ZMP
ACLY (2 of 2)
Ensembl ID:
Description:
ATP citrate lyase [Source:HGNC Symbol;Acc:115]
Human Orthologue:
ACLY
Human Description:
ATP citrate lyase [Source:HGNC Symbol;Acc:115]
Mouse Orthologue:
Acly
Mouse Description:
ATP citrate lyase Gene [Source:MGI Symbol;Acc:MGI:103251]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41986 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18271 | Essential Splice Site | Available for shipment | Available now |
sa14734 | Essential Splice Site | Available for shipment | Available now |
sa41985 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa6242 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35232 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41984 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41986
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078037 | Nonsense | 68 | 1096 | 2 | 27 |
Genomic Location (Zv9):
Chromosome 12 (position 15180278)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 14035931 |
GRCz11 | 12 | 14074234 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTTTTACTTGTGCAGAGGCTAGTTGTGAAGCCAGATCAACTGATTAAA[C/T]GAAGAGGAAAGCTGGGATTGGTAGCAGTTGACCTGAAACTTGAGAGTGTC
Long Flanking Sequence:
TAATTTGAAACATTTTACAGTATCTGACTTCTCTTGGTAGTGTAGTCATTATAGTGTATTTTAAAATTGTATTGAATCAAAATAGCATAATTTTGACAGATACTATAAAATTAATTCCCAGTCTTAAACAAGCATGAATAAAGCAAATGAAACAACAAATGTCTTAAATGACACTCGTGCTGTGGTGCATGAAGCTAACACTTTTTTTTTAATTTTCTGTAGTCGTTCTCAGCCGAGATGTCTGTAAAGGCCATTTCTGAGCGGACAGGAAAAGAGCTCCTGTATAAATACATCTGCACCACAGCAGTTGTGCGAAACCGTTTCTCCTGTGTGACGGTCACTACAGACACCAACTGGGACTGCATTACAGTGGACCACCCGTGGCTGCTAACAGAAGTAAGAACATGCATGTGTCTTGCTTTTCTATTTTGTAATACTGCATCATTTTTATATTTTTACTTGTGCAGAGGCTAGTTGTGAAGCCAGATCAACTGATTAAA[C/T]GAAGAGGAAAGCTGGGATTGGTAGCAGTTGACCTGAAACTTGAGAGTGTCCAGGAATGGCTGAAATCACATCTGATGACAGAAATTACAGTGGGTACTCCCTATGAATTTAGATTTTTTTGAGTATTAAAATATACCCTCACTTGCATGAACCCACTTTAATAAAATTGTTTCAGTTGTGAATAAATAATTTAATCATAGGTTCAAGGGATTTTTTCCACTGTTTTTCAGGTTGGGAATGCAAAAGGGGTTTTAAAGAAGTTCCTCATTGAGCCATTTGTTCCTCATATTCAGGTATATATTATTCAGTTTTAATCAGTGTTATAGATCTATGCCCAGGGTGTCTCCTGAGGCTTAAAATGTTTTAAAAGTTGATAAATCAATGTAGAATAATTTAAGGCCCTTAAAAAACCTTATTGCTATTTTGCAAGGTATTACTTTTTATATAATTTTTGATTATGCAACATATGGTTGTATGCCAAGGCTTGCCTGAATTAAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18271
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 |
---|---|---|---|---|---|
ENSDART00000078037 | Essential Splice Site | 292 | 1096 | 8 | 27 |
Genomic Location (Zv9):
Chromosome 12 (position 15150669)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 14006322 |
GRCz11 | 12 | 14044625 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGAACATAAACAGAACAGATAAYAAACGTGACCTCGTTATATYTGTTTTA[G/A]TGACACTATATGTGATCTGGGTGGAGTAGATGAGTTGGCCAACTATGGTG
Long Flanking Sequence:
