NP_001182055.1

Ensembl ID:
ENSDARG00000086055
Description:
forkhead box L1-like [Source:RefSeq peptide;Acc:NP_001182055]
Human Orthologue:
FOXJ1
Human Description:
forkhead box J1 [Source:HGNC Symbol;Acc:3816]
Mouse Orthologue:
Foxj1
Mouse Description:
forkhead box J1 Gene [Source:MGI Symbol;Acc:MGI:1347474]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa42007 Essential Splice Site Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
sa42007
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 2017.
Mutation:
T > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000123315 Essential Splice Site 37 220 1 3
Genomic Location (Zv9):
Chromosome 12 (position 19384264)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 18236425
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CGTCATGTGGCACTGATGAAGAAAAGAAAGTGTGTCGACCAGCTTACAGG[T/A]ATTTCATTGTTGTTGTTGTTGTTGTTGTTATTGCTATTTGTTTTTGTTGC
Associated Phenotype:
Not determined

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