ZMP
fbxo5
Ensembl ID:
ZFIN ID:
Description:
F-box only protein 5 [Source:UniProtKB/Swiss-Prot;Acc:Q0V967]
Human Orthologue:
FBXO5
Human Description:
F-box protein 5 [Source:HGNC Symbol;Acc:13584]
Mouse Orthologue:
Fbxo5
Mouse Description:
F-box protein 5 Gene [Source:MGI Symbol;Acc:MGI:1914391]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa31965 | Essential Splice Site | Available for shipment | Available now |
| sa8720 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa38972 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa42299 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa18636 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31965
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000056962 | Essential Splice Site | None | 384 | None | 6 |
| ENSDART00000112924 | Essential Splice Site | 57 | 182 | None | 5 |
| ENSDART00000113450 | Essential Splice Site | 39 | 346 | None | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 47400262)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 46652267 |
| GRCz11 | 13 | 46942102 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATACGGACATATGAGGACGACGTAAATATTGATTTTAACTTTTTAGAGG[T/A]AAGATAATAACGTTTTCCTGTCATATCCACGTATTTCCGTTAAAATTAAG
Long Flanking Sequence:
TAACTACGTTTTTATCTCTTCAAAACCTGAAAAGCACACACACACCCATGATTCCCTAATATTACCAGTATGTTTTGGCTGTGACATGCACATTATACACACACACACACGCTTGATTAAACTAAAAACAATGCACATTTAAAGTCCACATTATCGATTTATTTCAAAAAGGGCGCTTTTTTCCCTGAAGCGCTTCTTTCATTGGGTGGCGCTCTTTATGGGCGATGACGTTACGCTTGTATCTGCGTCATGACGTCACATCTGTATTCCGCCAAACGCGTTCATTGGCCGTGAGACCTTTAAAGGTATCTTGCAGCGCTCTGATTGGTCGGCGCGATTTGTCGCCAAATTCAAATCCATTAGCAGTGGCGCTTTTTCCTCAAACTCACAAACCATTGTGTTGCCGCTTAAATGCTTGAGCTACCACTGCAATAGCGACAAGGGCGCGTTTATACGGACATATGAGGACGACGTAAATATTGATTTTAACTTTTTAGAGG[T/A]AAGATAATAACGTTTTCCTGTCATATCCACGTATTTCCGTTAAAATTAAGACTTTTAAGAGGCTTTTAAATCAGTAGATACTAGATGTTCTGTCATGTTTGCGTTTCCCTTTTAAGTTATAAGCTCAGTTTTAGGTGTAGAATTGCGTTTTTGTTCAATATTAGTCAACTATTTTTTATCTAGAACGTATTTTATGTGTATAAACATATTTTGTAGAGTATGCTAAAGCTAATATGTGCCCTTAGTAGTGTACATCATGAGTTGTAGCCACGTCAGGAATGCAAGCATTAGGCGCGCAAAATGCAAAACGCACATAAATCGCGTTCAAATAAAAACTGCACTTCTTTAACTTTTAAGCACACTTAATATTAAGCATATGTATATATTTTAACATGCATATATAATCACAATGTCTTAAAATGTGAGGTCAAACTAATGTGCTCCGATTGGAGCATAAAAATGTGGAGTAAGTTAACATTTATTACGTAATACAGTTCTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8720
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000056962 | Essential Splice Site | 80 | 384 | None | 6 |
| ENSDART00000112924 | Essential Splice Site | 146 | 182 | None | 5 |
| ENSDART00000113450 | Essential Splice Site | 128 | 346 | None | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 47403035)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 46655040 |
| GRCz11 | 13 | 46944875 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAACTACCAGAACAAGAGACATTCACTGGATATGGCATCAGATGATGAGG[T/C]GAAACGACAATCATTTTTAGCCGTGTGTACATGTKGGACGCRTGTTAAAT
Long Flanking Sequence:
ATATATATATATATGTGTATATGTGTGTCTATATATATATATATATATATATATATATATATATATATATATATATATATATATAGACCTATATATGCATGTGTAACCATTTTTCTAACACGCTTAAAGGTCATATTTCTTATTTTCAGTACTTTGCTGTAAAATAATGTATGCACAATTAACCATTTATCCAACTAGCATCAACATGTCTTATTTCATTACTCTCTTCTAGTTTGCTGGTGTCCAAATTCTCCTCAATATGAAGTGTCCAAACTACACTGAGGATTCCACGGTTTTATGCCACATGGAGAAGACTGAAACAGACCTGGGTGAGGTGAAGGGCCATAAGGTTTCGCCACGAAAAACAGGAGCCCTCCCCCTGCGCTCCCCCGCAGCCACCAATGTCTCCACACCTCTGGAGAGCCGAAGCAAAGGCCCCCATAATAAAGAAAACTACCAGAACAAGAGACATTCACTGGATATGGCATCAGATGATGAGG[T/C]GAAACGACAATCATTTTTAGCCGTGTGTACATGTGGGACGCGTGTTAAATCTTTATATTCTGCACTATTTGTGTGTGTGTTTGTTTTGGTGGTGTAAAAAGACAGAATTTATATGATGACATGGGTATGACCTAGGCTGCGTTGCACTCCACTTTTAGAAATGCACTTGTGAACTTCTCCATTTTTTTCCCTAGAGGGAGTCCTGTCACCATTTTGAAGTGTTCCATTTTATCAAGTGAACAAGGGAAGCATGCATAGGCATACCCTCAATTTTGACTGAGGGAGTGAGTCGGCTTCATATGTCCATTCTATCACCTGTATCTCCCATAATGCAATGCGATAGTGATGTCACGACCGAGTAGTTCCCAAGTGCTCAAGGGTTTAGAGCACTTGATTTAAACCCATTCACATGTTCCAAATTCTAATTTTATTCATCAAATATCCATTAAAATGCTTGCACAACCACTCATGACCTTAAAAATTATAACAATCAGAATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38972
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 |
|---|---|---|---|---|---|
| ENSDART00000056962 | Nonsense | 101 | 384 | 3 | 6 |
| ENSDART00000112924 | Nonsense | 167 | 182 | 3 | 5 |
| ENSDART00000113450 | Nonsense | 149 | 346 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 47406081)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 46658086 |
| GRCz11 | 13 | 46947921 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGCAGCGGCCTGACCGAAGACAGCGGTTACCTTTCCCTCCATAACAGC[C/T]AGGTGGACGTGGACGGACTGGACTCATTAGAGAGGAGTGAAGAGAATTGT
Long Flanking Sequence:
GACACTTCTATACAGCTTAAAGTGACATTTAAAGGCTTAACTCGGTTAATTAGGTTAACAAGGCAAGTTGTTGTATAATGATGTTTTGTTCTGTAGAATATCTAAAAAATAGCTTAAAGGGGCTAATAATTTTGTCCTTTTAAAATGCTGTTAAAAAATTAAAAACTGATTTTATTCTCGCTGAAATAAAACAAAACACTTTCTTTAGAAGAAAAAATATTATCAGACATGCTGTGAAAATTTTCTTGCTCTGTTAAACATCATTTGGGAAATATTTAAAAAATAAAATAAAATTCAAAGGGGGGGGCTAATAATTCTGACTTCATCTGTTGATAGTGTTATGTTAATGTAAGATTTATCATCACGCAGTGCTAATCCTGCACACATGTGGATTTTTGATGTGGCAATAAAAGTGAATGTATTTATTTTGTTTTCATTAGGTGATCTTCAGTGGCAGCGGCCTGACCGAAGACAGCGGTTACCTTTCCCTCCATAACAGC[C/T]AGGTGGACGTGGACGGACTGGACTCATTAGAGAGGAGTGAAGAGAATTGTGTGTCCTCTCAATCCTTGGACGTTGAGTGTCATTCTGGACCCTGTTTACCTGTGCTGAACTTCCAGGAGGAGGCCTGCCGAGAGCTGCAGAGGAGCTACAAGAAGAACCGAAGCTACGATTGGACCGTCGTCGATAAAGTGGCGGAGAATTTTGGGTTGCATAATGTGATTGGTGGAAAAATGGGACGGCAGTTCGTGGATATCCTCTGCAAGCTGATGAGGAAGGACATGAGGCACATTCTTGCCAGGATTTTGGGCCTGCTGGGAGATTGTGACTTGATAAGGTACGCTCCATTTTTATATTATTGTATTTTTCTTGTATAAATGTTTTTACTGCTATTGCTGACATTGCATTACATTAAAATACAGTTCAAGTCATAATTAGCCCTCCTGTATATTTTTCCTCTATATTTTTATATATTTTTTCAACACATTTCTAAAGATAATAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42299
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000056962 | Essential Splice Site | 242 | 384 | 4 | 6 |
| ENSDART00000112924 | None | None | 182 | None | 5 |
| ENSDART00000113450 | Essential Splice Site | 290 | 346 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 47408670)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 46660675 |
