ZMP
per1a
Ensembl ID:
ZFIN ID:
Description:
period 1 [Source:RefSeq peptide;Acc:NP_001025354]
Human Orthologue:
PER1
Human Description:
period homolog 1 (Drosophila) [Source:HGNC Symbol;Acc:8845]
Mouse Orthologue:
Per1
Mouse Description:
period homolog 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1098283]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa16532 | Essential Splice Site | Available for shipment | Available now |
| sa14433 | Nonsense | Available for shipment | Available now |
| sa41652 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16532
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 |
|---|---|---|---|---|---|
| ENSDART00000079459 | Essential Splice Site | 385 | 1229 | 7 | 18 |
| ENSDART00000100468 | Essential Splice Site | 385 | 1352 | 7 | 19 |
| ENSDART00000121968 | Essential Splice Site | 420 | 1387 | 7 | 19 |
Genomic Location (Zv9):
Chromosome 10 (position 23019900)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 22850238 |
| GRCz11 | 10 | 22819690 |
KASP Assay ID:
2260-3205.1 (used for ordering genotyping assays)
KASP Sequence:
TTACCTGCATCCAGAAGACAGACTGCYCATGGTGGCCATTCAYAAGAAAA[G/A]TGAGTCRTTCATTCTGAATTCAGTGGTGAATGTTTGYAAAGTAAGACTCK
Long Flanking Sequence:
TCTCCAAACTCAAATAATTCAAGAAACTTCACATACCATCTATTATAGATTATAATAGCTTTAAACATTGTTCTAGTATCACTTTAATTACTCTAACTACATCTTATTATTAGCCAAACGTGCCCTTAATTGAACAATCACCCTTATGTAATATTGACACCTAATTAAACACACCCTACTCTCTGTTATTGTTGTCTGTCTCAGGTTCTGATGTGTTTTGCTTTTTTGAAACAGCGCCTCGTATCCCAGCAGACAAGAGAATATTTACCACCAGTCACACCCCGAACTGTCTCTTCCAGGAGATTGATGAAAGGTTCGCATGTTTTGTCACAATTTAACCATCCATGTCTATTTTGGAGTAGTTGCAATAATTTTCTCCCCTCTCGTTTGCAGGGCTGTGCCATTATTAGGTTATCTGCCTCAAGACTTGGTTGGGAAACCGGTGCTTGTTTACCTGCATCCAGAAGACAGACTGCTCATGGTGGCCATTCATAAGAAAA[G/A]TGAGTCGTTCATTCTGAATTCAGTGGTGAATGTTTGCAAAGTAAGACTCGTTAATCAAATTTTCATCTTCGCTAGTTCTTCAGTTTGCCGGACAACCTTTTGATCACTCGCCCCTGCGTATGCGTGCAAGAAGTGGTGAATATCTGACCATTGATACCAGCTGGTCTTCCTTTATCAACCCATGGAGCAGGAAGGTGGCTTTCATAGTGGGACGCCACAAAGTTCGAACGTAAGTGAAAATAAAAATATTCATGAGCTAAAACAGTTATTTTCGTAAACTAAAACCAAAACAAAGGCTAAAACTATTGGTCAAGACTTGAATGAAAAACTAAAACGGAAATTTGAAAAAAAGCTTTATTGTGAAGAAAATAAAAAACATGTTTTCAGATTTAACAAACATGCATCCTCTTGGCACCAATAACCTTAGTGGTAAAGTTTACTGTAGTGTTCATGATGACCTGAGTTTGATTCCCAACTCAAGGATCTTTGCTGATTCTTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14433
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 |
|---|---|---|---|---|---|
| ENSDART00000079459 | Nonsense | 774 | 1229 | 15 | 18 |
| ENSDART00000100468 | Nonsense | 813 | 1352 | 15 | 19 |
| ENSDART00000121968 | Nonsense | 848 | 1387 | 15 | 19 |
Genomic Location (Zv9):
Chromosome 10 (position 23015154)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 22845492 |
| GRCz11 | 10 | 22814944 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