GGGCTAATAATTTTGTCCCTAAAATGGTTTTGAAAAAATTTTAAACTGCTTTTATTCTCGCCAAAATAAAAAAATAAAGCTTTCTCCAGAAGAAAAAATGTTATCAGACATACTGTGAAAATTCCCTTGCTCTGTTTGTCATCGTTTAGGAAATATTCAAAAAGGAAAAAAAAAACTCAAAGGAGGGCTATTAATTCTGACTTCAACTGTATGTAGATATTTTTTTTTTAAAGTCTTATTTAAATTTTTTTTTTGTTAATGTAATTTATTTTTTGTGAAAACTCCTTCATACATCTCATCTCATTCTGTTTATTTATGAATATGTTTATTTTTGTAAACTGGTCAATCTTTATTTGTTTAATCATAATGTATTTATTTCAAATACTAGCACAAAACCACAAAATCATCTAATTTTGTGAACTGATTTAATTTTCATACTACGTTGATCTGCGAACATAAACAGAACAGATAACAAACGTGACCTCGTTATATTTGTTTTA[G/A]TGACACTATATGTGATCTGGGTGGAGTAGATGAGTTGGCCAACTATGGTGAATACTCTGGATCTCCCAGCGAGCAGCAGATGTATGATTATGCCAAGACTATCCTTTTACTTATGACCCGAGAAAAACACTCTGATGGTAAGATTAATTCTTTTATATTCTAGACTGTCACATCATATTACAAATATACATAGAATATAAACCAGAAGTTTACATGCAGTCTAAATGAGGAACATAACCATTTTTTTTATCAATTTATAAACAGTCAAAAGTTTTCATACATTTTCTTGTTTTTTTTTTTCTTTTTTTTAGCTTTGCTTTTAAACTGTGTTATTTTAATTAAACTTTGGTCAAATGTTTTGGATATGCTTCCACAAGCTTCTCACAATAGTTTGAAGTAATTTTGGCCCTTACCTCCTGACAGAATTGGTTTAAGTCAGTTTTGTGGGCTGTCTTGCCCACACAAGTTTTTTCAACTATGCTCACAAATTTTCTATAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14734
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 |
---|---|---|---|---|---|
ENSDART00000078037 | Essential Splice Site | 358 | 1096 | 9 | 27 |
Genomic Location (Zv9):
Chromosome 12 (position 15145850)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 14001503 |
GRCz11 | 12 | 14039806 |
KASP Assay ID:
2260-5132.1 (used for ordering genotyping assays)
KASP Sequence:
TCATYGGTGGCAGTATTGCTAACTTCACAAATGTAGCAGCAACTTTTAAG[G/A]TTAGACTATACGGCTTGWTCTAGATATTGATAGAGTATTGAYATATTCAC
Long Flanking Sequence:
ACGGAAAAACAGTTACTATAGATAACAATGTTTATGGATTTCCATCTTTCTTCAAAATATCTTCCTTTGTGTTTAACAGAAGAAAAAAGTCGGGTGAGTAAATGATGACAGAATTATCATTTTTGGGTGAACTATTCCTTTAATGAGAAATCCTCTGAATTTCAGGAGTTGGTTTAATTTTTAGGTATGATGGGTATCACCAGGTAGAAGCAAAAATAAATGGAGAATAATTAGTTAATATGTTTGTTGGACTCTCTGAATTGTTGGCTAAGAAGGATTATTTGTTGTTGCTAATGTTGTCTGGATTATTTTGAATTCAATTTTTACAAATTTCTCTTCCTGACAAACTAATTCATAATCTTGAATTGACTTTGCAAGTTATTATATTCAGGGAGTAATAGTGCTGAATTTTACTCCAGTTCAATCTTTTCTCTACAGGAAAGGTGTTGATCATTGGTGGCAGTATTGCTAACTTCACAAATGTAGCAGCAACTTTTAAG[G/A]TTAGACTATACGGCTTGTTCTAGATATTGATAGAGTATTGACATATTCACAAGTTTTATAGCACATCATTTTTCTTTACACCATGTTTGCTTCATCAAACTCATCAGGGTATTGTGAGAGCTATCAAAGACTACCAGGAGCCTCTAAAAGAACATGAGGTTACCATCTTTGTGCGACGAGGAGGTCCAAACTACCAGGAAGGATTGAGAGTGATGGGGGAAGTTGGTAAGTATTTTTGTTTCAAGTTTTTTTCAGTGCACATTAAAATGATATTTTGATAATAAATTTAGTTTAATGAAAAAATGCTCAATGCAGTGCACACACTTCAATCTAAATGTGTGCTCAGCTAAATAACAAATATTCATAAGGGATGCAACACCAAAGCTCACCATCAGTAGAGCTGGCATGCTCAAAACGTCACATGCTTTGTGATAGCTTTTTTAGGTTAACAAATTAATATTTATAGAGCTTTGGTTTTGCCACCTTTATTTAATTTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41985
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078037 | Essential Splice Site | 398 | 1096 | 11 | 27 |
Genomic Location (Zv9):
Chromosome 12 (position 15143799)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 13999452 |
