ZMP
camk2g1
Ensembl ID:
ZFIN IDs:
Description:
calcium/calmodulin-dependent protein kinase (CaM kinase) II gamma 1 [Source:RefSeq peptide;Acc:NP_0
Human Orthologue:
CAMK2G
Human Description:
calcium/calmodulin-dependent protein kinase II gamma [Source:HGNC Symbol;Acc:1463]
Mouse Orthologue:
Camk2g
Mouse Description:
calcium/calmodulin-dependent protein kinase II gamma Gene [Source:MGI Symbol;Acc:MGI:88259]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44771 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa31890 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa44771
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000105518 | Essential Splice Site | 392 | 560 | 16 | 21 |
ENSDART00000137139 | Essential Splice Site | 371 | 405 | 15 | 16 |
ENSDART00000105518 | Essential Splice Site | 392 | 560 | 16 | 21 |
ENSDART00000137139 | Essential Splice Site | 371 | 405 | 15 | 16 |
The following transcripts of ENSDARG00000071395 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 35961097)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz11 | 12 | 35361861 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGGAGAGCTGCAACACCAATGAAGAAGAGGATATGAAAGGTAGGAAAGG[T/G]ACACAGATCCTCTCCTCCTGTTCTCTGCATGCCTACTGCACTGCGGCCAT
Long Flanking Sequence:
TGATCCTCTCATTCGTTATTCACCTGCTTTCCTTTGCACAGCGAAAAGCTGTTTTTGTCAGTCGTGCTGCTTCTCGATTCTAAGATCACATTAGTACGCATATAGACAAACTGTCATAAACTCACAGTCTAATCTGTAGTGACGACGAGCCAGCACTGGCAATTTAAAAATGAGTTTCAGCCAGCCAAAGTGGCTAGTGGGAGTGGCTGTCTAGCCCGCCACAACCGAAATCTACCCGCATTTGGCGGGTGTTAATGTAAAGCCCTGGTTGTCTCTAAAATTGTCAACAAAAATTGTCAACTTTAAAATAGTCTCAAAAATAGAATTAACAACTACTCAGGCTTCATTTAGAATCCAGTTTCAGAGACCTTAATCTAACCCTATTTATTACATATCCTCATGATTTGTTTGTGTTGTATGTTCTTTGTTTGCTTCCGTCTGCAGGGCTCCACGGAGAGCTGCAACACCAATGAAGAAGAGGATATGAAAGGTAGGAAAGG[T/G]ACACAGATCCTCTCCTCCTGTTCTCTGCATGCCTACTGCACTGCGGCCATTCAGATCCCAGTGCTCATGTCAGAAGAGTAAACCCTCTCCTGTCCAGACCCTCCGCTGTCATGTCACCAAAAACACACCTCTGTGATTAAACAGCACACACAGCAATCTGAAAGATCAAACCCCTGAGGCTGATGGTCAGACAGGAGGGGAATTACAATCGATTAACATGCATGATGGCACAAGTCTTTATGTTTACAGCTAAATTGCAGTGTTACTAAAGGTGCACCATAGAGATTTAGCTATAAAGAAGGAGAATAAATATTTAGAGCACTGATAAACACTGCAATCTGGACGGGATTAGATTTCTCTGAACTCTAAGATAGCAAGAGAGAGATTAAGCATCCTTAGGGAAATTTAGTCCCGTCCAAATAGAGTTGAACAAGTATCTTTCTTTCAGATCACCCACAGTTCATTGTCACACTAATATATATCTCCAGCCAAGTTTAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31890
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 |
---|---|---|---|---|---|
ENSDART00000105518 | Essential Splice Site | 392 | 560 | 16 | 21 |
ENSDART00000137139 | Essential Splice Site | 371 | 405 | 15 | 16 |
ENSDART00000105518 | Essential Splice Site | 392 | 560 | 16 | 21 |
ENSDART00000137139 | Essential Splice Site | 371 | 405 | 15 | 16 |
The following transcripts of ENSDARG00000071395 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 35961097)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 35260798 |
GRCz11 | 12 | 35361861 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGGAGAGCTGCAACACCAATGAAGAAGAGGATATGAAAGGTAGGAAAGG[T/G]ACACAGATCCTCTCCTCCTGTTCTCTGCATGCCTACTGCACTGCGGCCAT
Long Flanking Sequence:
TGATCCTCTCATTCGTTATTCACCTGCTTTCCTTTGCACAGCGAAAAGCTGTTTTTGTCAGTCGTGCTGCTTCTCGATTCTAAGATCACATTAGTACGCATATAGACAAACTGTCATAAACTCACAGTCTAATCTGTAGTGACGACGAGCCAGCACTGGCAATTTAAAAATGAGTTTCAGCCAGCCAAAGTGGCTAGTGGGAGTGGCTGTCTAGCCCGCCACAACCGAAATCTACCCGCATTTGGCGGGTGTTAATGTAAAGCCCTGGTTGTCTCTAAAATTGTCAACAAAAATTGTCAACTTTAAAATAGTCTCAAAAATAGAATTAACAACTACTCAGGCTTCATTTAGAATCCAGTTTCAGAGACCTTAATCTAACCCTATTTATTACATATCCTCATGATTTGTTTGTGTTGTATGTTCTTTGTTTGCTTCCGTCTGCAGGGCTCCACGGAGAGCTGCAACACCAATGAAGAAGAGGATATGAAAGGTAGGAAAGG[T/C]ACACAGATCCTCTCCTCCTGTTCTCTGCATGCCTACTGCACTGCGGCCATTCAGATCCCAGTGCTCATGTCAGAAGAGTAAACCCTCTCCTGTCCAGACCCTCCGCTGTCATGTCACCAAAAACACACCTCTGTGATTAAACAGCACACACAGCAATCTGAAAGATCAAACCCCTGAGGCTGATGGTCAGACAGGAGGGGAATTACAATCGATTAACATGCATGATGGCACAAGTCTTTATGTTTACAGCTAAATTGCAGTGTTACTAAAGGTGCACCATAGAGATTTAGCTATAAAGAAGGAGAATAAATATTTAGAGCACTGATAAACACTGCAATCTGGACGGGATTAGATTTCTCTGAACTCTAAGATAGCAAGAGAGAGATTAAGCATCCTTAGGGAAATTTAGTCCCGTCCAAATAGAGTTGAACAAGTATCTTTCTTTCAGATCACCCACAGTTCATTGTCACACTAATATATATCTCCAGCCAAGTTTAAAT
Associated Phenotype:
Not determined