ZMP
fbxl22
Ensembl ID:
ZFIN ID:
Description:
F-box/LRR-repeat protein 22 [Source:RefSeq peptide;Acc:NP_001013297]
Human Orthologue:
USP3
Human Description:
ubiquitin specific peptidase 3 [Source:HGNC Symbol;Acc:12626]
Mouse Orthologue:
Usp3
Mouse Description:
ubiquitin specific peptidase 3 Gene [Source:MGI Symbol;Acc:MGI:2152450]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44315 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa30271 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa24690 | Nonsense | Available for shipment | Available now |
sa44314 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44315
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067114 | None | None | 227 | None | 2 |
ENSDART00000088884 | Essential Splice Site | 127 | 527 | 4 | 16 |
Genomic Location (Zv9):
Chromosome 25 (position 27616033)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 26306127 |
GRCz11 | 25 | 26749329 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACTTGGGCATGTGCAGAGGGTCAGAGAACATCTACAGAGTTTGGAGAA[G/T]TAAGACTGTAGTTTATAATGTATCTGTTTATCAATCAAACATCATAAAAC
Long Flanking Sequence:
GAATATACAAACATATTTATAACATGTTGAAGTACAATTCTACTGAAATAAATAACATTTAATCATTAAAATATACACACATAAGCATTTAATCTCTTTTCTTTTGTAGGTATGTTAATGGCCATGCCAAAAAGCATTTTGAAGAGATTGAAGCTCCAGGTTGCAGCCAAAGGAAGCCAGACAGAGAAAAGTTGAGGGAGAAGGGTCAACAGCACTCTGTGTGTATGGACTGTAACAGTTATAGCACATTCTGGTAGGTTTCTTGCCCTATTATTCATTCATCATTCATTTATTCATTCATATATTCATTCATTCATTCATATTTGTCAATGGACTTTAAAATTTAATATTGTTCAGTAAGCAGTGTTATATGTTAAAAAAAAACTATTTTTGAGTTTCTTACCTATTTCCTGCAGTTATAAATGCGACGAATTTGTGGTGAATGACACAAAACTTGGGCATGTGCAGAGGGTCAGAGAACATCTACAGAGTTTGGAGAA[G/T]TAAGACTGTAGTTTATAATGTATCTGTTTATCAATCAAACATCATAAAACTTTATTGACATTGTTGTGTTTAAATGGTTTATTCTTTGTCCAGCTCTGTGTGTAATACCGACAGACAGAGAAAGAGAAAAATGTCTGAAAGTTTTTCTCCTGACAGCAAGATGAAGCAAGACAGTGTAAGTTTAATTTGTTTCTATGCATCTTTGCAAAAATGTGCCAAGAAATAGCTTAGAAAAAATATTATGCACCCACCTACACATGCACATCTTTTGAAAAAGTTAGGACACCTTATTTAACTTGGTGGGTTTTTATCAGGAGAAAATAAACGAAATAAAAGTTTAAATGTCATTTTTTACTTAAAAATAAAGCCAAAATTTAAAAAAAGTGATGAGTGATGAGCTTAGGACACTCTTAAAATAGGGATTAAGAATGTAAGTAGCAGTCAAGCACAGCTAGTCAAATGCCATTTAATAAGCTGATCATCAGCAAGTGTGTGCCCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30271
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067114 | None | None | 227 | None | 2 |
ENSDART00000088884 | Essential Splice Site | 409 | 527 | 12 | 16 |
Genomic Location (Zv9):
Chromosome 25 (position 27607395)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 26297489 |
GRCz11 | 25 | 26740691 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAGCGACAGAAGTCCACCAAGAAATTCTGGATCCAGAAACTGCCCAAG[G/A]TAACCAAATATTTAAATATTTCGGTAATATGTTGTCCATATTTTTTCAGC
Long Flanking Sequence:
GTTTGTGTAGTAATGTTGAGCAATTCTGCAATTGTTTCTAGAAATGGGACATCCACTATTGTTACATCTGTGTTTGGTGGCGTTCTACAGAATGAGGTGTATTGCTTGATATGCGGCACGGAGTCTCGGAAATTTGATCCATTCTTAGGTAAGCATAATTTCACAAAAACTTGACTTTTGTAACTATTGTTGGAAAAGTTCACCTGTCTTATTCTCCTTCAGATCTTTCACTCGACATTCCCAATCAGTTCAGAATCAAAACCACAAAGGACCAAGAACCGGGGCCAACGTGCACTTTGAGTGGTAAAGGATTATCTGAAACGAAGTTGCTGCAGTTTGGTTAATTTTGGGCAGTGTATTTAGTTTTTCTGTTGGTTACAGATTGTCTTCGTAGTTTCACAGACCTTGAGGAGCTCGATGAAACAGAGCTATACATGTGTCATAAGTGTAAAAAGCGACAGAAGTCCACCAAGAAATTCTGGATCCAGAAACTGCCCAAG[G/A]TAACCAAATATTTAAATATTTCGGTAATATGTTGTCCATATTTTTTCAGCTATATGATGTCATATCCCTTTCAGGTGCTTTGTCTACATTTGAAGAGGTTCCACTGGACAGCATTTCTGAGGAATAAGGTTGACACCTATGTAGAGTTTCCCATGTGTGGCCTTGACATGAAAAGCTACTTGTTAGAGGTGAGAGCATTCAGTTTTGTTACACATTGTTTTGTTTTTTTTGTTATTTGTTTCTAATATTTAAATGAACATTACAAGAAAACAAATCATGCCAATATACTGTTATTTATTATTATATGTATAAAAGGATATTAATGAATAAAGTAATATTTATTTACATTGAAAATGCATGTTTTTCTTCAAAACACAGTAGACAAAATGATTGGCATCTCTAAAATTCTAATGAATAAAATATATCTGTGTAATACTTTTCTTTAAGTTTACATTTTTAGCACACTTGAGTGAGTACAAGCACAAAAGAATCCAGGCATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24690
