ZMP
zgc:194737
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100170786 [Source:RefSeq peptide;Acc:NP_001124097]
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 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42506 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16462 | Essential Splice Site | Available for shipment | Available now |
sa22600 | Essential Splice Site | Available for shipment | Available now |
sa28418 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42506
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000125864 | Nonsense | 18 | 484 | 1 | 16 |
Genomic Location (Zv9):
Chromosome 15 (position 14335411)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 15380374 |
GRCz11 | 15 | 15316396 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGTGCTGACACAGCCAGCAGACTGGATCTAGACTCTGATTATCATGCT[G/T]AACTGGCGGACATGGTGGCAGCCATGAGTGTGGCTGCCACCAGACTGACC
Long Flanking Sequence:
CAAAAATGGTAAAACTCAGTTGTTAAACTGTTGGGGACTTTAAAAAATGAGCATAACCCAACAGTGTTGTTTTTAAACATGAGCTGTAGCTAAACACATTCAGGTTTAAATGAAACATGACCAGCGTATCGTTTTTTGCTCTGCAGAAAAGTGAGCACTGTTTTTATAGCAATCATCTGTGAGTACTTCTCAAACTGCCAAAGAATTAAAAAAAAAAAGTTCAACTGGCTTTTCGGCAGCGCAAAAATTATACAGTGGCCCTCACTTCTGTTGTGTAAAGAGATGGATGTGTTTGTGCTTGAGAAATGTGCTTGTTAAACACAATTCTCTTGCTCTGCTTTTCCAGCTTGACTTGACCACGGCCCCTCTGAAGACACTGGACTCAGTGATGTCCACTGAGATGTGTAGTTTCTTATAATTTGCGAAGACAGACAGGAGGAAGGACAGCCATGAGTGCTGACACAGCCAGCAGACTGGATCTAGACTCTGATTATCATGCT[G/T]AACTGGCGGACATGGTGGCAGCCATGAGTGTGGCTGCCACCAGACTGACCCCACCAAACGGGTACAGGACCACACCACATCGCCTCAACCTGTCCGACCGGAAGCTTTCCCTGCAGGAGAGATCCAGCTGCCAGAATGGAGGTCCACGAATGGCCAGAAGACCTACTATTGAGTCCAAGCGTGTGTCTATTTCTGATGGAGACGTAAGTTTAGCGGGAATTCTTTTAGATTTGTGTTGACTATCTAAAAAACTTCTGTAGGATTTTTTAAACGTGATGGTTCACCCAAAAAAGAAAATCTCTGTATTCACTCAAATCAGAGGTATGGGATTTTCCTTCAGTAGAACATTAAAGCAGGTATTTATGTGAAACCGTGGTCCTTGGTGACTCATACAATGCAAGTCAATCACACTTTGAGAATCCCAAAAAATGATTACAGACAAAATATATTCAATATGCATACATGCTGTTGATAGGGAAATTAAGAAATTGAACATTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16462
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000125864 | Essential Splice Site | 204 | 484 | 8 | 16 |
Genomic Location (Zv9):
Chromosome 15 (position 14342705)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 15387668 |
GRCz11 | 15 | 15323690 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTNNTTAGTTTAGATTTTCTGTATTTTTTACTTCTTCTCCTGCCTGGTTCTA[G/A]CCCAGTGATGGAGGTCCCGACAGACAGCCCTCTAWCAGAAGAAATGGCCC
Long Flanking Sequence:
CTCAGGCCAAAAAACATGTGATCTGTGCAGCATGACTAGTCGATGTCGATCAAAAAGCGTCACGGCAGAGCATTAAAGTCAACTACACAATTAGTCGACTAGTCGGTGTAACCCCTACTATCTAATAATAAGGACCAATATCTAATGAATAAGTACTAGAAAGGTACTAGTACCTAAAGAATTAGTGCTAACAGCTATTAAATATACAACAATACTAATATGTTAAAAAAATACTAGTGGCATGAAAATGGTTACCAGTATGTCTCATAGCTAAGATGTTTAATGTAAAAACAACTTGCCATATTTAGATTTCACCCTATGATATCAAACACTTTGCTTTTTACTTAATGATCTATTTTATTCTGTTAATTCTGTATTCTTTTCATAGTGTTTGAGTTGGTACCTAAAGGGTAAGTATATGTACCTATAGATCACAGTCACACACATTTTTTTTAGTTTAGATTTTCTGTATTTTTTACTTCTTCTCCTGCCTGGTTCTA[G/A]CCCAGTGATGGAGGTCCCGACAGACAGCCCTCTATCAGAAGAAATGGCCCATTTGTACTTCAGAGACATCATTCTAGGAATCGAATACTGTAAGTCTGTCCTGTCTAGGATTTTTTGTGTGTTTTAATTCTCATTAATAAACTTCATGAGATTAAGTTTTTTGTTCATGTTTTATTCGTAGTGCACTATCAGAAAATCATACATAGAGACATCAAACCATCAAACCTCTTGCTGGGTGATGACGGGCACGTCAAGATTGCAGATTTTGGGGTCAGCAATGAGTTTGAGGGGAACGACGCACTCCTGTCGAACAGTGCAGGAACACCAGCTTTCATGGCACCTGAAACACTGACGGATCAGGACCAAAGATTCAGTGGAAAGGTAAGAAGAGTTGTTATGTTGGCTTTCAAGCATGAAAAACACAAAAAAGTATGTCAGTTAAGCACCTTGACTTTATAACGACATCAAATTGACATCTAACATTGATGTAAAAAAAACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22600
