ZMP
camkk1
Ensembl ID:
ZFIN ID:
Description:
calcium/calmodulin-dependent protein kinase kinase 1 [Source:RefSeq peptide;Acc:NP_001014361]
Human Orthologue:
CAMKK1
Human Description:
calcium/calmodulin-dependent protein kinase kinase 1, alpha [Source:HGNC Symbol;Acc:1469]
Mouse Orthologue:
Camkk1
Mouse Description:
calcium/calmodulin-dependent protein kinase kinase 1, alpha Gene [Source:MGI Symbol;Acc:MGI:1891766]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40469 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa6985 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa20454 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa40469
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:
C > A
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028237 | Splice Site, Nonsense | 279 | 434 | 11 | 15 |
ENSDART00000133743 | Splice Site, Nonsense | 326 | 481 | 13 | 17 |
Genomic Location (Zv9):
Chromosome 5 (position 33050920)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 30813152 |
GRCz11 | 5 | 31413305 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACTCATCCGTCTGTCTTCTTTTTTTATTTCTCTTCCTCGTCCTCCAGTG[C/A]CCATTTATTGATGAGTACATACTGGCTCTTCACAATAAGATCAAGAGTAA
Long Flanking Sequence:
CTGCTCTTTAATGTTTATTTGCTACCCATCAGAGAAAGACTTAAAATACGGGAAAATATCTTTACGGGATGATAACCGGATAGAACTGTGAAAAACGGGAGAATCCCAGGAAAAACAGGAGGGTTGACAGATATGCAACGTTCACACTAGCTAAACCTACAGAACTCTGACATCAAATGAACCCGGTTGTGGACCAAGCTAGTGTAAATGCAACCTAAAACTGTCCTACATCACTATAACAGAAGTTGTGTTCTGTTTAGGCTCTGGACGTGTGGGCAATGGGAGTGACCCTCTACTGTTTCGTCTATGGGAAGGTGAGTTTCCTCTTGCGCTGATATGATCAGAGTGATAGCAGTAATTCTTCATTGTGGGATTATATATCAGAATGATCAATGGACGGGCTGCCGCTGCTGCTGCTGCGGTGACATTTGTGTGATTGATGATTTAGATCACTCATCCGTCTGTCTTCTTTTTTTATTTCTCTTCCTCGTCCTCCAGTG[C/A]CCATTTATTGATGAGTACATACTGGCTCTTCACAATAAGATCAAGAGTAAAGTGGTGGAGTTCCCCGACACGTAAGTCACCCCACAGGAACAGATGCAGAGAAAGGAAATGTCAGAGATGTTTGAGTGCAGCGAATGTAAAGCTGATTCATGTTGGTTTATGCAGGATATTTGTGTATGCTTGTGCAGGTCTGTTTAAATGATGTGCTGATGAAGTGTGTGAAAGACCAGAGGGCATCCGGATGCATGTCATCTGGTGCCTGTGTTTGGAGTCATCAGCTAATAAAAGAGCAACTTGTCTATCTTACACACACACACACACACACACACACATACACAAACAAACACACACACACACACACACACTGCTCCTTGTTGTGTTCTCAGTGGCTGAACTAACTGAAACATATCACAGTGTCAGTGGCTCTCAGTAAAATAGTGTCTACATGACTAGGGGCTCTCAGTATTTTTGCCAGCAGAACCCTTCAGTATATTTTAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6985
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 |
---|---|---|---|---|---|
ENSDART00000028237 | Essential Splice Site | 303 | 434 | 11 | 15 |
ENSDART00000133743 | Essential Splice Site | 350 | 481 | 13 | 17 |
Genomic Location (Zv9):
Chromosome 5 (position 33050992)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 30813224 |
GRCz11 | 5 | 31413377 |
KASP Assay ID:
554-4606.1 (used for ordering genotyping assays)
KASP Sequence:
