ZMP
plrg1
Ensembl ID:
ZFIN ID:
Description:
pleiotropic regulator 1 [Source:RefSeq peptide;Acc:NP_998605]
Human Orthologue:
PLRG1
Human Description:
pleiotropic regulator 1 (PRL1 homolog, Arabidopsis) [Source:HGNC Symbol;Acc:9089]
Mouse Orthologue:
Plrg1
Mouse Description:
pleiotropic regulator 1, PRL1 homolog (Arabidopsis) Gene [Source:MGI Symbol;Acc:MGI:1858197]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa13503 | Nonsense | Available for shipment | Available now |
| sa38266 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa24845 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13503
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 |
|---|---|---|---|---|---|
| ENSDART00000054235 | Nonsense | 98 | 511 | 4 | 15 |
| ENSDART00000123032 | Nonsense | 98 | 265 | 4 | 16 |
| ENSDART00000125834 | Nonsense | 105 | 519 | 4 | 16 |
| ENSDART00000131111 | Nonsense | 98 | 510 | 4 | 17 |
Genomic Location (Zv9):
Chromosome 1 (position 24512254)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 24964025 |
| GRCz11 | 1 | 25654854 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTTGTGCAGACACTACTCCAGAATATTTGGTGACAGGAACACACCCTTA[T/A]CCATCTGCTCCAGGTWGAACCAGGATTTTTTTACTTATTTAGCCTAGATG
Long Flanking Sequence:
ATTAGCTGCTTTGTAATAGTAAGGTAGTAGTTGGGTTTAGGTATTTGAGTAGGATTAGGGATGTACAATAAGATCAAACTTTATGAGTGCTAAAACATTGTAATATCTCAATAATAGAAAGCTAATAAACCAGTAGTAAATGGTGTAAATTGTTACATTAATTGTTACTTTTGTTAATGTTATTTACGTTTTGTCTGTAGCTTCAAGGTGAAGATGGCAGCAAAGATGCGGGCCGAATACAAAGCTGTCTTACACATGCCTGTGCTGAAGGAGGGCCGAGAAAAGGGTTCTCTCCACACCTCTGACCCATATGGCCAATCGGCGTACCCTCTGCCTGGTATGCCTCATAAACCAATCCTGTTGGCTTTTTCTTTATATCAGTATTTTCATTTAGTTTGTTTTTTTAATAAACCTCTCAAAGATTTCATTAAGTATTAACTGTTTGACTTCATTTGTGCAGACACTACTCCAGAATATTTGGTGACAGGAACACACCCTTA[T/A]CCATCTGCTCCAGGTTGAACCAGGATTTTTTTACTTATTTAGCCTAGATGCTAAACATTTCAACCAATTTATTTGAGGCCTAATAATTTTTTTTTTTTTATTATTACGCTTTCAGGAGTTGCCCTCACTGCAGACACACAAATGCTGAAGATGCCCAGTGAAATGGGTGTTCACTCCATGGCCCTTGCTCTTCCTCCGTCTCAAGCTAGGTACTGAATTGTATTTCCTTATGGGTTGTTGTAGTTATTATTAAATGTTTTTAGAAAAAAAAAAATTATATATATATTTTTTGCCATAAAAAACATTTTAAAAAATTAAAAACCAGCACGACAACACTTATGCTTTTGTATTTAGGTTGCACAATTTGGCCTGAAATAATTATAATCATAGTTATTGTTATTATAAATAGTATAAATTTTTTTTTCAAACGAAAATTGTAAACAAAATAAGAAATGTTATTACTGTCGAATTTGATTTAAAGTAATTGTACAGATTTCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38266
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000054235 | Essential Splice Site | 276 | 511 | None | 15 |
| ENSDART00000123032 | Essential Splice Site | None | 265 | None | 16 |
| ENSDART00000125834 | Essential Splice Site | 283 | 519 | None | 16 |
| ENSDART00000131111 | Essential Splice Site | 276 | 510 | None | 17 |
Genomic Location (Zv9):
Chromosome 1 (position 24518175)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 24969946 |
| GRCz11 | 1 | 25660775 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTGGCGAGGACAAACAGGTTAAATGCTGGGACCTCGAGTATAATAAGG[T/C]ATGAGCTTTATATATATCACCACTGTCATACTCCATTTAGGTTTACAGAC
