ZMP
rrp12
Ensembl ID:
ZFIN ID:
Description:
RRP12-like protein [Source:RefSeq peptide;Acc:NP_001025447]
Human Orthologue:
RRP12
Human Description:
ribosomal RNA processing 12 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:29100]
Mouse Orthologue:
Rrp12
Mouse Description:
ribosomal RNA processing 12 homolog (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:2147437]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9602 | Nonsense | Available for shipment | Available now |
sa8658 | Nonsense | Available for shipment | Available now |
sa13242 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9602
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 |
---|---|---|---|---|---|
ENSDART00000034829 | Nonsense | 613 | 1283 | 16 | 34 |
ENSDART00000134343 | None | None | 100 | None | 5 |
ENSDART00000145887 | None | None | 276 | None | 9 |
ENSDART00000034829 | Nonsense | 613 | 1283 | 16 | 34 |
ENSDART00000134343 | None | None | 100 | None | 5 |
ENSDART00000145887 | None | None | 276 | None | 9 |
The following transcripts of ENSDARG00000022410 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 31579027)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 31224975 |
GRCz11 | 13 | 31355425 |
KASP Assay ID:
2260-6599.1 (used for ordering genotyping assays)
KASP Sequence:
TCAGCYGATGAACTGGAGCAGTCAGGGCAGAAGCTCATGGCAAAGGTTTA[T/A]CAGACGTTACAGATGCAGGTATGATGTGTATTTTAAGACTGTAAACACAT
Long Flanking Sequence:
TTATCAGAGTCTCCAGTCTCTCAGTGACCTGAGGGCCACCCCTCAGTTCCCCTTCACTGGTGAGCTGGATCTGGCTGTTGGTGGTGCGGTGGAAAGCATGGGTCCAGAGGTGGTGCTCAACGCTGTACCCCTCCTCATCACTGGAACAGAGTGTGTTTCTTTTTCAATGCTTTTCAATGTAAAAACCAATTAGTGCTTTAAATGAAAAGGTACAAATATGTTTTGTGTGTGTGTGGTTGCAGTGATGACCTTGAGTTTCCACGCAGTTGGTTGATTCCGGTCATTAGAGATCATGTAAAGAACTCTCAGCTGGCTTACTTCAATTCACACTTTTTCCCGCTGGCAAACAAACTTAAACAGACAGGTCTGTATAAGTCTCGCACTCACACGGTCCCAATGTTCTCTGGCGACAGTGTTGCTGTTATATAAACTCTTAATCTTTGGTTTATTTCAGCCGATGAACTGGAGCAGTCAGGGCAGAAGCTCATGGCAAAGGTTTA[T/A]CAGACGTTACAGATGCAGGTATGATGTGTATTTTAAGACTGTAAACACATTGTTTAGACCATAATTGTAAATTTTGTCAAGAAAATGAAATGATCTGATCTAAATAATGACATTATGATATACAGTTTAGTTTATTTATAAAGCACAATAAAACAACAGTTGTTGACTATTGTGCTGGACAAACCTAAAAGCTAGAGGCTGGGATGCACAAGAAAAGAAACCAAAGAGCCACTCTGGTGACATCCTTTTTTATTTACAATCTCTTCACTGCTGCCATACAGTTCTCTTTTTCGCATGTTTTGTTATTCTGACCTGAAGTGACAAGCACGAGCACATGCTTTGTGTCTGAGGTAATTAGTCTGCCGTTATTACTGAAATGTGTATTGCCCATACAAAGTGTAAAGCAGATTGGTTAGTTCTTGCTCCTGGGGCATTCTGAGAGTTCAGATGTTTTTCAACTAGGTGTACCTGGAAAATGTGTGTTTGTTATGTGCACGTCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8658
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 |
---|---|---|---|---|---|
ENSDART00000034829 | Nonsense | 613 | 1283 | 16 | 34 |
ENSDART00000134343 | None | None | 100 | None | 5 |
ENSDART00000145887 | None | None | 276 | None | 9 |
ENSDART00000034829 | Nonsense | 613 | 1283 | 16 | 34 |
ENSDART00000134343 | None | None | 100 | None | 5 |
ENSDART00000145887 | None | None | 276 | None | 9 |
The following transcripts of ENSDARG00000022410 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 31579027)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 31224975 |
