Busch Lab

ZMP

fbxo32

Ensembl ID:
ENSDARG00000040277
ZFIN ID:
ZDB-GENE-040426-1040
Description:
F-box only protein 32 [Source:RefSeq peptide;Acc:NP_957211]
Human Orthologue:
FBXO32
Human Description:
F-box protein 32 [Source:HGNC Symbol;Acc:16731]
Mouse Orthologue:
Fbxo32
Mouse Description:
F-box protein 32 Gene [Source:MGI Symbol;Acc:MGI:1914981]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa9611 Nonsense Available for shipment Available now
sa8703 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa6431 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa9611
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000058938 Nonsense 80 356 3 9

The following transcripts of ENSDARG00000040277 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 16 (position 27499665)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 25345352
GRCz11 16 25260384
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTGTCTACTAGTGTAAAAACTTAACTGACTGCTTTGTTTCAGATTTTTA[T/G]AAAGACAAATGGATTTATGTCCATAAAGGGAGCACCAAAGAGGTAAGATC
Long Flanking Sequence:
AAACATGCATACGTCTACGTAAATTTGTATATAAATATCTATCTTTATAGATGGTGATGCAGCACTGCAGTAAATAGCTTGCTGTGGTAAACACAAAATGCCTTTGTGTTTGCTCATCATCTTTTAATCACCTTGCTATTAATAGTGACCATAGGACAGGTCAGATCCTGGAACTATATACTGTTTCTAGAACGGTTGCTGTAAATGCAGACGAGAAATGACTACATTTGCATATCAATTACTTGCATAATTGACCTTTAACATGATATTAAACGAAAAGCACTTGTCTTTGTTTTCAGCTACTGCAAGGAAGAGCATGACAAAGAGAATTTGATCCTCAGCATTAATTATGATGTGGCTGCAAAGAAGCGAAAGAAGGACTTGCTGAACAACAACACAAAAATTCCATGTAAGTGTCGTCAGCGTGTCTCATGACTTTTTAAGATGTGAGGTGTCTACTAGTGTAAAAACTTAACTGACTGCTTTGTTTCAGATTTTTA[T/G]AAAGACAAATGGATTTATGTCCATAAAGGGAGCACCAAAGAGGTAAGATCTGTTAATGATTTCCTCCTGGGTTTCAGTGTGAACAAACAGTCCACTAACTCCTCTTTGATCATTTCTCACAGCGTCATGGATATTGTACTCTGGGAGAAGCATTCAATCGCTTGGACTTCTGCAGTGCCATCAAGGACACCAGGCGATTTAATTATGTCGTAAGGGTGAGTTTCCACTGTCTGTTTATAGCTAGGTGAATGGTGACTATAGCCAGGCTTAGCGTATGAAGAAGGAAGGGTTAGGTCCTGTGCTCAGGGTATCTGCTACTGTTTTCATTCTTATCATCACACACCAGACAAGAGGGCCTCTGGGGCTGTTTCATAGCAGATGCACATATGTCTCTGTGTGCATTTTTGCAGTGTTTCTAGTTATGGAAATATGAGTGTAACTGAGTGTAGATTATCACAGCAAACTTGAGCGGTGATAAATATAAATATTGTACTTTGTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8703
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000058938 Essential Splice Site 125 356 4 9

