ZMP
puf60b
Ensembl ID:
ZFIN ID:
Description:
Poly(U)-binding-splicing factor PUF60-B [Source:UniProtKB/Swiss-Prot;Acc:Q6IQE0]
Human Orthologue:
PUF60
Human Description:
poly-U binding splicing factor 60KDa [Source:HGNC Symbol;Acc:17042]
Mouse Orthologue:
Puf60
Mouse Description:
poly-U binding splicing factor 60 Gene [Source:MGI Symbol;Acc:MGI:1915209]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa13888 | Nonsense | Available for shipment | Available now |
| sa18886 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa9413 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13888
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 |
|---|---|---|---|---|---|
| ENSDART00000038487 | Nonsense | 21 | 516 | 3 | 12 |
| ENSDART00000052274 | Nonsense | 21 | 502 | 3 | 11 |
| ENSDART00000143285 | Nonsense | 21 | 499 | 3 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 43877681)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 40867981 |
| GRCz11 | 7 | 41148054 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACAAGGCACAGGGTCAAAGCTTGGATTACCGCCTCTTACTCCTGAGCAA[C/T]AGGAGGCGCTACAGAAGGTAAATAGTAGATCTTTKTTTTWCTTTAATTCT
Long Flanking Sequence:
CAGTTGATCTACTTTATTCATGCAAATAGTTCCTGTCATTGTTGCCTTAGTTTTGTGTGTGTGTGTGTGTGAGCGAGCTCTGTGGGTAAAAGTGTGTCAGTGATTCCTTTAATATCTTCTCATTGAACTTGTACAAGGATTTAAATCTAAATGTTGTATACTTTTCCATGAACCACAGATCACTGTAAAATTGTGAGTGCTTTGCAGACAAGTCACTGGCTTCACGACCCTGGTTGGCATATAAGGTTCGCCTCATAGGTAAACTGCGTTTATTTTACCTTCTCTTTCCCTTCTCTCTTTCTGTGACTCTTAAGTTGGAAGTTTACATGTGCAGATAGTGAGTAAACTGATAATCGGGTTTGGAATTTCACCTCATTATGCGCTTCCTTTTTCGTTCCATGTCCATTGTATCACTTTCCCAGTGAGGCAAAGGTCTGATGATGGAGAATGGACAAGGCACAGGGTCAAAGCTTGGATTACCGCCTCTTACTCCTGAGCAA[C/T]AGGAGGCGCTACAGAAGGTAAATAGTAGATCTTTGTTTTACTTTAATTCTGGGCTTCTTTTTTTTTTTTTTTTGTTGCATGATTTTCAGTTTCAGATTACACTACTTTCTGGGTTTGCCCTTGTGTGAACACTATACAATGGAACAGTGACTCAGACTCACATATTGCACACCTTTTTAAAATGAAATAATGGGGTATGTGCACACACACTTTTATTTTCAGTCAGCCAGCCCCAGGGCTTTCGATGAATTGTCATCCCATAAAAAAAACCCATACAAAATCGCTGCGTGATTTCTTTAAAAAAAAAAAAAAAAAACGCAGTCATCACTGCCAGGCTGAGATACGATATAAAGTGAGTATCAGACCAAACAAGAAGTACTGCATTAAATTAGATTTTCCAATCCATGTCTTTAAAATATGGAAATGAATTTTACCACAGTTTTTTTAATGTGTGTTTTTTTTTTGCGCTAGCCTGCATTTAAAACTGTATTTTGTCTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18886
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000038487 | Nonsense | 382 | 516 | 11 | 12 |
| ENSDART00000052274 | Nonsense | 368 | 502 | 10 | 11 |
| ENSDART00000143285 | Nonsense | 365 | 499 | 10 | 11 |
| ENSDART00000038487 | Nonsense | 382 | 516 | 11 | 12 |
| ENSDART00000052274 | Nonsense | 368 | 502 | 10 | 11 |
| ENSDART00000143285 | Nonsense | 365 | 499 | 10 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 43886658)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 40876958 |
| GRCz11 | 7 | 41157031 |
KASP Assay ID:
554-6149.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCTGCAGTGCAATTGCACACAGAAGTGAAGAGAGAGGAAGACAGCAGG[C/T]GAACTGCAGAAGATCACAGTGCACCGGTTGGCAATGGACAAGACAGTGAA
