ZMP
B8JLI4_DANRE
Ensembl ID:
Description:
Novel protein similar to H.sapiens FBXO11, F-box protein 11 (FBXO11, zgc:153171) [Source:UniProtKB/T
Human Orthologue:
FBXO11
Human Description:
F-box protein 11 [Source:HGNC Symbol;Acc:13590]
Mouse Orthologue:
Fbxo11
Mouse Description:
F-box protein 11 Gene [Source:MGI Symbol;Acc:MGI:2147134]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35300 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22100 | Nonsense | Available for shipment | Available now |
sa9441 | Essential Splice Site | Available for shipment | Available now |
sa18066 | Essential Splice Site | Available for shipment | Available now |
sa9342 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22099 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35300
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 |
---|---|---|---|---|---|
ENSDART00000112918 | Nonsense | 185 | 929 | 8 | 26 |
Genomic Location (Zv9):
Chromosome 12 (position 26403977)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 24776418 |
GRCz11 | 12 | 24897637 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCCTACCTGCTCGAGCAGGACCTGTGCCAGGCTGCCTGCGTATGCAAG[C/T]GATTCAGTGAGCTTGCAAACGACCCTATTCTCTGGTGAGAATTTATACAT
Long Flanking Sequence:
TTTCTAATCTCTGCTGTCTGTATATTTCATATTCCACTCCATACGTTCACCCCTGACAGTGGGGAGAGAACATTGGAAAATATGTAGTATCAACTATGATAGATAGATCTAACACTTTAATCTTAATGTTGTTTTAACCTAAAAAGTGGTAGTTTTCAGTGTCTGATTTATGTGATGCAGGGAGCCTCCACTTCAGCCACAGAAAACTTCGGTCACAGAGCTAAACGTGCAAGAGTGTCTGGAAAATCCCAGGACCTACCGGGTGAGTGAAGACTTGTGGTTTCGGTTTGCTCAGTTGTGGTTGCTATATTAATAGTTTAGCATTTTGTCAAAGGCTTTGGTCTGCAAACAGATTGGTTTAGAAACTTTCTCCTGTTGTTTCTGTTTTAGCTGCTCCAGCAGAGCAGTATCTCCAAGAGAAGCTTCCAGATGAAGTTGTTCTGAAGATTTTCTCCTACCTGCTCGAGCAGGACCTGTGCCAGGCTGCCTGCGTATGCAAG[C/T]GATTCAGTGAGCTTGCAAACGACCCTATTCTCTGGTGAGAATTTATACATACTGACAATAGATTGATTTGTGGAAGCGCTAGGACAGCATGATATTGGAAGAATTGGACATTGCGATATTTATGGTGGCTTGAAAAGCCAACATACTGTTATCTCACGTAAACTTATTATTATGGTGGCTTGAAAAGCCAACATACTGTTATCTCACGTAAACTTATTATTAGGCTGGCTTGAGAAACAAGCCAGACTACTGAAATCCTATTTAAACTTATTATTTTTTTTATATATTATTCTTCTTCTTCTGAGACTAAAATTCAAAATCTATCTCCTCCTAGAGCTTTCGAGCTATGACCCCCAAACTCACACCAGACCTCCAAACTGGTCTGACTCTTTATGCCATATCTTTTCCGACTGATCCGACTTTCGATTTTCCGAAAAACGTCCCGGGACTGTCGGAAAAATCCCATAGACTTAACATTGGATCAAACTTTGTGACCTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22100
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 |
---|---|---|---|---|---|
ENSDART00000112918 | Nonsense | 208 | 929 | 9 | 26 |
Genomic Location (Zv9):
