Busch Lab

ZMP

lonp1

Ensembl ID:
ENSDARG00000071674
ZFIN ID:
ZDB-GENE-030131-4006
Human Orthologue:
LONP1
Human Description:
lon peptidase 1, mitochondrial [Source:HGNC Symbol;Acc:9479]
Mouse Orthologue:
Lonp1
Mouse Description:
lon peptidase 1, mitochondrial Gene [Source:MGI Symbol;Acc:MGI:1921392]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa43743 Nonsense Mutation detected in F1 DNA Not yet available
sa39354 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa43743
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
ENSDART00000106143 Nonsense 844 966 16 18
Genomic Location (Zv9):
Chromosome 22 (position 1230420)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 3145013
GRCz11 22 3162286
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGCGCTAAGATTGCGTACACGTTTGCTCGCTCGTTCCTCATGAAGGAG[C/T]AACCAGACAATGAGTTCCTCGTGAGCTCCCATATTCACCTCCATGTGCCT
Long Flanking Sequence:
ACGTTATCATAGTTGACGGTAACTTAGTTGATGGTACTACAGTAACAGAGTTGACGGTTACTGGCTTGTTAGTACCAGAGTAACAGAGTTGACGTTATCATAGTTGACGTTATCATAGTTGACGGTAACTTAGTTGATGGTACTACAGTAACAGAGTTGACGGTTACTGGCTTGTTAGTACCAGAGTAACAGAGTTGACGGTAACAGAGTTGATTCTAACTTGTTTGATGGTAACTTGGTTGACGGTAGCAGAGTTGACGTTTAACTACTATTTGTGTACCCTAAACTTTTTGTATAAAACTATGAAAAAAACAATCATACTTTCCCCTGCAGGTGGTTCGACGCTGTTCATCGAGACGTCTCTGAGGCGGCCCAGAGATCCGCCGGGGAAAGATGGTCCCAAAGACGGATCGCTGGAGGTCACTGGACAGCTGGGAGACGTGATGAAGGAAAGCGCTAAGATTGCGTACACGTTTGCTCGCTCGTTCCTCATGAAGGAG[C/T]AACCAGACAATGAGTTCCTCGTGAGCTCCCATATTCACCTCCATGTGCCTGAGGTGAGTTACTTCTCTTTTTATTATTTGATAAAGTCATTTAAACATCTTGTCGAGTGCTTTGAAATGTGCATTTTTGTTTGATATGTGATATAATTTAAACTGAACGTTGAAGAGAGGGTGGGGCACATAGTTGCTCCGCCCCTTTATTAAAAACTTTCTATTACAGCTCTGTCGGTGAGAGTGGTTGAGCTCATATTGCAATAGTGTTTTGAATGAGGGAAAGCCAGACTTAGGTTGTGTTTGTTTTCAGGGTGCGACTCCTAAAGACGGCCCCAGCGCCGGATGCACCATCGTCACGGCTCTGCTGTCTTTAGCCACAAACACAGCTCTGCGTCAGAACGTTGCCATGACTGGAGAGCTATCCCTGACTGGCAAAATCCTGCCTGTTGGAGGAATCAAGGAGAAGACCATTGCTGTAAGCTAAAACAATTCAGAACACACTTTTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39354
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000106143 Essential Splice Site 862 966 17 18
Genomic Location (Zv9):
Chromosome 22 (position 1230118)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 3144711
GRCz11 22 3161984
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATAGTGTTTTGAATGAGGGAAAGCCAGACTTAGGTTGTGTTTGTTTTC[A/T]GGGTGCGACTCCTAAAGACGGCCCCAGCGCCGGATGCACCATCGTCACGG
Long Flanking Sequence:
ATGAAAAAAACAATCATACTTTCCCCTGCAGGTGGTTCGACGCTGTTCATCGAGACGTCTCTGAGGCGGCCCAGAGATCCGCCGGGGAAAGATGGTCCCAAAGACGGATCGCTGGAGGTCACTGGACAGCTGGGAGACGTGATGAAGGAAAGCGCTAAGATTGCGTACACGTTTGCTCGCTCGTTCCTCATGAAGGAGCAACCAGACAATGAGTTCCTCGTGAGCTCCCATATTCACCTCCATGTGCCTGAGGTGAGTTACTTCTCTTTTTATTATTTGATAAAGTCATTTAAACATCTTGTCGAGTGCTTTGAAATGTGCATTTTTGTTTGATATGTGATATAATTTAAACTGAACGTTGAAGAGAGGGTGGGGCACATAGTTGCTCCGCCCCTTTATTAAAAACTTTCTATTACAGCTCTGTCGGTGAGAGTGGTTGAGCTCATATTGCAATAGTGTTTTGAATGAGGGAAAGCCAGACTTAGGTTGTGTTTGTTTTC[A/T]GGGTGCGACTCCTAAAGACGGCCCCAGCGCCGGATGCACCATCGTCACGGCTCTGCTGTCTTTAGCCACAAACACAGCTCTGCGTCAGAACGTTGCCATGACTGGAGAGCTATCCCTGACTGGCAAAATCCTGCCTGTTGGAGGAATCAAGGAGAAGACCATTGCTGTAAGCTAAAACAATTCAGAACACACTTTTAAAATAAGCTTGTTTCATTGAACGAACATCATTTTTGGCCTACAGGGTTTTCAGGTCCAATTATGATGCTCAGTAAAGGAACAGTTCACCCAAAACTGACAACTCTGTCATCAATAATCACACTTTTACTTGTTTTAAACCAGTGTGAATTTCTTTACTATTAATGTGTGTTCATGTTTCCGGCAGGCGAAGAGAGCCGGCGTGACCTGCATTATCCTGCCGGCGGAAAACAGAAAGGATTTCTCGGATCTGCCTGAATACATCACTGAAGGCCTGGAAGTGCACTTCGTGGAAAACTACAGCG
Associated Phenotype:
Not determined