Busch Lab

ZMP

per2

Ensembl ID:
ENSDARG00000034503
ZFIN IDs:
ZDB-GENE-011220-2, ZDB-GENE-011220-2
Description:
period circadian protein homolog 2 [Source:RefSeq peptide;Acc:NP_878277]
Human Orthologue:
PER2
Human Description:
period homolog 2 (Drosophila) [Source:HGNC Symbol;Acc:8846]
Mouse Orthologue:
Per2
Mouse Description:
period homolog 2 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1195265]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa33027 Nonsense Mutation detected in F1 DNA Not yet available
sa25916 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa33027
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
ENSDART00000039735 Nonsense 272 1394 5 28
ENSDART00000098004 Nonsense 272 1399 5 22
Genomic Location (Zv9):
Chromosome 2 (position 48457563)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 48489227
GRCz11 2 48343391
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGATATCTTCGCAGTGGCCGTGTCTCTCATCACTGGGAAGATCGTCTA[T/A]ATTTCAGACCAGGCCGCCTCCATCCTCAACTGCAAGCGGGACGTCTTCAA
Long Flanking Sequence:
CTTAATTTTCCAAATTTTGCATTGTTTTTCCCACCATTTCTGTTTCTTTATTTTTTATTTTATGCATTTAATTTGTTTAGCAATTTTTTTAGATTATATTTTGTATTTACTTTTACTTTTTTTACTTTGTGCATTATTTTTGCTATTTATTTCTTTACTTTTCATAATTATTAATCTTTTTTTTCTTGTTATATTATGACAATTTAGTTCCTAGTTTAGACTATTTTTTGTGTATTTATAATTTATATTTTAGGTATTCTTCTTATTATATATTTATTATTTTGTCATTATTATTATTATTATTATTATTATTATTATCATTATTTGTGGTTTATTACTATTGTTTATTTTATTAATTTATTTTTTCAGAAACACTTCACTGATTGCATACAGTGAATTTCAGTAGTTCCCATCAGTAATCACTCATCATGCGATGTTTGTTTGTCTGTGCAGGATATCTTCGCAGTGGCCGTGTCTCTCATCACTGGGAAGATCGTCTA[T/A]ATTTCAGACCAGGCCGCCTCCATCCTCAACTGCAAGCGGGACGTCTTCAAGAATGCCAAGTTTGTGGAGTTTCTTACACCACAGGACGTCAGTGTGTTCTACAGCTTCACCACACCATACAGGCTGCCCTCATGGAGCATGTGCACTGGCGCAGGTAGAACACACACACACTGACAAATACACACTTACTCTATCACACACACTGACACCATCAGTCTTAACATATGTAGAGTAGCACATGACAATATTTAGCCAAACTATTTTTGAAAATCTGTAATGTGAGAGTTTAAACAAATCTAAATATTGAGGGAAAACTCCTTTAAATGTGTCCAAATTGTGTTTATAGCCATGCATATTACTAAAAAGTATATTTTGATATATGTACAATAGCTCCGGTTTCCCCCACAGTCCAAAGACATGCGGTAAAGGTGAATTGGGTAAGCTAAAATTGTCCTTAGTGTATGTGTGTGGATGAGAGTGTATGGGGTTTCCCAGTGATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25916
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000039735 Essential Splice Site 323 1394 5 28
ENSDART00000098004 Essential Splice Site 323 1399 5 22
Genomic Location (Zv9):
Chromosome 2 (position 48457408)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 48489072
GRCz11 2 48343236
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCACCACACCATACAGGCTGCCCTCATGGAGCATGTGCACTGGCGCAG[G/A]TAGAACACACACACACTGACAAATACACACTTACTCTATCACACACACTG
Long Flanking Sequence:
TACTTTTCATAATTATTAATCTTTTTTTTCTTGTTATATTATGACAATTTAGTTCCTAGTTTAGACTATTTTTTGTGTATTTATAATTTATATTTTAGGTATTCTTCTTATTATATATTTATTATTTTGTCATTATTATTATTATTATTATTATTATTATTATCATTATTTGTGGTTTATTACTATTGTTTATTTTATTAATTTATTTTTTCAGAAACACTTCACTGATTGCATACAGTGAATTTCAGTAGTTCCCATCAGTAATCACTCATCATGCGATGTTTGTTTGTCTGTGCAGGATATCTTCGCAGTGGCCGTGTCTCTCATCACTGGGAAGATCGTCTATATTTCAGACCAGGCCGCCTCCATCCTCAACTGCAAGCGGGACGTCTTCAAGAATGCCAAGTTTGTGGAGTTTCTTACACCACAGGACGTCAGTGTGTTCTACAGCTTCACCACACCATACAGGCTGCCCTCATGGAGCATGTGCACTGGCGCAG[G/A]TAGAACACACACACACTGACAAATACACACTTACTCTATCACACACACTGACACCATCAGTCTTAACATATGTAGAGTAGCACATGACAATATTTAGCCAAACTATTTTTGAAAATCTGTAATGTGAGAGTTTAAACAAATCTAAATATTGAGGGAAAACTCCTTTAAATGTGTCCAAATTGTGTTTATAGCCATGCATATTACTAAAAAGTATATTTTGATATATGTACAATAGCTCCGGTTTCCCCCACAGTCCAAAGACATGCGGTAAAGGTGAATTGGGTAAGCTAAAATTGTCCTTAGTGTATGTGTGTGGATGAGAGTGTATGGGGTTTCCCAGTGATGGGTTGCAGCTGGAAGGGCATCCGCTTTGTAAAAGGTATGCTGGATAAGTTGGCGGTTCATTCCACTGTGGCGACCCCAGAATAATAACGGAACTGAGCGAATGAATGAATATTTACAATTGGAAATCTACTAAATATCTCCCTGGATCATCTTCA
Associated Phenotype:
Not determined