ZMP
fbxw11a
Ensembl ID:
ZFIN ID:
Description:
F-box and WD-40 domain protein 11a [Source:RefSeq peptide;Acc:NP_958467]
Human Orthologue:
FBXW11
Human Description:
F-box and WD repeat domain containing 11 [Source:HGNC Symbol;Acc:13607]
Mouse Orthologue:
Fbxw11
Mouse Description:
F-box and WD-40 domain protein 11 Gene [Source:MGI Symbol;Acc:MGI:2144023]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa31968 | Essential Splice Site | Available for shipment | Available now |
| sa12221 | Essential Splice Site | Available for shipment | Available now |
| sa42328 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31968
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000036901 | Essential Splice Site | 13 | 527 | 1 | 13 |
Genomic Location (Zv9):
Chromosome 14 (position 2127792)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | KN150273.1 | 28829 |
| GRCz11 | 14 | 2588049 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAACAATAATATGGATCCGGACAAGGAGGACAAAACCCTGGAGCTGATG[G/A]TACGTGCCGCCCGGTATCCACGACACCTCCTGCTCTGTATGTTTATATTT
Long Flanking Sequence:
ATACAATTACTACTGCTACTACCAATTATTCTTAATATTATCTTATGTATGCGTGTGTGTCTTTTTATTTTAAAAATAATCATAACAATGTATTTTATTATTATTTACATTTTAATTATGACACTAAACATTTAAACCATATCTAATCCTATTGTTTGAATTTTTCTGCTTCAGCACGAACAGCTAACTTTTTATTGATAAAAGTTATGAATAAAATATTAAATTATAAATTAACTAAAATTCTACATTTTATTAATAATATCCTAATAATGGATGGGCAATGTATATAATTTGTGACATAGCTAGTCGTGTGTGTATGTGCGCGTGTGAAATAGGACTCTTATTATCGTATAATACCAGTAAGGCTCCATCTTTTGTAGCTGTGTGTTGTTTCGCTCTTCTCTCGGGTTCACCGACGGGTTTCCATTTTCACGGTTGGATTCAGCTAGAACAACAATAATATGGATCCGGACAAGGAGGACAAAACCCTGGAGCTGATG[G/A]TACGTGCCGCCCGGTATCCACGACACCTCCTGCTCTGTATGTTTATATTTATGTTTATATGTATCGGTATAACGTACATCGTAAACGCGGGCTAAAGAGGCAGGAGGACAAAAACACAGCAGCGGCCCGAATACTATAGCGTTCAACATTCTTCATGTTAAATTATAATGTTTGGTTTGAGTTTTGTCAGTAAACCGAGTTTCCGCTTATTATTTGATGAGCAAGTCGCGTATTAATGTCGAGGAATCGTTTGCGCGTCGCTGGAGCGGTCATTGCGGCACCGCTGCGCCATTTACGTTACATCTTCTATATATTACACTTATTAACGACTATGTGATGAAAACATTGTGTATATGAGCTTCATACATCACACAGCCAACATTCACTTATATAATTGATCAAATACTCCACCTTCAGCCTATTTGACCGTCATATATCACAATTGATATCCGCTTCATATATTAAACACTTAGCGACGATATCATATGGTATATCGACGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12221
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000036901 | Essential Splice Site | 172 | 527 | 4 | 13 |
Genomic Location (Zv9):
Chromosome 14 (position 2149257)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | KN150273.1 | 50294 |
| GRCz11 | 14 | 2567435 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGGTGCGAACCGACCCACTGTGGAAAGGCCTGTCAGAGCGGCATCAATG[G/A]TAAAAGAACATNNNNACACTACATGTCACAGACGTAATGATGTTTCTACTATAC
Long Flanking Sequence:
CTGTGTGTTTAAGTTTTTACTCTTCAGCCGTTTGCATTTCCCGTGGTCATAAAAGCTCCTTCCCTGTCATCTGACAGCAGAATACCTTGAGTGATTGACAGCTAATATGAACCAATATAGCGGCTTGAAAGAGCGATTCAGCACGTTTTTACAAAAAATCAAAACAGGTTGCACTACAACCACTATCTGCAGTCGCACTAATGCGCCCAAATATATTATGAAGTCGCATAGATTAATTTTCGGGCGCATATGCGACCAAAATGGTCGCAATTTCGAGCCCTGAGTAACTCTTAGTGCATCTGTGTGTTTGCAGCTCGGGGTCTGGATCACATCGCTGAGAACATCCTGTCGTTCCTGGACGCTCGCTCTCTGTGCTCCGCTGAGCTGGTCTGTCGAGAGTGGCAGAGGGTCATTTCAGATGGGATGCTCTGGAAGAAGCTCATCGAGAGGATGGTGCGAACCGACCCACTGTGGAAAGGCCTGTCAGAGCGGCATCAATG[G/A]TAAAAGAACATACACTACATGTCACAGACGTAATGATGTTTCTACTATACAAACTTTATATTCTCTCCCTCTACCCCTAAACTCAGCCCTCACCAATCTGCATTTTTACATTTTAAAATAATTTAATTCAATTCACCTTCATTTCTATAGCGCTTTTACAATGTAGATTGTGTCAAAGAAGCTTCACTTAGAAGATCATAGTAAATTGAAACAGTGTAGTTCAGTTTTTTAGAGTTTAAGTTCAGTTCAGTTTAGCTCAGTTCAGTGTGGTTTAATTTTCACTACTGAGAGTCCAAACACTGAAGGGTAAATCCATTGATGCGCAGCTCTACAGGTCCCAAACCTTGCAAGCTAGTGGCGACAGCGGCGACGAAAAAACTTCACCAATTGGCCAAAGTAAGGAATTAAAAAACCTCGTGAGAAACCAGGCTTAGTTGGGCACGACCATTTCTCCTCTGGCAAAACGTCTTGTGCAAAGCTGCAGTCTAGGCGCCGGAGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42328
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 |
|---|---|---|---|---|---|
| ENSDART00000036901 | Nonsense | 512 | 527 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 14 (position 2162985)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | KN150273.1 | 64022 |
| GRCz11 | 14 | 2553707 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGACGACACAATCCTTATATGGGACTTCCTGAATGTGTCCAGCAATGGG[C/T]AGTCGGACGGTCGGTCGCCCTCTCGGACATACACATACGTCTCCAGATAG
Long Flanking Sequence:
CAGACAAAGGAGACATCCAAAACATGCAGTGCTGGTGGTCCTCCAGAAATGTGGTTGAGAACCACTGATTTAAACTATTCTATGGTAGAAAAAAAATGCTTAAACACTTCCTAAAAACATTGCAAATCAGTTACATTAAATCATAAACTATTCACTTATTATTTGTGTCATCATTACTCAAACTTATTCATTTGTCTATTTTTAAAAATGCTGTTTCCTGTATCCTGTAGTTTGGCAATAGATATATATTTACTAAAGCATTATCCTGAAAGCAGAGCTCTTAATGTGCTGATAACATATGTTGTGTTTACTCTTGAGTTTACACGTTTGTGTGTGCACGCTGTATGTTGTCATGTGGGTTTAACTGTGTTTGTTGTCATCTGTCGCAGGAACATTCTGGCCGTGTGTTCCGTCTGCAGTTTGACGAGTTCCAGATCATTAGCAGTTCCCATGACGACACAATCCTTATATGGGACTTCCTGAATGTGTCCAGCAATGGG[C/T]AGTCGGACGGTCGGTCGCCCTCTCGGACATACACATACGTCTCCAGATAGCAGGTACACATTAGAACTCAATAAAATCAACATTTCGTTATTATTGTGGTTTGAATTTTTATTTTTTTTGATGGTTTTATATGTTGGTCTGAGAATCCTTCTGAATGGGTCTAGAGGTGATCTCTCTCCTTTTTGTCATTCTGTTTTGATCTTATATATATATAAGTGGTGTTAGTGGGTGCTAATGCCCCTGTATAGTGATGGGGACTCTATACTGTTCAGTGAGCGCTGTCTTTTGGATGAGACATTAAACTGAGGTCCTGACTCTTTGTGGACATTAAAAATTCCACAATGTCTATCAAAGAAGAGTATCCGTACGTTCACACCGAAAGCGGCGAGAGCGTCAAAGTAGCCGGAAGTCATTCATTTTCAATGAGAGCCGGCGACGATAGGTGGCGATAAGCGGCGAGGAGCAGCGCGGCGCGTCTTCGCCGGCGTGAGCGTCGAGGA
Associated Phenotype:
Not determined