ZMP
LOC100332846
Ensembl ID:
Human Orthologues:
ACSL1, ACSL5, ACSL6
Human Descriptions:
acyl-CoA synthetase long-chain family member 1 [Source:HGNC Symbol;Acc:3569]
acyl-CoA synthetase long-chain family member 5 [Source:HGNC Symbol;Acc:16526]
acyl-CoA synthetase long-chain family member 6 [Source:HGNC Symbol;Acc:16496]
acyl-CoA synthetase long-chain family member 5 [Source:HGNC Symbol;Acc:16526]
acyl-CoA synthetase long-chain family member 6 [Source:HGNC Symbol;Acc:16496]
Mouse Orthologues:
Acsl1, Acsl5, Acsl6
Mouse Descriptions:
acyl-CoA synthetase long-chain family member 1 Gene [Source:MGI Symbol;Acc:MGI:102797]
acyl-CoA synthetase long-chain family member 5 Gene [Source:MGI Symbol;Acc:MGI:1919129]
acyl-CoA synthetase long-chain family member 6 Gene [Source:MGI Symbol;Acc:MGI:894291]
acyl-CoA synthetase long-chain family member 5 Gene [Source:MGI Symbol;Acc:MGI:1919129]
acyl-CoA synthetase long-chain family member 6 Gene [Source:MGI Symbol;Acc:MGI:894291]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12007 | Essential Splice Site | Available for shipment | Available now |
sa18353 | Nonsense | Available for shipment | Available now |
sa15288 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12007
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 |
---|---|---|---|---|---|
ENSDART00000053750 | Essential Splice Site | 280 | 685 | 7 | 19 |
Genomic Location (Zv9):
Chromosome 8 (position 53109523)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 50872083 |
GRCz11 | 8 | 50860792 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTGTGTGCTTCACAGGATCTGGGAAGAGAAAATTTAAAGCCACCTGTGG[T/C]AAGAGCTTCTTTTAATTTCCCTTCATTAMTTAAAGGACTTTCAGCAYGTT
Long Flanking Sequence:
TGTTCTTCATTTAAGACAAAATAAATCTTTATTTATCCTGAAGGAAGGCCATTCGTTAAGAAAACAACAAAATACAAAGACATACTAAATATAGAAATAAATTAATCCAATAATAATAATAAAGAAAAAACAATAAATAAATAAATAAATAAATTAATTAATTAATAAAAATGCTCATTAAGTAACATATAACAATAATACTAATAGTAGTAATTATGATGATAATAATGATAATGATAATAATAATAATAATAATAATAATAATAATAATAATAATACTTTGAACTGAGTAGAAAGACAGAGACAGTATTTTACTTTCTAACTTTATTTATTATCTTTAAAATGAACACCAATAAAGTGTATGTAAACATCTTCTAGTGCAATTAAAATAATTAATATGATAAAGGTTTGCTTGTAAATATGGATGCTTCTGTAAGTTGATCCAAGGTGTTTGTGTGCTTCACAGGATCTGGGAAGAGAAAATTTAAAGCCACCTGTGG[T/C]AAGAGCTTCTTTTAATTTCCCTTCATTACTTAAAGGACTTTCAGCACGTTTACAGATATAAGAGGAGTATTAATGCAGTTGGTCTTCGTCATCTAGATCTGTTTCTTGGTGTTTTGATCTGTATTTGTGTTGCTTGCTTGTTTTGTATTGGTCTTAGCCTCCTAAACCTCAAGATCTGGCTGTTGTGTGTTTCACCAGTGGGACAACAGGTACTGAGAAACTAATGCTTCAAATCACACTTTATAGATTTCGTTTGCAAACCACAAAACTAATCATAAGAGTTCATGTTTTAATATTGAGATTTATACATCACATGACGAAAGGACAGGACAATATTTGGTGGAGAGACTACTGTTTGAAAATCTAGAATCTGTGGGTTCAAAAAACAAAACACTTAGAAAACACCTATACACACTCATACATTCATTTATTCATTCATTCATTTTTTTAAATCAGTCCCTTATTTATCAGGGGTTGCCACAGTGTAATGAACTGCCAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18353
