ZMP
camk2d2
Ensembl ID:
ZFIN IDs:
Description:
Calcium/calmodulin-dependent protein kinase type II delta 2 chain [Source:UniProtKB/Swiss-Prot;Acc:Q
Human Orthologue:
CAMK2D
Human Description:
calcium/calmodulin-dependent protein kinase II delta [Source:HGNC Symbol;Acc:1462]
Mouse Orthologue:
Camk2d
Mouse Description:
calcium/calmodulin-dependent protein kinase II, delta Gene [Source:MGI Symbol;Acc:MGI:1341265]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa2005 | Essential Splice Site | F2 line generated | Not yet available |
| sa32622 | Essential Splice Site | Available for shipment | Available now |
| sa19450 | Nonsense | Available for shipment | Available now |
| sa25543 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa2005
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000040049 | Essential Splice Site | 199 | 493 | 8 | 19 |
| ENSDART00000044896 | Essential Splice Site | 199 | 554 | 8 | 22 |
| ENSDART00000040049 | Essential Splice Site | 199 | 493 | 8 | 19 |
| ENSDART00000044896 | Essential Splice Site | 199 | 554 | 8 | 22 |
Genomic Location (Zv9):
Chromosome 1 (position 13078251)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 13506993 |
| GRCz11 | 1 | 14193506 |
KASP Assay ID:
554-3243.1 (used for ordering genotyping assays)
KASP Sequence:
GGTGCTGAGGAAAGATCCTTATGGCAAACCGGTGGACATGTGGGCTTGCG[G/A]TAAGAAATGAWTGAGCCACAGAAATATCAGCTTTATAAGTGAGCCGGTGT
Long Flanking Sequence:
CAGGAATAAATGATATTTTAAAATATTTTAAAACTAAAAACTGTTCTTTTTTTGTGAATTTGTTCCACAATATGTGTTTTTACTGCATTTTTGATCATAAAAATGCTTTGCTAAGCATAAGAGGTGCCTTGCAAAAGCAATAAAAAGTCAGCCTGACCCAAACTTTTAAACAGCACTTATCAGCATTTATAACACTTTAGAGTAATGTTGTAAAATATAGTATTTAATGAAAACCAATATTCCACAAACACAGTTCTCTTTTATTTAGAACTTATTTGGGACCAGTAAAGGCTAAACAGGGAACACTGCTTTATTAATCATTTTGCTGTTTGCAATTTTGCACGACTAAGCTTTTTCATGCCAACTTGGCCAAATAAACTGCCGTTTTAGTGCTCTCAACCACTCTCTCTGTTCAGGATTTGCTGGTACTCCAGGGTATCTGTCTCCAGAGGTGCTGAGGAAAGATCCTTATGGCAAACCGGTGGACATGTGGGCTTGCG[G/A]TAAGAAATGAATGAGCCACAGAAATATCAGCTTTATAAGTGAGCCGGTGTGATAGATGTCACTGTTGAAGCTCATTAACTGATTATTAAATTACTGCAGACTGAGTTTTTAAGCAGCGTTGAATCTAATCAGCTAAATGGAGTGTCCCTAGTAAATTGTCTTTCTGTTTTTAGGCTTAAAACGTGTTAGTCCAATCCAAGCAGTTAAATGAATGTTTCAATTTAGCCTTGAGGATTGCATAATTATTGAAGGCAGTTGGATAGTTGAAAATTACTGTAAGGACTACCATGTTACTCATGGTATTTTGGGAAGTACATTCTGAGTAATGCAGAATAATTAATATATTCATGCACACATACAAAAGACAATGTCTGCCTATTTTATTTTATTTTATTTTATTTATTTTTTATTTGTTTTTGTTTTATTTTATTTTATTTTGTATATTGTATATTTATTTTGTAAAAGTATATATATATATATATATATATCATATTTTAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32622
