ZMP
camk2a
Ensembl ID:
ZFIN ID:
Description:
calcium/calmodulin-dependent protein kinase type II subunit alpha [Source:RefSeq peptide;Acc:NP_001
Human Orthologue:
CAMK2A
Human Description:
calcium/calmodulin-dependent protein kinase II alpha [Source:HGNC Symbol;Acc:1460]
Mouse Orthologue:
Camk2a
Mouse Description:
calcium/calmodulin-dependent protein kinase II alpha Gene [Source:MGI Symbol;Acc:MGI:88256]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43723 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa10214 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43723
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 |
---|---|---|---|---|---|
ENSDART00000039571 | Essential Splice Site | 210 | 555 | 6 | 18 |
ENSDART00000039571 | Essential Splice Site | 210 | 555 | 6 | 18 |
Genomic Location (Zv9):
Chromosome 21 (position 42477940)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 43931591 |
GRCz11 | 21 | 43926757 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCTGTACTTCATTGCCATCAGATGGGTGTTGTGCACAGAGACTTAAAG[G/A]TAATTCAGCACTAAAATATGTCTTTAAGCATGTTTTTAGAGCACAATTGT
Long Flanking Sequence:
AATTAAATAATTCATCTATTTTTATTTTTATCATTATCACTATTATTATTATTAGTAGTATTAATTAATCTATTTTATTATTATTATTATTATTTATTTTATCTATTTATTTAATTGTTATTATTATTACTATTATTATTATTAATCTATTTCTTTTATTATTATTATTATTAATATTATTATTATTATTATTGATTATTTTAATTGTATTATTATTATATAGCAGATTTTGCATAAAACAAATGTTGCACATCTAGCCAAACTGCTATGTTTCATTTTTATATCCATATTTCTACAGTAAACAAAAAATAATAATAATTTGACAGGTTTAAATGCACATCTGTTGTGTGTTATTCATGTAAAGTGCAGCAAGTATATTATAACGAATTTAGTTTTTCTTTTTGTCTGTTTCCTTTCCCCCCTAAAGTCACTGCATTCAGCAGATTTTGGAGGCTGTACTTCATTGCCATCAGATGGGTGTTGTGCACAGAGACTTAAAG[G/A]TAATTCAGCACTAAAATATGTCTTTAAGCATGTTTTTAGAGCACAATTGTGATTAAATGATAAAATACAACACCAGTATTTACATTTACATTTAGTCATTTAGCAGACGCTTTTATCCAAAGCGACTTACAAATGAGGACAAGGAAGCAATTTACACAACTAAGAGCAACAATGAATAAGTGCTGTAGGCAAGTTTCAGGTCTGTAAAGTCTAAGAAGGAAAGTATTAGTAATTTTTTAGTAATTTAGTAATTTTTATTATTAATTTTATAATTAATTAGTATTAAATATATCATTAAATATTATTGATTTCACAAAATAAATATACATTTATTAAAGAGTAAATATGCATAAAGCATGCACATCTATTTACATGCTTTTTAAGGGGGCGTTTATAAAGAGAATTCAGCAGGTCTCGACACCGAGCCTTGGAGAACTCTTCAAGCTTTGTAAGATACTTGGCCACTGAACCAGGGAAGTTTATATTGAGTTTATATAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10214
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000039571 | Essential Splice Site | 210 | 555 | 6 | 18 |
ENSDART00000039571 | Essential Splice Site | 210 | 555 | 6 | 18 |
Genomic Location (Zv9):
Chromosome 21 (position 42477940)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 43931591 |
GRCz11 | 21 | 43926757 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGCWGTACTTCATTGCCATCAGATGGGTGTTGTKCACAGAGACTTAAAG[G/T]TAATTCAGCACTANNNNNNNNNNNAAATATGTCTTTAAGCATGTTTTTAGAGCACAATTGT
Long Flanking Sequence:
AATTAAATAATTCATCTATTTTTATTTTTATCATTATCACTATTATTATTATTAGTAGTATTAATTAATCTATTTTATTATTATTATTATTATTTATTTTATCTATTTATTTAATTGTTATTATTATTACTATTATTATTATTAATCTATTTCTTTTATTATTATTATTATTAATATTATTATTATTATTATTGATTATTTTAATTGTATTATTATTATATAGCAGATTTTGCATAAAACAAATGTTGCACATCTAGCCAAACTGCTATGTTTCATTTTTATATCCATATTTCTACAGTAAACAAAAAATAATAATAATTTGACAGGTTTAAATGCACATCTGTTGTGTGTTATTCATGTAAAGTGCAGCAAGTATATTATAACGAATTTAGTTTTTCTTTTTGTCTGTTTCCTTTCCCCCCTAAAGTCACTGCATTCAGCAGATTTTGGAGGCTGTACTTCATTGCCATCAGATGGGTGTTGTGCACAGAGACTTAAAG[G/T]TAATTCAGCACTAAAATATGTCTTTAAGCATGTTTTTAGAGCACAATTGTGATTAAATGATAAAATACAACACCAGTATTTACATTTACATTTAGTCATTTAGCAGACGCTTTTATCCAAAGCGACTTACAAATGAGGACAAGGAAGCAATTTACACAACTAAGAGCAACAATGAATAAGTGCTGTAGGCAAGTTTCAGGTCTGTAAAGTCTAAGAAGGAAAGTATTAGTAATTTTTTAGTAATTTAGTAATTTTTATTATTAATTTTATAATTAATTAGTATTAAATATATCATTAAATATTATTGATTTCACAAAATAAATATACATTTATTAAAGAGTAAATATGCATAAAGCATGCACATCTATTTACATGCTTTTTAAGGGGGCGTTTATAAAGAGAATTCAGCAGGTCTCGACACCGAGCCTTGGAGAACTCTTCAAGCTTTGTAAGATACTTGGCCACTGAACCAGGGAAGTTTATATTGAGTTTATATAAAG
Associated Phenotype:
Not determined