ZMP
acsl3b
Ensembl ID:
ZFIN ID:
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 |
---|---|---|---|
sa39930 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa2049 | Essential Splice Site | F2 line generated | Not yet available |
sa15610 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39930
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
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 |
GRCz11 | 2 | 47495086 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGAATGGGTCATAGCGGCACAGGCTTGCTTCATGTACAATTTCCCCTG[T/A]GAGCATTCGGAACACACACACACACACACACACACACAAACACACACACA
Long Flanking Sequence:
GCAAAGAGTCTTAAAAGGTATTAAATTTCCATCTCTGACGCCTGTATCCTGATCATGCGGCCCCAATTTAGAAACCAGCAGTTTAAATACTCAAGTATATTTCGAAGGTCTCTCTAAGATCATGTGTACACATCTCAAGAGACCTCACTCAAAGACTCTATTGAAAGAAGTTCATTGGCCGTCTATCTCTGTAAACACTGTGTATCTCTGCTCTGGTGTTGTCCAGACCTGTTTACATTAAACTGAAAAGCAGTCACATGCTGCTGTCAAGGCCATCGATACAATACAATGCCACTCTGACTTGTCTCTCGTTCTCTCTAGGTGATTTTGGGCGATTATAACTGGTTGTCGTATCAAGACACTTTCCATCTGGCTCAGAGGTTTGGAAGTGGACTGGCTGCGCTGGGTCAGAAGCCTCTCTGCAACATCGCTATTTTTTGCGAGACTCGAGCTGAATGGGTCATAGCGGCACAGGCTTGCTTCATGTACAATTTCCCCTG[T/A]GAGCATTCGGAACACACACACACACACACACACACACAAACACACACACACATACATAGTGTTGCCTCCAATAGCTGCCATATTGTGCTGACTAGGAAAAAATATTTGGCCAAAAATAGCACTGCTAGGGTGGTTGATGCTAGACAGTATCACTGAAATCAGAGCATTTACTCTCTTGAAATTGATACTATACATACAAAATATGCATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAAAAATATATATATATAAAAAAAAAATATATATATATATATGTTATATGTTAATTTCTTATAACTATAACTATTTATATTATTTGTTATATTCATTTACTATCCCTCGATATAACGCGGCCCTGCCTCGTAGTTCGCCAAATTTTTTTTTGTGCAGTTTGACATGCTTTTTTTAACAGCGCATTGTGTGCTACATCCTGATTAGCTGTAAACCATTGTCAATCAATCTCCTCATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2049
Status:
F2 line generated
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 |
---|---|---|---|---|---|
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 |
GRCz11 | 2 | 47503270 |
KASP Assay ID:
554-2998.1 (used for ordering genotyping assays)
KASP Sequence:
TACAAAATGGAGCAGATCTCCAAAGGATACACCACACCGCTYTGCGACAG[G/A]TACAACGCAATGCTMAATATRATATTAAAGAGCTCTATATAGTTTTTTNA
Long Flanking Sequence:
GTACTGAACCATGATTTTTGTGAACTTTACACCCCAAATATTTATAGTTATTAGACTGGATCAACAGATACTATTTTTGGAACACCCTCAAAATGAATGAGAAACAAATATTGGATTTCATTCAGTGAAAAGTGATGCAGGGGAGTAAAATAATGCAGAGTGAATCAAAGATTGTAATACTATATCATATTTTTCTCCTCACAGTCATCTAAAATTAAAAAGGGCAGTAAAGGAGACACCAGCGTCCTCAAACCAACACTGATGGCAGCTGTTCCTGTAAGAAACCTTGCATTCACACAAACACAAACACACACTGGTCAGAATAGCCGCATGTCTGTAAAACTTCCCTCTTTTCTTTAGGAGATTATGGATCGTATCTATAAGAATGTGATGACTAAAGTTGAAGAGATGAGCAGTGTCCAGAAAACACTCTTTGTTTTGGCGTACAACTACAAAATGGAGCAGATCTCCAAAGGATACACCACACCGCTCTGCGACAG[G/A]TACAACGCAATGCTAAATATGATATTAAAGAGCTCTATATAGTTTTTTTAGCAATCATGTAGTGTGTTTAGTGTGGTAAAAGTTTAAAATATCATAAAAAAGCAGCTAGCGTCTCTAATTAGAACCAGTTGTAGTAAAAAAAAAGGTAATGTCAGCCTTGCATTCTGGGTAAGTTTGTAAAAATGAGCATAACGCAAGCTTATGGTGTTCATTGGTCTTCTTTAACCCTTTAAACTCTATAGGTGTACCTGTGACCTAAAAAAAGTTTGGTTTTATGTGGTTAGCATGTTTAGAAGATGCTGTTTGGTTTGTGCTGCAAAAATGAATTGAAAAATCAATCACTGATGGGTTGAACAGACACTTTATTACAAGTACACCGTTACTAACAGCGTTACTTTTTTCTTTAACGAGTAATCAAATTAATTACTGTTTCCCCTGTTACAACGCCGTTACTATTATTGACAATAAAACGCGTGTTACTATAATTGAGAATGGTTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15610
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
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 |
GRCz11 | 2 | 47510934 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAAGTCATTTCTACACAATWTTTACTAATTAATTGTGACNTCTGTGTGT[A/T]GATCGAAAGAAGGACCTAGTGAAGTTGCAARCTGGTGAATATGTGTCTTT
Long Flanking Sequence:
GCAGGGCTGAGCCTGGTCAGTACCTATATGGGAGACCACATGGGAAAACTAGGTTGCTGTTGGAAGTGGTGTTAGTGAGGCCAGTAGGGGGTCTGCGTAAGTCCTAATGCCCCAGTAAAAGTAAAGAGGACATCTTTCGGATGAGACGTTAAACAGGTCCCGACTCTCTCTGTGGTCATTAAAAATCCCATGGCACTTCTCGTAAAGTGTACGGGTGTAACCCCGGTGTCCTGGCCAAATTCCCTTCATCAGCCCTTAACTATCATGGCTTCCCAATCAACCCTTATCTACCGAATTGGCTCTATCACTGTCTCTTCGCTCCTCCTATAGCTGGTGTGTGGTGAGCGCAGTTGCACCATTGACCTGTGGCTGCCCCCCCTCATGATTGTGAAGCGCTTTGAGTGTGTGCGCTATACAAATACTCACATTACATTTAAATATAAGCATTATCAAAGTCATTTCTACACAATTTTTACTAATTAATTGTGACATCTGTGTGT[A/T]GATCGAAAGAAGGACCTAGTGAAGTTGCAAGCTGGTGAATATGTGTCTTTAGGCAAAGTGGAGGCTGTGCTCAAAAACTGCCCACTCATCGACAACATCTGTGCTTACGCCAACAGGTACAATTACACAATAAACACACTTGCCAAAAAAAAAAAAAAAATACACACACTGTGACAGTTTGACATGCTCGCTTTTCAAATATAGCATTCATGTAAAGGCTGTTCTGTCTGAAATGTATAAACCTCTCCTTCTCTATACACAGCGATGAATCTTATGTGATTGGGTTTGTGGTGCCCAATCAGAAGCAGCTAACCGCTCTTGCTGGGCAGAAGGGCATCAGGGGATCATGGGAAGAGATCTGCAACCATGCAGAGATGGAGAAAGAGGTTCTACGTATCATCACAGATGCAGCGATTTCAGGTTTGTAAGCAGTGAAGCAAAATAAGTTGGAATTTAAAGAGCCCATATTATGGGTTTTTGAAAATGCCCCTCCATGTAGT
Associated Phenotype:
Not determined