ZMP
camk2d1
Ensembl ID:
ZFIN ID:
Description:
Calcium/calmodulin-dependent protein kinase type II delta 1 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 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa25374 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa41051 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25374
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000056466 | Essential Splice Site | 73 | 491 | 3 | 19 |
| ENSDART00000136175 | None | None | 289 | None | 10 |
| ENSDART00000138757 | None | None | 245 | None | 5 |
| ENSDART00000142259 | Essential Splice Site | 73 | 476 | 3 | 18 |
| ENSDART00000148369 | None | None | 264 | None | 11 |
The following transcripts of ENSDARG00000043010 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 59030856)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 57483465 |
| GRCz11 | 7 | 57785905 |
KASP Assay ID:
554-7310.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGAACGAGAGGCCAGAATTTGTCGTCTACTCAAGCATGCTAATATTGG[T/A]GAGTGCAACCACACACACACAAACACGCGCAAACACGCACACATGCACAC
Long Flanking Sequence:
AACAAACAGAGAAGGGAATCAATGAATGGATGTGGAAGGAGGGAGATAGAAGAGCAAGAAGTGTGTGTATTTACGTACACACATACATATATATCCTCACATATATAAATCCAACATTTCCTAAATGAAAAAGACTTGTCTATTTGTTTGTATATTGTGTCTGTTGTACTTGACTTCAATGGAATGGCTAAAGAAAACAGTTATGGCTTTTTGGGTTTTCCCTTAGATCTCATTGATCATTAAATCAATTAGAGAAAGCAGATTTCAGAACCATAACACACTGTATCTGTTGTGTGGTATTCACATTTTTTATAGATTTTTTTCAATAAAAGTTGACAATTAGCTAAAATGGTATTATCTGGATGCTAGTTAAATATTTTGGTGCTTAAACAGATTTGTATTATTTATTTTTTCCAACATGTCTTTTAATGTCTTTTAGATCACCAAAAACTGGAACGAGAGGCCAGAATTTGTCGTCTACTCAAGCATGCTAATATTGG[T/A]GAGTGCAACCACACACACACAAACACGCGCAAACACGCACACATGCACACACGCATGCACAGACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAGTTAAGGTTCCTTTACCACAGCCTTAAAGCACTTAATGTTCCACAGATTGATGAGCTGTTTTATGTACATTACATGTAGCATTTAAAATATACTAGTATTTAAACCAGATGTAAAATGACAGATTCAAACTTAAAAGTAATTTTTCTGTCCTCACTGAACACAGAAAGTTCACTCCCTGCTTGGTGAGTGCTGATGGTATGAGAAATAAACACAAAGCCCAGAGTGGATCTGGAGTAGAAGCGTTAACAGACTCCAGACATGCTGAAGACAGAGCACAGATGCAACATCAGACAAACAAACAGGAGCTGCAGTCAGATTGCTGGGCATCTCCCAGCCTAACCAGCTAAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41051
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 |
|---|---|---|---|---|---|
| ENSDART00000056466 | Essential Splice Site | 314 | 491 | 12 | 19 |
| ENSDART00000136175 | Essential Splice Site | 112 | 289 | 4 | 10 |
| ENSDART00000138757 | None | None | 245 | None | 5 |
| ENSDART00000142259 | Essential Splice Site | 314 | 476 | 12 | 18 |
| ENSDART00000148369 | Essential Splice Site | 236 | 264 | 9 | 11 |
The following transcripts of ENSDARG00000043010 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 59092896)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 57545505 |
| GRCz11 | 7 | 57847945 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTAGGGTGCTATTCTTACTACCATGCTTGCCACACGGAACTTCTCAA[G/A]TAAGAAACTATTGTATTCTGTATGTAATAATTGTTCCTTCTTTTAATTAA
Long Flanking Sequence:
AATATGACATACAGTGGTGTGAAAAAGTGTCAGCCTCTTACAGGTTTTTTTATTATTCTGCATGTTTATAACACTTTAATGTTTCAGATCATTAAACAAATTTAAATATTAGACAGATAACACAAGTAAACACATAATGCATTTTTTAAATGAAGGTGAAAAACCTGTGTGAAAACACTTTTTCTGTTTGCAGTTTTCCCTCTATAGTAAAAGCCTTCATTTGAATAAAGCACAATGTGTTTATTTGTGTTATTTTTCACTAATATTTACATTTTGTTTGACGATCTAAAACAATAAAGTATGAAAAACCTACAAAAAATAAGAAATCTTTTTCCACACTAGTGTACTTTAAAAGGTTAATCTGGATTAATCGTTATCCACTAGCACTGACTAATGTTTTACAAGACTTAAGTTTAAGTGATGTTTTTCCTTTCTGCTTTTTCTGGACTGTTTTTAGGGTGCTATTCTTACTACCATGCTTGCCACACGGAACTTCTCAA[G/A]TAAGAAACTATTGTATTCTGTATGTAATAATTGTTCCTTCTTTTAATTAAAAAAGTTGTAGTCAAGCTTTTTTTGCCTGAGATGATATAAAGCATGCTAGATGTTGTAGAAAATAATATTTTCATTGAAACATGAAAGCAGAAGCAACTCTGCAGATAGCAGATATACAAGCAGTAGCGTCTCTGCATATTTATTATTTCACAGTTTAAACAGCAATCACAATATGTTTCATGGTGTTTTTTTAGATCATTTTCTGTAGCCTTATGATCCTGCTTAAAAATAAGCATTTTCATTCTCAGAAATTAAATTTCATTTTTAACACTGCAAACATTAATTCATATTAAATAGGCTTCTTAATCATATTTCATTACATAATGCAAATCTTTGATTACAGACTATTCAGAGGTTTTGATTTTGAGGTCAATAGATTATTAATATTCATGGCATACTGCAGTGATTAAAGTTGTGAATTTTAATTTTGTACTCTTTTAGATGCGATC
Associated Phenotype:
Not determined