Busch Lab

ZMP

puf60b

Ensembl ID:
ENSDARG00000001241
ZFIN ID:
ZDB-GENE-040625-116
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
sa9413 Nonsense Available for shipment Available now
sa18886 Nonsense Mutation detected in F1 DNA Not yet available

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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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:
sa9413
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:
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

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.
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