ZMP
acsl3a
Ensembl ID:
ZFIN ID:
Description:
acyl-CoA synthetase long-chain family member 3 [Source:RefSeq peptide;Acc:NP_001038593]
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 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa8864 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16715 | Nonsense | Available for shipment | Available now |
sa32062 | Essential Splice Site | Available for shipment | Available now |
sa39067 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35990 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42620 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa8864
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042884 | Nonsense | 22 | 713 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 15 (position 41726681)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 43052088 |
GRCz11 | 15 | 43008520 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATTTGAGTCCAGCYGTGGTGCTTGTTTTCAGGCTGGTGGTTTGGCTGTA[T/G]TCCCTCATCTCCTACCTGCCGTACCTGTTGCTGAGATCACCTGAGTCTCA
Long Flanking Sequence:
GATTTGTTCATAAATCTGGCCTGAGAGTCAGTCGATCCACTGTTTGTTGCGCTTTCTAATCTCTCTCTCCTCTCACGGCTTCAGGCTTCTTTGTTTAGGTGAACGTCAAGATTATAAAACGGCCATCTACCAAATAATCTCCCATGATCTGCACTGGAATTTTCTGATGCTGGTTAACTGACTGCTTGCTTTTCTTGTTCAGGGTCAAGAGGCTTCGCCGACCGTCTCACAGGAGAAGAGCCAAAAGAAGAGGAGGAAGTGACTTCACAACTAGGTATGTGACGATATCAGATTGTCAAATAGTCATATGGGTGGTGCGGTGGCTCAGTGGTTAGCAATGTCGCCTCACAGCCAAAAGGTCTCTGGTTTGAGTCCTGGCTGGACTGGGATTTCACCACATGCCTAATCACAGCTCTTCCTCTTTCCTCTGTCAGGATGAGGCTGACGCAGGATTTGAGTCCAGCCGTGGTGCTTGTTTTCAGGCTGGTGGTTTGGCTGTA[T/G]TCCCTCATCTCCTACCTGCCGTACCTGTTGCTGAGATCACCTGAGTCTCAGTCGCTGTCGGAGTGCTCGCGGAGGCTGAAGGCACGGTCGGTGAGCGGAGACCCTGCAGGACCGTATCGGGATGTGGCGGCGCTGAAGGGGCTGGAGATGTGTCTGCACCCCGGGATCAACACACTGGATCAGGTGTTCCAGTCCTCCGTCTCCCACTTTCCTAACAGTGACTGTCTGGGCACCAGAGAGTTGCTGAGCGAAGAGGACGAGACTCAAGAGGATGGAAAAGTCTTTAAGAAGGTGTGTACGAGCTGTAAGTCCACAGATCTGAAGCTCTGCAGAAGCCTCTCACATGGGTTTTAAGCTCCACAGGGTGCAATATAATGTTGTCACAATGTTGAATTTCGGTACCTATTCGTTTTTCGATAAAGTTCAAGCGCTGCTCAACAGAAATGACTGTGATTGATCTTGAAGATCATCAGTTCACCGCACTTCACCACTGTTCACCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16715
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042884 | Nonsense | 408 | 713 | 8 | 14 |
Genomic Location (Zv9):
Chromosome 15 (position 41783126)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 43108533 |
GRCz11 | 15 | 43064965 |
KASP Assay ID:
2260-8978.1 (used for ordering genotyping assays)
KASP Sequence:
GAGCAAATGAGTGGATTTCAGAGGACTCTCTTTCTGCTGGCCYACAACTA[C/A]AAGATGGAGCAGCTGGCAATGGGATACAGCACTCCACTGTGTGATAAGTG
Long Flanking Sequence:
TGCAGATCCATCGTTTGAACCACGTTAGTTATAATGTAAAACGCCCATAATGATGCTCTAAACGATGTGGAAAGAATGATGGGGTTCTTCTTTTTGTGCAAATTATATTGTTTTACACGCATTTAAAAACAAACAATCCAATATTAGATTTGGTAAAAACATGAACTCGTTTTCCATATTAACTGAAATATTTGTAAACGTCACATGGACTATAATTCAGAAATATTATTGTTTACATGTTTATTGTTGATGTGTCCCTTGAGGGAAAACAATGTCCGCAAACATTAATATTATGAGGGAGAGAACGAAATCTGATGTTTCAGAACCGAAAGCTTGTGTTTCAGTGATGTCATCAGTTAAGTCTGCAACTTTTTTTTATGCACATACTTTCTCCGTCTCTGTTTGTAGGAAATAATGGATCGCATCTACAAGAATGTGATGCTGAGGGTGGAGCAAATGAGTGGATTTCAGAGGACTCTCTTTCTGCTGGCCTACAACTA[C/A]AAGATGGAGCAGCTGGCAATGGGATACAGCACTCCACTGTGTGATAAGTGTGTCTCTCTTTTACTCACATACACACACACACACACACAAACACAATCATAAACAAAATGTTAGGAACTCTTCAAGACTGGTTTTCAGTCAACACACACACTCTCTCAAGCTTCAGTTTTCCTGTATCCAGGCTGGTGTTCAGGAAGGTTCGGGCTCTGCTGGGTGGGCGTCTGCGTGTGTTGTTGTCAGGCGGAGCTCCTCTGTCTGCGGCGACCCAGCGCTTCATGAACATCTGCTTCTGCTGTCCTGTAGGTCAGGGCTACGGCCTCACCGAGACCTGCGGCGCAGGCACCATCAGCCATCGTGAGACTCGCATCTTCATCAGATACACCAGCACTTCATCATATATTGCATAGATTCAAAATCTCTTTACTGTCTTCACATTTGAAATATCAGATACAGTTAAAGTCAGAATTATTAGTTTGCCAAATGATGTCATTTTTCACAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32062
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042884 | Essential Splice Site | 424 | 713 | 8 | 14 |
Genomic Location (Zv9):
Chromosome 15 (position 41783175)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 43108582 |
GRCz11 | 15 | 43065014 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAGATGGAGCAGCTGGCAATGGGATACAGCACTCCACTGTGTGATAAG[T/C]GTGTCTCTCTTTTACTCACATACACACACACACACACACAAACACAATCA
Long Flanking Sequence:
ATGATGCTCTAAACGATGTGGAAAGAATGATGGGGTTCTTCTTTTTGTGCAAATTATATTGTTTTACACGCATTTAAAAACAAACAATCCAATATTAGATTTGGTAAAAACATGAACTCGTTTTCCATATTAACTGAAATATTTGTAAACGTCACATGGACTATAATTCAGAAATATTATTGTTTACATGTTTATTGTTGATGTGTCCCTTGAGGGAAAACAATGTCCGCAAACATTAATATTATGAGGGAGAGAACGAAATCTGATGTTTCAGAACCGAAAGCTTGTGTTTCAGTGATGTCATCAGTTAAGTCTGCAACTTTTTTTTATGCACATACTTTCTCCGTCTCTGTTTGTAGGAAATAATGGATCGCATCTACAAGAATGTGATGCTGAGGGTGGAGCAAATGAGTGGATTTCAGAGGACTCTCTTTCTGCTGGCCTACAACTACAAGATGGAGCAGCTGGCAATGGGATACAGCACTCCACTGTGTGATAAG[T/C]GTGTCTCTCTTTTACTCACATACACACACACACACACACAAACACAATCATAAACAAAATGTTAGGAACTCTTCAAGACTGGTTTTCAGTCAACACACACACTCTCTCAAGCTTCAGTTTTCCTGTATCCAGGCTGGTGTTCAGGAAGGTTCGGGCTCTGCTGGGTGGGCGTCTGCGTGTGTTGTTGTCAGGCGGAGCTCCTCTGTCTGCGGCGACCCAGCGCTTCATGAACATCTGCTTCTGCTGTCCTGTAGGTCAGGGCTACGGCCTCACCGAGACCTGCGGCGCAGGCACCATCAGCCATCGTGAGACTCGCATCTTCATCAGATACACCAGCACTTCATCATATATTGCATAGATTCAAAATCTCTTTACTGTCTTCACATTTGAAATATCAGATACAGTTAAAGTCAGAATTATTAGTTTGCCAAATGATGTCATTTTTCACAGTAATTCCTATAATATTTTTTATTCTGGAGAAAGTCTTATTTGTTTTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39067
