Busch Lab

ZMP

rrp12

Ensembl ID:
ENSDARG00000022410
ZFIN ID:
ZDB-GENE-050706-182
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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