ZMP
fbxw11b
Ensembl ID:
ZFIN ID:
Description:
F-box and WD-40 domain protein 11b [Source:RefSeq peptide;Acc:NP_998669]
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 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|
Mutation Details
This allele has been removed from public view.
Allele Name:
sa2566
Status:
Allele not cryopreserved
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:
n/a
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000019252 | Nonsense | 130 | 527 | 4 | 13 |
| ENSDART00000140113 | Nonsense | 127 | 524 | 4 | 13 |
The following transcripts of ENSDARG00000017230 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 21533578)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 21494992 |
| GRCz11 | 10 | 21452373 |
KASP Assay ID:
554-3259.1 (used for ordering genotyping assays)
KASP Sequence:
GATCATATAGCGGAGAAYATCTTGTCGTTCCTGGATGCTCGCTCGTTGTG[T/A]TCRGCTGAGCTGGTGTGTAAGGAATGGCARCGTGTCATATCTGAAGGCAT
Associated Phenotype:
Not determined
Mutation Details
This allele has been removed from public view.
Allele Name:
sa27592
Status:
Less stringent filtering
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:
n/a
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000019252 | Essential Splice Site | 371 | 527 | 8 | 13 |
| ENSDART00000140113 | Essential Splice Site | 368 | 524 | 8 | 13 |
The following transcripts of ENSDARG00000017230 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 21540715)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 21502129 |
| GRCz11 | 10 | 21459510 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTGATGACAAGTACATTGTCTCTGCCTCTGGGGATCGGACTATAAAGG[T/G]CAGCACTTCAGTATGTTATCAGCTGTCAGTCAAAGCACAAATCAGTGCTC
Associated Phenotype:
Not determined