ZMP
acsl1
Ensembl ID:
ZFIN ID:
Description:
acyl-CoA synthetase long-chain family member 1 [Source:RefSeq peptide;Acc:NP_001027007]
Human Orthologue:
ACSL1
Human Description:
acyl-CoA synthetase long-chain family member 1 [Source:HGNC Symbol;Acc:3569]
Mouse Orthologue:
Acsl1
Mouse Description:
acyl-CoA synthetase long-chain family member 1 Gene [Source:MGI Symbol;Acc:MGI:102797]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11697 | Essential Splice Site | Available for shipment | Available now |
sa13904 | Nonsense | Available for shipment | Available now |
sa19462 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11697
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000039917 | Essential Splice Site | 125 | 697 | 4 | 21 |
ENSDART00000125125 | Essential Splice Site | 125 | 697 | 4 | 21 |
ENSDART00000146946 | None | 125 | 125 | 4 | 4 |
The following transcripts of ENSDARG00000030514 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 16297838)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 16863006 |
GRCz11 | 1 | 17555943 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGGGTCGCGAAAGGCAGGCCAGCCATATAAATGGCTGTCRTATAAGGAG[G/A]TAAGATTTGTGAAATAATTATTGACCTAATTGCAGAACGCATTTAGCTTT
Long Flanking Sequence:
ATAGGTAAAAACATGACCTTGGAGTGTGTTTATTCCTGCTTTAAGCATTAAATGATTTGATCATTTATGTCTTCAAATCTAAATGGTGTTAAAAGATTGTACAGGTGAAGTTTCTCTTCATGGCCTTGTAGATTATCAACAGGCCTGGATTTGAGGAGCTGGTATTTGCTTGTTTGCTAAAGTTTATCATAGACTGTTGGTTGTGTTTTTCAGGGTAAGGAATATGCACGTCGCTCTATCCTAATGGACAATGACACACACATGACGTACTACTATAAAGACGCTCTGACACTGTATGAGTTTTTCTTACGAGGACTACGAGTGTCAAGTGAGTTATCCGGCCATTTAAAGCAGACATTGTGACAAAGGAATAGTTTAAAATAAGCTATTAAAATGGTTAAAATCATGATCTACATTTTTGTTTTACTCACACAGACAATGGTCCTTGTTTGGGGTCGCGAAAGGCAGGCCAGCCATATAAATGGCTGTCGTATAAGGAG[G/A]TAAGATTTGTGAAATAATTATTGACCTAATTGCAGAACGCATTTAGCTTTTTATTTTTCTCTCTATATTTTTTATTCCCTTAATATTTAGATATTATCAGATATGTATGTGCATTGTAATTATTAATCAGTTGTTATTACTTTATTTTGATGCTCTCTTTAACACATTTTGTTGATCGTTGGTTACATTGCAACTACGTTCCAACTAATTCTCAGTAGAGTATTAGTAGGCTGTAAGGTTTGGGTTAGTGTAAGTTGACATATTTGAAAGGTTTGTTATTATCGGTTGAATGTCTGTTGATGGTGTGGTATCAGCAGATATTGAGCAGACAGTCTTATAATCTAATTAGTTGGCATATAGTAGTTGCAATGCGACCTAAAGTCAATAAAATGTTCAAAAAGAACCAACAAATAAATGACAGCAATTAGTTTAGTATTTTTGTGTGTAGGTTGCAGACAGGGCAGAGTTTGCAGGTTCAGCTTTACTCCACAGAGGTCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13904
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000039917 | Nonsense | 212 | 697 | 7 | 21 |
ENSDART00000125125 | Nonsense | 212 | 697 | 7 | 21 |
ENSDART00000146946 | None | None | 125 | None | 4 |
The following transcripts of ENSDARG00000030514 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 16296041)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 16861209 |
GRCz11 | 1 | 17554146 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACYACCATCATCTGTGACATCGCGGATAAAGCTCGTCTGATCCTGGACTG[T/A]GTGTCTGGCCGGAAGCACAGCGTCACGACTATAGTKATCATGGAGAGCTT
