ZMP
prpf39
Ensembl ID:
ZFIN ID:
Description:
Pre-mRNA-processing factor 39 [Source:UniProtKB/Swiss-Prot;Acc:Q1JPZ7]
Human Orthologue:
PRPF39
Human Description:
PRP39 pre-mRNA processing factor 39 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:20314]
Mouse Orthologue:
Prpf39
Mouse Description:
PRP39 pre-mRNA processing factor 39 homolog (yeast) Gene [Source:MGI Symbol;Acc:MGI:104602]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13245 | Nonsense | Available for shipment | Available now |
sa23828 | Nonsense | Available for shipment | Available now |
sa23827 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13245
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 |
---|---|---|---|---|---|
ENSDART00000061672 | Nonsense | 46 | 752 | 2 | 14 |
ENSDART00000135114 | Nonsense | 46 | 391 | 2 | 13 |
The following transcripts of ENSDARG00000042080 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 54632876)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 54481354 |
GRCz11 | 20 | 54242499 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGGGACTGATGATGTCACAGGCTTGAGCACGTCCGATTTGACGACAGAA[C/T]AACCCCCAGAAAGCCAGGAGCAGACCCAGCCGGTGTCCGACATGGAGTTT
Long Flanking Sequence:
CAATCTTATTTATTTAATTATTATCATTATTTACTCTCTCTTTACTTTATTTCTTTTTCTGTCGAACACAAAAGATGTTTTGAAGAAGGCTGTCAATGCTGAAACCACTGACTTCCATGGTAGAAAAAACAATACAGTGGAAGTCAATGATTTTCAGCTGAATATCTTCTTTAGTGTTTGGCAGAAGATCCTTTAAGACAGGATGATGGCCATCCAGTTAAAGAAGGAACTCGGTTAAATTCTCTTGTTTATCTGTTTAAAGCTTTGAACAGTTTGTGCAGTCCAGCATATTGCGTCACATCTGACCGCTTCTGTGGGGTCTAAATGACAGAATTGCACAATCGTTTTTCAAATGTAATCAAATGTGATTTGCTCCAGGTGAGTCAATGACCGGGATGTTGGACTCGAAATCCCCGGAAAGCGGGGACTCTCCTGCTATGGAGGGCACAACGGGGACTGATGATGTCACAGGCTTGAGCACGTCCGATTTGACGACAGAA[C/T]AACCCCCAGAAAGCCAGGAGCAGACCCAGCCGGTGTCCGACATGGAGTTTTCGGTGGAGCATTTAAAGACTGCGGTACAGAACATTGACCAAAGTGCCAGTCCTGCAGAACCTGCTGCGGAAAACTCTGAGCAGCCGCCAGAGTCAAACGGACAGCAAGAGGACCAATCAGAACAGCCGGATGATGTGAAGGAGGCGGGACAAGGTGACTCTGAGAGTCCCTCCAATATGGAGCTGGAGGACGCGCCGAAAGAGCCAGCCGAACCCGCAGCAGAAGCAGATCCAGCGGCGCCACAAGAACCAGAACTTCCCACAGAATATGAGCGTTTGTCCAAGGTTGTGGAAGATAATCCTGAAGACTTCAATGGCTGGGTTTACCTCCTGCAGTATGTTGAACAAGAGGTAAGAGCCTTAAGTAAAATAATGAACCCTAATAAGCTGTGCTTTACAGGAAATTTATAAACAAATGGCAAAGAGAATGCGAACTACATAATAATGAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23828
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061672 | Nonsense | 152 | 752 | 2 | 14 |
ENSDART00000135114 | Nonsense | 152 | 391 | 2 | 13 |
The following transcripts of ENSDARG00000042080 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 54632556)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 54481674 |
GRCz11 | 20 | 54242179 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGAAGCAGATCCAGCGGCGCCACAAGAACCAGAACTTCCCACAGAATA[T/G]GAGCGTTTGTCCAAGGTTGTGGAAGATAATCCTGAAGACTTCAATGGCTG