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000053750 | Nonsense | 438 | 685 | 12 | 19 |
Genomic Location (Zv9):
Chromosome 8 (position 53102515)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 50864641 |
GRCz11 | 8 | 50853277 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGTCGTGAGGAACAMCAGCCTGTGGGACAGACTCATCTTCAATAAGATA[C/T]AGGTATAAGACTCGTAAGGTGTTTTTGGAAAAATAAAGATAYATRCAGTT
Long Flanking Sequence:
TGTCAAAAATCCCTGCTCTGTTAAACATCATTTGGGAAGTATTTAAAAATTCACAGGAGGGCGAATAATTTTGACTTTCCTTTTGTGTTTCTCTCTCCCTCAAGTTATCTTGACGTTTGGATGATGTTTTCCTCCTTCTCTCTTCCTCAGGTGTCGATGTTTTGTCACGGGGCGAGGGTCGGCTTTTACCAGGGTGATATTTCTCTGCTGATGGATGACATAAAGACCCTGAAGCCCACTTTTTTCCCTGGGGTCCCTCGATTACTCAACCGCATCTACGACAAGGTCTGTGCTACACATCAGTGTTTGACGGATTGAGTTGTTGGGTCTCTGTGTTAAAGTGATGGATGTCGTGAATCTGTGTGTAGATTCTGGGCTCGGTTACGTCTCCGCTGAAAAGAGTCCTCCTTCATTATGCCGTCAGGAGGAAACAGGCAGAACTGAGCAGTGGAGTCGTGAGGAACAACAGCCTGTGGGACAGACTCATCTTCAATAAGATA[C/T]AGGTATAAGACTCGTAAGGTGTTTTTGGAAAAATAAAGATATATACAGTTGAATTTAGAATTATTAGCCCGCATGTGATTTATCTATTTATTTTTTAAATATTTCCAAAATGATGTTTAACAGAGCAAGGACATTTTCACAGTATTTCTGATAATATTTTTTCTTCTGGAAAAAGGCGTAGTTGTTTTATTTAGGCTAAAATAAAATAGTTTTAAATTTTTTTATGACCATTTTATTAAAGCTCTTAAAGAATATTTTTATTTGATTGTCTACAGAACCACTGTTATACAATAACTTGCCTATTTAAGCACAGGAAGTGCTAATTTGTGATAATAATACTTTATTAATAAAACAACTTTTAAAGTGATAATTAATTTTTACTTTTTAAAATGATTAATTTATTTATTTTGCATTCTTTTTTATTTTTATATATTATTTTTTTGATTATTTTATTATTAAAATATTGTATTATTGTATTAATTTATTTTGTATATATAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15288
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000053750 | Nonsense | 560 | 685 | 16 | 19 |
Genomic Location (Zv9):
Chromosome 8 (position 53099117)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 50861243 |
GRCz11 | 8 | 50849879 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGCARAGGCTCTGGACACTGAAGGGTGGCTTCACACTGGAGACGTGGGA[C/T]AATGGCTGCCTGTGAGACTTTAAACAACTTTCACAACACTGACATTCTGA
Long Flanking Sequence:
CTGATATTCCTGACATGAACTACTATGCCAAGAACGGAGAAGGAGAGGTCAGTATTTGAACACAAGTGTTTCTGGGACTGTATATATCAGCTCTGGCGGGTCTGTCTTAACCGCCAGAGCTGAAATCTACCCGCATTTGGCGGGTCAGCGGGTGTTAATGTAAAGCCCTGTATGTGTGTGTGTGTATATATATATATTAGACAGTTAAAGTCAGAATATTAAACCCCCTGGTGAGGAGGAGGAAGAGTCTGCTCAGTTTTAATTTTTCTAGGAACTGCAGCACGTTAAAAAAAAAAAAAAAAAAAAAAAAGCTTCCCGTTCATGCAGACTTTAAATGAGGAGATTTTCTTGTATCATTAAAGACTTTCCTTGATGTGTGTGTTTGTGTGTGTCAGATCTGCATCAGGGGTCCCAGTGTGTTTCGGGGTTATCTGAAGGATGAGGAGAGGACAGCAGAGGCTCTGGACACTGAAGGGTGGCTTCACACTGGAGACGTGGGA[C/T]AATGGCTGCCTGTGAGACTTTAAACAACTTTCACAACACTGACATTCTGAAATTGAATGCACAATCAAGAAAATCCCCACTATTTGCGAAAGGTTGCAGTTTGTCTTCATTCATTCATTTCCTTTCGGCTTAGTTCCTTATTTATCAGGGTTCACCACAGCGGAATGAACCGACAACTATTTCAGCAAATGTTTTACGCAGCGGATGCCCTTCCAGCCACAACACAGTACAGGAAAACACATACACTCTCATTCACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACATATACACTATGGCCAATTGAGTTCATCCAATTCCCCTATAGTGCATGTGTTTGGATTGTGGGGGAAGCCGGAGCACCCTGGGA
Associated Phenotype:
Not determined