ZMP
fbxw2
Ensembl ID:
ZFIN ID:
Description:
F-box/WD repeat-containing protein 2 [Source:RefSeq peptide;Acc:NP_001018175]
Human Orthologue:
FBXW2
Human Description:
F-box and WD repeat domain containing 2 [Source:HGNC Symbol;Acc:13608]
Mouse Orthologue:
Fbxw2
Mouse Description:
F-box and WD-40 domain protein 2 Gene [Source:MGI Symbol;Acc:MGI:1353435]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa33642 | Nonsense | Available for shipment | Available now |
| sa8382 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33642
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000023977 | Nonsense | 299 | 455 | 5 | 7 |
| ENSDART00000141294 | Nonsense | 51 | 141 | 2 | 3 |
The following transcripts of ENSDARG00000009745 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 34020818)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 31783050 |
| GRCz11 | 5 | 32383203 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCATGATGCACAGTCCTGGTGACTACATACTACTGAGTGTTGATAAATA[T/A]GAAATAAAGGTAATGCATGCCATTTTTAAGAACCAAAGTGTTTTGCAGAC
Long Flanking Sequence:
GGTGCCAAAATCCAGCAGTTTCGAGGACATACTGGGGCAGGTTGGTTTCAGGCTCTCAAAGTAACATCATTATTCCTTTGTTTTTCTTCTCTGTTTTTTTGTGTCATGTTTATGGTTATGTCACAACATATCAATAGCAGAATTTTAAAGATTGACTTTTGTTGCAGTGTTCAGCATAGACTACAATGATGAGTTGGACACCCTGGTCAGCGGCTCTGCAGACTTCACTGTCAAAGTATGGTCCCTTTCTGCAGGAACGTGTGTCAACACTCTTACTGGACACACAGAGTGGGTCACTAAGGTAAGACTCGTATAAACCAGATCTCACTGTGGAACGAAACATAGTAGTTTTTATTCAACTGATTTTTATTTTGGAGTTGGTGATCAGTGGTAACTGTTCGCTTTTCATCTGTGCTTATTTAGGTGCACCTTCAGAAAAGCCAAGTGGAGTCCATGATGCACAGTCCTGGTGACTACATACTACTGAGTGTTGATAAATA[T/A]GAAATAAAGGTAATGCATGCCATTTTTAAGAACCAAAGTGTTTTGCAGACTGGTGTTCCGGGTTAAGAATAGTGTTTAGCACTTATAAAAGTAAGGTGTCTTAAAAGTCCTGGTAACATGGTCAAAAGAAATATTTAAAAAACAAGATGCCATGAGACGTTTTAATTTGTATATATATTTTTTCTTTATTTGTTTACAAATAAATTACAATTATGCACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACACATACATACACACACACACATCAAAAGCTTTATACAAAATCATAAAAATATTAATGCGCACTTACTGCAGATGGGATCTCTAAGTGCTGTTTTCTTAAAATTTCCATGGACTAAATCCAATCATTTTACTTGGAATTTCATTGCGCAACAGTTTTTGTTACTCCCAAGTTTGTTGTTGTCCAAGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8382
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 |
|---|---|---|---|---|---|
| ENSDART00000023977 | Nonsense | 451 | 455 | 7 | 7 |
| ENSDART00000141294 | None | None | 141 | None | 3 |
The following transcripts of ENSDARG00000009745 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 34019013)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 31781245 |
| GRCz11 | 5 | 32381398 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTAGTGTTTGCCACSAGTATGCCTGACCATAGCATTCATCTGGTTCTCTG[G/A]AGAGAGAATGGCTAGGACATGGAGGAGGCAAATACTAGCCCTGTGCTTTG
Long Flanking Sequence:
TCGCAAGCTTTGATGTCATCAGGTTCATGCATTTCATCTGTCCGTTTACATTATCTTCATTTTATATTAGAGACATAACTTTTAATATACATTTTAACATTTATGTCTGTAAGTAAATAATTAACATGATGTAAAATTAAATGTAAAAGGATTTGTGCAATTTTTTTTTTACTAATTTCACTAATTAAATAAGCTAAATTGTTTTATTGAATTGATCTTCTCAGAGTCATCAAGCCACAGCAGGACCCCTCCAGCCTCTCTCTGCTTAGTTTTGGTGAGGTTTTCGCTCTTCTCTTTGACAACCACCATCTCTATGTTCTGGACTTGAGGACTGAGGTTACTGTGGGCCGCTGGCCACTGCCAGCCTACCGTAAATCGAAACGTGGCTCTAGTTTCTTAGCAGGCGTCACTTCCTGGCTCAATGGACTGGATGGCAAGAATGATGCAGGCCTAGTGTTTGCCACCAGTATGCCTGACCATAGCATTCATCTGGTTCTCTG[G/A]AGAGAGAATGGCTAGGACATGGAGGAGGCAAATACTAGCCCTGTGCTTTGAAAGCAGGCAGAACTTTACAGCAAAAAGAAGAAAAAAGGGTGCTTTTCATTAAACTAAACAGCCAACATTGTTAGATAATGCATGGACCAAAGTGTTTCCCCCTCCTCAACTTTGTTTCCATTCGCATTATGGATTCACTCTTGCTTCACTTTCTTTCCTAGTTACTTGCAAACCATGCATTCAACACTCATAGAAAAGGAGACCACTGGAGATTGGCAGTAGCTTTTCTCCATCATGTGAATCCAATTCAAGGGTTTTGTTTGTTAAAGACTTGAGAGATTTCTCGCTGAACTTGAGTTGAGTCGCTTTTGCTTTCACACCAGTGAAAGTTGTTAAAATGCTACTGCACCACCAGAGCGCAGATCGCTCCACAGCAGGCACGAGCAGGGGAGGTGGCATGTTTTATAGCACAATCACCAGGATTGACAATGAAGTACGTTGTTTGTTTT
Associated Phenotype:
Not determined