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000040049 | Essential Splice Site | 272 | 493 | 10 | 19 |
| ENSDART00000044896 | Essential Splice Site | 272 | 554 | 10 | 22 |
Genomic Location (Zv9):
Chromosome 1 (position 13076051)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 13504793 |
| GRCz11 | 1 | 14191306 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTAAACGTATCACAGCTGCTGAAGCCCTCAAACACCCCTGGATCTGCG[T/G]ATGTTTTTTTAACACATAAACACACACTAGTAAACAAGCTTGTCTATACA
Long Flanking Sequence:
TTTGAAGTATTTGCTGTGAAGAAGTTTCCCCTCTGAATGTGGCCATAATAGGAGCTTTCTGGTTCTCACAGGTGTGATCCTCTACATTCTGCTGGTTGGATATCCGCCATTTTGGGATGAAGACCAGCATCGCCTCTATCAGCAGATCAAGGCTGGTGCCTATGATGTAAGACTGAAGTTGAAGATTTCTCCTGCAAAGTGTTCACACTATACAAGAAGACACTGTTAGAGCTACATATGCAGAATATGATGAGACTGTTGATAACCATTGGGCAACACTGATGATAACTTGATGATATCTTGGGTTCCACAGCATATATGTTCATACAAAATAATGAAACTATGCTCAATTGTGTTGTTTTATCTCCAAATGTAGTTTCCTTCTCCCGAGTGGGACACCGTGACCCCTGAAGCTAAAGATCTGATTAATAAGATGTTGACTATCAATCCCTCTAAACGTATCACAGCTGCTGAAGCCCTCAAACACCCCTGGATCTGCG[T/G]ATGTTTTTTTAACACATAAACACACACTAGTAAACAAGCTTGTCTATACACAGTACAACAAAGGACTGTTTTAATCTTTACTAATGACTAATTTTTCTATCTTCTTTCTCTTCCTTCAGCAACGCTCCACTGTTGCCTCAATGATGCACAGACAGGAAACCGTGGAGTGCTTGAAGAAATTCAACGCCAGAAGGAAACTCAAGGTTAGTTTTTAACTGATCTTTTACAGTTTTCTACTTTTGACCAAGCTTTAGCTTTCTCCACACCTTCAGAGTTTACTTCGCAGAGCTTCACCATTGTGTGTGCACTTGCTTTTTCTCTAAATCCGAGTCACAGAGACTCTGTTTACACCAGGTATTAATATGCATTTTCATCAATGTAATTACAAGTGGATGAATCAAAGGCCTGCTTTCACAGACAGGGCTTAGGGTGCACTCACACTATGCTATCTGAACCGTGTCCTGGCTTGTTTCCCGGTTCGTTTGACAAGTGTGAGTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19450
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000040049 | Nonsense | 296 | 493 | 11 | 19 |
| ENSDART00000044896 | Nonsense | 296 | 554 | 11 | 22 |
Genomic Location (Zv9):
Chromosome 1 (position 13075862)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 13504604 |
| GRCz11 | 1 | 14191117 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATGATGCACAGACAGGAAACCGTGGAGTGCTTGAAGAAATTCAACGCC[A/T]GAAGGAAACTCAAGGTTAGTTTTTAACTGATCTTTTACAGTTTTCTACTT
Long Flanking Sequence:
TCCTGCAAAGTGTTCACACTATACAAGAAGACACTGTTAGAGCTACATATGCAGAATATGATGAGACTGTTGATAACCATTGGGCAACACTGATGATAACTTGATGATATCTTGGGTTCCACAGCATATATGTTCATACAAAATAATGAAACTATGCTCAATTGTGTTGTTTTATCTCCAAATGTAGTTTCCTTCTCCCGAGTGGGACACCGTGACCCCTGAAGCTAAAGATCTGATTAATAAGATGTTGACTATCAATCCCTCTAAACGTATCACAGCTGCTGAAGCCCTCAAACACCCCTGGATCTGCGTATGTTTTTTTAACACATAAACACACACTAGTAAACAAGCTTGTCTATACACAGTACAACAAAGGACTGTTTTAATCTTTACTAATGACTAATTTTTCTATCTTCTTTCTCTTCCTTCAGCAACGCTCCACTGTTGCCTCAATGATGCACAGACAGGAAACCGTGGAGTGCTTGAAGAAATTCAACGCC[A/T]GAAGGAAACTCAAGGTTAGTTTTTAACTGATCTTTTACAGTTTTCTACTTTTGACCAAGCTTTAGCTTTCTCCACACCTTCAGAGTTTACTTCGCAGAGCTTCACCATTGTGTGTGCACTTGCTTTTTCTCTAAATCCGAGTCACAGAGACTCTGTTTACACCAGGTATTAATATGCATTTTCATCAATGTAATTACAAGTGGATGAATCAAAGGCCTGCTTTCACAGACAGGGCTTAGGGTGCACTCACACTATGCTATCTGAACCGTGTCCTGGCTTGTTTCCCGGTTCGTTTGACAAGTGTGAGTGTTCTGAATCGGGACATGTCATGCATATGAGCATTCCTGCAAAAGTGATATAGTGCTTGATTAAATAGGAGACAGGGGTTTTGTCAAAATCACAGCGATCACAAATAATGCATTTGAATGCATGTTAATAAATATAAATGGATTGAAACAAGGCCAGGGTATTTGTGCTTTAAAAGTATTTCAGTACACTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25543
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 |
|---|---|---|---|---|---|
| ENSDART00000040049 | Essential Splice Site | 343 | 493 | 14 | 19 |
| ENSDART00000044896 | Essential Splice Site | 363 | 554 | 15 | 22 |
Genomic Location (Zv9):
Chromosome 1 (position 13063294)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 13492036 |
| GRCz11 | 1 | 14178549 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTAGGAGCCACAAACTACCGTGATCCACAACCCAGTGGACAGAAACAAG[G/A]TAATGTTCATTGTTAAAATCCAACTGAAGCCAATATCAGAGTTTTTGGGG
Long Flanking Sequence:
CATCATGTTTTATTAGCCAAACTGCAATGAAGCCATTTTATATAACCAATGCACAAATAATGAGTCGACTTTAAAAATATTATTAGACAAATCCACACGCAGAGATGTTTTAAGTATACTCCAGGTTTATTTTTGGAAGAAATGTGATTTATTTCTTAGCAGGAATGGAAGATTGTGTGTGTTTTAAGTTTGTGTGCTGTGATTGAGATTCAGATTGTTTTCCACGTGTACTATATAATAAACCACTAATGGAAATAACGAGTCTACATTTGATAGTCTTGTTCTGCTGATTGGATGTATTTAGTGGTTTGTTTTTTCCCCTTCAATAGCTTCAAAAAATCATTTGCTTTTCCATGCATGTTGTGTCTAGTACACAGCCATTATCTGCCATTATGCTTTATTAAGCTTCTTTTCCACATACAAATAATATTTTGTATTACCTTTCACTCTTTTAGGAGCCACAAACTACCGTGATCCACAACCCAGTGGACAGAAACAAG[G/A]TAATGTTCATTGTTAAAATCCAACTGAAGCCAATATCAGAGTTTTTGGGGGGTGTTAGTAACAATTTGTTAGTCTTGAGGTTAGAGCTACACAATATATAATTTCAGCATCGATATTACCGTGTGCGCACCTGCAATTGTCAAAATATGCAATGTTGTGTCTCAATTATAGTTAAACAAGAGCCACAGAATTGTATAAACTGCTGTATGTACATGAAATATATGTGATTAATCCAAAAAAAAAGAAATCTTATAATTTTTGTCATGTTTTTAGTTCAAATATCTACATTTCAAAGTGAAAACAAGATTATTTTACTTATTTTACTGGCAGATAATTTAGCTTGTTGATTTGTTTGATTTATTTCTTCACAAGTTGAAAACAAAACAATATTTTTTTTTGAAAATTAGACTAAAAATGAGACAAAGAAAAGCATTTATTGCATAGTGATTATTCAATTTCTGTACCTGAATATCATTAGGCTTCCCAGAAAACCATCAAAT
Associated Phenotype:
Not determined