Long Flanking Sequence:
CTAAATGACAGAATTGCACAATCGTTTTTCAAATGTAATCAAATGTGATTTGCTCCAGGTGAGTCAATGACCGGGATGTTGGACTCGAAATCCCCGGAAAGCGGGGACTCTCCTGCTATGGAGGGCACAACGGGGACTGATGATGTCACAGGCTTGAGCACGTCCGATTTGACGACAGAACAACCCCCAGAAAGCCAGGAGCAGACCCAGCCGGTGTCCGACATGGAGTTTTCGGTGGAGCATTTAAAGACTGCGGTACAGAACATTGACCAAAGTGCCAGTCCTGCAGAACCTGCTGCGGAAAACTCTGAGCAGCCGCCAGAGTCAAACGGACAGCAAGAGGACCAATCAGAACAGCCGGATGATGTGAAGGAGGCGGGACAAGGTGACTCTGAGAGTCCCTCCAATATGGAGCTGGAGGACGCGCCGAAAGAGCCAGCCGAACCCGCAGCAGAAGCAGATCCAGCGGCGCCACAAGAACCAGAACTTCCCACAGAATA[T/G]GAGCGTTTGTCCAAGGTTGTGGAAGATAATCCTGAAGACTTCAATGGCTGGGTTTACCTCCTGCAGTATGTTGAACAAGAGGTAAGAGCCTTAAGTAAAATAATGAACCCTAATAAGCTGTGCTTTACAGGAAATTTATAAACAAATGGCAAAGAGAATGCGAACTACATAATAATGAGCTACATAATGATGAGCTACATAATGATGAGCTACATAATGATGAGAACTACATATAAAATGAGCCGTAATGCTGGCAAAAGAAACATTTAGAGTTTCTCCAACTGGTTGGATCAGTTTTTTTGCACTCTGTAAAATCAGGCACGCTAGGATGTCACAAGCTTTACATTCTTGTAGATGATCCTCTGTGCTATTTCTAAAGCACTTTAAAGGGTCATCCAACACTGAAACACACTTTTTGATATGTTGACAGATATCGGTGTTCAAAATTGCAACCGTTTTGGTCGCATATGCGCCTGAAATTATATCCAATCCACCTCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23827
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061672 | Essential Splice Site | 317 | 752 | None | 14 |
ENSDART00000135114 | Essential Splice Site | 317 | 391 | None | 13 |
The following transcripts of ENSDARG00000042080 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 54623430)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 54490800 |
GRCz11 | 20 | 54233053 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCGTCTGCTCTGCATTCCCACACAGCTGTACTCGCAGCATTTCCAGAAG[T/C]GAGTGTCCGACACAGCACATGTTAGAGCTGTACGATAGTGGAGAGATGCG
Long Flanking Sequence:
TTACTGTTTCTGCTTTTACTGTGCATTTCAGTTTATACTTTTAATTACATTTAAAATACAAACAAGGATAGAAACCGTATAAAAAGCAGACAAACCTACTGACTGACAGTTATAGGTTGCATAGATTGATGTGTGTCAGGGATGCTAACATTTGCCTCAAATCCGAAAATTTCCCCTTTCTAGCTGATCTTTCTGTGAGAATTATGCAGAGCACAGGCATGTCTCGTGCATGGTAAAGCATTACTAACCAACAAAAGGATTCAACATAGAAAAATAATAATATAAACACATTAGAATTAATAAGAATCTAAAAATGCTTGTTTTCCTTCAGGTCCTATGAGCATGCAGTTCTGGCCTGCGGGACAGATTTCCGCTCGGACCGTCTGTGGGAGGCTTATATCGCATGGGAGACGGAGCAAGGGAAGCTGGCCAATGTCACCGCCATCTACGACCGTCTGCTCTGCATTCCCACACAGCTGTACTCGCAGCATTTCCAGAAG[T/C]GAGTGTCCGACACAGCACATGTTAGAGCTGTACGATAGTGGAGAGATGCGACATTGTATCACAATGTTTATCACAGAAAAACGAAATATCGCAATGTCAAATTTTTTTATATCATGCAGCCGTTTGTCATCTGGTGAAAGTGTGTCCGTATCGTAATGTTTATCGCAGAAAAACAAAATATCGCAATGTGCTATTTTTCATGCGTCGCAGATTTATAAAATGTAATTAAAAATCGTTGCTGCATTTTCAGGTTTAAAGACCACGTGCAGAGCAACAACCCCAAGCACTTCCTGTCAGAAGAGGAGTTCGTGTCGTTGCGAGTGGAGCTGGCGAATGCAAATAAACCCAGCGGAGACGAGGACGCAGAGACTGAAGCTCCTGGGGAAGAACTGCCGCCAGGCACCGAGGACCTGCCAGACCCTGCTAAGGTAAGAGCGCTGTCTGCATCTGTGGGGTTTCAGACGTGGCACAGGTAGGCAGGGGCGTCTGATCCTGGAGAC
Associated Phenotype:
Not determined