ZMP
clock
Ensembl ID:
ZFIN ID:
Description:
circadian locomoter output cycles protein kaput [Source:RefSeq peptide;Acc:NP_571032]
Human Orthologue:
CLOCK
Human Description:
clock homolog (mouse) [Source:HGNC Symbol;Acc:2082]
Mouse Orthologue:
Clock
Mouse Description:
circadian locomotor output cycles kaput Gene [Source:MGI Symbol;Acc:MGI:99698]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39276 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa14713 | Essential Splice Site | Available for shipment | Available now |
sa23683 | Nonsense | Available for shipment | Available now |
sa17257 | Nonsense | Available for shipment | Available now |
sa37017 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39276
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025575 | Essential Splice Site | 27 | 892 | 2 | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 22216712)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 22244879 |
GRCz11 | 20 | 22144552 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTATCTTTGATGGGTTGATGGAAGAAGATGAGAAGGACAAAGCAAAAAGG[T/C]GATTATACAAGTAAAACTTTATGATTTTAATTGCTCACAGCGATATCCTT
Long Flanking Sequence:
AAAATCAAAAGGTGGCCAATAATTTAAACTCAATTGTATATTCAAAATATGAAAAAAAACACACAAAAATGCAAAGGGGTATCTAAAATTAACAGAATATGAAAAAGAAAGTTCAGCTGAAAACAAAAAGTTAAACATGAATATATCAATATATCAGTAATACTAAAAACTTTTTTACTTTAGTTGAATCACTAGACTCTTTCAAGATTTTGTATGACATTTTAAAAAGCTTGAGTCCCTCACTATTGCATATTGGGGAACAGTCTATTAAAATAATGTTTAACAGCTTCAAATATGAACTGATTGGGTTGGCATGGGAATTTCTGTCAGTTCACTGGAATTTTATCACAGTTAAAGCTGTTATGATCACAAACACTGTCGTTGATTGGTTGAATTTGGGCAAGCTAGTCTAACTACTCTTAATTTTGCTCTCTTTCAGGGATGACAGCAGTATCTTTGATGGGTTGATGGAAGAAGATGAGAAGGACAAAGCAAAAAGG[T/C]GATTATACAAGTAAAACTTTATGATTTTAATTGCTCACAGCGATATCCTTTGTCTTGTCCTGAGCTGAACTCTTTTTGTGATATATTGGCGTATTCCATTATCTCATGCAAGAGTGGTTTAAACATGATTCATTACACTAGATGATTGTATAGACAAGTCCTTTTTCGTGGTAGAGGATCTGAAGTGGTTTTTTGCACCGGGAATAGAAACTTAAGTGTGACCTAGTTATGACTGTTTAAACCTGAGCGTACGCCTTCACCCTCGTCGTCTGTATACAATCACCACACCGTGAAATGGTTTCTCTCAGCATTGCTGGATTCCTCTGAGATTAGATAGAGCTCGACTGTGACTTTGAAAGCTTCTGCAATAGCAATGGAATTATGCTATCATCCTATTATCTTAAAGTCTACAATTGGCTTCCATTGTTGAATTTTCCACCTTTTTGTTTTTGATTTTTCTCATCTTTCTATAGAGTTTCTAGAAATAGGTCGGAGAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14713
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 |
---|---|---|---|---|---|
ENSDART00000025575 | Essential Splice Site | 76 | 892 | 3 | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 22217335)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 22245502 |
GRCz11 | 20 | 22145175 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAGTYTACCATCCTACAGAAGAGCATCGACTTCCTGCGCAAGCACAAAG[G/A]TTACTCTTGTTGCATAACAATTATTGTTTATYATTTGGAAAATTTAAGTA
Long Flanking Sequence:
ACATGATTCATTACACTAGATGATTGTATAGACAAGTCCTTTTTCGTGGTAGAGGATCTGAAGTGGTTTTTTGCACCGGGAATAGAAACTTAAGTGTGACCTAGTTATGACTGTTTAAACCTGAGCGTACGCCTTCACCCTCGTCGTCTGTATACAATCACCACACCGTGAAATGGTTTCTCTCAGCATTGCTGGATTCCTCTGAGATTAGATAGAGCTCGACTGTGACTTTGAAAGCTTCTGCAATAGCAATGGAATTATGCTATCATCCTATTATCTTAAAGTCTACAATTGGCTTCCATTGTTGAATTTTCCACCTTTTTGTTTTTGATTTTTCTCATCTTTCTATAGAGTTTCTAGAAATAGGTCGGAGAAGAAGAGGCGAGACCAGTTCAATGTGCTCATCAAGGAACTGGGCACCATGTTGCCGGGCAACACCCGCAAGATGGACAAGTCTACCATCCTACAGAAGAGCATCGACTTCCTGCGCAAGCACAAAG[G/A]TTACTCTTGTTGCATAACAATTATTGTTTATCATTTGGAAAATTTAAGTATACATAAAAATAGGGTGGGCGAATTCAAAGTATCTAGCAGCTGTTAAAGATCAAGATCTGGACCTCCCTGTACACTGTAAAACGTTTTACTTGGTTAAACTTACAAACTCACGTTCATCAGCTGACATATATCAACTAAAACTCAACATCTTTAGTTGTAAACAAAGAGTCTCTCTTGAGTTGACTCACATTTTCAAGGCAGCTGGTGAACTTGAGTTTGTAAGTTTAACCAATGTCAAATGTTGTACTGTGTATAATCAATGCTCAAAGTCACATCTTCTCCAAAACACATGATCGCCCACAGGCTGATCTGAGACCAGAAGTGACAAGAATATTCAAATATTCGACTCTGAACTTAAGTTAAATGCAGCTCTGTAGAAGAGCTCTCAAGTTGAACATATTTGGAAGATCGCAGGCAATTTTAACCGTTTCAGTGGACTCGCGTCTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23683
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 |
---|---|---|---|---|---|
ENSDART00000025575 | Nonsense | 203 | 892 | 7 | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 22222543)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 22250710 |
GRCz11 | 20 | 22150383 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACATGCTCCGGGGCACCATCGACCCCAAAGAGCCGCCCGTTTATGAATA[T/A]GTCAAGTTCATCGGAAACTTTAAGTCCCTCAACACTGGTGAGTGTCAGAA
Long Flanking Sequence:
TGGTTATACTCACGACAGGTATTGTTTGGTAGTTTGGTCATTTATTTTACTAATTTGGCAACCGTCAAACGCCATCAGAGAAACCGTTTGAAAAAAAACATTGGTGTTCCATTTGGGACGACGCTGTGTTCATATACTATGCTGCTGAGTGTGTAAGTCCATAAGTACATGCATAAGTGTATAGTGTGTCATTTGGGATGCAGCTTTTGATTAAACTTTGCAATGACTCAAAACATTTTTATTCGAAAAATGAAAAAATATTAGAAATGATCTCCTCATGATCAAATCATTCTTAGCATTCTCATTCAGCTTCCTTCAGTACCTCTCCCTGCTATTGTCTCATTTCTATGAGCACCGATCACTAAGCTGCAGCTTGTTAATGTTGTTTTCTTGTTTTTGTTTTGTTGCGTTCGCTTCCCTGCAGCAAAGAACCAGTTGGAGTTTTGTTGCCACATGCTCCGGGGCACCATCGACCCCAAAGAGCCGCCCGTTTATGAATA[T/A]GTCAAGTTCATCGGAAACTTTAAGTCCCTCAACACTGGTGAGTGTCAGAAGCAGCGCCAGCCTTTCATGTGGATCTGTTTATTGAATTATCCAGCCAAGTGCTTGATTGCTTGTGCTTCTTATGAGAGTGGCAGGAGCAAGCATCGTTATTTAAAAAGGAAGCGCTGCAAAGAAAAGCCAGAGGAACAGGCTTCTGACCCAGATTTTAAGACTGGAAGTTGAATGTTTTGTGGTGAAGTGTGTAATTAGACCAGTGTTGAAGAATATAAGTGCAAAAAATAATGAATGAGAGTTATGTTTTTACACAGCTGTTATTTGCTCAAGCAGAATGTCCTGTCCTGAATTCATATAGTGATAGCTGCTTGGGACTATCAAACGGTGTGTTGTTTCTACCTACAGAGCTGCTGTGTTCAGATTTTCTAGAAAATCAACCTACTAAAATTGACTTAATTATAGTTTATACATGATTATGTAAACATTTTAACCATTACAGATTTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17257
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 |
---|---|---|---|---|---|
ENSDART00000025575 | Nonsense | 414 | 892 | 13 | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 22232759)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 22260926 |