Long Flanking Sequence:
GGCAGATGCAAATGCTGTAACTGAAGTCAGTTCAATATAAATGTCATTGTTGAAGTGCTGCTTTTATTAACACTTGTAAGTCACTTTGGTTAAAAGCGTCTGCTAAATGAGTCTACTAGTGCACATGTGCAGTAACACTAATGGCGTGTATCGAGCGTTTTCTGTTTATTTATATGGAAGTTCAGGGTAAATGGTCATGCAGTGCATTATGGAATTTAAAGCAGCACGGAAAAACATTAAGAGCAGCTGACGTATAAAACATTTTAGAATGTTAAGTTAGTATTTATAAATATTATTGTTAATTATTGTTTTCATTTATTTTGAAATTTTTTCTCTTTTTTTGTGCCAGATTTGGGATCTTGCCAGTGGTAAGCTAAAGTTGTCTCTAACTGGGCACATCAGCACAGTGAGAGGGGTGGCCGTCAGCAACCGCAGCCCGTACCTCTTCTCTTGTGGCGAGGACAAACAGGTTAAATGCTGGGACCTCGAGTATAATAAGG[T/C]ATGAGCTTTATATATATCACCACTGTCATACTCCATTTAGGTTTACAGACTAAAATTGTGTGTAATCTACAGGTTATACGGCATTATCATGGTCATCTGAGTGCAGTCTATGACCTTGACCTCCATCCAACCATTGATGTGCTGGTTACTTGTAGTCGAGATGCCACAGCTAGGGTAAGATGTCTTATAAGTCTTTTTTTTGTGTGTGTGTGTGAATAATTGTTTGCATTGTTTATATATATATTTGTTTTTTTTTCTCTCTCATTTTTTCCTTTTTGTTTCTTTTCTTTCTTTTTTTCCTCTTCTATTTCTTCATGCAATCATGTTGGCATCTTTTGGTGCTATATTGCAAGATATGGTTTGGTATGGTTCACTTTTGCGTGGGTTTCCACTGCATACTGTAACTGGTTGGGTTTGCACCGTCAGTAAGTTCTTGCTTCAACTGGAACACCCTAGTCCACTCTAGGGGCTAGCATGAATTACTATCTAGTTTGTAACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24845
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000054235 | Nonsense | 442 | 511 | 14 | 15 |
| ENSDART00000123032 | None | None | 265 | 15 | 16 |
| ENSDART00000125834 | Nonsense | 450 | 519 | 14 | 16 |
| ENSDART00000131111 | Nonsense | 441 | 510 | 16 | 17 |
Genomic Location (Zv9):
Chromosome 1 (position 24522543)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 24974314 |
| GRCz11 | 1 | 25665143 |
KASP Assay ID:
554-7460.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATCAGCTGATAACGGCACTATTCACATGTGGGATTGGAGAACTGGCTA[T/G]AACTTCCAGAGGATTCATGCAGCGGTGCAGCCTGGTTCTCTGGACAGCGA
Long Flanking Sequence:
AAACTTTGAGTTTTACATTTTACTACATAACAGTATTTTTTTTTCTTCTATTCACTTGATTTGAGCTTTCATTTTGGTGTAATACTGACTAAAGACATCGACATTTCCTTACATTTTCATCATTCACTTCTAATTGAATCGAATTCAATCATATTCTTTTTTTAATAGGTACACCTTTGCCTCCGGCTCTCCAGACAACATTAAGCAGTGGAAATTTCCTGATGGGAACTTCATCCAAAACCTTTCAGGACACAACGCAATTATAAACACATTGGCTGTCAATTCTGATGGTGTTCTGGTGTCAGGAGGTGAACTATTCCTTCACACTTTCTTACAATCCCTATTCTGCTAAAAATAGAATTTTATTTTTTATATTTTTTGTTGTCTTTTCTGCTTTGTTTGAGCTGTAAAAATTTGCATGTTTTGTTTACTGTCTTTTTATCATTTTTCCCATCAGCTGATAACGGCACTATTCACATGTGGGATTGGAGAACTGGCTA[T/G]AACTTCCAGAGGATTCATGCAGCGGTGCAGCCTGGTTCTCTGGACAGCGAGTCTGGCATTTTTTCATGCGTGTTTGATCAGTCTGAGAGTCGCCTCATTACAGCAGAGGCTGATAAAACTATAAAGGTCTACAAAGAGGATGACACAGCGGTAAGTTCTGACTTCACTGGTAATTCATTAGTTAACAATAATATTAACAAGAATTACAGTACAGTTTAATAATATGCAATGTAATATTTATAAGGTTCTCTGAACTCAAATTCTTGATTGAAGAGAATTGCTGCATAATTTTATATACAGTTGAAGTCAGAATTATTAGCCCCCCATTTTCTTCTTTTAAAAAATTTTCAAATGCTGTTTAACAGAGCAAGAAGATTTTCACAGTATGTCTGATAATATTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTCAACTAGATTAAAAGCAGTTTTTAATTTTTTAAAAACCATTTTAAGGTCAAAACGATTAGCCCCTT
Associated Phenotype:
Not determined