ZMP
per1b
Ensembl ID:
ZFIN ID:
Description:
period homolog 1b [Source:RefSeq peptide;Acc:NP_997604]
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 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa31594 | Nonsense | Available for shipment | Available now |
| sa41011 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa41012 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa21065 | Essential Splice Site | Available for shipment | Available now |
| sa21066 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31594
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 |
|---|---|---|---|---|---|
| ENSDART00000011082 | Nonsense | 939 | 1398 | 15 | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 52296435)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 50566185 |
| GRCz11 | 7 | 50841255 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGTCCTGGCCCACATCAGGGTCACAAGCCAGCGTTCCCAATGTCCAATA[T/A]CCACCCACCGTCCTTCCTTTTTATCCAGTCTATCCCCCAATCTCCCATCC
Long Flanking Sequence:
TGATTGATTGACATATGCATGGATGGATGGATGAATGGCTGGTTGGTTGGTTGGATGGGTGGATGGATGGATGGATAGATTGATTATATGGATGGATAGATTAATGGATGGATAGATGGACAGACAGACAGACAGAAAGATTGATCGATCTGTGGACTTTCTTAGTCTTTGTCAACCTATCAGCTTTTATTTTGCTGTAAGAACGGACTGAATATACAATATCCCTCTTTTCTTTTCTTGACAGGTGTGCGCTGCTCTCGTGATTATCCAGCAGCAGGCAGCAGTGGGCGCAGACGTGGTCGAGGAGGCAAAAGACTGAAGCATCAGGAATCTTCAGAGCAAACAGGTTCTTGTAGTCCAGCCGGACCAATAAGAGGCCTCCTCCCTGGAGTTCCCGCTCTGGGCAGACCCTCTAACCCCTCCATACCCATGGGTCCTACAGCCAGCTCCTCGTCCTGGCCCACATCAGGGTCACAAGCCAGCGTTCCCAATGTCCAATA[T/A]CCACCCACCGTCCTTCCTTTTTATCCAGTCTATCCCCCAATCTCCCATCCCGTCTCAGACCCCAGCATGCAGTCAGGCCTTCGCTTTCCCCTTCAGAACTCACAAATGGCGCCTCCGATGGTCCCCCCAATGATGGCATTGGTATTACCCAACTACATGTTCCCACAGCCCAGCGTAGGCATGGCTCAGCCCTTCTTCAGCCCAAACTCAGCTTTCCCCTTCGCCGCTGCCAACATGGGCTCGCCTGCTCCCTGTCAGATCCAGACCCCAATACAACGCGCTCATTCTCGCTCCAGCACACCTCACTCCTATAGCCAAAGAGAAAACGGTGCAGAGAGAGAAGGAGCAGAGTCTCCCCTCTTTCAGTCCCGATGCTCATCGCCCTTAAATCTGCTGCAGCTGGAAGAGTCGCCAAGCAATCGGTTCGAGGTGGCGTCAGGACAGCAGACTACATCTCCTATGGTGGGACAAGGAGGTGGAGCTGGAGGACAGGCCTCGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41011
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000011082 | Nonsense | 1115 | 1398 | 15 | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 52296962)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 50566712 |
| GRCz11 | 7 | 50841782 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGCTGGAGGACAGGCCTCGTCTAACCAGAGAGGGTCAGCGGTGGATT[C/A]AAAAACAAACGAAAATGTAAGTAGTTAAAAAGAAAATTTGATTTAGGTAG
Long Flanking Sequence:
AGTCTATCCCCCAATCTCCCATCCCGTCTCAGACCCCAGCATGCAGTCAGGCCTTCGCTTTCCCCTTCAGAACTCACAAATGGCGCCTCCGATGGTCCCCCCAATGATGGCATTGGTATTACCCAACTACATGTTCCCACAGCCCAGCGTAGGCATGGCTCAGCCCTTCTTCAGCCCAAACTCAGCTTTCCCCTTCGCCGCTGCCAACATGGGCTCGCCTGCTCCCTGTCAGATCCAGACCCCAATACAACGCGCTCATTCTCGCTCCAGCACACCTCACTCCTATAGCCAAAGAGAAAACGGTGCAGAGAGAGAAGGAGCAGAGTCTCCCCTCTTTCAGTCCCGATGCTCATCGCCCTTAAATCTGCTGCAGCTGGAAGAGTCGCCAAGCAATCGGTTCGAGGTGGCGTCAGGACAGCAGACTACATCTCCTATGGTGGGACAAGGAGGTGGAGCTGGAGGACAGGCCTCGTCTAACCAGAGAGGGTCAGCGGTGGATT[C/A]AAAAACAAACGAAAATGTAAGTAGTTAAAAAGAAAATTTGATTTAGGTAGTGAAAGTAGGGTGGCACAATGGTGGCACAATAGGTAGCATGATTGCCTCACAGCAAGTAGGTTACTGGCTCTCTGTGGTCATTAAAAATCCTATGACACTACTCGTAAAGAGTAGGGGTGTAAATCCGGTGTCCTGGCCAAATTCCCAGAATAGTATTTATATCAGGAATAAAAGATGCATTTTAACTAGATTTTTTTGCTCAAGGCTAAAAGCTATAGTTGAAACCCCATACAATTTGTGACACCATTTCTGATTGCTCTGTAATCAGCTATCTTTGATGAGAAAAATGCAGGTTTCCATATAATTCATTCATGTTGTCCCAATGCAAATTAAGTTCGCTTATAACTTGTGGATTGAATATAAAACAATTAAGTTGCCCAAAAAAACCTTTTTGCATGGATTTGTGTGTTTATTCGTATCAATTAATCACAGTCTGTGCTTGATTTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41012
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000011082 | Nonsense | 1257 | 1398 | 18 | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 52298982)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 50568732 |
| GRCz11 | 7 | 50843802 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAATTGACCCAGTATATGTCTTTTTTTCAACAGAGACAGAGATTCAGTGT[T/A]GAAAGAGGACCGAGCTGCGCTGAGAGCCATGCAGAAACATCAGCCTCGCT
Long Flanking Sequence:
TAATAATAAAAGTAATATTTAACGTGTCTATTTTGTGTCTGACACATTAAATATTGCATTTTAAAATACTAATTATTAAAAATATGTCTGTAAGCATGTGTGATTACACGTGTTTCCCTCATGCCAGTTAACAAATGTGTTGCACAATTTATGCAGCCAATTTAAAAAAATAATATTTTTTAATAGTTTAACTGAAACTATCAATCGGTTAAAAACGCACCCTTTTGGTTAATAGTAAATTGGTTATTATGAGTATCCCTAATTCATGATATTTAGTAACTCACTAAATGACATCCCTTGCAAATTCTACAATTTGTATTTGGTTTGCTTTTTTTTTTTGCAACCTTACCTTTTGTACTCACAATATCACAACACACATAGTAAAAAAAAGCTGCTTCCTGCTAACGCCCTAAAATCACACATTCCCAAAGACCCACTGTAAATAGCCAATAATTGACCCAGTATATGTCTTTTTTTCAACAGAGACAGAGATTCAGTGT[T/A]GAAAGAGGACCGAGCTGCGCTGAGAGCCATGCAGAAACATCAGCCTCGCTTCACTGAAGAACAGAAGAGCGAGTTGAGTCAGGTTCACCCATGGATCCGCACCGGACGCCTTCCTCGTGCCATTAACATTTCAGTGAGTTCAATTCTCAGACAGTAACTCCCAAAATGATAACACTCAGGTGTAGAGAGGTTTATATTTATAATGCTTTGTGTGTCTTTCAGGCATGTGCAGGCTGTAGATCCCCTCCTTCAGTCCCCTCTGCGACACCATTCGACGTGGAGATCCACGAGATGGAGTTCTGCAGTGTTTTAGCGGTGGCGGAAGAGAAACAAACCCCTGCAGATACAGTTATGGAGAAAAGCGAAACTGACGGACAAAATGAGACATGCAAAGAGAACAATGGGACTGTTACGACAGCACAAATCAATGATCAAGAAATGCTGACGGAAGAACAGGAAATGACCTCGCAGATCGAGGAAGAAATGGGTGCCTCACATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21065
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 |
|---|---|---|---|---|---|
| ENSDART00000011082 | Essential Splice Site | 1301 | 1398 | 18 | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 52299116)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 50568866 |
