ZMP
fbxl5
Ensembl ID:
ZFIN IDs:
Description:
F-box/LRR-repeat protein 5 [Source:UniProtKB/Swiss-Prot;Acc:Q2YDQ5]
Human Orthologue:
FBXL5
Human Description:
F-box and leucine-rich repeat protein 5 [Source:HGNC Symbol;Acc:13602]
Mouse Orthologue:
Fbxl5
Mouse Description:
F-box and leucine-rich repeat protein 5 Gene [Source:MGI Symbol;Acc:MGI:2152883]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa24418 | Nonsense | Available for shipment | Available now |
| sa44065 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa7510 | Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa24418
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 |
|---|---|---|---|---|---|
| ENSDART00000102891 | Nonsense | 16 | 694 | 1 | 12 |
| ENSDART00000123100 | None | 1 | 679 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 23 (position 46157634)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 46024253 |
| GRCz11 | 23 | 45869044 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGATCTGGCGCCCGCGTGTTCAGTCCGCGGCAGTGGAGCTGATGGAGGCG[C/T]GATGGCTCCTTTTCCCGATGAGGTGGATGTTTTCACGGGCCCTCACTGGC
Long Flanking Sequence:
ATTCCAGATTTTAAAATAGATTTGTTTACCATGGTTTATTATTACTATTATTAATTATTTTCTTTATTTAAATTTCAATCATAGCATAATCGTACAATCATGACATCCACAACATGACAGAAAACAGCAAAATTGTACAATTAAACTAATAGAATAAAACAAATAAAACAAGAAGGGTATATATTCATATTTATAATTAGTTTAGTTGTTTGAGTATGTTCATACTATATTAGTTGTTTGAGTATGTTATTAAAAAAATAATACGTACTTTAAAACATTAGATAAATCTTTAAATCAGCCTTGAAATATAATATATGTGGCATCCTTTTTAAAATTTTACTTCAATCCATGTCTTTCTTTATCATGAAAATAATCTACTCTCAACAACTCTGTTGTTTTGTGTATGTTTTTGTGCAGATGTTCAGCGTCGGCAGAGGATTTTGAGCTGGAGGATCTGGCGCCCGCGTGTTCAGTCCGCGGCAGTGGAGCTGATGGAGGCG[C/T]GATGGCTCCTTTTCCCGATGAGGTGGATGTTTTCACGGGCCCTCACTGGCGCATGAAGCAGCTGGTGGGTCTTTACAGCGAAAAGGTTCGTCTATTACCCATTTTACATCGCATTTCACACTTAATCTGCTTTTTAACATCCCCGAAGCTGTGTTTACGCAGAGCTAATGCTAGCCGCACTGCTAACAGACAGCGATCAGAGTTTAATGTCAACGTCTGACAATCATCTGATCTCAGATCGGCGCTTCTGTCATCATTTCTGCATATTATACGTGTAATTATGATTATATTAACTCATTGTGATCCGTGTGAGTTAATGTAAACATATTATAAGAGGTTAATGTGCACGTCTGACCTCAGATCTGTGGCGAAACAAACTGCTAGCATTGTGTGTGAGGATGATTTGAAGCACACACTGATCTCAGACCTGTAATACACTTCATTTCTGGGCAATAATGATAATATAAACACGCAAATAGGTGCAGATATGATCATGTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44065
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000102891 | Nonsense | 31 | 694 | 2 | 12 |
| ENSDART00000123100 | Nonsense | 16 | 679 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 23 (position 46157586)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 46024301 |
| GRCz11 | 23 | 45869092 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCGATGGCTCCTTTTCCCGATGAGGTGGATGTTTTCACGGGCCCTCACT[G/A]GCGCATGAAGCAGCTGGTGGGTCTTTACAGCGAAAAGGTTCGTCTATTAC
Long Flanking Sequence:
TATTAATTATTTTCTTTATTTAAATTTCAATCATAGCATAATCGTACAATCATGACATCCACAACATGACAGAAAACAGCAAAATTGTACAATTAAACTAATAGAATAAAACAAATAAAACAAGAAGGGTATATATTCATATTTATAATTAGTTTAGTTGTTTGAGTATGTTCATACTATATTAGTTGTTTGAGTATGTTATTAAAAAAATAATACGTACTTTAAAACATTAGATAAATCTTTAAATCAGCCTTGAAATATAATATATGTGGCATCCTTTTTAAAATTTTACTTCAATCCATGTCTTTCTTTATCATGAAAATAATCTACTCTCAACAACTCTGTTGTTTTGTGTATGTTTTTGTGCAGATGTTCAGCGTCGGCAGAGGATTTTGAGCTGGAGGATCTGGCGCCCGCGTGTTCAGTCCGCGGCAGTGGAGCTGATGGAGGCGCGATGGCTCCTTTTCCCGATGAGGTGGATGTTTTCACGGGCCCTCACT[G/A]GCGCATGAAGCAGCTGGTGGGTCTTTACAGCGAAAAGGTTCGTCTATTACCCATTTTACATCGCATTTCACACTTAATCTGCTTTTTAACATCCCCGAAGCTGTGTTTACGCAGAGCTAATGCTAGCCGCACTGCTAACAGACAGCGATCAGAGTTTAATGTCAACGTCTGACAATCATCTGATCTCAGATCGGCGCTTCTGTCATCATTTCTGCATATTATACGTGTAATTATGATTATATTAACTCATTGTGATCCGTGTGAGTTAATGTAAACATATTATAAGAGGTTAATGTGCACGTCTGACCTCAGATCTGTGGCGAAACAAACTGCTAGCATTGTGTGTGAGGATGATTTGAAGCACACACTGATCTCAGACCTGTAATACACTTCATTTCTGGGCAATAATGATAATATAAACACGCAAATAGGTGCAGATATGATCATGTTGTTGACATAACTAGTTCTGTTTATTCAGATTGGGGTTTGTCAGTGTGTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7510
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:
Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000102891 | Missense | 32 | 694 | 2 | 12 |
| ENSDART00000123100 | Missense | 17 | 679 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 23 (position 46157584)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 46024303 |
| GRCz11 | 23 | 45869094 |
KASP Assay ID:
554-4192.1 (used for ordering genotyping assays)
KASP Sequence:
CRATGGCTCCTTTTCCCGATGAGGTGGATGTTTTCACGGGCCCTCACTGG[C/T]GCATGAAGCAGCTGGTGGGTCTTTACAGCGAAAAGGTTCGTCTWTTACCC
Long Flanking Sequence:
TTAATTATTTTCTTTATTTAAATTTCAATCATAGCATAATCGTACAATCATGACATCCACAACATGACAGAAAACAGCAAAATTGTACAATTAAACTAATAGAATAAAACAAATAAAACAAGAAGGGTATATATTCATATTTATAATTAGTTTAGTTGTTTGAGTATGTTCATACTATATTAGTTGTTTGAGTATGTTATTAAAAAAATAATACGTACTTTAAAACATTAGATAAATCTTTAAATCAGCCTTGAAATATAATATATGTGGCATCCTTTTTAAAATTTTACTTCAATCCATGTCTTTCTTTATCATGAAAATAATCTACTCTCAACAACTCTGTTGTTTTGTGTATGTTTTTGTGCAGATGTTCAGCGTCGGCAGAGGATTTTGAGCTGGAGGATCTGGCGCCCGCGTGTTCAGTCCGCGGCAGTGGAGCTGATGGAGGCGCGATGGCTCCTTTTCCCGATGAGGTGGATGTTTTCACGGGCCCTCACTGG[C/T]GCATGAAGCAGCTGGTGGGTCTTTACAGCGAAAAGGTTCGTCTATTACCCATTTTACATCGCATTTCACACTTAATCTGCTTTTTAACATCCCCGAAGCTGTGTTTACGCAGAGCTAATGCTAGCCGCACTGCTAACAGACAGCGATCAGAGTTTAATGTCAACGTCTGACAATCATCTGATCTCAGATCGGCGCTTCTGTCATCATTTCTGCATATTATACGTGTAATTATGATTATATTAACTCATTGTGATCCGTGTGAGTTAATGTAAACATATTATAAGAGGTTAATGTGCACGTCTGACCTCAGATCTGTGGCGAAACAAACTGCTAGCATTGTGTGTGAGGATGATTTGAAGCACACACTGATCTCAGACCTGTAATACACTTCATTTCTGGGCAATAATGATAATATAAACACGCAAATAGGTGCAGATATGATCATGTTGTTGACATAACTAGTTCTGTTTATTCAGATTGGGGTTTGTCAGTGTGTCTGA
Associated Phenotype:
Not determined