CTGGCTCTTCACAATAAGATCAAGAGTAAAGTGGTGGAGTTCCCCGACAC[G/A]TAAGKCACCCCACAGGAACAGATGCAGAGARAGGAAATGTCAGAGATGTT
Long Flanking Sequence:
TAACCGGATAGAACTGTGAAAAACGGGAGAATCCCAGGAAAAACAGGAGGGTTGACAGATATGCAACGTTCACACTAGCTAAACCTACAGAACTCTGACATCAAATGAACCCGGTTGTGGACCAAGCTAGTGTAAATGCAACCTAAAACTGTCCTACATCACTATAACAGAAGTTGTGTTCTGTTTAGGCTCTGGACGTGTGGGCAATGGGAGTGACCCTCTACTGTTTCGTCTATGGGAAGGTGAGTTTCCTCTTGCGCTGATATGATCAGAGTGATAGCAGTAATTCTTCATTGTGGGATTATATATCAGAATGATCAATGGACGGGCTGCCGCTGCTGCTGCTGCGGTGACATTTGTGTGATTGATGATTTAGATCACTCATCCGTCTGTCTTCTTTTTTTATTTCTCTTCCTCGTCCTCCAGTGCCCATTTATTGATGAGTACATACTGGCTCTTCACAATAAGATCAAGAGTAAAGTGGTGGAGTTCCCCGACAC[G/A]TAAGTCACCCCACAGGAACAGATGCAGAGAAAGGAAATGTCAGAGATGTTTGAGTGCAGCGAATGTAAAGCTGATTCATGTTGGTTTATGCAGGATATTTGTGTATGCTTGTGCAGGTCTGTTTAAATGATGTGCTGATGAAGTGTGTGAAAGACCAGAGGGCATCCGGATGCATGTCATCTGGTGCCTGTGTTTGGAGTCATCAGCTAATAAAAGAGCAACTTGTCTATCTTACACACACACACACACACACACACACATACACAAACAAACACACACACACACACACACACTGCTCCTTGTTGTGTTCTCAGTGGCTGAACTAACTGAAACATATCACAGTGTCAGTGGCTCTCAGTAAAATAGTGTCTACATGACTAGGGGCTCTCAGTATTTTTGCCAGCAGAACCCTTCAGTATATTTTAGGTTTTTCAATTATCAGATTTTTTATATTAGTAGAATGTGATTTATATCATATGCTGTGTACACTATCATTTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20454
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028237 | Nonsense | 316 | 434 | 12 | 15 |
ENSDART00000133743 | Nonsense | 363 | 481 | 14 | 17 |
Genomic Location (Zv9):
Chromosome 5 (position 33055587)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 30817819 |
GRCz11 | 5 | 31417972 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGATATCTTAGACCGACTGTCAGCGAGGGGCTGAAGAGCCTGGTCTCA[C/T]GAATGCTGGACAAAAACCCAGACACCAGGATCACCATTCCTGAGATCAAA
Long Flanking Sequence:
TTTAGACTATACAGGTAATAAATGTTTTCTTTTAACAAATGCTGAAATTATGTTATTTGAAAAAGATACAACACATGGTGGTTTTGTGAATGCTATGCTTGTGTATATGAACCATGTGATCACTGATTTGTGCATAATTTTACTGTGTTGCTGCAGAATTTGGCATTACAATGTGGTGTAAATTATGCAAAAGCAGTGCAAGGAGCAGGGGTTCATAACCCGTTTGTGGTAAACATTCCTATACAGTACCTGGGGTTACTTGCAGAGTTTTTCAGTGCAGTTTGAAGTTCAGCTTGTTTAGTGGTCTACAGCTCTCATGAAGCATTCTGAATCAGTTTTGGGGTTAACATTGAAATTCCTATGCCTCCAGTGAGTCTCATGCCTTATAAAAATGTGCTGTTGTTGTTCTGATATAGTTTTTTACCACTTCAGCTGTTTGTTCTGTGTTTTTGTGATATCTTAGACCGACTGTCAGCGAGGGGCTGAAGAGCCTGGTCTCA[C/T]GAATGCTGGACAAAAACCCAGACACCAGGATCACCATTCCTGAGATCAAAGTAAGTCTACACAAGGCGCATTTCTGAAATCCAGAGTGGCAAGTAATCCGTTTTACGTTCATCCTCACAAATCTGTATTGCAAGATATTTTAAAGACTAGAGTATATCTTCTTACACACAAAAATATGTTTGCATTTGGCCTTTTCGGCAGACTTAGCATTATTAATTTGTGCATTTTCCTTCAGAAATTCTTTGTTTTCTTCTATACTGGCAAGACAGTATATCCTCTTTAAATATTGAAATTATAGTCAGCATCTTTAAAAGAAATATACCAAGAACATTCCAGAGAGTAAGTCTCATTAGTTTTCTCTCACAATACCAGCCCTGTTTTTATCATGGAGACACATTCAGGCATGTTGTTGAAATATGACACAGTACCTTTGATAGCTTCTGCTTTATCAAGCTGACTTGAAATTTGGATAGAAACACATCAGCTTATCCCAATGGAGA
Associated Phenotype:
Not determined