ZMP
zgc:86598
Ensembl ID:
ZFIN ID:
Description:
casein kinase II alpha 1 subunit [Source:RefSeq peptide;Acc:NP_001002164]
Human Orthologue:
CSNK2A1
Human Description:
casein kinase 2, alpha 1 polypeptide [Source:HGNC Symbol;Acc:2457]
Mouse Orthologue:
Csnk2a1
Mouse Description:
casein kinase 2, alpha 1 polypeptide Gene [Source:MGI Symbol;Acc:MGI:88543]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11456 | Essential Splice Site | Available for shipment | Available now |
sa7459 | Missense | Mutation detected in F1 DNA | Not yet available |
sa36759 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32228 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11456
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 |
---|---|---|---|---|---|
ENSDART00000020344 | Essential Splice Site | 122 | 393 | 6 | 14 |
ENSDART00000125504 | None | None | 105 | None | 6 |
Genomic Location (Zv9):
Chromosome 19 (position 3784655)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 3281228 |
GRCz11 | 19 | 3222126 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCGAACTCCGGCTCTGGTTTTTGAAMATGTGAACAACACAGACTTCAAGG[T/C]AAAKCACTTTAAATCTACCTCAGCTTATTGCATGATGAAATWAARCTCAA
Long Flanking Sequence:
GCGTTTTTTTTTATTTTTTTTTATACCGTGCCAACTTTTTCTGATTTGGGATTGTATAAATATTATCGTTTTTTATTTAATAGCTACATTTAACACATCCATATCCACAATGTTCAACTTTAAAATGCGATTGTACAGTAGTTAAAGGTGTTGCTATCGCATTGTTTACTTTTAATGATTTTGTTCTTTGTTTCCATCTTTGTTTCCAAACACAGCCAGTAAAGAAGAAGAAAATCAAGCGAGAAATCAAAATTTTGGAGAATTTGAGAGGCGGCCCCAACATTATCACACTTCTAGACATTATCAAAGATCCAGTGGTCAGTTGGCTTTCTCTCAGTATAAAACTGCACTTGAAACACAGCATTTGAAATCAACTGTGTGCACATACTTCTTTAAAATAGGTTTCAAATATGTGTCTGACTGAAGTCTTTTATGTTTCTCCCTGAAGTCTCGAACTCCGGCTCTGGTTTTTGAACATGTGAACAACACAGACTTCAAGG[T/C]AAATCACTTTAAATCTACCTCAGCTTATTGCATGATGAAATAAAACTCAATTCACTCATGTTGTTGTTCTGTTGTGCAGCAATTGTATCAAACACTATCAGACTACGACATTCGGTTCTACATGTACGAGATCCTAAAGGTAAGTTCTTTCAGATATCATCTTAAATCCATTCACAGAAATTAAACGATTTTTGTTTTTGTTTTTTAAATAAATTTCCAATATTCCAAGTATCTTTCCCACTTTACTAAATTTGAGTCATTGATGCTGACATTTTGGATCCGAGTCAGCCGGTTTTTATTTTGCCACTTTCAGTTGTACAAACGTTACGCACTTTGCCTTTAAGTGCTACTGAAAGATCTTATTGCTTGCATTTTTAGGCCTGTGTACATGCGGTAAAAAGTGCATTTTTGCATGTGATGTCAAGTTAATAAGGGTAAATGCTGGTTTAAATGGCAGTTTCTGAAATGTTTTGAGCCTGTTTACATTCAACAACTTCTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7459
