ZMP
lonp2
Ensembl ID:
ZFIN ID:
Description:
Lon protease homolog 2, peroxisomal [Source:UniProtKB/Swiss-Prot;Acc:Q5PQY6]
Human Orthologue:
LONP2
Human Description:
lon peptidase 2, peroxisomal [Source:HGNC Symbol;Acc:20598]
Mouse Orthologue:
Lonp2
Mouse Description:
lon peptidase 2, peroxisomal Gene [Source:MGI Symbol;Acc:MGI:1914137]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36621 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13813 | Nonsense | Available for shipment | Available now |
sa29014 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36621
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000027791 | None | None | 840 | None | 15 |
ENSDART00000028806 | Essential Splice Site | 241 | 840 | 4 | 15 |
Genomic Location (Zv9):
Chromosome 18 (position 18300397)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 18528979 |
GRCz11 | 18 | 18518045 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGTTGCTTCAAAAGACCCGCAAACTCAGACCGGATGATGACAAAAGAG[T/C]AGGACAACATAAAAATTAGCACAGACAAACTCATCCACAGCTTCCTGTTT
Long Flanking Sequence:
TTTGTTAAACAATAAGTTAATTTGAAAAATGTTGGAACCCTGTAACCATTGACCTCCATTGTGTTTATTTTGTATTAATTTTTCAATAATAATTAATGATTTCCAAAGTAAAAAAAAAAACATGGCATCTTTGTGTTCAACATAAAAAAAATCTAACAAAAAGGTTTGTTAGCACTTGAGGGTGAGTAGATATTTTATAAAGTATGTATAAAGTACATTTTCATTTTTAGATTAACTATCCCTTTAATTTTTTTTTTGGTTTATTCAGAGGTTGTCCTTACGATAGCCTTGTTGCTGGCATGGTGTAAAAAGTAAATAGAAATGAAAAAAAAAAGTTAAATAGTTTCAAAAAACTTAATGTTGGTGTTGATGGCAGGTTCTAGATGCAGTAGACTTGGAGGAACGCTTTAAGAAGGCCCTTCCGCTGCTCACCAGACAGATTGAGGGCCTCAAGTTGCTTCAAAAGACCCGCAAACTCAGACCGGATGATGACAAAAGAG[T/C]AGGACAACATAAAAATTAGCACAGACAAACTCATCCACAGCTTCCTGTTTGAGTCACAGTTTTGTTTGGTTTCTCCTAGGTTCTGTCCATCCGTAAAGGTGGTGTGTTCCCCGGTCGCCAGTTCTCTCTAGATGAAGAGGTGGAGGATGAGGACAGTGATGACACTGCTCTGCTGGAGAGAAAGGTGAAGGCAGCTGCTATGCCTGAGGCAGCTCTGCGCGTCTGTCTCAAAGAGCTCAGACGGTGTGTAATGCTCATTTTACAGCTAATCATGTTCATATTTTAGCTGCATTTTAAATAGTAAGGGACTTGTCATTTTATCTGTAGTTTTTAGATCTTCAAGAGTGTCTAATTATCCTCCTGGAAGGCAGATGTTTTATAAATCTAGATCCAGCCAATTCCAAAACACATGCCTAGAAGTTTTCAGGGAGTCTAAAGAGACCTTAGTTAGCTTAATCAGTCAGCTTAATCTAAACTCTGTAGGGCAGTAACCCTTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13813
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000027791 | Nonsense | 565 | 840 | 11 | 15 |
ENSDART00000028806 | Nonsense | 565 | 840 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 18 (position 18153799)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 18505565 |
GRCz11 | 18 | 18494631 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTTGCGTGTGTKTGCAGGTACACACGGGARGCTGGCGTTCGCTCTCTG[G/T]AGAGGAAGATCGGGGCTGTCTGTCGAGCYGTGGCTGTGAAGGTTGCTGAA
Long Flanking Sequence:
GGGCTTTTCATTTTCAGTCAGCCAGCTCAAGTGCTTCCGGCATTTAAGTTTAAGTTCTAGTTTCTTTAAAAATCAATGATTTTCTCTACCTGATTGATATACGATATAAAGTGGGTCTCAAAACGGACAAGAAGCACTGCATTAAACTCAATTGTTTATCTATTGCATGTGTTTAAAATATAGAAATGTATTTTTAGTGCTCCTGATGTTTCTGACAATGATTAATTTAAACAGCCTTTCATCTTGTTTAATACTTGAACAGCTAAATGAAAGCCTAAGTCTATTAATAAGATTATATTTAAATTAATTTACATCCTCTATGCTGTAAAAGCAAGCTTATGAAATTAAAAATGGTCACATCAGCCTTCCAGGTTTTATAGTTTTTTTTTATCACAGGAAGCTATTTCTCGTCCTGAGCAGAATTTATAAGATACTGATGTTGTAAGAACTTTCTTGCGTGTGTTTGCAGGTACACACGGGAGGCTGGCGTTCGCTCTCTG[G/T]AGAGGAAGATCGGGGCTGTCTGTCGAGCTGTGGCTGTGAAGGTTGCTGAAGGTCAGAAGGTCTCTAGATCAGAGGCGCCCACTGAGCAGCATGCTGGTAAGACTGTTTTCATGTCATGTTATTTACTGCTAGATTTACTCCAGCTCTGCTCCAGGATTATTGCTAGTAGTCTTTGAGCAAAGATAACTTACACGCTGGGTTTTCTTATTTATGTAGTATCCTGATGGCAAGATCTCATTGGATGAAAATACTGTCACTGCATTTTAAAAGAATAATACTTTATGAAGTATTTTGTTTTCAGAATAGGAAAAATCTGTTAGTATATTGAAATAAATATTAAGTTAAATGAAAATATTTTTTACCTATAAATTGTTTTTATTTAATAAAAAATATATACATTTGGAATTGAAATTAATATTAAGTCAAATGAAATTGTATTTTTCATCTTCAAAAATGTTTGATTTTATAAAAGAAAATATAATTTTGTTCAGTGTACTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29014
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000027791 | Nonsense | 614 | 840 | 12 | 15 |
ENSDART00000028806 | Nonsense | 614 | 840 | 12 | 15 |
Genomic Location (Zv9):
Chromosome 18 (position 18146595)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 18498361 |
GRCz11 | 18 | 18487427 |
KASP Assay ID:
2261-2064.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAGAATACAGACAGTAAGGTGGAGGATTCTGGGATTGCAGCACCTCCT[G/T]AAATGCCAATTGTCATTGACCACATTGCCCTGAAGGATATTCTTGGACCG
Long Flanking Sequence:
TAAAGTCAATTCACCCTGAAGCTGCTTCCGTTATAATGTTTGATATTAAAACCCATAATACCTTATTGTTTCCTCCCAAAATGAAGACAGCACCTGCTCTCCCCCTTCACTGGACCCCTATGGCATTTTCTCTCCAGCCTATAATTCTCCATTATTCCAGACAGCTCTCTTTCTCGCCTTTGCTTTCTTTTCACTTTTCCCCCCTCTGGCCTCGATGTCTGTCACCTTGCTTAATGAAAAGCTTCAAATAGACGTGATAATGGAAGTGCAGACCTGATCAAATTTTATAGCGCCATTTGTCTCTTGTAATTCACTTTCCTTTTTTTTGCATCTCCGCTTAAATGGACTTTACTTTTAAGTTTGTGAAATGTCAGTCACCCACCTCTTTTATATCGACACAAGTTTTAAACAAATAAAACCCACCTGTACTTTTCTGTTTGTACATTTCAGAGCAGAATACAGACAGTAAGGTGGAGGATTCTGGGATTGCAGCACCTCCT[G/T]AAATGCCAATTGTCATTGACCACATTGCCCTGAAGGATATTCTTGGACCGCCTCTCTTTGAAATGGAGGTTAGCATCACTGAAATGCCTGAAAGCTCATTATGTCTCAAATACATATAGAAAAAAAGGATCAGGGTCTAATAAAATGAAGGGTGGTTATTTATTTTACAGTCCTATTTTACCTGTACTAACTATGTATTTATCATAGTCATCATTACATAAACCTAACCATGAACCTAACCTTACCCATGTAATTACTATTATAACCCAATTTTTTTTTTTTTTTTTAGATATAGTTCATGACAAAACTTTTAGCCCTTAAATTTAAATTCTTTTTCAGTTATTTCCCAGGTGCTGTTAAATGGAGTGAATTAAATAAAATAAAAAAAGTTTATTTTTTGTCTTTGCCGTGATGACTGCACAAAAGATTTGGTTAGCTATTTTGCAAGATAGTTTTCAGTTCAAAGTATGATTTCAATGCCTGACTAGTTTAATTGGGTT
Associated Phenotype:
Not determined