Busch Lab

ZMP

penk

Ensembl ID:
ENSDARG00000036045
ZFIN ID:
ZDB-GENE-030729-3
Description:
proenkephalin [Source:RefSeq peptide;Acc:NP_878303]
Human Orthologue:
PENK
Human Description:
proenkephalin [Source:HGNC Symbol;Acc:8831]
Mouse Orthologue:
Penk
Mouse Description:
preproenkephalin Gene [Source:MGI Symbol;Acc:MGI:104629]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa41053 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa21103 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa41053
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
ENSDART00000052332 Essential Splice Site 19 266 1 3
Genomic Location (Zv9):
Chromosome 7 (position 59931867)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 58384476
GRCz11 7 58686916
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGACTTTACACGCACCGGACAGACTGCAGTAACTGCCTCAGTAATGAAG[G/A]TCAGTACAACATTTAAAGAATTGTTCCAATTGTTTTGACCTGTTTATTCT
Long Flanking Sequence:
CAGTCGAGGCTTGAACCAGCAACATTCTTGCTGTGAGGCAACAGCACTACCTACTACGCCACCAAGTCGCCAATAATATTAATAATAATAATAACAATATTATTATTATTTTTATATAAGTATAGTATTTTTATTTGGTTTAAAGTGTAATGTCTTTTCAGTGTATAACCTAAAGACACATTTGACAACAGAAATTAATATTTATTGCATAATAACACGTTAATGAACTTTTTGATTTAAGATTTTCCTTTTATAAATTCGTAAATTATACTGTGCAGTGCGTACATTGGATTTGTGAGATTTAATAAATAACCCCATCCCCCCTTACACCCTCTCATGCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTTATTCTGTCGCTCTCTCTTAAACGCTCAACATCCACTCTAGGGAATAACGCAGACTTGTGCCCTCAGACCGACGAGACTTTACACGCACCGGACAGACTGCAGTAACTGCCTCAGTAATGAAG[G/A]TCAGTACAACATTTAAAGAATTGTTCCAATTGTTTTGACCTGTTTATTCTTAATTTTGTTTTTACGGCACTGACTTGAACACATTAAAAGAAAAAAACATTGTCAAATAAGTCTTGATAACACTGAGAAAGGAGTTTAACTGTTTTATTTCTTCCCTTTAAGACCTTGACAGTTCCCATAAGCTGCAGATGGACACTGTTGCTGAGCGCGTGCCTGACGCTGACAGCGCGTGCGGACTGTGGAGAGGACTGCGCGTACTGTCTGCAGCAGATGCCCCTTCAGCTCAAACATCTTAACTCAATAGTAAGTCCGCTGTGTTCTTCACGTGTAATCAAACGAGTTCTTCCAAAAGTTTATCCACTTATTTATTTATTTATTTTTTACCTGTGCACTTTCGCATTTTTATTTTTACATCCATTTTAAATGATTATTTCCCTTTTGCATAATTAAAACAACAATCCACTGTTGAAGCCCTTTGGATTTTTTTTCAAAGGCTTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21103
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
ENSDART00000052332 Nonsense 195 266 3 3
Genomic Location (Zv9):
Chromosome 7 (position 59940298)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 58392907
GRCz11 7 58695347
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGGCTCTGACACGTTCAAAGGGAGGTGAAGAGGGAACTGCAAAACGTTA[T/A]GGGGGTTTTATGAGAAGGGGAGGGCTTTATGACTTGGAGAGTGGGGTTAG
Long Flanking Sequence:
AGAGATGAAGGTTGAGGGAGAGACGAGGGATATCCTCTCAGCCATTCATTTCTGGGACTGCTGTGTACGTCTCAACGACTATACATTCACGTTTTGTTTTGCTTTTTCTCGCAGGAATGTGTGTTGGAGTGTGAGGAGCAACCGAACGCAGGCAGCTCTTGGAGTCAGTGCAAACATTTCATGCAGAATGCTGATAACAGTCCTGAGGGTAACCGAGCAGCCACACAAATCGAACACTCAAACAGCCAACAGCACCAGGTAGACAAAAAATATGGCGGCTTCATGAAACGTTCTGAAAGTTTAATCAAGCGTTATGGAGGATTCATGAAGAAGGCAGCTGAATTCTATGGGCTGGAGCCAGAGGATGTTGATCAGGGCAGAGCAATCCTGACTAATCATGATGTTGAAATGCTGGCCAATCAAGTTGAGGCTGACGGGGAGAGGGAGGAAGCGGCTCTGACACGTTCAAAGGGAGGTGAAGAGGGAACTGCAAAACGTTA[T/A]GGGGGTTTTATGAGAAGGGGAGGGCTTTATGACTTGGAGAGTGGGGTTAGGGAACTGCAAAAACGTTATGGGGGCTTCATGAGGAGAGTAGGCCGACCAGATTGGTGGCAGGAGTCTAAACGTTACGGAGGCTTCTTAAAGCGGTCTCAAGAGCAAGACGAGGATGAAAATTCATCAGAGGTAGAAAAGAGGTATGGTGGATTTATGGGATATTAAGATGATGTCCGCGATGTCCAAGTTCACTTCCTCTTGAAGATAAAAAAACACCTGAAAACTGAACAGAAAATATGCTTAAAACACGCTAATGTAATGTATTAATAAAGTGTTCATTATGTCTTTATTGTGATGTTATTGTGTGAGTAAGACCATTTTAACAGTACACATTGCATCTGAAGTCACAATCATAGTCAAGTTGTGTAGCATATTTTAATAAACAGGGTTATCTGTTTTTGACCGAACAAGAATATTGTAATATGTTTTCATCAACACTGCAATTCTGG
Associated Phenotype:
Not determined