGTCC
Long Flanking Sequence:
CTTGAATCTAGGCCCAAATGCTGACGCTACGGTCTCTTAAATAACTAAATGACCCCTTTGGTGGTTGTTTGGCACAGTTTAGCACTTACTAGCGGTCATTTCTCTAAATAGCCGTATCCTTTTTCTCCTCTCTCTAAATATGTGGCTCCAGTACCCTGGCCTGTTTAGCTGCATAGCCATATGATGCAGCAGGTTAACGTTCAGGGTCTTCACACTGATGCCAATTAAATCACACGAGTCCATTTAGGAGTCCATTATAGTAGCCAGTAGACATTCATATACTGGATCGCATAAGCTCTCCTATCTGTAGATTTTTGACCTTCTGCTGGATATGAATCTCTGACCTCTGTATGCTAACCCTGTGTTTTTCCTTCATTCTGACCTTGCAGCAGGCCTGGCCATCTGGTACTCAACAGATTCTCCTTCCTCCAGCGTGGCAGCAGCTCACACACACTTCAGTGCAACACGCCACCGTCATCCCAGACTCCATGACCAGCTCA[C/T]AGCCTCTGGCTAACTGGAGGTGAGACAGCACTACATCAATTTGACTGTCCACCATTGCCTTTCGGTTTTGAGAAAGCGTTATTATTTTTAAAATAGAGTGCAAATTAGTTCTTCAGTCATTTTCTCTTTTGGAAATTGATTTTTAACAGTGACTAATAAACTGTTGAAGAAGGGCCTATTGTGAGCTCTGATATTGTCAATCGATTGTACATGCTTTTGTTGTGTAATAGTGGAATTTGTGCTGAAAATTTGCAGAAAATTCCCCAATCTGAGAGAAAGCCTGTCAGTCATTTTTTAGCTCCACCCACTCCCCCCAAAAAAATCTAAATACATACAGCCATGAAAACAATTCTGGTTAAATAAAAACTTGTGGATTTTTTAGGTTCAGGTAAAGCTTGACCCTTGACCACAAAACCAGTAATAAGGATCTTCTTATGGAAATTGAGATTTATACATTTTATATAAGCTGTAAAAATAATGTTTTGATAGTATATGATCAT
Associated Phenotype:
Not determined