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 |
---|---|---|---|---|---|
ENSDART00000067114 | None | None | 227 | None | 2 |
ENSDART00000088884 | Nonsense | 446 | 527 | 13 | 16 |
Genomic Location (Zv9):
Chromosome 25 (position 27607211)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 26297305 |
GRCz11 | 25 | 26740507 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCTATGTAGAGTTTCCCATGTGTGGCCTTGACATGAAAAGCTACTTGT[T/A]AGAGGTGAGAGCATTCAGTTTTGTTACACATTGTTTTGTTTTTTTTGTTA
Long Flanking Sequence:
TATTGTTGGAAAAGTTCACCTGTCTTATTCTCCTTCAGATCTTTCACTCGACATTCCCAATCAGTTCAGAATCAAAACCACAAAGGACCAAGAACCGGGGCCAACGTGCACTTTGAGTGGTAAAGGATTATCTGAAACGAAGTTGCTGCAGTTTGGTTAATTTTGGGCAGTGTATTTAGTTTTTCTGTTGGTTACAGATTGTCTTCGTAGTTTCACAGACCTTGAGGAGCTCGATGAAACAGAGCTATACATGTGTCATAAGTGTAAAAAGCGACAGAAGTCCACCAAGAAATTCTGGATCCAGAAACTGCCCAAGGTAACCAAATATTTAAATATTTCGGTAATATGTTGTCCATATTTTTTCAGCTATATGATGTCATATCCCTTTCAGGTGCTTTGTCTACATTTGAAGAGGTTCCACTGGACAGCATTTCTGAGGAATAAGGTTGACACCTATGTAGAGTTTCCCATGTGTGGCCTTGACATGAAAAGCTACTTGT[T/A]AGAGGTGAGAGCATTCAGTTTTGTTACACATTGTTTTGTTTTTTTTGTTATTTGTTTCTAATATTTAAATGAACATTACAAGAAAACAAATCATGCCAATATACTGTTATTTATTATTATATGTATAAAAGGATATTAATGAATAAAGTAATATTTATTTACATTGAAAATGCATGTTTTTCTTCAAAACACAGTAGACAAAATGATTGGCATCTCTAAAATTCTAATGAATAAAATATATCTGTGTAATACTTTTCTTTAAGTTTACATTTTTAGCACACTTGAGTGAGTACAAGCACAAAAGAATCCAGGCATTACCTTGTCACAAGAGCACAGAGATAGAATTACAACTTCTGTATGAGCCCAGTTAAGAGTATTGAGTACTTTTCTGATATAAATCAAAAGATTCAAAGAAAACAGATTTAAAATATCAAGTATTTAAAATTCCCATTTCCACTAATACAATACAACATTACTTGCAATGAAGTTGAAATAAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44314
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067114 | Essential Splice Site | 112 | 227 | 2 | 2 |
ENSDART00000088884 | Essential Splice Site | 497 | 527 | 16 | 16 |
Genomic Location (Zv9):
Chromosome 25 (position 27594481)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 26284575 |
GRCz11 | 25 | 26727777 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAGTAGTAATTATATTTAGCATGTCAAAATTGTGCTTTTTGTTTTTTTA[G/A]GTGTCCAAATCTGATCTCACTGACTCTGTCTGGATGTGGGCACATAATGG
Long Flanking Sequence:
GGTGCAATAAATAAAATCTTAGGCTAAATGAATAATTTTATTTGGTTCTTTCTCATAATGTGGCATAGGAGTTAAGATAAATAAATAAAAAAAATACTAGTCATTGTAGTAGTATCAGTAGTAGTGTTAGCAGTAGTTGTTGTGGTAATAGTAGTAGTAGTTGCTGTATTAGTTGTGGTAGTAGTAATTTGTGTACCTCTTTGAATACTACTACTACTACTACTACTACTACTACTACCACTACTACCACTACTACTACTACTACTACTACTACTACTACTAATAATAATAATAATAATAATAATACACCTTTAATAATAAACCTTTGACTTGATTTCTCTCCAGTACCGTGGGCTGACAGAGCATTACTGTACGTTGCAAAACGTCCCCAAAGACTCTTCTGCATTTTAACAATCTCAACAAATTAAACAAACAAAAAATGTTTAGAGCATAGTAGTAATTATATTTAGCATGTCAAAATTGTGCTTTTTGTTTTTTTA[G/A]GTGTCCAAATCTGATCTCACTGACTCTGTCTGGATGTGGGCACATAATGGACAACAATGTCATCAAAGTGCTACAAAGCTGCAGAAGGCTACGTAGCCTGAGTCTAGAAAACTGTGCTCGGATAACAGACTCTGTACTCAAGGCTGCGGTGGAGCATGGCCACAATCTCACAGAGGTGAGAGTGGACTTTTGCCGCAATGTGACCCAGGCAGGGTTGCAGGAGCTAAAAAACAAGAGACCAGAAGTACTTCTGAGTGCATTACACAGTGCGGATATGATTCCAGATTGCAAGCCTGAGGAGAAAACACATATCAAGAGAGCTCTGCAGAAGTTCTTGATCTTCTCTTGACTGACCGTTGTGACCTTATGTCAAGATGATATTTATTTTCTAATTCTATTATAAATGTTTTTTTTCACCAATTTTTTGATTCCTTATTTTATGACATGCTAATTTTATTGCTAACATTTTATATTTTATTAGTTCCCTCTTTTCACCCACC
Associated Phenotype:
Not determined