Busch Lab

ZMP

LOC794026

Ensembl ID:
ENSDARG00000029474
Human Orthologue:
CAMK1
Human Description:
calcium/calmodulin-dependent protein kinase I [Source:HGNC Symbol;Acc:1459]
Mouse Orthologue:
Camk1
Mouse Description:
calcium/calmodulin-dependent protein kinase I Gene [Source:MGI Symbol;Acc:MGI:1098535]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa41768 Nonsense Mutation detected in F1 DNA Not yet available
sa21838 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa41768
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041417 Nonsense 45 382 2 11
Genomic Location (Zv9):
Chromosome 11 (position 4148678)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 4067182
GRCz11 11 4086569
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGAGGGGCTTTTTCTGAGGTGATGCTCGCTGAGGAGAAGAGGACGAGG[A/T]AACTGGTGGCCGTAAAGTGCATAGCCAAAAAAGCTCTGGAGGGAAAGGAG
Long Flanking Sequence:
GTATGTATAACGTAAAATAGTTACGCTTCCCACATAAGCGTGGAACAGAGATGTGTACCTGTAAAAGACATTGTTCAATCTGAAATGAGTAAGTGAGTGAGTGAGTTGGGGTGGTGTGTATGGGGATGTTTTCTGTCTAATGGTTGAAAATAGTCTGGATAGCCATTCATTTCCTATGGTGATCACTTTTGACCGGGAACACCACAGGTGTAACAAGGTTGATTAAAATACTCAAAATTCAGTGAAGGAGGTGATCATTACTTTTATATGTTTAAGCACACAGTGTGAAGAATATGACGCAACCAGATGTAAAACACAATATTTATGAGTGATTTAAGCTGTAAATCGGTCAGATTTGACCCGAACACGACAGGAAGGTTAAATATTTCAATATGTTCTGAAATTATTGCCTTTTGCTGGTTTATGTCTGATTGTGCTTTATCATTTGTTTCAGAGGGGCTTTTTCTGAGGTGATGCTCGCTGAGGAGAAGAGGACGAGG[A/T]AACTGGTGGCCGTAAAGTGCATAGCCAAAAAAGCTCTGGAGGGAAAGGAGAACAGCATTGAAAATGAGATCGCCGTCCTCCACAAGTGAGTCATTCATACAGCTGTTCCACTTCACTTACAGATATACAGATGACACACACACACACACACTGTTCGATGTAAAATACAGACTGTGGAATGTATTTTTAACAGAAATATTCTGTAGATAAAATTTTTGATTGAAAAATGTTAAAAACAGTAGATTACTGGCAACCACAGCTGCCGGTATTTTTCAGTAAAATCAAGAAAAGAAAAAAAACAGCAAAGCTTTTTTTTGTGTGTCACCATTGTGGTGGATATTAGCATCTGTGTTCAAGTCCAGGATGGACTAAGAGTATTTGATGTTATGCTGCATCTTCTTTTGCTCAAAGTTAACTGTGTAGTTACTAACGCAGTAAAAATCTGTTTGCTAATTGCAATCACACATGTGTCAGGGTTCTGCCACTCTGGTCTTGGAAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21838
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041417 Essential Splice Site 73 382 2 11
Genomic Location (Zv9):
Chromosome 11 (position 4148764)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 4067268
GRCz11 11 4086655
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGAGGGAAAGGAGAACAGCATTGAAAATGAGATCGCCGTCCTCCACAA[G/A]TGAGTCATTCATACAGCTGTTCCACTTCACTTACAGATATACAGATGACA
Long Flanking Sequence:
GAGTAAGTGAGTGAGTGAGTTGGGGTGGTGTGTATGGGGATGTTTTCTGTCTAATGGTTGAAAATAGTCTGGATAGCCATTCATTTCCTATGGTGATCACTTTTGACCGGGAACACCACAGGTGTAACAAGGTTGATTAAAATACTCAAAATTCAGTGAAGGAGGTGATCATTACTTTTATATGTTTAAGCACACAGTGTGAAGAATATGACGCAACCAGATGTAAAACACAATATTTATGAGTGATTTAAGCTGTAAATCGGTCAGATTTGACCCGAACACGACAGGAAGGTTAAATATTTCAATATGTTCTGAAATTATTGCCTTTTGCTGGTTTATGTCTGATTGTGCTTTATCATTTGTTTCAGAGGGGCTTTTTCTGAGGTGATGCTCGCTGAGGAGAAGAGGACGAGGAAACTGGTGGCCGTAAAGTGCATAGCCAAAAAAGCTCTGGAGGGAAAGGAGAACAGCATTGAAAATGAGATCGCCGTCCTCCACAA[G/A]TGAGTCATTCATACAGCTGTTCCACTTCACTTACAGATATACAGATGACACACACACACACACACTGTTCGATGTAAAATACAGACTGTGGAATGTATTTTTAACAGAAATATTCTGTAGATAAAATTTTTGATTGAAAAATGTTAAAAACAGTAGATTACTGGCAACCACAGCTGCCGGTATTTTTCAGTAAAATCAAGAAAAGAAAAAAAACAGCAAAGCTTTTTTTTGTGTGTCACCATTGTGGTGGATATTAGCATCTGTGTTCAAGTCCAGGATGGACTAAGAGTATTTGATGTTATGCTGCATCTTCTTTTGCTCAAAGTTAACTGTGTAGTTACTAACGCAGTAAAAATCTGTTTGCTAATTGCAATCACACATGTGTCAGGGTTCTGCCACTCTGGTCTTGGAAATTCTTGTTTTGGTGGCAGAGCTCTGACACTAGCTGTGTCTGGTCGTGAGTACGCAGAGTGTGCGCGCTCCCGCTTGATGCGGCCGCG
Associated Phenotype:
Not determined