GRCz11 | 20 | 22160599 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGCTCCGAGTCTCAGTTGAACACCWCCAGCTTGAAGGAGGCSCTAGAG[C/T]GATTCGATCACAGCCGCACACCCTCAGCCTCKTCACGCAGCTCCCGCAAG
Long Flanking Sequence:
AATTAAAACTGCTTTTGTTTTAGCCGAAATAAAACAAATAAAACTTGTATAAAAAGAAAAAATATTATCAGACATACTGTGAAAAATTTCCTTGCTCTGTGAAACATAATTTGGGGAATATTTAAAAAAAAGAAAAAACAAAAAAATAAATCAAAGTGGGGCTAATAAATCTGACTTCAACTGTATACTGTATATGAATTTATTTTTGTACATGTTTTAAAATACACATTTTTTTCCTTTCGTTATTTTTGTCTTTTTCTTTTTTTCCATTTACAAATGTATGTTAATTGCATTAAAACATTTGACATAATCATTTTTAAACATATGATATTAATCAAACTTTTCCATTACCTTTTTTATTTCTGTGGTAATCAACATAGTATGACGCAGTTGATCTTAACTTAAAGAACAATCTTTTAACACTGTTTTGCTCTGCTCAGTCTCAGGACTCTGGCTCCGAGTCTCAGTTGAACACCTCCAGCTTGAAGGAGGCGCTAGAG[C/T]GATTCGATCACAGCCGCACACCCTCAGCCTCGTCACGCAGCTCCCGCAAGTCCTCCTCACACACCGCTGTCTCTGACCCCACCTGTATGTACTTCCTCAACAATGCATACACACATACAGACATATTTTAATAGTGTTACTAACTTATGTGTGTTTATTTGTCTGTAGCCACACAGACCAAGCTGCAGACAGATCGCAGCACACCACCTCGCCAATCAGTGTCAGCCATTGAGATGACATCACAGCGGAGGTCCTCCATTAGCAGTCAGGTTAGTTCTTGTCATCATCACTTGGTTCCCAACCTTTTTTAAGACCCCCTTTCCCCCTGAAAAATATTGTAAGGCCCACATTTAATGATATTTACACTCATATATTAAAAGTTTGCAGTAGATATGACAAAAAAGTGGTTTTCAAACAATAGGTATGTTTATTACTTTATCTAGATAATAGCCTAATGTGAAATATAAAAGCAAAACATCAGTAGGCCATTTGTAATGGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37017
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 |
---|---|---|---|---|---|
ENSDART00000025575 | Splice Site, Nonsense | 476 | 892 | 15 | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 22235745)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 22263912 |
GRCz11 | 20 | 22163585 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTAGTTTGTCTCTGTTCAGGCTGTTTACTCTTGTGTTTGTGTGTTCAGT[C/A]GATGAGTTCTCAGACCACAGGACAGACGATGGGAACATCTCTTGTGTCTC
Long Flanking Sequence:
TGAATGACCCTCAACTCGTTTTTTTGTTTTCCATTGGTATTCATGAGTACCTTGTTTGCCCTGAACAGTTCAACTGCAGAGAAGCCTTCAGATTCCATAAATTGTTTGGTTTTGTGTATTTAAAATAGGGGTCAAAACAATTATTTACTTTTGAAATCCGTCTTTTCACACTTCTTCATTTGCAGCTAATACAGCAGTTTTAAATACTCAATGTAGTTCTAAAAGAAAAACAAAACAAACAATTCATATAGAGCGGAGGAAATTTTGCCTTAATATCAAATTTAGTACTTTTTTTTTTTTTTTTTGCATTTGGCCTCTTTAATTACTTTTATCGAAGTTGCTTTCAGATTACAAAAAAATAAAAAATAAATAATAGAAAATTCTGTGAAATACTGCAAATATTGTAATTGCTAGATAACTAATCAAATGATTATATTACTAAAGAATATGTGTAGTTTGTCTCTGTTCAGGCTGTTTACTCTTGTGTTTGTGTGTTCAGT[C/A]GATGAGTTCTCAGACCACAGGACAGACGATGGGAACATCTCTTGTGTCTCAGCCTCAGCAGCCTCAAACACTTCAGGCCACTGTTCAGGTGATTCTGCTTCAGTTACTGCATGCACTATCAGCGCTCTTGCTCATTAGTGTTCCACTGATATGGGTCTTTCAGCGCCTGCTGTGGTGAGAGCGAGTGGGGTGGTCAACGTGTGTATAGAAATATTGAACTTTTGACACGTGTGATCAATAAGGGGATTGACACTGACCCAGAGAGTGGGACTGGGTAAACATGCCACTTGAATCAATGAAACGGCTACTGAAACCTTTTTGTAGTTTTCATAATATAACAATATGCACGCTAATAATTATTTTATTTAGCAAGGATGCATTGATTAATAAGTCTTTAAGTAAAAAGTAATGTTTAATTTGCTACAAAAATCTGTTACACATAAACATTGTTCTTTTCAACTTTGTATTCTTAGAATTTTTCACGTAATTCACAAAAAAAA
Associated Phenotype:
Not determined