Busch Lab

ZMP

pds5b

Ensembl ID:
ENSDARG00000061312
ZFIN ID:
ZDB-GENE-091217-2
Human Orthologue:
PDS5B
Human Description:
PDS5, regulator of cohesion maintenance, homolog B (S. cerevisiae) [Source:HGNC Symbol;Acc:20418]
Mouse Orthologue:
Pds5b
Mouse Description:
PDS5, regulator of cohesion maintenance, homolog B (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:2

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa35942 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa35943 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa35942
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087246 Essential Splice Site 133 1415 3 33
Genomic Location (Zv9):
Chromosome 15 (position 32076519)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 33940028
GRCz11 15 33798007
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGGACACAAAGAGTGCTCAGTTTAATCGATATTTTTATCTACTGGAG[G/A]TATGGCACCCAACTAATAGACACCGTAATAAGGTCTAATGGTTTAAAACA
Long Flanking Sequence:
ACTTAAGTTTATATAATAATTAATTCAGTAGACAGAGAGAAGTTTTTGTTGCACATTTAATAAAGAGCGTTTGCTGTATGGAAAGCACTCTGCAAATATGTCTTCAGCTGCTTCTGGAAGATGTCAAAAGTGTCAGACCTTGGTAATGCATGTATTAAGCACAGGATGCATATAAATGCATCATAATGCCAGTTGTAATTGCAGTATTACAATCCTACAATGTTTGCTCGTGTTGTAATACATAAAAACATTTGTGGGTGTTTCATGTGTGCATGTTTTCTATCATTTGAACAGAAGGCAGCAGTTGCTCATTGTTCAGCGGAAAATACCAAAATATCACTGTGGTCTCTCATGCATTGCCTTCGTAGGTGTTTAAACTATTAAAACTGTCTGCTCTTTTGTTTTTCACTCAGGATATTTTCATGTTCATAACTCGGCAGCTGAAAGGTTTGGAGGACACAAAGAGTGCTCAGTTTAATCGATATTTTTATCTACTGGAG[G/A]TATGGCACCCAACTAATAGACACCGTAATAAGGTCTAATGGTTTAAAACAAGCATCTGACCTTGTCTTTCTGCCTCTGGCTCTCTAGAACATCGCTTGGGTGAAATCCTACAACATCTGCTTTGAATTGGAGGACAGCAATGAGATCTTTACTCAGCTCTACAGAACGCTGTTCCAAGTGATAAAGTGAGTCTGTTGTTCATATTTGTCCACTAGGGCATTTCGTGTGTGTGTGTGTGTGTGTGTGTATATATATATATATATATACACATACACACAATTATAAGCTTTTTTTGGCTTGTTTTCGTGTGTGATTTAGTGCTGGGCAAAAATGAATCGTGATTAATCAAAGGAAATCCAAAATAAAAGTTTGTTCTGCCAATATATGTGTGTGCGCTGTGTATATTTACTTTGCATATATAAATAGACACATGCATGCATATATTTAAGAAAATGTTTATTTATATGTATATGGTGGCACAGTGGCTGTGTGGAGTTTGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35943
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
ENSDART00000087246 Nonsense 171 1415 5 33
Genomic Location (Zv9):
Chromosome 15 (position 32079584)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 33936963
GRCz11 15 33794942
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTTTACAATGTTTTTTCTCTCTCGTTTTCTTTTAGCAATGGACACAAT[C/T]AGAAAGTTCACATGCATATGGTGGATCTCATGAGCTCAATTGTGTGTGAG
Long Flanking Sequence:
TAGTAATGCTATAATAGAGCTGCCATTTAGTTAGAAAGTACAACGATGAATTCTGCAATAACTATTGTCGTAAGTCAGTGAAGCACCTCCTCGCTTTACTGTTTTCTATTTGAGATGTAAATGTGAAGCTGCAGCCTATTTGTTATGTCCTAATGAGCTGTCAGCCTCCTGCTCTCCGATATTATTTCCCTGCATTCGGTCAGATGACAATGATGCGTGCGAATCCCAGGTGGAAACCCTTCATTGCATGTGCGCCATAAAGGCTGCATATGGGGGGCGATTTATCTCAGCCACTGTTGTTCAGTCATTCGGAAATGTCCTCTACGAGCGGGACACTGCAGCGATCTGCTCTCATGTGTAAATGGGAAAAACCTAGAAGAGTTTCTGTTTTCTCTGCCTCATTGCACGCTCTTCCCATTTTCATTCGTCTGATGGACCTGATGTTAGGTCAGTTTTACAATGTTTTTTCTCTCTCGTTTTCTTTTAGCAATGGACACAAT[C/T]AGAAAGTTCACATGCATATGGTGGATCTCATGAGCTCAATTGTGTGTGAGGGCGACTCTGTATCACAGGAGCTCCTGGATACGGTTCTGGTTAACCTGGTTCCAGCACACAAGGTACAGAGAACAAATGAATTCAAATGAGAGGAAAATATGCATGCTAATTGTGTATTTATGCATTTATGTTAATTTTTACTTTATAAAGGTCTCAAAACATTTATTTCAAATACTAAAATCATGTAGAGCAGGGGTGGTCAACCCTGTTCCTGGAGAGCCAACTTCCTGCAGATTTCAATTGCTGCCCATATCAAACACACCTGAACCAATTTATTAGGACCTGAACACCACGTGATAATTACAGGCAGGTGTGTTTGATATGGATTGCAACCGAAATCTGCAGGAAGGTGGCTCTCCAGGAATAGGGTTGACCACCCCTGATTTAGAGCATTTATTGTTGATGTAAATAAGGGGTTTTTCTGCCAAATTTTAATATCATACAATAAA
Associated Phenotype:
Not determined