ZMP
wu:fb99d03
Ensembl ID:
ZFIN ID:
Human Orthologue:
FBXO34
Human Description:
F-box protein 34 [Source:HGNC Symbol;Acc:20201]
Mouse Orthologue:
Fbxo34
Mouse Description:
F-box protein 34 Gene [Source:MGI Symbol;Acc:MGI:1926188]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19164 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11291 | Nonsense | Available for shipment | Available now |
sa6461 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa19164
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 |
---|---|---|---|---|---|
ENSDART00000105251 | Nonsense | 10 | 652 | 1 | 3 |
ENSDART00000105251 | Nonsense | 10 | 652 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 17 (position 10647594)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 10630683 |
GRCz11 | 17 | 10786717 |
KASP Assay ID:
2261-0692.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCCTTTGTTTAGGTTGAACAACATGCACCTCAAGCCATACCCTAAACCA[C/T]AAGATAAAGAGATACATCGGGAATCTGTGCGCGATGCAACACGAGGCCTC
Long Flanking Sequence:
TTAATGTCTGGTTCAAAAAAAGCAAAAAAAAAAAAAAGCAAAAAAAAAACCACCAAAATACCTTTGTCATTGAATACCTGTAATGTACTGTACTTTTTGTCATAAAAAAAAAAAAACACGAAGATAAGGGAGTAAAGTTAGATGGGATATTCATGTTAAATTTGGAATGATTTGATTGGTCCCCCATTCAAGCCAATCATATTATGTGCTCCTCTCAAAATTAGTTTGTGAAACTTCACTTAGTTTGTGACCTTGGATCAGTTGGTGACCTTGAATTATTCAGCTATTAACTGCAATTCAAATTCTCAATTGAGCAATAATCTTATTTTACATCATACAGTATTATTGTCTTTATTATTGGATTGAAATTGTATAAAGCCTTTTTCTCGTAATTAATCTGTTTATTTTAATGTGGCACATTGGATTTGTTTTAAAATTCTTTGCATTTATTCCCTTTGTTTAGGTTGAACAACATGCACCTCAAGCCATACCCTAAACCA[C/T]AAGATAAAGAGATACATCGGGAATCTGTGCGCGATGCAACACGAGGCCTCCATGCCGACCAGCAGGGAGTACTCAGGAAAGAGTGGGGCGTTCACCAGTCGTGTGGCCTTATGGGCTCACCTGGCAACGGCACAGCCAACCGGTGTCCCCTCGGTGTCATCTCCCCCAACACCCTCCGATGTAATACCAACAGTGGAAGCAATGTACCAACTAGAGTTAGTGGGGCCCGCAAAAGCAAATCACTTCCCATCACAACATTTACTAGTTCTTTAGTCCTGCTCTCACCTTCGACTGGTTTGGAGAATGAAGGCTCACTTGGGATCTATCAAGGAGAGGATGAAGAGGGATCTTTGGATATATGGGCTGTCATTAAACCTGGTAACACAAAAGAGAAAATTGCTATTTTTGCATCTCAAATGTGCAGCAGTACTTGCGATAGTGTTATTGACGATGGCTCAGAAACAGAAGCCATTGCCCCTGAGCTGCGGACAGCTTCTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11291
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 |
---|---|---|---|---|---|
ENSDART00000105251 | Nonsense | 10 | 652 | 1 | 3 |
ENSDART00000105251 | Nonsense | 10 | 652 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 17 (position 10647594)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 10630683 |
GRCz11 | 17 | 10786717 |
KASP Assay ID:
2261-0692.1 (used for ordering genotyping assays)
KASP Sequence:
TCCCTTTGTTTAGGTTGAACAACATGCACCTCAAGCCAYACCCTAAACCA[C/T]AAGATAAAGAGATACATCGGGAATCTGTGCGCGATGCAACAYGAGGCCTC