Long Flanking Sequence:
CATGTTGTGACCAATACAAATAGGTATCTATTTTCAACTTCCCCTTGGAAAAATGTAACTGGGCAACCACTAAGATTTAAAATTCTGGCCATGTAGCTGCTGGTGTCACATAAAACTAGCTCATTTCTCACATAAAGTGTTCACTGGTTAATGACTTTTTGGAGATTGTGTGAACTGGACCTTAAAAAAGAAGAAAAAACAGCCATCGAAGCAGTCCATACTTTAGGGCTATTAAAGGATTGTGAAAATCTGACTGGTTAAAGATGTAGCAATAATAAAGAGTATAAATATTTCAATCTGTACTAATAATCATAACTCTCTCTCTTGCAATCCATTTGATAGGTGTGACACCTGCTCGCCCCACTCTCCCTGTAGTCCCGCAGGTGGGTTTGGTCAACCCAGTTCTGGCATCCCCACCAGTCACAGCACCTGCTTCTATGGGAACACCAACATCTGCAGTGCAATTGCACACAGAAGTGAAGAGAGAGGAAGACAGCAGG[C/T]GAACTGCAGAAGATCACAGTGCACCGGTTGGCAATGGACAAGACAGTGAACTGGAGCGTCTCAGCGTCAGCGCAAGTGCAGGAAGACAAGCGGCCATTCAGTCCAAGGTTAGATAGCATCACTGTGGTTCTGTTAAAGGGATAGTTCACTCAAAAATGAAAAGTACCTCAGTGTTTACTCTCGCTTGTGTGGTTTTAAATCTGTGAGTTTCATCTGTTAGTAACACAGATTAAAGTAAGGTATTTTGAAGAATGCTGGTTGATGGTATCCATCGAGTTCCATTGTATTTTTCCCTACTATGGAAGTCAGAATAAATTAATAAATCAGATGTTTCTGCTAGGAAGTCTAGTTTAAGCTTCACGTTAATTTGCCAGCTTTTCTCTCTTTGCTTGCAGTCAACGGTTATGGTGTTGCGCAACATGGTTGGTCCAGAGGACATTGACGATGACCTGGAAGGGGAAGTGATGGAGGAATGTGGGAAGTACGGGGCTGTGAACCGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9413
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 |
|---|---|---|---|---|---|
| ENSDART00000038487 | Nonsense | 382 | 516 | 11 | 12 |
| ENSDART00000052274 | Nonsense | 368 | 502 | 10 | 11 |
| ENSDART00000143285 | Nonsense | 365 | 499 | 10 | 11 |
| ENSDART00000038487 | Nonsense | 382 | 516 | 11 | 12 |
| ENSDART00000052274 | Nonsense | 368 | 502 | 10 | 11 |
| ENSDART00000143285 | Nonsense | 365 | 499 | 10 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 43886658)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 40876958 |
| GRCz11 | 7 | 41157031 |
KASP Assay ID:
554-6149.1 (used for ordering genotyping assays)
KASP Sequence:
CATCTGCAGTGCAATTGCACACAGAAGTGAAGAGAGAGGAAGACAGCAGG[C/T]GAACTGCAGAAGATCACAGTGCACCGGTTGGCAATGGACAAGACAGTGAA
Long Flanking Sequence:
CATGTTGTGACCAATACAAATAGGTATCTATTTTCAACTTCCCCTTGGAAAAATGTAACTGGGCAACCACTAAGATTTAAAATTCTGGCCATGTAGCTGCTGGTGTCACATAAAACTAGCTCATTTCTCACATAAAGTGTTCACTGGTTAATGACTTTTTGGAGATTGTGTGAACTGGACCTTAAAAAAGAAGAAAAAACAGCCATCGAAGCAGTCCATACTTTAGGGCTATTAAAGGATTGTGAAAATCTGACTGGTTAAAGATGTAGCAATAATAAAGAGTATAAATATTTCAATCTGTACTAATAATCATAACTCTCTCTCTTGCAATCCATTTGATAGGTGTGACACCTGCTCGCCCCACTCTCCCTGTAGTCCCGCAGGTGGGTTTGGTCAACCCAGTTCTGGCATCCCCACCAGTCACAGCACCTGCTTCTATGGGAACACCAACATCTGCAGTGCAATTGCACACAGAAGTGAAGAGAGAGGAAGACAGCAGG[C/T]GAACTGCAGAAGATCACAGTGCACCGGTTGGCAATGGACAAGACAGTGAACTGGAGCGTCTCAGCGTCAGCGCAAGTGCAGGAAGACAAGCGGCCATTCAGTCCAAGGTTAGATAGCATCACTGTGGTTCTGTTAAAGGGATAGTTCACTCAAAAATGAAAAGTACCTCAGTGTTTACTCTCGCTTGTGTGGTTTTAAATCTGTGAGTTTCATCTGTTAGTAACACAGATTAAAGTAAGGTATTTTGAAGAATGCTGGTTGATGGTATCCATCGAGTTCCATTGTATTTTTCCCTACTATGGAAGTCAGAATAAATTAATAAATCAGATGTTTCTGCTAGGAAGTCTAGTTTAAGCTTCACGTTAATTTGCCAGCTTTTCTCTCTTTGCTTGCAGTCAACGGTTATGGTGTTGCGCAACATGGTTGGTCCAGAGGACATTGACGATGACCTGGAAGGGGAAGTGATGGAGGAATGTGGGAAGTACGGGGCTGTGAACCGG
Associated Phenotype:
Not determined