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 |
---|---|---|---|---|---|
ENSDART00000125864 | Essential Splice Site | 300 | 484 | 9 | 16 |
Genomic Location (Zv9):
Chromosome 15 (position 14343088)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 15388051 |
GRCz11 | 15 | 15324073 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGGCACCTGAAACACTGACGGATCAGGACCAAAGATTCAGTGGAAAGG[T/G]AAGAAGAGTTGTTATGTTGGCTTTCAAGCATGAAAAACACAAAAAAGTAT
Long Flanking Sequence:
CATAGTGTTTGAGTTGGTACCTAAAGGGTAAGTATATGTACCTATAGATCACAGTCACACACATTTTTTTTAGTTTAGATTTTCTGTATTTTTTACTTCTTCTCCTGCCTGGTTCTAGCCCAGTGATGGAGGTCCCGACAGACAGCCCTCTATCAGAAGAAATGGCCCATTTGTACTTCAGAGACATCATTCTAGGAATCGAATACTGTAAGTCTGTCCTGTCTAGGATTTTTTGTGTGTTTTAATTCTCATTAATAAACTTCATGAGATTAAGTTTTTTGTTCATGTTTTATTCGTAGTGCACTATCAGAAAATCATACATAGAGACATCAAACCATCAAACCTCTTGCTGGGTGATGACGGGCACGTCAAGATTGCAGATTTTGGGGTCAGCAATGAGTTTGAGGGGAACGACGCACTCCTGTCGAACAGTGCAGGAACACCAGCTTTCATGGCACCTGAAACACTGACGGATCAGGACCAAAGATTCAGTGGAAAGG[T/G]AAGAAGAGTTGTTATGTTGGCTTTCAAGCATGAAAAACACAAAAAAGTATGTCAGTTAAGCACCTTGACTTTATAACGACATCAAATTGACATCTAACATTGATGTAAAAAAAACAAAAAACATCAACACTCAATTACAGTGCAGTCCTGTAATCAATTCTTTTACTTTTGTTTTTGACGCCAGTGTTATTAATGTGCAGTTGAAGCTTTTAGATGAATAGGTGCCAATAGGGTATTTTCTAACAGATTTTATTTACACTTTTTTGAAAACTGACTCCTGACTTTTGAAAACTGACTTTTGAAAAAGTCCCGTTCACTTGACAGTGGACCAGATTTTTGAGCTCACACTCCACATCTTAATGTTGAAGGGGGACATATCTGCTTCTTAAAGGGAAAGTTCACCCAACAATTTTCTCGTCCTCCACTTGCTATTTTTTTTAACTATTTAAGAGTCTTTCTTCTGTTGAACAATATATATATCGTCACCTTAAAATTATAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28418
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000125864 | Essential Splice Site | 459 | 484 | 16 | 16 |
Genomic Location (Zv9):
Chromosome 15 (position 14349996)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 15394959 |
GRCz11 | 15 | 15330981 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTTTGTGTTTGCGTCTATCTTCATATTTTGCTGGTGTGTGTCTCCAAC[A/T]GCAGAGGGAGTAACAGTAACAGTAACGGGAGCAGAGAAGGGGAGCTGGAA
Long Flanking Sequence:
AAAATAATGTCCCCACAAGATAAAGATTTACAGGTATTGTTATACTTGTGGGGACATATTTTTGGTCACATGAGGAAAATGACTCATAAATCATCCTGAATTTAGTATTTTGAAAATGTGAAAGTGCAGATTAGTGTAGTGGATAGAAAATACACTCTGTCTGGTATAAAAATCATTACCACTTTAGCAATCCCTGTAAAGATAGCTGTACGTATGTGTGTATACTGGTTTTAGTGGTTTGTGAGGACATGTTTTTATAATGACGTGCATAATGTTGATGGGGTTTATGAGGACATGTCCTGTGTCCTCATAATTCAAAATGCTTAAAAATAATCTTTCAAAATGTTTCCTCTGAGGATTGGGTTTAGGGCTAAAGGTGGGTTAAGGTCATATAATAAGCAGCTTTTACAGTGTTAAATATAGGCCTATGGGGAGTCCTCATAAACCACCAGTTTTGTGTTTGCGTCTATCTTCATATTTTGCTGGTGTGTGTCTCCAAC[A/T]GCAGAGGGAGTAACAGTAACAGTAACGGGAGCAGAGAAGGGGAGCTGGAAAACCTTATCGAGGATGAAATTTTTCCATGAATCAGCTCAAATCATTTTGCAGACCGACCCAGTTGTGCGATGTGACCATTTTTCACATCTTCATTTGATTATTTTATAATCAACATGCTTTGTTTCTACTGTACATCACAGAGTGATGTAAGGATAGACTTTGAGGTATACGTTAAAATATAAAGCTGAATCTGGTTAACAATACTTCACATTTGTGTAACAATTAAGAAATTGTTAACATCTGCATGCATTTAACAGCAAAAGGTTACGTCTCATGGAATGGAATTTTAACTTTAATCAGTATTTATATAAAAAGATTGTAAGACTGAGTATGACTGAGTAGCATGTAATGTGGCAGCAGCAACATTAGCGATAATCAAGTAACTTTTGCTTATGATGTAAGTAAGCTGTTGAGTTTTGTTGTTGTACTGTATTTTTGTTCATTCAATG
Associated Phenotype:
Not determined