GRCz11 | 13 | 31355425 |
KASP Assay ID:
2260-6599.1 (used for ordering genotyping assays)
KASP Sequence:
TCAGCYGATGAACTGGAGCAGTCAGGGCAGAAGCTCATGGCAAAGGTTTA[T/A]CAGACGTTACAGATGCAGGTATGATGTGTATTTTAAGACTGTAAACACAT
Long Flanking Sequence:
TTATCAGAGTCTCCAGTCTCTCAGTGACCTGAGGGCCACCCCTCAGTTCCCCTTCACTGGTGAGCTGGATCTGGCTGTTGGTGGTGCGGTGGAAAGCATGGGTCCAGAGGTGGTGCTCAACGCTGTACCCCTCCTCATCACTGGAACAGAGTGTGTTTCTTTTTCAATGCTTTTCAATGTAAAAACCAATTAGTGCTTTAAATGAAAAGGTACAAATATGTTTTGTGTGTGTGTGGTTGCAGTGATGACCTTGAGTTTCCACGCAGTTGGTTGATTCCGGTCATTAGAGATCATGTAAAGAACTCTCAGCTGGCTTACTTCAATTCACACTTTTTCCCGCTGGCAAACAAACTTAAACAGACAGGTCTGTATAAGTCTCGCACTCACACGGTCCCAATGTTCTCTGGCGACAGTGTTGCTGTTATATAAACTCTTAATCTTTGGTTTATTTCAGCCGATGAACTGGAGCAGTCAGGGCAGAAGCTCATGGCAAAGGTTTA[T/A]CAGACGTTACAGATGCAGGTATGATGTGTATTTTAAGACTGTAAACACATTGTTTAGACCATAATTGTAAATTTTGTCAAGAAAATGAAATGATCTGATCTAAATAATGACATTATGATATACAGTTTAGTTTATTTATAAAGCACAATAAAACAACAGTTGTTGACTATTGTGCTGGACAAACCTAAAAGCTAGAGGCTGGGATGCACAAGAAAAGAAACCAAAGAGCCACTCTGGTGACATCCTTTTTTATTTACAATCTCTTCACTGCTGCCATACAGTTCTCTTTTTCGCATGTTTTGTTATTCTGACCTGAAGTGACAAGCACGAGCACATGCTTTGTGTCTGAGGTAATTAGTCTGCCGTTATTACTGAAATGTGTATTGCCCATACAAAGTGTAAAGCAGATTGGTTAGTTCTTGCTCCTGGGGCATTCTGAGAGTTCAGATGTTTTTCAACTAGGTGTACCTGGAAAATGTGTGTTTGTTATGTGCACGTCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13242
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 |
---|---|---|---|---|---|
ENSDART00000034829 | Nonsense | 735 | 1283 | 19 | 34 |
ENSDART00000134343 | None | None | 100 | None | 5 |
ENSDART00000145887 | None | None | 276 | None | 9 |
The following transcripts of ENSDARG00000022410 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 31576142)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 31222090 |
GRCz11 | 13 | 31352540 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AKGTTTGTTCCTGTTGTTTCAGATGGTGTGCACATTTCTTCAAAAAGCAT[T/A]GGAGAGACTCAATGCWGACAACACTGAGTTTACCAGGTAATACAGCTTCA
Long Flanking Sequence:
TCACTTAAATTGCGCGTGAGCAGTGAGGCAAAAATAGACCCAGCACTGAAACTATTGCGGCACTGCTGCTTCTGCAACGCTTGTTTTTTGCGCTGACGCGATGCTTCTGCGTATGATATGAAAGCTCTTATCTGGTAACATGGACGCCAAAAAATATGCTGCTCACACTCTGCTCGCGCTTGTGGTGTAAAATAGGCTTAAGTATCTGCAAGTAAAAAGTTATGTAGTTGCATATTTTTTGCTCGCTTTATGTTAATTACATTTATATACTGCTTATATTGCAAAAAAAAATACTGCATGTTCTTGCCTTCCTGTAGCTCAAACAGAAAAGCCACTAATTGGTTTAATTTCACATGAAAACTTTAAAAACAGTGCAAGTATTTCTTGATTAAAATAATAAATGTCCTGCGGTTTGTGCCGTTGGCTCTTTTCACAATGTCAATACCAAATAGGTTTGTTCCTGTTGTTTCAGATGGTGTGCACATTTCTTCAAAAAGCAT[T/A]GGAGAGACTCAATGCTGACAACACTGAGTTTACCAGGTAATACAGCTTCATACCTTTACAAGGCATTATAGAATACGTTATAGTGTGAACAGAAACCTGATGCATGCATAAAGTGACAAGATAATTTAATGGCCGTGCTGCCTAAAAGATGTGCTTTGTTTTGTTTAAAATTAAATTTTGAGTCTAGCATTTTAATATTAGTGTTTGTTATTTCATAGGCTTGCAGTCATTGACCTGGTTGTAGCCATGGCTCCGTTTGTGGATGAAGCGTCTATGAGCCAGATACTTGAATTCATAAAACCTTTTGTGGAGGTGAGAATCTTCCTAATAAATCTTTTGTTTTCATTTGTTTTGTCATGAGTGCACTTTACATTTGTTTGTGTGTTTATAGAGCAAGGATACTGGCATCCAGAAGAAAGCCTACAGAGTCCTGGAAGAGATCTGTGGAGGAGAGAGAGCGTCCTGTAAGGCTTTTGTTCTGGCAAACCTGGAGCAGCTGA
Associated Phenotype:
Not determined