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042884 | Nonsense | 443 | 713 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 15 (position 41783364)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 43108771 |
GRCz11 | 15 | 43065203 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCAGGAAGGTTCGGGCTCTGCTGGGTGGGCGTCTGCGTGTGTTGTTGT[C/A]AGGCGGAGCTCCTCTGTCTGCGGCGACCCAGCGCTTCATGAACATCTGCT
Long Flanking Sequence:
GTTTATTGTTGATGTGTCCCTTGAGGGAAAACAATGTCCGCAAACATTAATATTATGAGGGAGAGAACGAAATCTGATGTTTCAGAACCGAAAGCTTGTGTTTCAGTGATGTCATCAGTTAAGTCTGCAACTTTTTTTTATGCACATACTTTCTCCGTCTCTGTTTGTAGGAAATAATGGATCGCATCTACAAGAATGTGATGCTGAGGGTGGAGCAAATGAGTGGATTTCAGAGGACTCTCTTTCTGCTGGCCTACAACTACAAGATGGAGCAGCTGGCAATGGGATACAGCACTCCACTGTGTGATAAGTGTGTCTCTCTTTTACTCACATACACACACACACACACACAAACACAATCATAAACAAAATGTTAGGAACTCTTCAAGACTGGTTTTCAGTCAACACACACACTCTCTCAAGCTTCAGTTTTCCTGTATCCAGGCTGGTGTTCAGGAAGGTTCGGGCTCTGCTGGGTGGGCGTCTGCGTGTGTTGTTGT[C/A]AGGCGGAGCTCCTCTGTCTGCGGCGACCCAGCGCTTCATGAACATCTGCTTCTGCTGTCCTGTAGGTCAGGGCTACGGCCTCACCGAGACCTGCGGCGCAGGCACCATCAGCCATCGTGAGACTCGCATCTTCATCAGATACACCAGCACTTCATCATATATTGCATAGATTCAAAATCTCTTTACTGTCTTCACATTTGAAATATCAGATACAGTTAAAGTCAGAATTATTAGTTTGCCAAATGATGTCATTTTTCACAGTAATTCCTATAATATTTTTTATTCTGGAGAAAGTCTTATTTGTTTTATTTTGACTAAAATAAAAGCTGTTTTTACTTTTTTAAGGTCAATATTATTAGCCCCCTTAAGCAATATTATTTTTTGATTGTATCCAGAACAAACCATCGTTATACAATAACTTGCCTAATTAATTTAATTAACCCAGTTAAACATTTAAATGTCACTTTAAGCTGTATAAGTGTCTTGAAATTACTGTCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35990
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042884 | Nonsense | 504 | 713 | 10 | 14 |
Genomic Location (Zv9):
Chromosome 15 (position 41785532)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 43110939 |
GRCz11 | 15 | 43067371 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGAGAGTTGGAGCACCGCTGGTCTGCTGTGAACTTCAGCTGAAGGACTG[G/A]ATAGAGGGTGAGTCTCGTAGCATACACACATGCATATATCTGCTCTTATG
Long Flanking Sequence:
CAGACTGACATTATAAGTGAACCCGAGAGTCCAAACAAACAAACATGATGTTACCATATTAATATGCACCAATCATAATATTCAAAATATCTGTAATTGTGTGATTAATAAGAAAATTACATTAACCAGAAGTCCATCCAAATAAAACTAGGTCACCAAATCCTGATCCTCGGCATTCGCAGGGAAAACAAAGCATCATCATGAACATGTGCAAAAGATGTAAAATGATTTGAGTTTGAGTTCTCGGAGGACTCTGTGGTGAGCCCCATGCAGCTGCTGACTTCTCAAATATGAGCGTTTTTATTGAAGATGCATATTTAGTCATCACTGTTTTTTTTTTGTGTGCAATGGAAATAATTACATAACTGCAGCCTTACAGCCAAAGCACAGATTGTTTTATGTGATGTTATTGTCTATATGTGTGTGTGTGTAGTGTGGGATTACAGTACAGGGAGAGTTGGAGCACCGCTGGTCTGCTGTGAACTTCAGCTGAAGGACTG[G/A]ATAGAGGGTGAGTCTCGTAGCATACACACATGCATATATCTGCTCTTATGAAAACACTGTCACACGCGTTTACCCATCCGTCAGGCCATATGTCTGCTCGTTTGCTACCTCGAGGGAAGGACGAGCAATAAAACAACAGAACAAAAGAGAAGGAAGTGGAACAAAAAAAAGTATTTATGGTTATCATTTGCGGCCTTGTAAGGAAGACATTTTTAGCGGCTGCTTCTTTAGTGGTTTTCGGTTTTTCTCTTAATGAATCAAACTCAGTCCGGAGGTTATGAATATCAGAAGAGTATACTTTATTGTGGACAACAAAGGAGATTTTTCAGGAGACCCCCGGTAACATCTCTGCCTGAAAATCAAGGAATCAAGTCTCACTGATGTTCTGGCCTGCTTATATACTCTTTTGCAACTGTTTTTCACATTGTTCTACATATGTCACACAAGATCCCACCTAGTTTAACCCCTGACCCCAAATTACACCTAGTTTAACCCCTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42620
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042884 | Nonsense | 694 | 713 | 14 | 14 |
Genomic Location (Zv9):
Chromosome 15 (position 41796641)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 43122048 |
GRCz11 | 15 | 43078480 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAGCCCTGGACCCCAGACACCGGCCTGGTTACAGACTCTTTCAAACTC[A/T]AGAGAAAGGAGCTAAAAACTCACTACCAGAACGACATCGAGAGGATGTAC
Long Flanking Sequence:
TTTCAAACCTTTATGAGTTTCATTCTTCTGTTAAAGAAGATATTTTAAAGAATGCTGAAAACCATTGACGTCCATAGTATCAGTTTTTCCAATGTAAGTCAATGGTTACAGGCTTTCAGCATTCTTCAAAATATGTTCTTTGGTGTTCAACAGAAGAAAGGAACTCATAAAGGTTTGTAACCTCTTAAGGATGAATAAATAGTGAGTAATTTTACATTTTTGGGTGAACTATCCCTTTAATTGTGTATATAGAAGTGTTTCATTAAATTCTATAAACATGACCAATGTCACAGCATGCTGATAAAGTTTTAGGAGCTCCAGCTATTTGTTGTTCTTCCTGTTTCACCACTGTATATAACCATCTGTGATTATGATTCATTTCCTGCTGCTGTGTGTATTTAACAGCCCAGCTAGAAAGATTCGAGATTCCCCGGAAGATCCGCTTGAGCGTTGAGCCCTGGACCCCAGACACCGGCCTGGTTACAGACTCTTTCAAACTC[A/T]AGAGAAAGGAGCTAAAAACTCACTACCAGAACGACATCGAGAGGATGTACGGAGCCAAGTAAGAGGCAAATCACGGGACAGGAAGGCAAGAAAAAGTAACTGATCTCATTACAGCAACATCCAATCAGGATGGAGATTTCCAGTGGACGCTGCAGACCTGAACACTGATCATTTGGAGATGTTTACACACAACTGAGTGGTGTTTTTGTGTGATATCAGAAAATGGTACTAAAACACTAAAGCAGTACTTAAAGGAATAGTTCACCCCAAAATGACTCTCATTTAAGGCATCTGTAAACAGTTGAAGTCAAAATTATTAGCCCTCCAGTCAATTCTTTTTCAAATATTTCTCAAATAATAATTAACAGATTTAGGAATTTTTCACAGTATTTCCGATAATATTTTTTCTTCTGGAAAAAGTCTTATTTGTTTTATTTTGTCTAGAATAAAACCAGTTTTAATGTTTGTTTAATTATTTTAAGGTCAATATTATTAGCCCC
Associated Phenotype:
Not determined