ZMP
si:ch1073-440b2.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
LONRF2
Human Description:
LON peptidase N-terminal domain and ring finger 2 [Source:HGNC Symbol;Acc:24788]
Mouse Orthologue:
Lonrf2
Mouse Description:
LON peptidase N-terminal domain and ring finger 2 Gene [Source:MGI Symbol;Acc:MGI:1920209]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25590 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32691 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32690 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39626 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25590
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000129204 | Essential Splice Site | 116 | 488 | 3 | 11 |
ENSDART00000148175 | None | None | 157 | None | 3 |
Genomic Location (Zv9):
Chromosome 1 (position 27488740)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 27734827 |
GRCz11 | 1 | 28428541 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTAATACCATTATTCCTAGAGATGGAACCAAAGCAGGCTGTTCGAAGG[T/G]TACTGTATGATTTAACCATGATTTAACATATACAACAGGGCTACCAACTC
Long Flanking Sequence:
ATCTTGATTGTGTATTGTGGTTGTGTTGTTACATGAAGAAATCTGTGTTACAAGTTAAACAAAAATTATTTTAAACAATTATATGATTGATCATTTATCATAAATTTGAGAACAATTCTATAATGTTTATACAGTGCTTTGCCTCTCTAGTTCAACCTAGTGGATGTATGAATGTATGTACAGTATGTGATCAAACTTTTAGGATTCAAACTTATGCAGTTACAAATGTTTATGCAAAAGGTATGAAGATTGTTTAAAGACATAATTACATACTGATTTCTTATATTTATGAAATTGTCAGTGGTGGATGATTTTAAGTATTATGTTTTATGTATTTGTGTATTTACAGATTCTGAGCCACATGTTCTCTTCAGTCTTTGTAAATGATGGTCTGGCTACGTCCCTTCCAGCCTGCACCTCTCGTATTAAACCCACATCTCTCCTCAGTTCTCTTAATACCATTATTCCTAGAGATGGAACCAAAGCAGGCTGTTCGAAGG[T/G]TACTGTATGATTTAACCATGATTTAACATATACAACAGGGCTACCAACTCTCACACAATTGTCATGAGATTCACACGATTGACAGTATTGTCAAGCTCTCATGCCACACACACACACACACACACACACACACACACACACACACACACACACACATTTCAGAATAAATCCCATCAAACAGTCACTCAAACCATATTTTTCTTTCTTTTTTTTTTTTTTTTTTTTTTGGTAGGATCTGACTCTCAGTTGCAGTAAAATCAAAGATGGGAACTCTCAATTATCTGAAAATGTGAATTGTGTTGGCCTCTCTTCACTATTTATTCCACCAGTTCTAAAAAGGAAATGGACTGAAAATTCTAAACAATCTGAGCCTCCAAGTAAACAGCTCAAAGAAGGTATGTGGTTTAAAGCCATGATTTCATGAATAGCTAATACTGGATAATATAGTCTTTAGTATGAATAAATAAATTTTACTTAGGTTATTGTTGATTTTATTTCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32691
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000129204 | Nonsense | 247 | 488 | 7 | 11 |
ENSDART00000148175 | None | None | 157 | None | 3 |
Genomic Location (Zv9):
Chromosome 1 (position 27482757)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 27728844 |
GRCz11 | 1 | 28422558 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAACATATCTTTCTTTTTTTGCAGTATCTGGCCACTAGAGCGTACTGC[A/T]AAACTCTTCTAATTGAAGAACTATTGCAGCAGTACTTGAGTGATGAACTA
Long Flanking Sequence:
TAATTTGGTCTGCAAAAACATGGCATTCCCTAGGCCCAGTAATTGTGCTAGATAGGCAGGATCCTGAGGGTGGTGCATCAGGATGTATCAGGATAATAGTGCACCAATACACCAATACACACAGCAAGACTGGTAACAGAGTGGTTTGATAAACATAAAAGTGAATTTGAACATCTCCTATGGTCTGCAGAGTTATCAGATCTATATACACCATCTATCTATAGTCTGACAAGACTTTATAATGTTATAAAAAAAGTTATGTAAAATTGAGTTATTGTTTTTTTTTTACATTCAGAGTTATCATTAAGGCCAAGCGCAATGGGAAGCACTAATGAACTGATGTCAAACCATAATGCCTAAAAACTTTTTTCTCTTCCCTATTTCAGTCCTCATGTGTTGAATGAATACTAATCCTTATGTTGTTTCATGAAGTTGTTAAAGTTATCCAACATGAACATATCTTTCTTTTTTTGCAGTATCTGGCCACTAGAGCGTACTGC[A/T]AAACTCTTCTAATTGAAGAACTATTGCAGCAGTACTTGAGTGATGAACTAACAGAAAGGCGAAAAGTTTATGAAGAAGAGATGAAAGAACTGTCAAAGTAAGCTGTCTTTTTTATTGTGAAGTAAAATAACACTTTAATTTGCACACTATGAATCATTTATTTAGGATTAGCAAATAGTTAATAAATCATTTGTAAAGAATTATATCATCATTGACTGTGTTGGTAGTGCTGTGACGGTGACAATTTTTGATTACCACTATTAATATTATTATTATTATTATTATTATTATAACCTTTATTTTACCAGGAAAGACACATTGAAATCTCTTTCACAAGAGCGTCCTGGCCAAGATTAGGCAGTACATAAGTCACATGAGTCCAACAGACAAAAACAACTTACAGTTAACATGAAACACACTGACAAACTATTCAAAACATCTACAAACCTGTTTCAACTTCCAAATCTTTGATATTCTTTTTAAAAGCATGTAGAGAAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32690
