ZMP
si:ch1073-193f3.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
LONRF1
Human Description:
LON peptidase N-terminal domain and ring finger 1 [Source:HGNC Symbol;Acc:26302]
Mouse Orthologue:
Lonrf1
Mouse Description:
LON peptidase N-terminal domain and ring finger 1 Gene [Source:MGI Symbol;Acc:MGI:3609241]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa19088 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa9353 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa35722 | Essential Splice Site, Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa19088
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 |
|---|---|---|---|---|---|
| ENSDART00000109513 | None | None | 311 | None | 8 |
| ENSDART00000109935 | Essential Splice Site | 192 | 605 | 5 | 13 |
| ENSDART00000114153 | None | None | 588 | None | 14 |
| ENSDART00000135556 | None | None | 596 | None | 12 |
| ENSDART00000137512 | None | None | 539 | None | 11 |
| ENSDART00000109513 | None | None | 311 | None | 8 |
| ENSDART00000109935 | Essential Splice Site | 192 | 605 | 5 | 13 |
| ENSDART00000114153 | None | None | 588 | None | 14 |
| ENSDART00000135556 | None | None | 596 | None | 12 |
| ENSDART00000137512 | None | None | 539 | None | 11 |
Genomic Location (Zv9):
Chromosome 14 (position 35164196)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 33737234 |
| GRCz11 | 14 | 34077548 |
KASP Assay ID:
2260-7752.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGATAATAGCAACATGCAATACATCAATAAAAGATGTATAATTCTTGTA[T/G]AATATGCAGATCTTGGAAGCAGAGGGCATGGCTGTGCCGGAGGAAGTTCC
Long Flanking Sequence:
ACTGAGGCTGAAACAATGGAGCTTTACCATCACATGAATAAATTTCTTTGTGTAATATATCAAAATGGAAAGCAGTTATTTTAAAATTCTTATGACATCTCACATTTAATAATATCTCTGCATTGGTGAGCTGAAAACATTTTTCCAAAACATTCCAAAAATTCTTGCATAGCCCAAACGTTTGAAATGTATTGTACTGCGCTGGCACAGGAAAAAAAACGTAAAATGTAAAACAGGTTGGAAATCATTTCTGTCTTCATAAATATTCACACAGTCACTGAATTCTGTATTTTACAGGGTTTCTTTCGTAAAGGGAATGTGCTGCTTGAAATGGGCAGACAGACCGAAGCCCTCATCCAGTTCTACCGTTGTCTGAAACAGCATCCTGACTTTGCCCCTGCTAAAAACCAGATTAAAAAGGTGGGCATTTCTGAAATTATTACATAGTGCATGATAATAGCAACATGCAATACATCAATAAAAGATGTATAATTCTTGTA[T/G]AATATGCAGATCTTGGAAGCAGAGGGCATGGCTGTGCCGGAGGAAGTTCCACGGATCCTGCATGTTGTGTCTGAGTTTTTGCAGGATCCCTGTCCAATCACCAGCTCCGTAAGCCCCTCATGCACAGATGCTCAGCGCTACTCCCACACCAATGCTGAAGGTCAAAGTGATTCCGGGCAGGTGAGATGTGCTTGCAGCACTGATGCTCCTGTGTCATTTCTGAACTGTAACATTGGTAATGCAAGCAGAAATAGCCGAAAGATCTGGGACTAGATCTAGAAACAGATTGCAGTAGTGCCAACCTTCCTACTGTAAAAAATGAATTCTATACTAGGTCTGTTTGATTAATTGGAGAAAAAAATAAAATAAAAATCACAATCTTGATTTGACCCTACACACAATATTAATTCTGCTTTTTTTCTACAGTAGCCAAATATATTTTTACATACATATACATATATATCTTCACATTGTTTTATATACATTGACATATTGTTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9353
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 |
|---|---|---|---|---|---|
| ENSDART00000109513 | None | None | 311 | None | 8 |
| ENSDART00000109935 | Essential Splice Site | 192 | 605 | 5 | 13 |
| ENSDART00000114153 | None | None | 588 | None | 14 |
| ENSDART00000135556 | None | None | 596 | None | 12 |
| ENSDART00000137512 | None | None | 539 | None | 11 |
| ENSDART00000109513 | None | None | 311 | None | 8 |
| ENSDART00000109935 | Essential Splice Site | 192 | 605 | 5 | 13 |
| ENSDART00000114153 | None | None | 588 | None | 14 |
| ENSDART00000135556 | None | None | 596 | None | 12 |
