ZMP
lrpprc
Ensembl ID:
ZFIN ID:
Description:
leucine-rich PPR-motif containing [Source:RefSeq peptide;Acc:NP_001136064]
Human Orthologue:
LRPPRC
Human Description:
leucine-rich PPR-motif containing [Source:HGNC Symbol;Acc:15714]
Mouse Orthologue:
Lrpprc
Mouse Description:
leucine-rich PPR-motif containing Gene [Source:MGI Symbol;Acc:MGI:1919666]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17469 | Nonsense | Available for shipment | Available now |
sa22236 | Essential Splice Site | Available for shipment | Available now |
sa42148 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35428 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22237 | Nonsense | Available for shipment | Available now |
sa12060 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17469
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034230 | Nonsense | 409 | 1461 | 9 | 38 |
ENSDART00000126427 | Nonsense | 395 | 1447 | 9 | 38 |
ENSDART00000128868 | Nonsense | 384 | 795 | 9 | 23 |
Genomic Location (Zv9):
Chromosome 13 (position 10375319)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 10677648 |
GRCz11 | 13 | 10810123 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGTCATGAAAAGACTGCCTTTTCKGTGCTGAAAAGCTWAACCGGGATGT[T/A]AGAYACACATMCGGGTGACACTCCAGATTTTGGMAACTTCTTTCTTCGCC
Long Flanking Sequence:
ATCTCTTGCATATCTCCTCTAGACTCTCGATGTGGTGGAGAACGCAGATTTCTTTCTGATGGACCGAGATCTGATGCAGTTGGTTTCCAGTCTGGCTAGAACTGGCCATGAGCAGCACGTGCCCGAGATTGTGTCACGTATGCGTCATGAGAGAGGATATGTGCCAGGTCTGACATCAGTTTGTCCCTGACCACTTACCACAGTGGTCCATAGTTAACCATAATGGTCGCAAATGTATTCATAACAGTATACTATTTGATGTGTTTTAAATATGAACTCAAACCAATTAGAGAAATGCGATACATAAAACATTGATGCCGTGAGATGAAGTTCTGGGATTTTGGGAAAGCCATTAATGATTGATAGATTTTTTTTATTTTGATCTTGATGCATCCGTTTGCTTCACTTTTTTTCAGATGCTATCAACCTTTGCTTGAATTTGATTACCCACGGTCATGAAAAGACTGCCTTTTCTGTGCTGAAAAGCTTAACCGGGATGT[T/A]AGACACACATACGGGTGACACTCCAGATTTTGGCAACTTCTTTCTTCGCCATTGCGTCAATATGGACAAGGTGAGGGACCCAAACATGACTGTTATGCATATAATTAACTTCTACCAAGCATTGTGCAATACTGAAGCCAGGTTTTTTTAAACTTCACACACATTCAGAATTGCCAACATAATAATTTACCAAACATTTGAGCTTAGACCAACACAACAGTTCATATAACAGACCCCCTAGTTTTTAGCGATTTTATGATTGCTGAATCCAATGTAAAATTAACAATTAACAACGATCCTGCAAAATTTGTTATTAAACACAGAATAATTACACAAAATGTAAATAATCTCATAAAATATCCAATTCAAAACCATAAAATCTAATTATATTTATTTCAGTTTGTAATTAATTGTTTTACATGACTTATTGACATTGCATATGCAGCGCATGTGATTTATTTAAGTGTCTCCTGAAAAATGACGTCTCACATGCACCCTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22236
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034230 | Essential Splice Site | 543 | 1461 | 12 | 38 |
ENSDART00000126427 | Essential Splice Site | 529 | 1447 | 12 | 38 |
ENSDART00000128868 | Essential Splice Site | 518 | 795 | 12 | 23 |
