LOC562292

Ensembl ID:
ENSDARG00000059503
Human Orthologue:
ACSF3
Human Description:
acyl-CoA synthetase family member 3 [Source:HGNC Symbol;Acc:27288]
Mouse Orthologue:
Acsf3
Mouse Description:
acyl-CoA synthetase family member 3 Gene [Source:MGI Symbol;Acc:MGI:2182591]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa31603 Essential Splice Site Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
sa31603
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:
G > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000082780 Essential Splice Site 270 564 4 11
Genomic Location (Zv9):
Chromosome 7 (position 57219175)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 55654501
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TGTGGGTCGGAGCCACCTGTATCATGCTGCCAGATTTCAGTGCTCAGAAG[G/A]TAAACCTTTAGCTTTAAATACACCAAATTTGAATATCACACTTTCACGCA
Associated Phenotype:
Not determined

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