acsl3b

Ensembl ID:
ENSDARG00000014674
ZFIN ID:
ZDB-GENE-030131-492
Description:
Novel protein similar to H.sapiens ACSL3, acyl-CoA synthetase long-chain family member 3 (ACSL3) [So
Human Orthologue:
ACSL3
Human Description:
acyl-CoA synthetase long-chain family member 3 [Source:HGNC Symbol;Acc:3570]
Mouse Orthologue:
Acsl3
Mouse Description:
acyl-CoA synthetase long-chain family member 3 Gene [Source:MGI Symbol;Acc:MGI:1921455]

Alleles

There are 3 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa39930 Essential Splice Site Mutation detected in F1 DNA During 2016
sa2049 Essential Splice Site F2 line generated During 2016
sa15610 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa39930
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:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000074968 Essential Splice Site 189 723 4 16
ENSDART00000141974 Essential Splice Site 177 711 5 17
Genomic Location (Zv9):
Chromosome 2 (position 47517216)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 47642582
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GCTGAATGGGTCATAGCGGCACAGGCTTGCTTCATGTACAATTTCCCCTG[T/A]GAGCATTCGGAACACACACACACACACACACACACACAAACACACACACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2049
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:
G > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000074968 Essential Splice Site 434 723 10 16
ENSDART00000141974 Essential Splice Site 422 711 11 17
Genomic Location (Zv9):
Chromosome 2 (position 47509032)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 47650766
KASP Assay ID:
554-2998.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
TACAAAATGGAGCAGATCTCCAAAGGATACACCACACCGCTYTGCGACAG[G/A]TACAACGCAATGCTMAATATRATATTAAAGAGCTCTATATAGTTTTTTNA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15610
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
A > T
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000074968 Essential Splice Site 581 723 14 16
ENSDART00000141974 Essential Splice Site 569 711 15 17
Genomic Location (Zv9):
Chromosome 2 (position 47501368)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 47658430
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
CAAAGTCATTTCTACACAATWTTTACTAATTAATTGTGACNTCTGTGTGT[A/T]GATCGAAAGAAGGACCTAGTGAAGTTGCAARCTGGTGAATATGTGTCTTT
Associated Phenotype:
Not determined

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