Busch Lab

ZMP

fbxo3

Ensembl ID:
ENSDARG00000029242
ZFIN ID:
ZDB-GENE-050522-269
Description:
F-box only protein 3 [Source:RefSeq peptide;Acc:NP_001018538]
Human Orthologue:
FBXO3
Human Description:
F-box protein 3 [Source:HGNC Symbol;Acc:13582]
Mouse Orthologue:
Fbxo3
Mouse Description:
F-box protein 3 Gene [Source:MGI Symbol;Acc:MGI:1929084]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa21023 Essential Splice Site Available for shipment Available now
sa38630 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa21023
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
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000139382 Essential Splice Site 31 451 None 11

The following transcripts of ENSDARG00000029242 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 7 (position 40106553)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 38443193
GRCz11 7 38714451
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCCTTACTTCTGGTGCTGTCATTCCTGGACTTCCGAGATCTTATCAGG[T/C]AGACATTACACTCGAGCCATACCGTTAGTCCGTGCAACAGCAAGCACGAT
Long Flanking Sequence:
ATTCTGTCAAGACGTGCTTAGTTTTGCTGTAAATGTTTTTATTTATTCATTGTTGAATATTGTTCTGGGCTACATATTGCAGCTTTATATTGTTTATTAAAAAAGTCATTACAAAGTCAATTTTTAAACATCATTTACATAAATTATATATGTGTTAGCTACATTACTCTATTTGGTCGATCTTATAATTGGCAACAAGTTTTATTCATTTTTTATTAATACTTCTTCTATAAAAGTAATGAGAACAAAAATCGTAAACATTATCTCGATCTCATCTCCTCACTTGGTTAATCGTCAAGTTAAAGCAGGCGACATGTGCGCAGTATTTGATAACAGAACAGCGTGCGGACACGCCCTCTTGTCATCGCATCAAGGGGCGGAGTTTCGCTTCTGCATTCGCCACCAAGATGGCAACGTCCATAGCGCTCAGCTTGGATAACTTACCGTCTGATCCCTTACTTCTGGTGCTGTCATTCCTGGACTTCCGAGATCTTATCAGG[T/C]AGACATTACACTCGAGCCATACCGTTAGTCCGTGCAACAGCAAGCACGATTTAAGCAAGTTTCTTCCTTGAATGATCTTGAAGAATAATATCAGCTGCACAGTTAGCTTGCTAAGCTAATGGTATAGCAAATGATTTTACTCTAGCAAGTGCTTTTGATAGGCATATTCTACGGCGATATTCTCCGTTTTTAGTCACTATTAAAATACATCTATCACAGTATGAACTGTTACACCGGTCATCTCCTGCATCTTTTTCTTTAAAGATGAAAGTGCATGACTTTATGTAAGTTGACAGTAAGAATGCGATAGGAGACTGCACGGATGGACATCACTAAAGCTTTATTTCTCCTTCAACTGCAAGTTTACTGTATGTGCACTGATGGTTATGAAATTGAGGTAAAGCTGGTTTTATATTCGCACATTCAGAGACATGCTCCCTTTGAACAATTTTTTTCTGAAGTCGCAAGTATGGCTATTTAATTCACTGTTAAAAATGTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38630
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
ENSDART00000139382 Nonsense 394 451 10 11

The following transcripts of ENSDARG00000029242 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 7 (position 40097396)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 38434036
GRCz11 7 38705294
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTCCACCGGCTCAAGAACAAAGAGGAAGTGTTTGACGTTTCCATCCCA[C/T]GATTCCACATGGTGTGCCCACCATTCCGCGAGTCAGTGGTGCGCTCCGTA
Long Flanking Sequence:
GCTTTGTGCTGTAACTTGCTGTAACGCCACACAGCTGTGCTAAGACTTGACACAGGATGATGCATTGAGTTGACTCTATGACGTCTGAGCTGTACCATCATCCTATATGCATCAGGATCGAGATGGCGAAGTCGGCCCTGCCAGAGAAAGCTTGCCAGCTGGACAGCCGCTACTGGAAGATCACAAACGCAAATGGAAACGTGGAGGAGGTCCGAGGACCTGGCGTTGTGGGTAAGAGCCCGTCCCTGTCTGTAAGTGAAGAATAAACTAGAACAGTTTAGTAACCAACATATTTAAGGCTCATCTTGATTCATAATGTGATGTTTACATTGTTTGTTTGTGTCGATGTAAACACAGGTGAGTTTCCAGTGATGACACCTGGCAAAGTTCACGAGTATGCCAGCTGCACCACGTTTTCCACTACTTCGGAGTACATGGAAGGCCACTACACATTCCACCGGCTCAAGAACAAAGAGGAAGTGTTTGACGTTTCCATCCCA[C/T]GATTCCACATGGTGTGCCCACCATTCCGCGAGTCAGTGGTGCGCTCCGTAAGTCCCCATTTGTCCCCCATCCAATTGAAAAAAATTGAAGATGCTAACGTGTGTCATTTTAAACCCCACGCTGTGTGTGTCTCTCTTATTTAGAGCTCGGTCAGCGAGGTGTCTGCTCCTTATGATGATGAGAATTCATCAGACACTGATGACTACGAGGAGGGAGAAATGCGTGGCATGAACATGGCTGACCCAGGGGGACGCTGTCCTCGGCATGTCTGATGCACTTTTTAAGCGTCTCCGGCCAGCAAGCGCCTACAGACACACTCGCACAAACAGGAGAGCAGGAGGACAAATGGAGCTTTTAGGCCTCCATTGTTTATTGTTCAGCGCCTTTGTGCCTGTCACCTCTTGAACGTTTTCTCCCGTTTGTGAGGGCATGTGTCTGGTTGTGGCGTGTTTGTGTCTGTGCGCGCTCGTGGATGTGTGAGATCATTGTGTGTGTTTGAT
Associated Phenotype:
Not determined