Long Flanking Sequence:
TTAATGTCTGGTTCAAAAAAAGCAAAAAAAAAAAAAAGCAAAAAAAAAACCACCAAAATACCTTTGTCATTGAATACCTGTAATGTACTGTACTTTTTGTCATAAAAAAAAAAAAACACGAAGATAAGGGAGTAAAGTTAGATGGGATATTCATGTTAAATTTGGAATGATTTGATTGGTCCCCCATTCAAGCCAATCATATTATGTGCTCCTCTCAAAATTAGTTTGTGAAACTTCACTTAGTTTGTGACCTTGGATCAGTTGGTGACCTTGAATTATTCAGCTATTAACTGCAATTCAAATTCTCAATTGAGCAATAATCTTATTTTACATCATACAGTATTATTGTCTTTATTATTGGATTGAAATTGTATAAAGCCTTTTTCTCGTAATTAATCTGTTTATTTTAATGTGGCACATTGGATTTGTTTTAAAATTCTTTGCATTTATTCCCTTTGTTTAGGTTGAACAACATGCACCTCAAGCCATACCCTAAACCA[C/T]AAGATAAAGAGATACATCGGGAATCTGTGCGCGATGCAACACGAGGCCTCCATGCCGACCAGCAGGGAGTACTCAGGAAAGAGTGGGGCGTTCACCAGTCGTGTGGCCTTATGGGCTCACCTGGCAACGGCACAGCCAACCGGTGTCCCCTCGGTGTCATCTCCCCCAACACCCTCCGATGTAATACCAACAGTGGAAGCAATGTACCAACTAGAGTTAGTGGGGCCCGCAAAAGCAAATCACTTCCCATCACAACATTTACTAGTTCTTTAGTCCTGCTCTCACCTTCGACTGGTTTGGAGAATGAAGGCTCACTTGGGATCTATCAAGGAGAGGATGAAGAGGGATCTTTGGATATATGGGCTGTCATTAAACCTGGTAACACAAAAGAGAAAATTGCTATTTTTGCATCTCAAATGTGCAGCAGTACTTGCGATAGTGTTATTGACGATGGCTCAGAAACAGAAGCCATTGCCCCTGAGCTGCGGACAGCTTCTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6461
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 |
---|---|---|---|---|---|
ENSDART00000105251 | Nonsense | 24 | 652 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 17 (position 10647552)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 10630641 |
GRCz11 | 17 | 10786675 |
KASP Assay ID:
554-4895.1 (used for ordering genotyping assays)
KASP Sequence:
CTAAACCACAAGATAAAGAGATACATCGGGAATCTGTGCGCGATGCAACA[C/T]GAGGCCTCCATGCCGACCAGCAGGGAGTACTCAGGAAAGAGTGGGGCGTT
Long Flanking Sequence:
AAAAAAACCACCAAAATACCTTTGTCATTGAATACCTGTAATGTACTGTACTTTTTGTCATAAAAAAAAAAAAACACGAAGATAAGGGAGTAAAGTTAGATGGGATATTCATGTTAAATTTGGAATGATTTGATTGGTCCCCCATTCAAGCCAATCATATTATGTGCTCCTCTCAAAATTAGTTTGTGAAACTTCACTTAGTTTGTGACCTTGGATCAGTTGGTGACCTTGAATTATTCAGCTATTAACTGCAATTCAAATTCTCAATTGAGCAATAATCTTATTTTACATCATACAGTATTATTGTCTTTATTATTGGATTGAAATTGTATAAAGCCTTTTTCTCGTAATTAATCTGTTTATTTTAATGTGGCACATTGGATTTGTTTTAAAATTCTTTGCATTTATTCCCTTTGTTTAGGTTGAACAACATGCACCTCAAGCCATACCCTAAACCACAAGATAAAGAGATACATCGGGAATCTGTGCGCGATGCAACA[C/T]GAGGCCTCCATGCCGACCAGCAGGGAGTACTCAGGAAAGAGTGGGGCGTTCACCAGTCGTGTGGCCTTATGGGCTCACCTGGCAACGGCACAGCCAACCGGTGTCCCCTCGGTGTCATCTCCCCCAACACCCTCCGATGTAATACCAACAGTGGAAGCAATGTACCAACTAGAGTTAGTGGGGCCCGCAAAAGCAAATCACTTCCCATCACAACATTTACTAGTTCTTTAGTCCTGCTCTCACCTTCGACTGGTTTGGAGAATGAAGGCTCACTTGGGATCTATCAAGGAGAGGATGAAGAGGGATCTTTGGATATATGGGCTGTCATTAAACCTGGTAACACAAAAGAGAAAATTGCTATTTTTGCATCTCAAATGTGCAGCAGTACTTGCGATAGTGTTATTGACGATGGCTCAGAAACAGAAGCCATTGCCCCTGAGCTGCGGACAGCTTCTGTAAAAAACAAAGGTTGCTGGGATGTTGACTGTTCTTTGCCTAAG
Associated Phenotype:
Not determined