Busch Lab

ZMP

per1b

Ensembl ID:
ENSDARG00000012499
ZFIN ID:
ZDB-GENE-040419-1
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.
Availability:
Order Allele From ZIRC
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.
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.
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
Availability:
Order Allele From ZIRC
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