ZMP
CAMK2G (1 of 2)
Ensembl ID:
Description:
calcium/calmodulin-dependent protein kinase II gamma [Source:HGNC Symbol;Acc:1463]
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 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15148 | Essential Splice Site | Available for shipment | Available now |
sa12015 | Nonsense | Available for shipment | Available now |
sa35467 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15148
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 |
---|---|---|---|---|---|
ENSDART00000078652 | Essential Splice Site | 153 | 598 | 6 | 23 |
Genomic Location (Zv9):
Chromosome 13 (position 22339579)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22068917 |
GRCz11 | 13 | 22199367 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCTTGAGAAAGGACCCTTATGGCAAGCCAGTTGATATCTGGGCCTGTGG[T/G]AAGGTTATAAAATATTACAGTGTTTCCATGAATGGTGTCTTTGTTCATGT
Long Flanking Sequence:
GTCCTTTTTGAGTCAAAACTACTATGAGGTCAAAAGTCACAGACGACAAAGCCAGTGAGCAAATTGGATTGAGCTATTCTAATAGCATGGGAATTTATTGGATGTTATTCCACATTGTGCAGCCTTGATAAGAATGATTTTTTAAAATATAAATAAACAAACCTGTTGCTTATTTAATACAAACTTAACAGTTATTGCCATATTTGTAATGCTTAGCTGCTCATTGAAATACACTCTGAGCTTTTATTCTTCGCTATACAAATATATGTGTATGTATTATTATTATTATTAAATTGTAATTATTGTCAATGAAGCTACCATTTATGGTTCTACACCCCATAGTTGGTATTGTTTTAAAAAATGATTCTGTTCATATTAAATACTACATGTATGCAATAACAGCATGGCCTTACAGGTTTTGCTGGCACCCCTGGATACCTCTCTCCAGAAGTCTTGAGAAAGGACCCTTATGGCAAGCCAGTTGATATCTGGGCCTGTGG[T/G]AAGGTTATAAAATATTACAGTGTTTCCATGAATGGTGTCTTTGTTCATGTGTAATGTGTTAGTCCATATATATATACACACAGATTAAAGAATTCAGCTTCTTTTGGAATAAGAGTATACAATGTATGTGTCCTGGCCAGGTGTGATCCTGTATATTCTGCTGGTGGGTTATCCTCCTTTCTGGGATGAGGACCAGCACAAACTGTATCAACAGATCAAAGCTGGAGCCTATGATGTGAGTAATCACACTCACTCTTTGCCTTAATGGGCCCTCACTGCTTTATAATCAAATGACACTGCTTTAGATCTAATCAAGCCTTTTGCCATTGAAGCAAACACATCCTCTTCAATATGCAGGTTGACCGGTAGGATTTTTCAATGCTTGGTTTTTAAAATCATCATTATTTTGCTATTTAAAAGGTTAAACATTTTGTTTTAGAGGTCACCTACAACATGTTTGGACTAATCCAAGGTAAAAAAAAAAAAACACTTAAAAAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12015
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078652 | Nonsense | 242 | 598 | 9 | 23 |
Genomic Location (Zv9):
Chromosome 13 (position 22347197)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22076535 |
GRCz11 | 13 | 22206985 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAACGCYCCACCGTCGCCTCCATGATGCAWYGTCAAGAAACCGTTGAGTG[T/A]CTGCGCAAGTTCAACGCYCGCAGAAAACTGAAGGTCTGATTCATTCATTA
Long Flanking Sequence:
ATCCTGTTAATTCCCAGGTCTGAACAAAACTCAGTCATCATTCATCTCTCTTGTCTTTTCATGTTTTAGTTTCCCTCTCCAGAGTGGGACACTGTTACTCCAGAGGCCAAAAACCTCATCAACCAGATGCTGACCATCAACCCAGCAAAGAGGATCACGGCTGACCAGGCACTCAAGCATCCATGGGTCTGCGTAAGTAGCCTGAACCTCTAGTGATTTTCAATGCATCTTTCAAAGCTGGTTTATATCGTGTCACCCTGAGTTACTTGAAGCAACTGGCGTAATGTCGTAGAGCTTACATCTGTAATGAAATACGCATCTGCTAGCCTGTTTGACTGATGAAAAATATTAAATGAGGCTTTATACCCATTTTGTATTATTTACAGTCTGTTATAGCATTTCTAAGTAAAGATTTTGTCCTGAAGACTGTGATGTCTCTCTCCCACTTAGCAACGCTCCACCGTCGCCTCCATGATGCATCGTCAAGAAACCGTTGAGTG[T/A]CTGCGCAAGTTCAACGCCCGCAGAAAACTGAAGGTCTGATTCATTCATTAGTAACACAACAAGGCTCAATTTGTTAACATAAGTGTAAGCAGTAGCTCAGTGCTTTTCTGTCTTTTAGACGCCACGGGCTCTCAAGTATGATCATCCTCATGCAAGGGACCTGATCTTAAAACATAATAAAGACCCAATTTATTTCATTTAAAAATCTATAAGTGTCTGAAATGTTGATAATATATAGTTTCTAAGTTACATTATTACATTTTCTACTCATATTAATGATGTATTCATTCATTTACTCTGTTTATTGTTATTCTAAGTCTCGGTAGGATTGCTAAACTAGTGTTTGTTTGTCCTACAGGGAGCCATTTTGACCACTATGCTGGTGTCCAGGAACTTCTCAGGTAAATGCCCTGTCATCTAAATTTTCATTAAGAGAATGCTCATACATTGAGGAATCAGTATTTTGTTTATGTAGTTTCTTTCCAAACTTGGATTTTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35467
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078652 | Nonsense | 373 | 598 | 16 | 23 |
Genomic Location (Zv9):
Chromosome 13 (position 22363763)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22093101 |
GRCz11 | 13 | 22223551 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATTGTCTCTCTCTCTGTCTCTCTCCTCACAGGGATCTACAGAGAGCTG[T/A]AACACCACAGAAGAGGAGGACATGAAAGGTAGGAAAGGTACAATATCAAC
Long Flanking Sequence:
TCATTCTGGCTCCTGTCCGTCAAGCTGGTGTAGTCCAGTGTCCTCATGCTAGTTGAGTTCCCTCAGCGCTGCATGGTAAACTCTCTCCTGCCTCCCCCCAGGAACCACAGACCACAGTCGTGCACAATCCAGCCGATGGCACCAAGGTAAGCCAGCTCTCTTAGCTCTGCCATTCAATTTGAGCTACTTCAAAAGCCACAACCTCAAACATTCACAAATAACACTCTAAACAGGGGCTTCCCTCATGCTCGTCTGGCTGGTTTGTGCAGGGCTTGGTGTGTTTTTCTGTGTGTGTGATGATGGGGTTTATCTGTGCTTGCTGGTGATTTTAATGTCTGTGTATTTGCTGATTTACAGTGTGTGTGCTATAGTTTATAGACATGGTGTATAGACTCTGTTTCTGTACTTCTTCTGTCTTCCCGCCTTCATCCAACCGTGTCTCCATCTTGCCCATTGTCTCTCTCTCTGTCTCTCTCCTCACAGGGATCTACAGAGAGCTG[T/A]AACACCACAGAAGAGGAGGACATGAAAGGTAGGAAAGGTACAATATCAACTCTTTATGTACTCTGCATGTCTTCCTCTTCTTCTATGAGATTTACTGAACGAGGTACATGTACAGAAGTCAACTGGATCAAAATAGTTTCTGAAAGTTGTCCTAAGACAAGAGTGGATGTTGTTCAATAGTTTTAGGACAACTTGCTGATGATCCACTTCAAATGTTGACTTCTGTATGTGTGTGCATATCGAATGCAAATATTGCTCAAACAGAATAATAGTTTGAATATCGATGGCCCCGTTTACACCTGATATATAAATCTGTTCTGTGACCACAGATTTTGAGGAGAGTGTCTGATTTTGCGATCTTGTAGTAGACTATTCTTTCAGGACAGCTATATTGGTTTCTTTTGATTTAGAGTGTCAGTATAAAACCTTGTTTAATAAATCAAATTTAAGTTTTTTTTTTTTTTTTTACAATACAGTGTATAAGAAGTAGAGCTGGACAA
Associated Phenotype:
Not determined