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000129204 | Nonsense | 298 | 488 | 8 | 11 |
ENSDART00000148175 | None | None | 157 | None | 3 |
Genomic Location (Zv9):
Chromosome 1 (position 27465257)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 27711344 |
GRCz11 | 1 | 28405058 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGAAGTTCCCATCTTTGTTTGCACCATGGCATTTCCTACCATTCCCTG[T/A]CCACTGCATGTGTTTGAGCCTCGATACAGGCTTATGATTCGCAGATCATT
Long Flanking Sequence:
CCTGAGGATTAAGCACATTATATATGTGTGTATAAGTCAAGAATACAGCATTTGTTACATTTTGCTAAACTGTCTATTAATGTAGTGTTAATGTAGAGTTTACAAATGATTCATTAACTATTTGCTTAATAAGTGATTCATAGTGTGCAGTTATTATAGTGTTACCTTATTTTATTACATTTTTTTCGTGTCTTTCTGGAATTTTGTTCTGACATTTCTACACCCTCTTTTCAAATGTGTTTTTTAAAATCATTGCATATGTGTTTGTTATGCGAGTAATAATTATTTGTTTTCTTGTTCTGAACTGTTTGTTGTTCATATGTATATTTCTATTGTATTAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTATATATATAAATATATAATTTTTTTTTTTTTCAGCTTAAACCAGGAAGTTCCCATCTTTGTTTGCACCATGGCATTTCCTACCATTCCCTG[T/A]CCACTGCATGTGTTTGAGCCTCGATACAGGCTTATGATTCGCAGATCATTGGAAACAGGGACCAAACAGTTTGGCATGTGTATTGCTGATGAACTGAAAGGGTAAGAGGCCTTGAATCAAATTTAAGTTCATATAATATAAGCTTATCAAAATAAGCTTATATTAAAGTTCCACTCAGTGATCAGTCTGGTGATGGTGAGCTTTAAGCATTTAAAGGCAAAAATTTCCAAAAAATAAAGCTTATAAAAAAAGTTTTCATACCTTACCGTTGCCTCGAACCAGGCCAAAGCACGCTTGTCCCCCCTCCCGTCTCCCCCGACGGCCCGCACTCACACCACAATCGGGCCTGGGCACGCTTACATCATCGATGCTGCGCTGTTCAGTGAGAAGCACTCTCACTCAGCAGCACAGTGGAGTTTTCTCTAGTTATATCGTTTTTTTGCTTTAAATCAAGCAAAAATTAAAGAACTTTGCCCTTCATTTTGTGTCAAGCATCTGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39626
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000129204 | Nonsense | 314 | 488 | 8 | 11 |
ENSDART00000148175 | None | None | 157 | None | 3 |
Genomic Location (Zv9):
Chromosome 1 (position 27465210)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 27711297 |
GRCz11 | 1 | 28405011 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTCCACTGCATGTGTTTGAGCCTCGATACAGGCTTATGATTCGCAGAT[C/A]ATTGGAAACAGGGACCAAACAGTTTGGCATGTGTATTGCTGATGAACTGA
Long Flanking Sequence:
GCATTTGTTACATTTTGCTAAACTGTCTATTAATGTAGTGTTAATGTAGAGTTTACAAATGATTCATTAACTATTTGCTTAATAAGTGATTCATAGTGTGCAGTTATTATAGTGTTACCTTATTTTATTACATTTTTTTCGTGTCTTTCTGGAATTTTGTTCTGACATTTCTACACCCTCTTTTCAAATGTGTTTTTTAAAATCATTGCATATGTGTTTGTTATGCGAGTAATAATTATTTGTTTTCTTGTTCTGAACTGTTTGTTGTTCATATGTATATTTCTATTGTATTAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTATATATATAAATATATAATTTTTTTTTTTTTCAGCTTAAACCAGGAAGTTCCCATCTTTGTTTGCACCATGGCATTTCCTACCATTCCCTGTCCACTGCATGTGTTTGAGCCTCGATACAGGCTTATGATTCGCAGAT[C/A]ATTGGAAACAGGGACCAAACAGTTTGGCATGTGTATTGCTGATGAACTGAAAGGGTAAGAGGCCTTGAATCAAATTTAAGTTCATATAATATAAGCTTATCAAAATAAGCTTATATTAAAGTTCCACTCAGTGATCAGTCTGGTGATGGTGAGCTTTAAGCATTTAAAGGCAAAAATTTCCAAAAAATAAAGCTTATAAAAAAAGTTTTCATACCTTACCGTTGCCTCGAACCAGGCCAAAGCACGCTTGTCCCCCCTCCCGTCTCCCCCGACGGCCCGCACTCACACCACAATCGGGCCTGGGCACGCTTACATCATCGATGCTGCGCTGTTCAGTGAGAAGCACTCTCACTCAGCAGCACAGTGGAGTTTTCTCTAGTTATATCGTTTTTTTGCTTTAAATCAAGCAAAAATTAAAGAACTTTGCCCTTCATTTTGTGTCAAGCATCTGGCTGGGAGATGCAATTTGACCTAATAATGATACTCGTCTTACCATAGGA
Associated Phenotype:
Not determined