GRCz11 | 12 | 14037755 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACACAAATAATCTTATCTAATCTTTTTGTTTCTTTGTTTCCTTTTTGTT[G/T]CAATAGGAAAGACTACTGGTATTCCCATTCATGTCTTTGGCACAGAAACA
Long Flanking Sequence:
ACGTTAATGTTCAAAGTCACTTAAATCACCTTTCTTTCCCATTCTGATGCTCGGTTTGAACTGCAGCAGATCGTCTTGAACGTGTCTACATCACTAAACTCATTGAGTTGCTGCCATGCAATTGGCTGTTTAGAAATTTACGTTAAGAAAGTTGGACATTTGTAAATAATAAACTGGCTGGTGAGTGTGCATATATCAAGGTATATTATATAAGACAACAGTGCTGCACAGATTTGCATGTTTGTGTAATTATAGTGCAGTCTTTGGGATATATTGATATCCAACTGGCAGGTAACACTATTTCTTATTCTTGACAATGATGGTTTTAAATCTCATTTGGCTCAGGGCAAATGTTAAATTTACAACCTGAGTGTATGGTTTTAAGGTATAATTTTCACATGCCGAAAAGGATATGTGTTACTATGCTTGCATGGAAGCAATTACATATCACACACAAATAATCTTATCTAATCTTTTTGTTTCTTTGTTTCCTTTTTGTT[G/T]CAATAGGAAAGACTACTGGTATTCCCATTCATGTCTTTGGCACAGAAACACACATGACTGCCATTGTTGGCATGGCACTGGGTCATCGGCCAATTCCCAATCAGCCTCCAGTGGCAGCACACACTGCCAGTTTCCTGTTGAATAGCAGTGCTAGTGCTGCTGTAAGTGTTTTCATATTTAGTCTGTATATTTAGGCCTTTTTTGATCTTTCAACCTAATAGTCTTTAGTTTAATTTTTTCTTTAATTTTTCTAGCTTTCTTTAAAAATAATTTAATTAGTTAATATTTTTAATTAACATTTTAACAGTAAACCTCTTAGCCAGAATGAAAAAAGAAAATCACTGCAATCAATTAAATTTTTAACTATGTAGATGTAAGTGTATAATATAATTCTTTATTTTCTGTGAATTCCTAATGCTGCATTTATACAATATTTATATAGATTATCGTCTACATTTACACTCATATTTTAGAAAATCTAAATTAATGAGATTGTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6242
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078037 | Essential Splice Site | 529 | 1096 | 14 | 27 |
Genomic Location (Zv9):
Chromosome 12 (position 15126959)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 13982612 |
GRCz11 | 12 | 14020915 |
KASP Assay ID:
554-4118.1 (used for ordering genotyping assays)
KASP Sequence:
CCTGTAATTTTGAAAGCATGGTTTTATGATTTTTCATTTTTRTGTGTGCC[A/G]GTGGTGACCACAAGCAGAAATTTTACTGGGGTCAWAAGGAGATCTTACTG
Long Flanking Sequence:
GGAATGACAGCATTTTGCGTGTTAAATTATGCTAAGCATTGTTAAATTTGACCACACCTTTATTCTCATTTTCTCTGTCTGTTTTCAAATTTTTGGAAATCTTTCACAGCTTTGATGATGTCAGTTGTTTTCCTTTTGTAGAACCTCATAAAGTTTATGTAGATGAAGCAACAAACATATTTTGTGCATGGCTAAATTAATGTCTGTTCATATTTACATAGTTTTGATTTGGCATTGACAAATCAGTTGAATTTAATATTGTCCCTCCCCTTTTAGCTAAACCCACGACTCTGTTCAGCAGACAGACCAAGGTAATCGTGTGTGGCATACAGACACAGGCAGTTCAGGGCATGCTGGACTTTGATTACGTGTGTTCTCGTGATGAACCCTCTGTTGTCGCAATGGTCTACCCCTACACGTCAGTACGTTTAAAAATAACCTTAGGATTTGCCTGTAATTTTGAAAGCATGGTTTTATGATTTTTCATTTTTGTGTGTGCC[A/G]GTGGTGACCACAAGCAGAAATTTTACTGGGGTCATAAGGAGATCTTACTGTCTGTCTATAAGAACATGGCTGATGCTATGAAGAAACATCCAGATGTTGACGTACTCATTAACTTTGCCTCCCTTCGCTCAGCCTTCGACAGTACCATGGAAACACTTCAGTACCCTCAGGTAATATCCCATACTGACAGCGCAGTGTTTCCACTTGCTAGCTAAAATAGCAGTTGTTTTTTTAAATCACAGTAACATCAGTCCTGTGGAAAGTAATGAAACAAATCCTGAAAATCCAATTTTATTGACTGAACAATACATTCCGTACCCACTGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTATATATATATATATATATATATATATATATATATATATATATATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35232
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 |
---|---|---|---|---|---|