Chromosome 12 (position 26364758)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 24737199 |
GRCz11 | 12 | 24858418 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGTTTGTTTCATAGGAAGAGACTATACATGGAAGTGTTTGAGTACACG[C/T]GACCCATGATGCATCCAGAACCAGGGAAGTTCTACCAGATCAACCCGGAA
Long Flanking Sequence:
GTAAGGATTCTCTTTAGAAATGAGCATTATACTAACATGCACAATCATGGCTGGATTTTCTCTTTAGGGCTTTTTGATATCCGTCTTGTGTAGAAGAACGTACACTACTGTTCAGAAATCGAGTAATTAATTGTTTACACAAGACTATAATTTAGGTGGACTGATACATTTTTGTTTACCTATTTTATTCTGTGACGTTAAACCAGTCATTACTCCAGTCTTCAGTGCCATGTATTCCTTCAGATATCTTTTTAATATGCTGATTTGGTGCTCAATATTTAGGTTTTTTTGATCAAGTAAATGAGTCCTTACTGAATGAAAGTATTAGTTTGAAATAGCCGTTTGAACGGTGTATTTTAAAAGCACAGCACTAGACTGGCATTTGGTCTCAATGTTTATTTTCCACAGTAATGTGTTGTCATTTAGTATTTTTACTCTTGTTTGTGTTTATTTGTTTGTTTCATAGGAAGAGACTATACATGGAAGTGTTTGAGTACACG[C/T]GACCCATGATGCATCCAGAACCAGGGAAGTTCTACCAGATCAACCCGGAAGAGTATGAGCAACCAAACCCATGGAAAGAGAGCTTTCAGCAGTTGGTATGAGAGCTTGTGTTTCTGTTTTCTTTCCTCAGTCAGATTATGGATAATCACACTTTAACGTCAAGGTGGATATGAATGATGGATGATTTTTTTCCATGCAAGGCCTTTTGTGTTTAATATATTTGAGTAACAATGGTATTCACTCTTCTAAAGGTCATGAAATGACTAATGCCACATTTACTCATGTTAACTGTCCATCTCGTGGACAAAAGTGATGCTGAAATGTAAAGAAAGATTCGCCACTAAATCTTTGCATTTGTTTCTCTTTCTACAGTATAAGGGAGCACACGTAAAGCCTGGTTTTGCAGAACACTTTTATAGTAATCCAGCCAGATACAAAGGCAGAGAAAATATGTTGGTATGGACATTTGACTTCAGTGGTTGAATTTTTTTTTTAAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9441
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112918 | Essential Splice Site | 347 | 929 | 12 | 26 |
Genomic Location (Zv9):
Chromosome 12 (position 26363558)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 24735999 |
GRCz11 | 12 | 24857218 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTATGGAGGGATCTGAAGATGCATATGTGGGCTACATGACTATCAGGG[T/C]AAGACYAACAGTATTTTTATTTTTTAAGTTATTTACATTTAGCGCATTAT
Long Flanking Sequence:
TAAACCTGATGGCTTTGTTTTTGTTATGTATATTCTTAACTTTAAAAGGATAGTTCACCTAAAACTGAAAATCCAGACATCATTTACTCACACTTCACTTGTTCCAAACCAGTTTGACTTTTTTATTTTTATTTATTATGTTGAGCCCAAAATAATAGATTTTAAAGAAAGCTCAAAACCAGTAACCATTGACTTCCATAGTCCATCAAATACTATGGAAGACAATGGTTACAGGTTTTGGTCTTTCTTCAAAATACCTTCTTTTGGGCGTAACATCATAAAAACACTCCTAAAGGTTTGAAACTATTAGAGGTGAATATATAAAGTGCACATAAAAGTGCACCAGACTGTTATCCTAAAGTCACCAACATCCCTGTTTTCCGTCCTTTCAGCCTCAGGGAAGGTAGCTGATAAGGTCGTCATTGAAAACACTAGAGATTCAACGTTTGTTTTTATGGAGGGATCTGAAGATGCATATGTGGGCTACATGACTATCAGGG[T/C]AAGACCAACAGTATTTTTATTTTTTAAGTTATTTACATTTAGCGCATTATTTTATTGCAAACATCAGTTTTTATTATTTTAATCATGATGTTAAAAGTTGCAACAAATCATGTTTTTGCATGTGTGTTGTATTGCTGTTTCGCACACAGTTCAACCCTGATGATAAGTCAGCACAGCATCATAACGCTCATCACTGTTTGGAGATCACGGTTAACTGCAGCCCCAATATCGACCACTGCGTTATCCGCAGCACCTGCACAGGTACCTTTCATTTAGATTACAGACTTAGTAAAAACATTTGTTGGAAATAAATATTTTATATCAGTATTAAGGAGAGAGTTCATCAAAACTGGATCAAAACCTTTGAGTTTGTTTTTCTGTTAAAGACAAAAGAAGTTATTTTGAAGAATGTTATAAATTGGTAACTATTTACCTCTATAGAAAAAAATATATATATACAGAAGATTTTCTTATATCATTTTTTAACATTTTTTAAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18066
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112918 | Essential Splice Site | 385 | 929 | 13 | 26 |
Genomic Location (Zv9):
Chromosome 12 (position 26363295)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 24735736 |
GRCz11 | 12 | 24856955 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACTGCAGCCCCAATATCGACCACTGCGTTATCCGCAGCACCTGCACAGG[T/C]ACCTTTCATTTAGATTAYAGACTTAGTAAAAACATTTGTTKGAAATAAAT
Long Flanking Sequence:
TTGGGCGTAACATCATAAAAACACTCCTAAAGGTTTGAAACTATTAGAGGTGAATATATAAAGTGCACATAAAAGTGCACCAGACTGTTATCCTAAAGTCACCAACATCCCTGTTTTCCGTCCTTTCAGCCTCAGGGAAGGTAGCTGATAAGGTCGTCATTGAAAACACTAGAGATTCAACGTTTGTTTTTATGGAGGGATCTGAAGATGCATATGTGGGCTACATGACTATCAGGGTAAGACCAACAGTATTTTTATTTTTTAAGTTATTTACATTTAGCGCATTATTTTATTGCAAACATCAGTTTTTATTATTTTAATCATGATGTTAAAAGTTGCAACAAATCATGTTTTTGCATGTGTGTTGTATTGCTGTTTCGCACACAGTTCAACCCTGATGATAAGTCAGCACAGCATCATAACGCTCATCACTGTTTGGAGATCACGGTTAACTGCAGCCCCAATATCGACCACTGCGTTATCCGCAGCACCTGCACAGG[T/C]ACCTTTCATTTAGATTACAGACTTAGTAAAAACATTTGTTGGAAATAAATATTTTATATCAGTATTAAGGAGAGAGTTCATCAAAACTGGATCAAAACCTTTGAGTTTGTTTTTCTGTTAAAGACAAAAGAAGTTATTTTGAAGAATGTTATAAATTGGTAACTATTTACCTCTATAGAAAAAAATATATATATACAGAAGATTTTCTTATATCATTTTTTAACATTTTTTAAAATAACTTTTGTGTTCAACTGAAAAAGAGACTTAAGGCTGGCTTATACTTCTGTGTCAAGGCTGCGGCGGCCTATACCTGTGTGATTGACGCAGAACTATAAATCAGCCTTTAAACAGGTTTATTTTTGACTATGTTTTTGGTTTTATTTATCAGCGATCCCTTTAATGTATTTTACTCCCACTTTGATCAGTATATAGAAAACCTGACTCTTAATTTTTGGATAGGAATTTATATCCTGTTTCGAAACAGATGCTTTATACTTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9342
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 |
---|---|---|---|---|---|
ENSDART00000112918 | Essential Splice Site | 781 | 929 | 22 | 26 |
Genomic Location (Zv9):
Chromosome 12 (position 26354650)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 24727091 |
GRCz11 | 12 | 24848310 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGCCACCCGGTGCTGCGGAAGAACCGGATATTTGACGGATTTGCTGCAG[G/A]TCAGTTAAAGGTCTAGGTCAGAAGTGCATACATCTTATGTAACAGTTGTT
Long Flanking Sequence:
TGTTTGAAATCTATTTTTAGGGCTGGGTTTCATTGAGGACAATGAAATCTTTGATAATGCCATGGCGGGGGTGTGGATTAAGACGGACAGCAACCCTACGCTACGCAGGAATAAGATCCATGATGGACGGGATGGGGGCATTTGCATATTCAATGGTGGGAGGGGTAAGAATGCATGGAGTTTTTTTTTTACATTTTTGTTTTCTAAACACAATACAGAAAGTAAAGCTAGTCTGATACCTAGACACGGATCATGGGTCATCTTGAGCTAAATCGCACAATCCTCCTAAGAACGTCTAAAAACTAGGCTTTATCTGTGTCATTAAAGCTAGCCAGTTTGTGTAGCATGATTATCAGAGAAACTAATAATGAATCTTCATGCATGTTCAGGGTTGTTGGAAGAGAACGACATCTTCAGGAATGCACAGGCTGGTGTTCTCATCAGCACGAACAGCCACCCGGTGCTGCGGAAGAACCGGATATTTGACGGATTTGCTGCAG[G/A]TCAGTTAAAGGTCTAGGTCAGAAGTGCATACATCTTATGTAACAGTTGTTTTGCTATATTAATAACTCGTTTAATCCCCCTTTACTTCTGAAGTTCAAGTGCATTGTACTCCTTTGAATATTATACTTGTGAAATTCACTTTATTATTAGGTCACAGTAGTAATCAGTGGAAAACAGCATAGTCACATCTACATTGTCTCAGTTGAAAACAATCAAATTGCAATGTGTTCTACCAACGTGTTACACTATTTAGATGTTCTATATGTGCAAGCAGAAACAATGTAAACAATTCGTGTCATATTTTCATTTAAAAGTTGAATTTGTTGGCCACCAACAAAACTTTTTTAACTTCCAGTTACAGGAACAAAAAACACAGTGGGATTAAATGGTGTTTATTTGTAAATTATGGTAAAATAATTTTATTTAAAAAATCTTAGTTGTCAATAAAACTTGTAGACGTTTTGGAGTGCATGGGATTGGGCTGTTTTTATTATTATTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22099
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 |
---|---|---|---|---|---|
ENSDART00000112918 | Nonsense | 858 | 929 | 25 | 26 |
Genomic Location (Zv9):
Chromosome 12 (position 26353691)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 24726132 |
GRCz11 | 12 | 24847351 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTATTTCACCCTGTTCCATTTTCTCATCTCATCTTAGGTGTCACACCTG[T/A]AACACGACAGACCGGAACGCAATTTGTGTGAATTGTATTAAGAAGTGCCA
Long Flanking Sequence:
GTTTTGGAGTGCATGGGATTGGGCTGTTTTTATTATTATTATTATTATTATTTTTTTTTTTTTTTAATTTGCTGCTCTTTTCCCTGATTTAGGCATTGAAATCACAAATCATGCCACAGCGACTCTCGAAGGCAATCAGATTTTCAACAACAGATTCGGAGGTTTATTTCTAGCCTCTGGTGTCAACGTTACAATGAAAGGTAAGCACTGAAAACTCATTACCAGACAGTTATTTTTACTTTAAATGTCTGTTAATATACATTTTTTCCCATACCTTTCTAGATAATAAAATCATGAACAATCAGGATGCCATAGAGAAGGCGGTGAGCAGAGGTCAGTGCCTGTACAAGATTTCCAGTTACACCAGCTACCCCATGCACGATTTCTACAGGTAAACTGAAAGCAGGCGACACCAAACGGTCTGCTTTGAAAACTAACAGTAATGGTTGCAGTATTTCACCCTGTTCCATTTTCTCATCTCATCTTAGGTGTCACACCTG[T/A]AACACGACAGACCGGAACGCAATTTGTGTGAATTGTATTAAGAAGTGCCACCAAGGGCATGATGTGGAGTTTATACGGCATGATAGGTCAGTGCTATAGCTTCTTGTATGCTGGGATATATATATATATATATATATATATATATATATATATATATATATATTCATGCTTGATACTTTTGTCAAAATACTCCTTTCATTGTTACTGTACTGACGTTGAATGTATGTGATTTCTTTTTTTCTTAGATTTTAATTTGTCTGTAAATATTTTTCAAATTTCTGAAAGTATTTTACTGTCATTGTGTGTGTACTTTTGAGTAAAATCGAGATGAAACAGATTGTTATTAATTTTGTTAATGTTTAGTTTTATTCATTTTTTTTTACGGTTAACTAACTGTTCATTAAATTAGCTGAAAAATTACCCCCAAAGAAAAAGAGCAAAAACATTTGAAAAGTAGCTTTAGAAATAATAGATCATGAAAGTAGATGATTTGAGAAATG
Associated Phenotype:
Not determined