Long Flanking Sequence:
CACAGGCTGGATTGCTGCTATTCGTGACAACGGTGTTACACCAGAAGTCAGTCAAGAAGTGCACATTCGGTAGTTGCCGGTATTCAGTGATTTGAGTTTATAATTAAAAAATGACACATCAGTCAGCTTAAGATGTCCGTTATCCCCCTGGTGGTGTATGGGTTAATTTTACAACACATTATTGCACTTTTGTAAACTTAAAATGCAAATGGAAAAGCCAGGATGAAATTTAAAACTACTTTAACTGTGCTCATCTGAAAGACAAAAGTCATACACACCGTGGATGGCTTAAGGGTTAAGTACATTACAGTTAAATTGTCATTTTTGGATTAGCTAACTCATTAAATAATTAAATAATGGCTTAAAGCTTGTATCACATGACTGCACAAAAACAGTAAAACTTGTGAGAAATGTGTTTTGAGTAACAGAGCTTTTGTCGTAGCTTCCATCACCACCATCATCTGTGACATCGCGGATAAAGCTCGTCTGATCCTGGACTG[T/A]GTGTCTGGCCGGAAGCACAGCGTCACGACTATAGTGATCATGGAGAGCTTTGACAGTGAGCTGACAGCACAAGCACAAAACTGTGGCATCGACATTATCAGCCTCAAGGAGCTGGAGGTTTCTCTCCCACACGCACACACACACACCCTTCTTTTGTAAATAGTGATCCCATTAAACGTGTATTTACACTGCACTAAATAAAGTCTTTTTTTTTCAGGCTATTGGCAAAGCAAACCACAAGACACCCATTGTAAGTTAAACTGAGCACTGTATTGATTTACAGACATGCAACATTGTGTTCTGTATACTTGGTGCAATGTGGCCCTAGGCGCAGGGCAAGTGCTTTTGGCTAGTTTCGACCTGTTGCAGTTATCATTTTCATGTTTTATGCCACCCTTTGATGCTTACGATAACATTGATGTGATCAGTAAACTGATTTTTAACAGACTTAATCGTTTATTTTATTTTCAATTGTGTAATGTTTGTTATGCATTTTATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19462
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000039917 | Nonsense | 614 | 697 | 19 | 21 |
ENSDART00000125125 | Nonsense | 614 | 697 | 19 | 21 |
ENSDART00000146946 | None | None | 125 | None | 4 |
The following transcripts of ENSDARG00000030514 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 16284825)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 16849993 |
GRCz11 | 1 | 17542930 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGTGTTGTGGTTCCTGATCCAGACTTTTTGCCAGGATGGGCAAAGAAT[A/T]GAGGCATTGAGGGATCCTTCAATGACTTGTGCAAAAGCAAGGTAAAACAC
Long Flanking Sequence:
GTCGTGTTTTATTTTTTACATTATTGCACATCCCTATGTAGGAAGAACGTCCAGTGTTCTCCAACGCTGAGGAGAAATGGTCATGCCCGACTGAGCCTGGTTTCTCTAGAGGTTTTCTTTTTCCTTCACTTTTGTCAATTGGTGAAGTTTTGTTCCTCGCCACTGGCTTGCTTGGTTTGGGACTTCCCATCGATGGATTTGCTCTTCAGTGTTTGAACTTTCAGCAGTGAAATTTAAACCACACTGAACTGAACCAAAACTGAACTTCAACTCTGAAAACTGGACTAACACCATCTCATTTACTAAAACCTCTATGTTAAGCTGCTTTGACACAATCTACATTGTAAAAGCGCTGTAGAAATAAAGATGAATTGACTTCAAAAGAAGTGTGAGAATAGAATATATGTGAGCATAAACCCATCCTGTTTCTCTCTTTTTAGGCATGTTTAGTGGGTGTTGTGGTTCCTGATCCAGACTTTTTGCCAGGATGGGCAAAGAAT[A/T]GAGGCATTGAGGGATCCTTCAATGACTTGTGCAAAAGCAAGGTAAAACACGGAACACAGAAAAAAGACGTTTACAAGATCTGGATTCAGCATAGTAGAGTACAGATAATAGTGTTCAGAGGTTTACTACCATTTTCAGCTAAAACATTTAATTGAAGAAATGGCTCCATTGGGGCATTACAAGTGATGCAAATTACTGTATATAATAGAATGACATTTCTAAGTAACTATAAAGTAAATGAATTAAAATTAGTCACAATGATTGTAGTCATAAGCAGTCAATGAAAGAATGTGCTCAATATTTTGAACGCATCGAGGAAAAGGGGATTGTCTTAATGGACAGTGATTTATCTTAAGATAAATAGTAGAAAAGAAGCAAACACATTGCTTTAAACTTTCATTAATCTGTGTATACACCGGCATGAAGAGCTCTGAGGTCAGATAACATTATCCTAAAATATATATTTGATGTGTTTTGTCAAAGGTAAATGAATGTGTAGG
Associated Phenotype:
Not determined