YCCTGACTCCCTTTTTATTTGATTTTAGGAGTGAACAGCTCCCAGAACTA[T/A]CCTTCTGTAGGYAACACCAGCAGTCGTCGGCATGGCAGRGGTGGGAAAAG
Long Flanking Sequence:
GCCTTCCCCCACTGCAGCTGTGCATGAGAAAGAAAAGGAGAAAGAGAGGAGAAGTGGAGGAAGCGCAGGGAAGGGTCTCACGAAAGCCGTGTTATCCGCACATACTCAACAAGAAGAGCAAGCCTTCCTCAACCGCTTCAGAGACCTCAGCCAGCTGCGGATGGTCCAACCTAGTGGGCTGCCACCACCACGCAGATGCACATCTATACCTGGAACAAAAGGTACCTGAATTGTGCAGTTTTCAAGAATTTGTTATTTCGACCCATGCACAAGATGAAAAACTCTCTTTCTGGAGGGCCACAGTCCTGTAAAGTTTATCTACATTCCTAATCAAACTCACCTTTAAAGACAGAACCAATGTTTTTAGGATTACCTGAATATCATTGGTAGGTGTGTTTGATTAGGAATAGAGATGAAAGGTAGTAGCCCTCCAGGACTGAAATTGAATATCCCTGACTCCCTTTTTATTTGATTTTAGGAGTGAACAGCTCCCAGAACTA[T/A]CCTTCTGTAGGCAACACCAGCAGTCGTCGGCATGGCAGGGGTGGGAAAAGACAGAAACATCAAGTAGATGGCAACATTCCAAACAATACCCCAATTTCTGCATCTGGCCCCTATAGAGGACCTAATCCTGCTCAGATAAGACCCAACTTCCCCTCTGTCCAGCAATCTTCCAACTCTTGGGCTCCATCTGCTGCATCCCAAACCAACGGTGCTCCAGTGGGTACATCTTTTCCTCCAAGCTACATGACCATGTTTCCAACTTCCTCACCATTCTCAGTAACCCAGATGGGAACTGATCCTTCCCTGCAAACAGGAGTCCCTAGATTTCCAGCGCAAGGCTTTCCTTCAGTGATGCCACCAGTCATGACATTCATGATGCCCAACTACATGTTTCCACAACTCTCTAATCCAGGATCACAGTTGAACCCAGCCAACTCCCAGCTCAACGCCCAAATGAACTCCTTTGGGCAGTTCCCTCCCCCTGTTGTTCAAATGAGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41652
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 |
|---|---|---|---|---|---|
| ENSDART00000079459 | None | None | 1229 | None | 18 |
| ENSDART00000100468 | Essential Splice Site | 1119 | 1352 | 15 | 19 |
| ENSDART00000121968 | Essential Splice Site | 1154 | 1387 | 15 | 19 |
Genomic Location (Zv9):
Chromosome 10 (position 23014235)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 22844573 |
| GRCz11 | 10 | 22814025 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAATTCCAGCAATCGCAGCAACACTCAAGATGCCAAACTAAATGACCAT[G/A]TAAGTATTAAGGACTATTTTAAACTCTTTGGTTTTTCCAGAACCTTGCTT
Long Flanking Sequence:
AGTTGAACCCAGCCAACTCCCAGCTCAACGCCCAAATGAACTCCTTTGGGCAGTTCCCTCCCCCTGTTGTTCAAATGAGTGTACCAATGTTCAATCCTGCAATGGGGCAATTTTATCCTTTGGGCTCCCAAATGAACCCTGCTATGCCTGCAATGATTCCCCAGCAGTTCTACAACCCAAATTATCAGTTAAATTTTTCCAACTCTCCATCAATGCCTGCTGCAAATGTCAGCACTACACCACATGGACAGTCTCGCTCCAGCACACCCCAGTCCACTGGGCCACAGGCTGGTGAGAGGGATGGGGCTGGATCTCCTTTGTTTCAGTCTCGATGCTCTTCCCCACTTAATCTTCTACAACTTGAGGAATTGCCAAGCAACAGAACGGATGCTACACAACAGACTCCACCTCCAGGGGGTGGGGCAACACAAGGCGGTGTGGTAGTGGTGCAAAATTCCAGCAATCGCAGCAACACTCAAGATGCCAAACTAAATGACCAT[G/A]TAAGTATTAAGGACTATTTTAAACTCTTTGGTTTTTCCAGAACCTTGCTTCTTAGCTAATTTGACCTAATTTACTTTAGCCTGAAGTCAGTGAGTCCAACCAGGATGCGCTGTCAACGTCCAGTGACATGTTGGACCTACTCCTGCAAGAGGATTCCCGCTCAGGCACTGGGTCATCAGGGTCAGGGTCAGGGTCTGGCTCCTTCGCTTCTGGATCAAATGGATGTAGCACATCTGGAAGTGGCACTAGTGAGTAATTTGTTCCTGTATGCTAAGTTCTTAAAGTGATATATCACCAATGTACTGGTCACTCATGCAATTCCATTTTTCCCCTTTATAAATGTTAATCTTAGGGAGCAGTAATACTAGCAAGTACTTTGGAAGCATAGACTCCTCAGAGAATGACCAGAATCACAAACCAGCATCTGGAGACCTGGGAGGGGAACAGTTTATCAAATTTGTCCTGCAGGACCCAATATGGCTCCTCATGGCCAACACAGA
Associated Phenotype:
Not determined