ENSDART00000078037 | Nonsense | 572 | 1096 | 14 | 27 |
Genomic Location (Zv9):
Chromosome 12 (position 15126829)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 13982482 |
GRCz11 | 12 | 14020785 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGAAACATCCAGATGTTGACGTACTCATTAACTTTGCCTCCCTTCGCT[C/A]AGCCTTCGACAGTACCATGGAAACACTTCAGTACCCTCAGGTAATATCCC
Long Flanking Sequence:
TCCTTTTGTAGAACCTCATAAAGTTTATGTAGATGAAGCAACAAACATATTTTGTGCATGGCTAAATTAATGTCTGTTCATATTTACATAGTTTTGATTTGGCATTGACAAATCAGTTGAATTTAATATTGTCCCTCCCCTTTTAGCTAAACCCACGACTCTGTTCAGCAGACAGACCAAGGTAATCGTGTGTGGCATACAGACACAGGCAGTTCAGGGCATGCTGGACTTTGATTACGTGTGTTCTCGTGATGAACCCTCTGTTGTCGCAATGGTCTACCCCTACACGTCAGTACGTTTAAAAATAACCTTAGGATTTGCCTGTAATTTTGAAAGCATGGTTTTATGATTTTTCATTTTTGTGTGTGCCAGTGGTGACCACAAGCAGAAATTTTACTGGGGTCATAAGGAGATCTTACTGTCTGTCTATAAGAACATGGCTGATGCTATGAAGAAACATCCAGATGTTGACGTACTCATTAACTTTGCCTCCCTTCGCT[C/A]AGCCTTCGACAGTACCATGGAAACACTTCAGTACCCTCAGGTAATATCCCATACTGACAGCGCAGTGTTTCCACTTGCTAGCTAAAATAGCAGTTGTTTTTTTAAATCACAGTAACATCAGTCCTGTGGAAAGTAATGAAACAAATCCTGAAAATCCAATTTTATTGACTGAACAATACATTCCGTACCCACTGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACTTACCCGCCACTTTAATAGGTACACCTGTTCAACTGCTCTTTAACACAAATTTCAATCACATCAACTTAATTAATTTAGCCATGTAGAGATGGTCAAGATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41984
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 |
---|---|---|---|---|---|
ENSDART00000078037 | Nonsense | 872 | 1096 | 21 | 27 |
Genomic Location (Zv9):
Chromosome 12 (position 15098462)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 13954115 |
GRCz11 | 12 | 13992418 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGTGTTTAAAGAGGAAATGGGTGTCGGAGGAGTGCTGGGCCTGTTGTG[G/A]TTCCAGAGGAGGTTTGTCATTTAAAATTGGATCATTATGAAAATACAGAA
Long Flanking Sequence:
ACCTTTATTTCTGAGAGTGTAGATCGTCTTTATTATGTCCATAATAATAGTATATAAATAAAAGATCACTTTCAAAAATTTCAACAAAAAAATCAATCACTCAGAAATAAAGATATTTGTGCTTATTTACATGCCCTGTTATGGATTTCCTCCTTTTGTTGAACACAACACAAGATATTTTGAAAAATATGGGTAACCAAAAATTGCCTGTCCTCATTGACTCCCATGGTTTGGAATGAGGTCAGGCATCTGCTTAGTTACTATTTTCTTTGAAATGTTTGTCACAATGTCACAATGCTACTAAAATGCGTTGCATAAGGAGGAAATCTGACCAAATTGATGTATTTATGCCTATAGGAGCTGGGGTTGATTCGAAAACCTGCGTCGTTCATGACTAGTATTTGTGATGAAAGAGGCCAGGAGGTCATATACGCCGGTATGCCCATCACAGAGGTGTTTAAAGAGGAAATGGGTGTCGGAGGAGTGCTGGGCCTGTTGTG[G/A]TTCCAGAGGAGGTTTGTCATTTAAAATTGGATCATTATGAAAATACAGAACAAGTAATATTTTACAATATTATTACAAAGTAAATGTTTACCTTTTTAAAAATGTTTTAGATTAGATTAAATTAAACTTTATTTTCATTACACATGTACAATTATAAGACAACTAAATGCAGTTTTGGTCTAACCAGGAGTGCACAAGGAACAAATTTAGGATGTAGGTATAAATTATAAGGAGCAATTATAGAAGTAACTATGGCGATATTTACAGATGGATGTACTATGACCATTATATACAGGTTGTATTATTTTTGAACAGAGATTTACAATAGATGAATATACTGTATGTACTGTACCAGTTGCTTTTGATAATCAGAGGTATGCAGTAGGGCTGTTACGGTGGCAATTCTTTACTAGCCCGTTGGTAAGTCACCAACAACCTCCGGTGTTGCAGTGGTGGTGTTTTTGTTTGTTTGTTTTTTGTGGGAGTGGGGAGGTGGAATC
Associated Phenotype:
Not determined