Busch Lab

ZMP

si:ch1073-193f3.1

Ensembl ID:
ENSDARG00000075048
ZFIN ID:
ZDB-GENE-100922-9
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
sa9353 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa19088 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:
sa9353
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:
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:
sa19088
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:
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:
sa35722
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:
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