ZMP
prpf31
Ensembl ID:
ZFIN ID:
Description:
U4/U6 small nuclear ribonucleoprotein Prp31 [Source:UniProtKB/Swiss-Prot;Acc:Q7SXM7]
Human Orthologue:
PRPF31
Human Description:
PRP31 pre-mRNA processing factor 31 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:15446]
Mouse Orthologue:
Prpf31
Mouse Description:
PRP31 pre-mRNA processing factor 31 homolog (yeast) Gene [Source:MGI Symbol;Acc:MGI:1916238]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa15636 | Nonsense | Available for shipment | Available now |
| sa11927 | Nonsense | Available for shipment | Available now |
| sa22886 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15636
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 |
|---|---|---|---|---|---|
| ENSDART00000039845 | Nonsense | 297 | 3209 | 9 | 27 |
| ENSDART00000137029 | None | None | 508 | None | 14 |
| ENSDART00000140794 | None | None | 240 | None | 6 |
Genomic Location (Zv9):
Chromosome 16 (position 34381998)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 32113498 |
| GRCz11 | 16 | 32067528 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTAATTTGCANNNNNNNNNNTTTTCATTTTCATATTTTACACAAACAGGAGGATTATTA[T/A]CTAACCCCAGACAAATTGTGGATACCTCTCCGCTGGATTGCTCCTGAACT
Long Flanking Sequence:
AACATTACTTAACAAGCATTTGGATTGTAATAAACTTTGGATCTTAATAATCTATTAGTAAATGTTGAACTATGATTGAGAAATGTTCTAAAAGTACTGTTCGTATTTGGTTCATGTTTGCAAATACATTAACTAATAGACCCTTATTATAAAATGTGACCAGAAAACATATATTAAAATGGAGAATTGTGAAAATATCAAATACATTTTTTACAATTGTCTATTTGTCATTTGTTCTTCAGTGATTTGGCACTGAGGAACTGCCTCCTCACCTCAGATCTCACGGTTAGGATTGGAGACTATGGCCTCTCACACAATCAATACAAGGTATTTAAACGATTACTGAACTCCAGATCAAAAAGACTTTTTTGACCAGGCCTTCAATCAGTCAGTGGTATAGCTGGCTTTTTCTGTTCACCATCAAAGAATATTTGTCAGTTTATTGTATTGTTTAATTTGCATTTTCATTTTCATATTTTACACAAACAGGAGGATTATTA[T/A]CTAACCCCAGACAAATTGTGGATACCTCTCCGCTGGATTGCTCCTGAACTCTTGGAGGAGTTTCGTGGAAATCTGATTGTCACCGATCAAACCAAAACTAGCAATGTGTGGTATGGAAAATTCTGGACTAATGTATTTCTGAGAGAAATTTTAATGGAGGATTCCAATAATAGGACAAATGAAAAGTATCATTTAATTAGTTTGTTTTAATTAAAAAGCAACACATGCTTAAGGTACTTGAATTGGTCATGCTTCTGCTACTCTTGGCTGTTTCTAATGTTTAAACACTTTTTCCCCCAAAATGACAACCTATAGGTCTTTGGGTGTTGTGATATGGGAGCTGTTTGAATTTGGGGCTCAGCCGCACAGACACCTGAGCGATGAAGAAGTTCTCACCTTTGTCATCAGAGAACGACAGATCACTCTCGCTCAACCTCGCCTCAAACTCGCTCATGCAGACTATTGGTCAGTAATTTTAAACGCTTTAGCTTGATGAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11927
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 |
|---|---|---|---|---|---|
| ENSDART00000039845 | Nonsense | 2697 | 3209 | 14 | 27 |
| ENSDART00000137029 | None | None | 508 | None | 14 |
| ENSDART00000140794 | None | None | 240 | None | 6 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 34392095)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 32123595 |
| GRCz11 | 16 | 32077625 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACCGTRACCGTGGGAGGAATGTGTCATTTTTCGATGACGTCACAGTCTA[T/A]MTTTTCGATCAGGTATGTCAAGGGTGTTTATACAAGCATCTTCAATTACG