| GRCz11 | 7 | 50843936 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCACCCATGGATCCGCACCGGACGCCTTCCTCGTGCCATTAACATTTCA[G/A]TGAGTTCAATTCTCAGACAGTAACTCCCAAAATGATAACACTCAGGTGTA
Long Flanking Sequence:
ATGTGTTGCACAATTTATGCAGCCAATTTAAAAAAATAATATTTTTTAATAGTTTAACTGAAACTATCAATCGGTTAAAAACGCACCCTTTTGGTTAATAGTAAATTGGTTATTATGAGTATCCCTAATTCATGATATTTAGTAACTCACTAAATGACATCCCTTGCAAATTCTACAATTTGTATTTGGTTTGCTTTTTTTTTTTGCAACCTTACCTTTTGTACTCACAATATCACAACACACATAGTAAAAAAAAGCTGCTTCCTGCTAACGCCCTAAAATCACACATTCCCAAAGACCCACTGTAAATAGCCAATAATTGACCCAGTATATGTCTTTTTTTCAACAGAGACAGAGATTCAGTGTTGAAAGAGGACCGAGCTGCGCTGAGAGCCATGCAGAAACATCAGCCTCGCTTCACTGAAGAACAGAAGAGCGAGTTGAGTCAGGTTCACCCATGGATCCGCACCGGACGCCTTCCTCGTGCCATTAACATTTCA[G/A]TGAGTTCAATTCTCAGACAGTAACTCCCAAAATGATAACACTCAGGTGTAGAGAGGTTTATATTTATAATGCTTTGTGTGTCTTTCAGGCATGTGCAGGCTGTAGATCCCCTCCTTCAGTCCCCTCTGCGACACCATTCGACGTGGAGATCCACGAGATGGAGTTCTGCAGTGTTTTAGCGGTGGCGGAAGAGAAACAAACCCCTGCAGATACAGTTATGGAGAAAAGCGAAACTGACGGACAAAATGAGACATGCAAAGAGAACAATGGGACTGTTACGACAGCACAAATCAATGATCAAGAAATGCTGACGGAAGAACAGGAAATGACCTCGCAGATCGAGGAAGAAATGGGTGCCTCACATACACAGATGACACACTAAAGACACTACGAGCCAGTGCGATGCCGGTGACATCCTTTGTGTACTCGTTAAATTGTCCTGTTGTATTTATTTTTATACACGAATGCAAATTAGCCAGGAAGGCTGACAGATGATGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21066
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 |
|---|---|---|---|---|---|
| ENSDART00000011082 | Nonsense | 1368 | 1398 | 19 | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 52299403)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 50569153 |
| GRCz11 | 7 | 50844223 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGGACAAAATGAGACATGCAAAGAGAACAATGGGACTGTTACGACAGCA[C/T]AAATCAATGATCAAGAAATGCTGACGGAAGAACAGGAAATGACCTCGCAG
Long Flanking Sequence:
ATTCCCAAAGACCCACTGTAAATAGCCAATAATTGACCCAGTATATGTCTTTTTTTCAACAGAGACAGAGATTCAGTGTTGAAAGAGGACCGAGCTGCGCTGAGAGCCATGCAGAAACATCAGCCTCGCTTCACTGAAGAACAGAAGAGCGAGTTGAGTCAGGTTCACCCATGGATCCGCACCGGACGCCTTCCTCGTGCCATTAACATTTCAGTGAGTTCAATTCTCAGACAGTAACTCCCAAAATGATAACACTCAGGTGTAGAGAGGTTTATATTTATAATGCTTTGTGTGTCTTTCAGGCATGTGCAGGCTGTAGATCCCCTCCTTCAGTCCCCTCTGCGACACCATTCGACGTGGAGATCCACGAGATGGAGTTCTGCAGTGTTTTAGCGGTGGCGGAAGAGAAACAAACCCCTGCAGATACAGTTATGGAGAAAAGCGAAACTGACGGACAAAATGAGACATGCAAAGAGAACAATGGGACTGTTACGACAGCA[C/T]AAATCAATGATCAAGAAATGCTGACGGAAGAACAGGAAATGACCTCGCAGATCGAGGAAGAAATGGGTGCCTCACATACACAGATGACACACTAAAGACACTACGAGCCAGTGCGATGCCGGTGACATCCTTTGTGTACTCGTTAAATTGTCCTGTTGTATTTATTTTTATACACGAATGCAAATTAGCCAGGAAGGCTGACAGATGATGAATGTAAAGCAGAAGTGCTTTTCGAAAGACTGTGATGTCACAATTTTTGGCTCCCACGAAGAGGTTGTGGTCTGTTTGCAAGCTCGATTTGGGCGGAGATATGGAATACTTCGCTTTAGCCCACTCTGGATTTGACCTCAAGACGCCACCTGTTCAGTTCCATCTCTAGAGACCCGCAGAAACCCGTTTCGTGGCGTCCTGAACTTTCAGATGTTGTTCAATGGGAAAAGGAGCGTTCACAGCTAGAGCGACAGCTATGACGATAACTATAAGATTTTATAAATCAAGCA
Associated Phenotype:
Not determined