fbxl18

Ensembl ID:
ENSDARG00000007443
ZFIN ID:
ZDB-GENE-050913-65
Description:
F-box/LRR-repeat protein 18 [Source:RefSeq peptide;Acc:NP_001025416]
Human Orthologue:
FBXL18
Human Description:
F-box and leucine-rich repeat protein 18 [Source:HGNC Symbol;Acc:21874]
Mouse Orthologue:
Fbxl18
Mouse Description:
F-box and leucine-rich repeat protein 18 Gene [Source:MGI Symbol;Acc:MGI:2444450]

Alleles

There are 4 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa39545 Nonsense Mutation detected in F1 DNA During 2016
sa767 Nonsense F2 line generated During 2016
sa9554 Nonsense Available for shipment Available now
sa19420 Nonsense Mutation detected in F1 DNA During 2016

Mutation Details

Allele Name:
sa39545
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
T > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103644 Nonsense 118 720 3 5
Genomic Location (Zv9):
Chromosome 1 (position 7720202)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 7960007
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GGCCGGCTCTACAGTGGATCAGGTCACCCGCTGTAAGTCTTTGGTCAGTT[T/A]GGACCTTTCCGGCTGCAGATTGACATCAGTTCGCCTCTCGCATCTGCTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa767
Current Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
T > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103644 Nonsense 307 720 3 5
Genomic Location (Zv9):
Chromosome 1 (position 7719635)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 7959440
KASP Assay ID:
554-0673.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
TTTGCAGCTTCCACGTACATGGTTGGACGGTGCTATACTTGGGCGGGTRT[T/A]AGCGCATGGATGTCCTGCATACCTGAATGTCTCCCGGTGTTCATCTCCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9554
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103644 Nonsense 598 720 3 5
Genomic Location (Zv9):
Chromosome 1 (position 7718762)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 7958567
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
CACGCAGGCCCTGCTGGAGGCTCTTTCCTACTGCACACAASTCAGGGAST[T/A]AAGGTGAGCGTGCAYGCCAATACTCAAAAKGTAATCAATAAGGTTGTTGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19420
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
T > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103644 Nonsense 625 720 4 5
Genomic Location (Zv9):
Chromosome 1 (position 7716045)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 7955850
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GCAGCGTTTTTCGAAGCGCTCAGTCAGTGTGGTCAGCTGCGGCGTCTGTG[T/A]TTAGTTTCTCGACACGGCACTTTCCAACCCGCCGCTGTGACGGCCTTCAT
Associated Phenotype:
Not determined

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