| GRCz11 | 13 | 46950510 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGATCAGTTGGCTCTTCAGCGCTGGAAAAAAGCAGAAAAAACACGCAGGG[T/C]AAGAATGGATGAACGTAACCCACACATTGATTCACTTCTGTGACACTTGC
Long Flanking Sequence:
AGTTTCTTCCAACTACCTCTGTTGTATTGTGATGACAAATGTCGTGAGCGTAGTATTACAAGTCGAGATTGCATTCATGTAATACAAGCGGGGCTTGACATTAACTTTTTTTGATCACCTGCCACTGTGGCTATATTGACCTTTTAAAATGGTTTTTAAAAAAATTTAAAATGTCTTTTATTCTAGCTAAAATAAAACAAATCAGACTTTCTCCAGAAGGAAAAATATTATAGGAAATACTGTGAAAAATTCTTTGCTCTGTTAAACATCATTAATGAAATTTTAGAAAAAGAGAAATTTACAGCAAGGCAAATAATTTTGACTACAACTCCTGTATGATATGTATTTTCCTGTGAATGAAGCAAATCACACCTGTTTATTTATTTATTTGTTTATGATCTATTACAGCTGTACGAAAGTAAGCCGGACGTGGAGGAAAATAATTTGTCAGGATCAGTTGGCTCTTCAGCGCTGGAAAAAAGCAGAAAAAACACGCAGGG[T/C]AAGAATGGATGAACGTAACCCACACATTGATTCACTTCTGTGACACTTGCTGAAGGGATAGTTCACCCAAAAAAAAAGAAAATTCTGTCATCTTACTCATCCTCCACTCATTCTAAAGCCTGGTTTATACTTCTGCGTCAAGTGACCGGCGCAACTCACGGCGCAGGCAACGCGCGTGGCTGTGCATTTATACTTCTGCGCGCTGTCTCCGTTGGTCTGCATTAACACTTCCGAAACGCTAGTGGGCAGTGAGGTGTAAATGTTCCTCTGTGTCGAGTTTCTTCGCTTCTGTTTTGCTATTCTGAACACTTCCTGGATGTACAAGTGACTCAAACTCGCTCATTTTGAGGCAGGAACCGGCGGACGTACAACAACTTTAACCATGAGGTAAACACAGAACAAAACTTTCCATCCGGAGCTCCTTCACGGGACTCCACACTTGTAAACAATCGCTCGCGCCATTCGCGCGGCTCTCGGTCCCGCCCAGACTCGTCGGCGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18636
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 |
|---|---|---|---|---|---|
| ENSDART00000056962 | Nonsense | 253 | 384 | 5 | 6 |
| ENSDART00000112924 | None | None | 182 | None | 5 |
| ENSDART00000113450 | Nonsense | 301 | 346 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 47410316)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 46662321 |
| GRCz11 | 13 | 46952156 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTTGTCTCTTGGTTTCAGGACTCGGGCCGGTCTATGGGATCTTTATCT[C/T]GAGACTTCACCTTGGACAGGGTGGTGTTCTCCTGCATGCAGACMGTTTCC
Long Flanking Sequence:
AATCTCATTAGCAAATGTTTTTATAACAATAAAATCTAATTATTATTATTATTATTATTATTATTACTACTTTTTAAGGCTAATAAACCTTTCTGTAGTTGTCAGACTAACATGAAATGTAATATTTGTAAATTAATCACCTATAAAACACCTATAAAGTCGTCAAGAATTAAACACTATGTGGGCTGGTCTGATAAATTATCTCAAATCCTGATCAAATTTGTCAAATAACAATAAGCTCTGGACTTTTTTTTTTTTTTTACTTTATAAGGATCTAAGAACCAATCACACAGTAGAAATGTGCAACAATGGGAATCTAGAAGTGTGTTAATTATTAGAGATTGGTCAGATATTCCTGGATATTTGTAGCTCAAAACATCCATTTAGCTCCTTTTCGTTGTTTCCGGATCGTCCTTCATCATTGTGGTTTAGCTGTTTGAGTTCTGATGGTGTTTGTCTCTTGGTTTCAGGACTCGGGCCGGTCTATGGGATCTTTATCT[C/T]GAGACTTCACCTTGGACAGGGTGGTGTTCTCCTGCATGCAGACCGTTTCCTCTCCACCCGCTCACAAGGCTGTTAAGAAGCCGCCATGCCAGATGGGTGGAGCGCAAAATGCGACTAAATCAAGCCGGTTTCAACAGTATGTAGAGGTAAGGGGAACACAAACTAAACCAAACACCTTATGGTGCCTTTACACAGTTTGTATTTTCAGTTACTACCAAAGTACTGGTTATCTTATTTATTACATTTATACACTGCAAAACACTTTACTTAAGGTTTTTTTGGGGGGTTTCTAGTCCAAATAGCTAAATCAGGTCAAGAAGCATTTTTAAGACCAGTACAATAAATGTTTTGTACTAATATTAAGTCAAATCTAAGTGAGCTTTACCTTAAAACAAGGTAAATAATCTGCCAGTGGGTTAAGAAAAATTATCTGGCAACATTATTTTACTTGTTTGTGTTTCAAGTTGCTAACAACTAGTGTTTTTGTACATTTATACACT
Associated Phenotype:
Not determined