Long Flanking Sequence:
TGACAACAGAAATAGGAATAACTGTGTAATATACTGTACTGAACCGTTTACTCTGTGGTAATGAGCTATTAGTGTCAGTTGTACTTTTTTAGTGGCTGTTCACATTTTGGTTGTTAGATAACCGACATGCCATCTTGGATGTTTATCTTTTATCTCTCCCACTCCACCTTTATTTCAGCTAAGTTGGCCCGTCTCTCCTTATCCCTCCCTCCACTTGCTCTTTCTCTTCCTCTCTCACCAAATACCAAAGGAGGATTCTGGGAAGGGAGCGAGTACAGAGGGGGCAGGAGGAGGGCTGCATCGACAGGTAGCGATCCAGATGAAGATGAAGAAGAGGAACAGGAGGAGGAGTCTCCCAGGCGCGTCATCGTTGTCACGGAAACAGATGTTGACAAGAGAGTTGGTTTGCGTAGCTTGTTGAAATCGCCAAAGGAGCCCGTGGACAAAGAGAACCGTGACCGTGGGAGGAATGTGTCATTTTTCGATGACGTCACAGTCTA[T/A]CTTTTCGATCAGGTATGTCAAGGGTGTTTATACAAGCATCTTCAATTACGAGGTTTCACACTGGGCTGTTAAACATCATATGTTTTATTATATTTCAATGGCTTGGCACTCTTCATATCAGGAAACTCCAACCAATGAGCTGAGCTCTGGATCTACTAGTACATCTCCTCATGGAAAGCACCCTAGCACTGATGGTTTAGGTAGGTGTATTCAGCAGAGTGTATTATAGATTGGCCCTGATCTGCATAACCCAAATGCAAAACTTGTGATTATCCGAAATGAGTAAAAGCTTTTTAAGCCAATTTTAAGGCTGACAACAAACTACAAAAAATAGACAGCCATTAATTAATTACATAAAAGATTTTAAAAATGAACACTCTAACATTCTGACATTGTGTCCTAACAACACGCAATGCAACTAGATTCCAGCAACAAGCAATTTGGTTATCCACACAATACGAGACATGACTGAGACATTTAAATACCAGAGCCATTCTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22886
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000039845 | Essential Splice Site | 2852 | 3209 | 18 | 27 |
| ENSDART00000137029 | Essential Splice Site | 151 | 508 | 5 | 14 |
| ENSDART00000140794 | Essential Splice Site | 151 | 240 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 16 (position 34399528)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 32131028 |
| GRCz11 | 16 | 32085058 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGGAGTCTCTGGTGCCAAATGCACTGGACTACATCAGAACTGTTAAGG[T/A]ATGTAGAAACCTGCCTGTCTGTAATTTAGCTTTTATGAGCAGACTATTTC
Long Flanking Sequence:
CTGCATACATTATTTAATTACGTTGTATTATTATCAATATTATTATTATTATTATAGTTTTTTTCATAAAATGTTATAATGCTTTTGAAGTGGCTCTTGGAGCATAGCAGATGAAGTTAATGTCCTCGTATAATGAAATGGCAGACAGTGCTTGAGTTTGTCTGTAGTAAACAAAGCCACGTGACTGATTTACACACAACATGCAGACTTTATTAAACCGCAAAAATACAGTTTATATATATTCACAAGCACTAGTCTGTATTCAATTGGATTACAGTTAATGGATGACTAGATTTTGTTAGCTTTTTCTGCATCATGAAGCCTCTTTAACCCTTTCAAACATTAGAATTATAAAACTTCTTACACATTTTGAGATCACTTTTGCTTTATTTCTTCCTCAGATATCATTCACAAGTTTGTTCGTGACAAGTACTCCAAAAGGTTTCCTGAGCTGGAGTCTCTGGTGCCAAATGCACTGGACTACATCAGAACTGTTAAGG[T/A]ATGTAGAAACCTGCCTGTCTGTAATTTAGCTTTTATGAGCAGACTATTTCTGTCAAAACTGTGTTTTGTGAGTTACACTTTCTAATCAGCTGGGGTTTTTTGTTAATGAAGTTTAAACATTAATACTTGTGTGTTCGATAATTTGATGTGTTTGTGTGTCTTTAGGAGCTGGGCAACAATCTGGAAAAGTGCAAAAACAATGAGACCCTTCAGCAGATTCTCACCAATGCCACCATTATGGTGGTCAGCGTCACAGCCTCTACCACACAAGGGTGAGTGAGCGAGCAGATACAGCCAGAATGGTTATAGCATAGGTCTCTAACTCAGTTGCTGGAGTGCCGCAGCTCTGCACAGTTTATACAGTACTATGCAGAGCTGAGGCCCTCCAGGAATTGAGTTTGAAACCAAAAATCTTTATTTATTGTGTTTGTTATTGCTTTATTTTTTGTAAAGAAAATTTTAAAACATTAAAAATATGTAAAATAGTGATAAAAATGTGT
Associated Phenotype:
Not determined