The following transcripts of ENSDARG00000040277 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 16 (position 27499882)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 25345569
GRCz11 16 25260601
KASP Assay ID:
2260-9673.1 (used for ordering genotyping assays)
KASP Sequence:
CTTCTGCAGTGCCATCAAGGACACCAGGCGATTTAATTATGTCGTAAGGG[T/G]GAGTTTCCACTGTCTGTTTATAGCTAGGTGAATGGTGACTWTAGCCAGGC
Long Flanking Sequence:
ATGACTACATTTGCATATCAATTACTTGCATAATTGACCTTTAACATGATATTAAACGAAAAGCACTTGTCTTTGTTTTCAGCTACTGCAAGGAAGAGCATGACAAAGAGAATTTGATCCTCAGCATTAATTATGATGTGGCTGCAAAGAAGCGAAAGAAGGACTTGCTGAACAACAACACAAAAATTCCATGTAAGTGTCGTCAGCGTGTCTCATGACTTTTTAAGATGTGAGGTGTCTACTAGTGTAAAAACTTAACTGACTGCTTTGTTTCAGATTTTTATAAAGACAAATGGATTTATGTCCATAAAGGGAGCACCAAAGAGGTAAGATCTGTTAATGATTTCCTCCTGGGTTTCAGTGTGAACAAACAGTCCACTAACTCCTCTTTGATCATTTCTCACAGCGTCATGGATATTGTACTCTGGGAGAAGCATTCAATCGCTTGGACTTCTGCAGTGCCATCAAGGACACCAGGCGATTTAATTATGTCGTAAGGG[T/G]GAGTTTCCACTGTCTGTTTATAGCTAGGTGAATGGTGACTATAGCCAGGCTTAGCGTATGAAGAAGGAAGGGTTAGGTCCTGTGCTCAGGGTATCTGCTACTGTTTTCATTCTTATCATCACACACCAGACAAGAGGGCCTCTGGGGCTGTTTCATAGCAGATGCACATATGTCTCTGTGTGCATTTTTGCAGTGTTTCTAGTTATGGAAATATGAGTGTAACTGAGTGTAGATTATCACAGCAAACTTGAGCGGTGATAAATATAAATATTGTACTTTGTGATGTGGTAATTCAATTAAAATGGGTGAGGAAACAAATGATAAAGCAACGCTATCATCAGATACTGTTTACAGTTCAAAATTCTCAAATATGAACTCTATAGTCTGAACTGAAGAAATTAACTTAAGGAAAATTGCATATGAAAGAACAGGGAGTCCTATTTAGCCATCTCCACAATTAATGCTATTTTAATGGTATCATAAATTTCACACTTTGATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6431
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000058938 Nonsense 294 356 8 9

The following transcripts of ENSDARG00000040277 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 16 (position 27511077)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 25356764
GRCz11 16 25271796
KASP Assay ID:
554-5294.1 (used for ordering genotyping assays)
KASP Sequence:
TTCACAGATCCGCAAGCGCCTCATGGTTTCAGATAAAGGGCAGTTGGAAT[G/A]GAAAAAGATGTATTTTAAGCTGTGTCGGTGTTACCCTCACAAAGAGCAGT
Long Flanking Sequence:
ATGATAATTTGCTTTATCACGTAATCACCAAATGCTTCGAAATCTTTTGAGTTTTTTCCCTCTTGTTGAACATAAAAGAAGATATTTTGAAAAATGTTGGTTTCCATTAGAAACTGACGTGCAAATTATGATATCAACAGAATATTGTTCTTCTGTTCAACAGAAGAAAGAAGCTCCTATAGGTTTAAAACCACCAAATAGTGTTTGACTAAATTCAGCAGCCCAGAGCATGTTAACAAAAGCGCTAAATTTATTGGTCGACCACTTTTTAATGTGGCACATTAAACCAAAATAACGAGTCTTTATGTTTTTTAGTAATAAGCCATTAATAATCAAAAATAAAAATAAGTGAAATTCGTAAATGGGTGCATGACCATTAACTAGGAAACATCATATTATTTACATAATTTTTTGTTCAGCCTCATGATTTGATATAAAGTTGCCATGTTTTTCACAGATCCGCAAGCGCCTCATGGTTTCAGATAAAGGGCAGTTGGAAT[G/A]GAAAAAGATGTATTTTAAGCTGTGTCGGTGTTACCCTCACAAAGAGCAGTACAGCGACACATTACAGTTCTGCACACACTGCCACATCCTCTTCTGGAAGGTGAGCTTTTAGTTTATTTTTTGGTCACTGTCTATAGCCAATTTTTTGGCACTAACAGAATTCTCCTTTTTTTCTCTCTTCAGGATACAGACCATCCTTGCACTGCCAATAACCCAGAGAGCTGTTGCAAAGCAGTGTCTCCACAGGGTTTCATCAACCTCTTCAAGTTTTAGCAGCGCTGCATTGCTGCCATGATGTACATAGTGTCAATAGTGCAAAGATTCCTGGATGACTTGAGGCAGGGAGAAGACGACTTGCATTAAAAGCAGATGCCTGTGTTACGTGGAGGAGTTTGGAAACTGAATGTACTCAAATATGCACGACGAAAAACCAAAAAGCTGCGTTGGGGAAAACATGCTCTGTTTATTTAAAAAGATTGTTTTATTTATTTATTTAGCAT
Associated Phenotype:
Not determined