Genomic Location (Zv9):
Chromosome 13 (position 10389397)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 10691726 |
GRCz11 | 13 | 10824201 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCCTGCCGTCTTTTCCATCATTGGACAATGCTAAGGCTTCTCTTAAGG[T/G]AACTGTACTGGATATGTGAATACATTGTTGGTTTATGTGACTGATTTGGA
Long Flanking Sequence:
ATATGTATATATATATATACTTATATATATATATATATATACATATATACATATATATATATATATATATATACACACATATATATATATATATATATATATATATATATATATATACATACACATACACATACACAAGTATGTATATGTTTATGTAATTTAATTATTTATTTGTTATGTAGATAGACATATGAAGTGTCCTATTTGTCACAAATTTAGTTAGTTTTAGTTTTAGTTAGTTAGTTAGTTTTGCTCAATAGACCTGCAGTCATCCATTCCTAAACTTACTTTGGTGCAGATGAAACCTTTGCATGCCATGATTTACATTTTATAATGCACATTTGATTTCACCAGTTTTTTTTTTGTTTCTTTCTTTTCAGCTATTATAGAAGTTCTGAGAGGCATGCAAGAAATGAGCGTCTCGCCAGATGTTGATGCTTTTAGTTTCTATATCCTGCCGTCTTTTCCATCATTGGACAATGCTAAGGCTTCTCTTAAGG[T/G]AACTGTACTGGATATGTGAATACATTGTTGGTTTATGTGACTGATTTGGAAAACTCTAACATGGGTTTGATAATTGCAGGAGGCCGGTGTTGACGTGAACACAGATGGCTTGATTGTGGCAGAATTACGAGTCCAAGCATATTCTGGAAACCTTGCAAAGCTACTATCTCTGAGTAAGCATTAGCTTCCATGAAAATTACTTTCCCTCAACCACTCTCTGTCAATTTTCCTTATACCTTTACATATATATGCTCATGTTCTTTCACAGACATAACTCTGTGGAGAGATTTATTTTTAGATGTACCCTGTATGATAGCACTAATCACTTAAAGGCTAATAGCCACCTCTCAGAACAGCACACACTAACAGACAGATATATGATCCATTAGGCTTTTTACGTTAGGGTTGTTAAAGTAAAGCACAGAGTCTCTTTATTTCATTCTTTTGCTTCAGGTTGCTTAATTGGAAGACTTCTAAACTTTCCTGTGTCATAAATTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42148
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034230 | Essential Splice Site | 745 | 1461 | 20 | 38 |
ENSDART00000126427 | Essential Splice Site | 731 | 1447 | 20 | 38 |
ENSDART00000128868 | Essential Splice Site | 720 | 795 | 20 | 23 |
Genomic Location (Zv9):
Chromosome 13 (position 10405284)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 10707613 |
GRCz11 | 13 | 10840088 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCCCATTTAACCCTCAAAAAACTCATCAACGTCCTGAGTATTGAGGAG[G/T]TGAGGTTGATTCTTGTATCACTATCAATGTGTGCTGTTCGTGTTCAATTC
Long Flanking Sequence:
TTATTGTATTAAATACCTGTTTAAAAAATCTGTTATGTTTAAATGCACTAAAATACATTACCTATATTCACTGAGAAATGGATAAAAAAATATTCGTTTTAAAAAGGGGTGTACTCAGTTATGCCGAGCACTGTATATTAACTACATTACAACACCCTTTCATCATGGTAATGTCAAATCTGAGTTGTTCTGGTAAGGTCTGTAATAATACTGTTAATAAAGCAGCTTATTCTTGTATACCTTTTAGGAGGCTCTTACTCTTGTGGATAAGACGGATGATATGACTGAGGTGATGATGTTTAGAGTAAGTGTGTGCATTTGGTTTATTTCTACCGAAAGCTCAATGTATCAGATGTGTCAGTCAGCTATTCTCTTGTTTGCAACAGAGTTCTGAGGGAAGAATTTCCGCCTTGGTGAAAACACTGGCAGAGCAAAAAGCTGAGGGCAAACCTGCCCATTTAACCCTCAAAAAACTCATCAACGTCCTGAGTATTGAGGAG[G/T]TGAGGTTGATTCTTGTATCACTATCAATGTGTGCTGTTCGTGTTCAATTCAAATTTTCATTTCTATAGCACTTTTACAATGTAGATTAGCATAGGAGTTCTAGTAAACTGAAACTGTGTCAGTCCAGTTTTCAAAGTTAAAGTTCTGTTGAAAGTCAAAACACTGAAGAGCAAATCCATCAATGCGCAGCTCCACAAGTCTTAAAAAAAAGCAAGCCAGTGGCGACAGGGGCAAGGAACAAAACTTAACCAATTGACAAAAGTAAAGGAAAAAACCTTAAGAGAAACTAGGCTTAGTTGGGCTCAACCATTTCTTCTAGTGTTCTGGATTGTTGGGCTTTTATTTCCATTTATAGAGATCAACTGATGTAATAAATGTAATAACTGTTAACAAAAACACATTTTTAATTATGTCAATTCTCAACATTACTATTTTACTGTTTGTTTTTGCAAATAAATGCAGACTTCAGCATAAGAAGCTTTCAAAGCTTACCAAAGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35428
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 |
---|---|---|---|---|---|
ENSDART00000034230 | Nonsense | 757 | 1461 | 21 | 38 |
ENSDART00000126427 | Nonsense | 743 | 1447 | 21 | 38 |
ENSDART00000128868 | Nonsense | 732 | 795 | 21 | 23 |
Genomic Location (Zv9):
Chromosome 13 (position 10406700)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 10709029 |
GRCz11 | 13 | 10841504 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTCTGTTTTCAGAAACTGGAGCAAGCTCTCGATCTGAAATCTAAATA[T/A]GAGGATGACATGACGCCTGCTGCTTATGCCACTCTCATCAATCTGTGCTG
Long Flanking Sequence:
AATACATCTCAATAAAACTTTTAGAAAAAAAAACTTTTTTATAATAGTCTGTTTGGTTTATTAAGTTTTTTTTTTTTTTTTTTTTGTATGTAAACAACAACAAACGTCTGCTTGTTTTGACATTATTTAAAATGTGTGACTAAGAAATAATTATTTACAATTATTTTTTTTTTATTTTGGATGAGGCAAGTAAAAAGTTGGGGCAAGTTCTGCTGGACCATTAAAAAAAATCCTTAGCATTTAGTTATAGTTAAGTCTGAAATTTCATTCTTGATGGTCTTAAAAAAAGTCTTAAATTTGACTTTGTGAAACCTGAAAAAATCCTGAGTATCTTTTAGCTATACAAAAACAATCCATCATGTTGTTACTTATAGCAACTGAAGTCTTGGGCATTTGGAGAAAATAACTTGCTCTCTGAAAAATGAAATAAAATAATATTATTTGTAACTTTTTCTCTGTTTTCAGAAACTGGAGCAAGCTCTCGATCTGAAATCTAAATA[T/A]GAGGATGACATGACGCCTGCTGCTTATGCCACTCTCATCAATCTGTGCTGTCGACATGATAATGCTGAGGAAGCTCTCAAACTGAAGATTGAGATGTGAGTTGGACATTTCTCTTCATTAAACAAATCTATTTTGAAGGAAAGGAAAACAGTTAACCGAGTAATTAGAATAAGCATCATTCACTTGCTCCCATATACGAATTATTTACTCACTCACTGGAAGACTGTAGAACATGAAATGTAATTCACAAACTGGATGACAAAGTCTTAAAAGTCACAGTTCACCCAATATAGTTATGTTATTGGAAAGTTTTAAAAAAAACTATGCAGGCTAAACAAAAATCAGACTGATTGTAATTACTTTTATTGATTAAATTGATGATTAATAATCACATGACTTTGAAAACATCACACAGAAGGATTTATATCATGACAGTTGACTGACGTCATGAGGGGAGTAATTAAATGAGGTATTTTCACATACTTTCAGTTGTAGCAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22237
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034230 | Nonsense | 1339 | 1461 | 35 | 38 |
ENSDART00000126427 | Nonsense | 1325 | 1447 | 35 | 38 |
ENSDART00000128868 | None | None | 795 | None | 23 |
Genomic Location (Zv9):
Chromosome 13 (position 10475616)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 10777945 |
GRCz11 | 13 | 10910420 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTTGAGAGTTTTGAGGTCTCTTGTGTTTCTCTGATTGCTTTAGCGCTG[T/A]GCGGCTGTCGGCGAGCAGAAGGACTTACTGTTCTCCTATGTGTTACGAGC
Long Flanking Sequence:
GAAATTCACCGTGCCTTCGTTTAACTTGCGTTATATTGTCCTGATTAAAGAGTGTGGAAATTGCACACCGACGCTTGAAAGCTCAGGAGCACGCCGATGCAATTCAAAGCCTTTATACGGCTAAGTGTAGATAATTGTACTTTAAATTGGGCGGACACTGTACATTTTAATTTTCATAAAGAAATAAGTGGTTATTTGCCTGACTCCCCTATTAGCTGTATAATTAACCCTCAACTATAGAGCACTGCGCTGAGTGCTAAAGGATGAAATGGAAGATGGATACGCTCAAAAACACACGTTCCCGTCATGCTGTTGTACACACACACACCTCTGTATGCTCCGTATTTTTACTGCCTGCTGTGTGGATTCAAGTAAATGGCAAGGGTTATGTTTTGCTCAAGGGCAGATACTGTGAACACGCTCAGGCGTTTTGATATGCGATAAATGTTTGTGTTGAGAGTTTTGAGGTCTCTTGTGTTTCTCTGATTGCTTTAGCGCTG[T/A]GCGGCTGTCGGCGAGCAGAAGGACTTACTGTTCTCCTATGTGTTACGAGCGTCCCAGCAGCCCGGACAGGTAAACAGAAGCTGTTTGTTTTTATATAGTCCATGCTTTTTGTTTAATTTATGCATGAGTTTTGATCGGAGGAGGAGAATGTTGCACTAAATGGGGACATAGTATGTGAATTAATTAATAAATACTGAATTAATAGCTTGAAGTTGTTTATGAATAATGATGGTTGATTGTCTTTTTGCAGGCTGCTAAAGTCATGAGTCTTATGGAACTGATTCCTGACATTCGAGAGAAGGAGGATATTTATTCGCAGCTGATGAAATGCCATGGTAAGACCACCATTTGGCAGGGGGATTTACAGTACAGAACTGTGCATCGGTGGTCCAATGTGGCAGTATAAATGTTGTTACAAAACATTTGAAGTTAAGGGTTTAAGGAAAATCTGTGTCCACAAAAAACAAAGATGTACCACTTATCTCTGAGTTGTTGATAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12060
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034230 | Nonsense | 1355 | 1461 | 35 | 38 |
ENSDART00000126427 | Nonsense | 1341 | 1447 | 35 | 38 |
ENSDART00000128868 | None | None | 795 | None | 23 |
Genomic Location (Zv9):
Chromosome 13 (position 10475662)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 10777991 |
GRCz11 | 13 | 10910466 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTGTGCKGCTGTCGGCGAGCAGAAGGACTTACTGTTCTCCTATGTGTTA[C/T]GAGCGTCCCAGCAGCCCGGACAGGTAAACAGAAGCTGTTTGTTTTTATAT
Long Flanking Sequence:
AAAGAGTGTGGAAATTGCACACCGACGCTTGAAAGCTCAGGAGCACGCCGATGCAATTCAAAGCCTTTATACGGCTAAGTGTAGATAATTGTACTTTAAATTGGGCGGACACTGTACATTTTAATTTTCATAAAGAAATAAGTGGTTATTTGCCTGACTCCCCTATTAGCTGTATAATTAACCCTCAACTATAGAGCACTGCGCTGAGTGCTAAAGGATGAAATGGAAGATGGATACGCTCAAAAACACACGTTCCCGTCATGCTGTTGTACACACACACACCTCTGTATGCTCCGTATTTTTACTGCCTGCTGTGTGGATTCAAGTAAATGGCAAGGGTTATGTTTTGCTCAAGGGCAGATACTGTGAACACGCTCAGGCGTTTTGATATGCGATAAATGTTTGTGTTGAGAGTTTTGAGGTCTCTTGTGTTTCTCTGATTGCTTTAGCGCTGTGCGGCTGTCGGCGAGCAGAAGGACTTACTGTTCTCCTATGTGTTA[C/T]GAGCGTCCCAGCAGCCCGGACAGGTAAACAGAAGCTGTTTGTTTTTATATAGTCCATGCTTTTTGTTTAATTTATGCATGAGTTTTGATCGGAGGAGGAGAATGTTGCACTAAATGGGGACATAGTATGTGAATTAATTAATAAATACTGAATTAATAGCTTGAAGTTGTTTATGAATAATGATGGTTGATTGTCTTTTTGCAGGCTGCTAAAGTCATGAGTCTTATGGAACTGATTCCTGACATTCGAGAGAAGGAGGATATTTATTCGCAGCTGATGAAATGCCATGGTAAGACCACCATTTGGCAGGGGGATTTACAGTACAGAACTGTGCATCGGTGGTCCAATGTGGCAGTATAAATGTTGTTACAAAACATTTGAAGTTAAGGGTTTAAGGAAAATCTGTGTCCACAAAAAACAAAGATGTACCACTTATCTCTGAGTTGTTGATAATAGCATCAAATCAGCATATTAAAATGATTTCTGACAGATCATATGAT
Associated Phenotype:
Not determined