Busch Lab

ZMP

per3

Ensembl ID:
ENSDARG00000010519
ZFIN ID:
ZDB-GENE-000804-1
Description:
period homolog 3 [Source:RefSeq peptide;Acc:NP_571659]
Human Orthologue:
PER3
Human Description:
period homolog 3 (Drosophila) [Source:HGNC Symbol;Acc:8847]
Mouse Orthologue:
Per3
Mouse Description:
period homolog 3 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1277134]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa21969 Nonsense Available for shipment Available now
sa41903 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa21969
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
ENSDART00000024304 Nonsense 293 1281 6 23

The following transcripts of ENSDARG00000010519 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 11 (position 41458254)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 39717935
GRCz11 11 39982080
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTGTACCATCAGGACGTCAATGTGTTTTACTCTCATACCGCACAGCCA[C/T]GACTGCCATCCTGGAACTTGGGCACAGACAGCGGTGAGTCTCTCTAGAAC
Long Flanking Sequence:
TGTAAACTTCAACATACATGCTGAAAAATACAGTAAGCTTTAAAATATAGCCTTAAAAACACAGTATACGCTTAAAAACCTGCAAACTGCATAGAACACAGTTAAAACACTGTACCCTACCATACAAAAACACGGTAAACTACAGGATACACACTTCAAAAACCCCACTGAACAGATACTCCAAAAACATGGTACGGTACGAGACTACAGGTCCTTCAATTGGTAATGTGATTTATCAGCTGGTTACTGGGTGTGGTAATAAAGAAAGTGACTCTGTTTGTCTTCCTGTAATGTGTGCATCAAGGAGTTCACAAGCTCTCTGGTTTCCTCAGGACTCTTTTGTGGTAGTTTTCTCTCTGGCCTCGGGGAAAGTGGTTTATGCGTCTGAGCAAGCCTCCAGTGTGCTCCACTGCAAGAGGAAGTTCCTGGAATCGGCCAAGTTTGTGGAGATGCTGTACCATCAGGACGTCAATGTGTTTTACTCTCATACCGCACAGCCA[C/T]GACTGCCATCCTGGAACTTGGGCACAGACAGCGGTGAGTCTCTCTAGAACAAGTTATACTCCAAATTAAATCAAAATTAAACTATTAAGAGTATCCAATGTTGTTCTAGAGGTCTTCTTGTCGTTATAATGGGTTCACATCTGTTCAAGGTCAAAAATATCACCTTTGTTTTCTCATAATAGGCACTTGAGCATCAGCTCTTTTTCATTAGGTCTGAAAGAGCTGGTTTAAATATCTGGGGCAATATCGTACACCCGGCGCAATGTGGCGCAAGGCGAGGCGCAATACTTGTTTGCTAGTTTTAGCTTGGCACAAGAGTTGTTTTGAGGCGTTGCGCTACGCTGTTTAATTAGCAAATGCATTTGCGCTCATATGTGCGCCCATAGGCGTTCTGGTCTAAAAAGGAAGGCGTTCTGAGGCGCACTGCTGACACGTTGCTAAAAAAACTAAAATATATTTTTCATTAGACCAAAACAAACCCGGTCTAAGCTCCAGAGCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41903
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000024304 Nonsense 1155 1281 21 23

The following transcripts of ENSDARG00000010519 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 11 (position 41485188)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 39744869
GRCz11 11 40009014
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCCTCAGACACGTCCCGGAAAGCACGCAAATCCGCCGAGGCCCAGGAA[C/T]GAGAGCGAAGCGGCTTCAAGAAACATGTGGACGACCCTCTGTGGAGCATG
Long Flanking Sequence:
GTTATTAGTAGTAGGATTATTGTATCAATAAAATATGTAGGTGAAATAATATTAAGATATATTTATAATTATTTGTAAAAAAGGATATTGGCAGTTTTATTAATCATTTTTAAATTATTATTATACTGCTCAAACAGTTATACAACACAAGGTAGCTCCAAGTTTTCCCTTAATTTTCTGAGCAGTATATAGTTTAATTGTATATAATTATTGTGTAGTTTAAGTGTATATATTGTTGTTGCTTTTTAAGTATTTTCTTGAAGAATGTGCTCCAATGAGAATGTTTTTTTTATTATTTACAATTTAAACAATTAATGTTGTACTCTTTCTGTGATGTCTTTATATATTTTGAGTTATTTATAAAACCGCAGTGTTTTCTTCATCAAACTGACCCATGGCATGCCTGGTTCACAGGCAGCAGCAACAGCAGCAAGTATTTCGCCAGCAACGATTCCTCAGACACGTCCCGGAAAGCACGCAAATCCGCCGAGGCCCAGGAA[C/T]GAGAGCGAAGCGGCTTCAAGAAACATGTGGACGACCCTCTGTGGAGCATGATCAAGCAGACGCCCGAACCCGTCATGTTAACCTACCAGATCAGCTCCAGGTATCAGACACTCTCCTGCCGTCTCTCTCTCTCTCTCTCTGTCCCGGGATCATTTCTATGACCAGCCTGAGTCAGTCACGTTCAGCATCTCTCTCCACAGGATTAAAAGAGAGCGCCACCTGCCTCTCGCTGAGGTAGTTCTGCTTTAAATATATCATTGTGTCGTCAGACCTCAGGTAGGTGATGGCAGGTATGGCATAGCAGCATTTCCACTGTCAGGCCTAAAGCTGCACTCACACTGGAGTTTGAGTGAAGTTCTGACATACAACACATGCGAAAAGCAGCAGGATAACAAAACAAGATGATTAGCCGTTGATAAAGCAAGCCATTGCACCATGAGTTCCAGCTCCAGGTCTGCTGTGAATGAATGGAAGTCTATGGTCTAGCTGGAAAAGCAGCT
Associated Phenotype:
Not determined