| ENSDART00000137512 | None | None | 539 | None | 11 |
Genomic Location (Zv9):
Chromosome 14 (position 35164196)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 33737234 |
| GRCz11 | 14 | 34077548 |
KASP Assay ID:
2260-7752.1 (used for ordering genotyping assays)
KASP Sequence:
ATGATAATAGCAACATGCAATACATCAATAAAAGATGTATMATTCTTGTA[T/G]AATATGCAGATCTTGGAAGCAGAGGGCATGGCTGTGCCGGAGGAAGTTCC
Long Flanking Sequence:
ACTGAGGCTGAAACAATGGAGCTTTACCATCACATGAATAAATTTCTTTGTGTAATATATCAAAATGGAAAGCAGTTATTTTAAAATTCTTATGACATCTCACATTTAATAATATCTCTGCATTGGTGAGCTGAAAACATTTTTCCAAAACATTCCAAAAATTCTTGCATAGCCCAAACGTTTGAAATGTATTGTACTGCGCTGGCACAGGAAAAAAAACGTAAAATGTAAAACAGGTTGGAAATCATTTCTGTCTTCATAAATATTCACACAGTCACTGAATTCTGTATTTTACAGGGTTTCTTTCGTAAAGGGAATGTGCTGCTTGAAATGGGCAGACAGACCGAAGCCCTCATCCAGTTCTACCGTTGTCTGAAACAGCATCCTGACTTTGCCCCTGCTAAAAACCAGATTAAAAAGGTGGGCATTTCTGAAATTATTACATAGTGCATGATAATAGCAACATGCAATACATCAATAAAAGATGTATAATTCTTGTA[T/G]AATATGCAGATCTTGGAAGCAGAGGGCATGGCTGTGCCGGAGGAAGTTCCACGGATCCTGCATGTTGTGTCTGAGTTTTTGCAGGATCCCTGTCCAATCACCAGCTCCGTAAGCCCCTCATGCACAGATGCTCAGCGCTACTCCCACACCAATGCTGAAGGTCAAAGTGATTCCGGGCAGGTGAGATGTGCTTGCAGCACTGATGCTCCTGTGTCATTTCTGAACTGTAACATTGGTAATGCAAGCAGAAATAGCCGAAAGATCTGGGACTAGATCTAGAAACAGATTGCAGTAGTGCCAACCTTCCTACTGTAAAAAATGAATTCTATACTAGGTCTGTTTGATTAATTGGAGAAAAAAATAAAATAAAAATCACAATCTTGATTTGACCCTACACACAATATTAATTCTGCTTTTTTTCTACAGTAGCCAAATATATTTTTACATACATATACATATATATCTTCACATTGTTTTATATACATTGACATATTGTTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35722
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:
Essential Splice Site, Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109513 | None | None | 311 | None | 8 |
| ENSDART00000109935 | Missense | 212 | 605 | 5 | 13 |
| ENSDART00000114153 | Essential Splice Site | 176 | 588 | 5 | 14 |
| ENSDART00000135556 | Missense | 203 | 596 | 4 | 12 |
| ENSDART00000137512 | None | None | 539 | None | 11 |
Genomic Location (Zv9):
Chromosome 14 (position 35164259)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 33737297 |
| GRCz11 | 14 | 34077611 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGAAGCAGAGGGCATGGCTGTGCCGGAGGAAGTTCCACGGATCCTGCA[T/A]GTTGTGTCTGAGTTTTTGCAGGATCCCTGTCCAATCACCAGCTCCGTAAG
Long Flanking Sequence:
AATGGAAAGCAGTTATTTTAAAATTCTTATGACATCTCACATTTAATAATATCTCTGCATTGGTGAGCTGAAAACATTTTTCCAAAACATTCCAAAAATTCTTGCATAGCCCAAACGTTTGAAATGTATTGTACTGCGCTGGCACAGGAAAAAAAACGTAAAATGTAAAACAGGTTGGAAATCATTTCTGTCTTCATAAATATTCACACAGTCACTGAATTCTGTATTTTACAGGGTTTCTTTCGTAAAGGGAATGTGCTGCTTGAAATGGGCAGACAGACCGAAGCCCTCATCCAGTTCTACCGTTGTCTGAAACAGCATCCTGACTTTGCCCCTGCTAAAAACCAGATTAAAAAGGTGGGCATTTCTGAAATTATTACATAGTGCATGATAATAGCAACATGCAATACATCAATAAAAGATGTATAATTCTTGTATAATATGCAGATCTTGGAAGCAGAGGGCATGGCTGTGCCGGAGGAAGTTCCACGGATCCTGCA[T/A]GTTGTGTCTGAGTTTTTGCAGGATCCCTGTCCAATCACCAGCTCCGTAAGCCCCTCATGCACAGATGCTCAGCGCTACTCCCACACCAATGCTGAAGGTCAAAGTGATTCCGGGCAGGTGAGATGTGCTTGCAGCACTGATGCTCCTGTGTCATTTCTGAACTGTAACATTGGTAATGCAAGCAGAAATAGCCGAAAGATCTGGGACTAGATCTAGAAACAGATTGCAGTAGTGCCAACCTTCCTACTGTAAAAAATGAATTCTATACTAGGTCTGTTTGATTAATTGGAGAAAAAAATAAAATAAAAATCACAATCTTGATTTGACCCTACACACAATATTAATTCTGCTTTTTTTCTACAGTAGCCAAATATATTTTTACATACATATACATATATATCTTCACATTGTTTTATATACATTGACATATTGTTTTATAACATGGACACTTTCAAATGGTGTTGTATTTATAAAGTATAAGTCACCCCATTATACAATTA
Associated Phenotype:
Not determined