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020344 | Missense | 164 | 393 | 8 | 14 |
ENSDART00000125504 | None | None | 105 | None | 6 |
Genomic Location (Zv9):
Chromosome 19 (position 3787818)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 3284391 |
GRCz11 | 19 | 3225289 |
KASP Assay ID:
554-4133.1 (used for ordering genotyping assays)
KASP Sequence:
CCACAGTATGGGGATCATGCACAGAGACGTGAAGCCACACAACGTCATGA[T/A]CGACCATGAACACAGAAAGGTACTGTTCTCCTGCAGTTCACGCCATTACC
Long Flanking Sequence:
TACCTTCACCACTCATGCTATACTGCGTTTCCCTCACTTTGTCATTGACTCCCAGTTGTACACTGTAAAATGTTATTTGATATATTGTAATGCAGTTTAGTATGTAATGTATTCCTGAAATTTGTATTTTCAGTATTGTTTTCCACTCTTCTGTGCTATATGATTCATCAAAAATCATTGATATGATTTAATGTCAAGAAAAATGTTGTTGTTCTATAATAAAAACATTGAAAGTTTTCATTCAAATTTAGTTTACATTTTGTTTTCCCAATAACTTTTGAATTTAAATGTATTTTCTTTAAATTTTTAAAGATGTCTTCTAAAGATAACTCTTATTTTTATAAATATATCGGTTTAATAAAACCGATATATAATAATATTTTGTTTAAAAGCTGTCTGTGTAGTGTGTTTTTAAGCGTCTGTGTGTTTCTCTCAGGCGTTGGATTACTGCCACAGTATGGGGATCATGCACAGAGACGTGAAGCCACACAACGTCATGA[T/A]CGACCATGAACACAGAAAGGTACTGTTCTCCTGCAGTTCACGCCATTACCCTCCTCACATCTGATTGGCTGGACACTCCATGCAATCTTAATTCTAAATCATCGCAATTTGCATGTTTATTGAACTCATGACAATCGCTGTCGTACATTCAAATCAGTCATCATCTGTGGTTAAAACATGTTCAGGGTTTAGTCTTTTCAACGCTGATTTCTATGGTTGTCATCAATCCATTTTTAAAAGCACCTTGATGCTTCAAATGAGAAACTTATGTTTTTTTTTGTCTGTTCAGATGTTTGTTTTTTTGTATTTATTATGTTTGTATTATTCTGAAGTGCTTTGCCCAGAAGATAGCCAATGTTGCTCACATGACGTTAAATAGAAGATGCAATGTGATACATCAAATAGAAAATTTATAATAAAAAATAATAAAAAATATGCATGTATACATACATATTATAATTATAATAATTATTATTATTATTATTATTATTATTATTTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36759
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020344 | Nonsense | 307 | 393 | 12 | 14 |
ENSDART00000125504 | None | None | 105 | None | 6 |
Genomic Location (Zv9):
Chromosome 19 (position 3792915)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 3289488 |
GRCz11 | 19 | 3230386 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCTGGTGAGCACTGAAGCTCTGGACTTCCTGGATAAACTCCTGCGCTA[C/A]GACCACCAGGCCCGACTGACTGCCCGCGAGGCCATGGAGCACCCTTACTT
Long Flanking Sequence:
TTTTTTTTTTTCATGTTTTAATATCTCAAAAACATCCTTTTCTTTCTTCTTTGTTGATCATATTTCTTTCCTGTTATATTTGGAAAGCTTTTTTTGCTCAAAGTTTACTGCATGCTTTCCTTTGTCTGGATGATAGTTTGTAGTGTTATAGCAAGTAAACATCAGCAGCTTCAAATTAAATATTTTTTACTCCATATTGGCACTTTCTTCTTCTATTATAATCATACTATATGAGTAATTAAAGCCTAATGTATTCAAATATTGTAAATAAAATTTTGATAAAATTTAAATAAATCTTGTTTCTAAAGGCACTTCTTACTAAAATTATGAATTACTTTTTAAATTATTACTATTTTCTTGCCCTGTGTGTATTTCTGCTGAACTGTGCTTTCTTTTCCCTCCAGACATTCCCGGAAGCGGTGGGAGCGGTTTGTGCACAGTGAGAACCAGCATCTGGTGAGCACTGAAGCTCTGGACTTCCTGGATAAACTCCTGCGCTA[C/A]GACCACCAGGCCCGACTGACTGCCCGCGAGGCCATGGAGCACCCTTACTTCTGTCAGTTTCTGCTCTCTCTGACTGACTGTCTAGATCAACATCAACTTTTGGCATCTGTAACACCGCTTAGCACCTGCAAAAGATTTTCTAAATCAATAAGAGGGTTTTAGGGTCTTAATTTGTTAAGAAAAATCCTTATTTTGTGTTTGACTGTTTTGCTAATCCCATTTTATGTAGCAGTTTAATGTAGTATTCAGAGTTTAATCAAAATGTTTTACAATTATTTATAAAACAAAAATCCAAACGACTTAAGTTTTTATGTCCCTTTAAAGGGATGGTTCACCCCAAAATTAAAATGTACTCACTTTTCACTCTCCGTCAAGTAGTGCCAAATTATTCCGGTTTTATTTCATCTGTTAAATACAAAAGAAGATATTTTGAAGAATGCTGAAAACCTGTAACCATTCACTTCCATTGAGAAAAAACTAATACTATGGAAATCAGTGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32228
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 |
---|---|---|---|---|---|
ENSDART00000020344 | Nonsense | 392 | 393 | 14 | 14 |
ENSDART00000125504 | None | None | 105 | None | 6 |
Genomic Location (Zv9):
Chromosome 19 (position 3794947)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 3291520 |
GRCz11 | 19 | 3232418 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCGTCTCCCAGTGCTCTCGCCACACAGGTTCCTGCCGCCGCCGGAGCG[C/T]AGCCCTGAACCTCCGTCTCTCTGCCCTGGCCCACAGTACACTAACCAGAC
Long Flanking Sequence:
AATTGTCATTTAATTCTATGATTTAAAGTTTCATAAATCATTCTAATGTGATGATCTGAAAATCAGGAGTTTTCCTTCTTTATAAATGCATAAATATTTGTAATATTTAATTTTATTATAAATAAAACATTAAAAGTAATATAGTCTTTTTTTGTCAATGTAATCAGTGTAATGCATCTTTGCTACAAAATGTTTAGTTTTTTTTACAAAAACCCAACACTTTGAATGGTAGGTTGTTTGTTCGGATTTTTAAAAAAAACCTTATTATATACCATAAACCAACAAAAAACTGTTTAATTACTACAACACATTTTGTGAAACCTGCAGAAACCCTATGAATTGACATTTCTCTTCTGAACGTGTGTGTGTGTGTGTGTTTGTGTCCAGCAGGAGGCGTCACGTCTCTGTCGTCGTCTCAGCCGATGGCCAACATGGCGGGTTCTCCAGTCATCTCGTCTCCCAGTGCTCTCGCCACACAGGTTCCTGCCGCCGCCGGAGCG[C/T]AGCCCTGAACCTCCGTCTCTCTGCCCTGGCCCACAGTACACTAACCAGACACAGAGACTCACTTAGCTTTCTTTCGTTTTTCTCTTTTTTTTCTCTCTTTTCATTTCTTTTTTTCCATACAATAATTATATATTGAAGCTCGGACACACAGCAGACAGTTGTTATGTTGCGTCAGTGTCCGGCAGTCTTTCCTGATGATGATGATGATGATGATGATGGTGTCTATATAGAAGCCAATACAGTGTAGAAATTCTGAAAAATGGATAATAAAATTTATTTTATATGTCCCTACTTTGCTTCCGTTTCTATTTAAATAATACAAACTTTTTTTAGCAAGCCTGAAAATGTTTGTCAAATTGGTTCGCCTACTATTTGAGTAGATGCCAGTTTTCAATTTAGGTTTACGACACGACTGTTAGAAAAGTGTGTTGGATACAGGATGAATGTGAGCAGTATGAATGGATTTCTCATGATCATGTGACCTTCCCGCATCAGTTGGT
Associated Phenotype:
Not determined