Busch Lab

ZMP

camk2g1

Ensembl ID:
ENSDARG00000071395
ZFIN IDs:
ZDB-GENE-050913-146, ZDB-GENE-070323-2
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
sa31890 Essential Splice Site Available for shipment Available now
sa44771 Essential Splice Site Mutation detected in F1 DNA Not yet available

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.
Availability:
Order Allele From ZIRC
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

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.
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