Busch Lab

ZMP

acot11

Ensembl ID:
ENSDARG00000058229
ZFIN ID:
ZDB-GENE-050522-538
Description:
acyl-coenzyme A thioesterase 11 [Source:RefSeq peptide;Acc:NP_001093445]
Human Orthologue:
ACOT11
Human Description:
acyl-CoA thioesterase 11 [Source:HGNC Symbol;Acc:18156]
Mouse Orthologue:
Acot11
Mouse Description:
acyl-CoA thioesterase 11 Gene [Source:MGI Symbol;Acc:MGI:1913736]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa12527 Nonsense Available for shipment Available now
sa12500 Nonsense Available for shipment Available now
sa12913 Nonsense Available for shipment Available now
sa19688 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa12527
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
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Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000076725 Nonsense 50 579 1 15
ENSDART00000081058 Nonsense 50 577 2 16
ENSDART00000145093 Nonsense 50 154 1 5
ENSDART00000076725 Nonsense 50 579 1 15
ENSDART00000081058 Nonsense 50 577 2 16
ENSDART00000145093 Nonsense 50 154 1 5
ENSDART00000076725 Nonsense 50 579 1 15
ENSDART00000081058 Nonsense 50 577 2 16
ENSDART00000145093 Nonsense 50 154 1 5

The following transcripts of ENSDARG00000058229 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 10822815)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 11247911
GRCz11 2 11031510
KASP Assay ID:
2259-1648.1 (used for ordering genotyping assays)
KASP Sequence:
AGATCGTGTTGCCCTGCYATGCCAACCACTGCGGAGAGCTGAGCGTCGGG[C/T]AGCTGCTCAAATGGATGGACTGCACAGCATGTCTGTCTGGTGAGTTTGCA
Long Flanking Sequence:
AATCCTGTCTAGGAGGTCTACAGATAATTCCTTTGTCTTCATGCTTGGTTTGTGCTTTGACATGCACTGTCCCCTTTGACCTTATATAGACAGGTGAATGCCTTTTCATTAAATGATGATCAATGAAAACAGAATGCACCTGAGCTCAATTTAGAGCTTCACGGCAAAGGCTGTAAATATGTGGTAGTCATTATTATGTTGTTCTGAAAAAAAATAAGGTCAGTATGCATTCTACTGAACAGAAAAAAAGAAAGCAACACATCTCCATGCCGTATTGCACTTTTATTCTTTTGATGCTTATAAACCACATGCGTGATTGTATTGAAGATTTCCGGTGTCCTCAACAGCTCATCATGGCATCATTAGAGTCCAGGCTAAAGGAGGATCTGCATGACCTTCATCTGGAGGATGGAGCTCAGCATCGCAACCCTTCAGAAGTGAAGATGAGCCAGATCGTGTTGCCCTGCCATGCCAACCACTGCGGAGAGCTGAGCGTCGGG[C/T]AGCTGCTCAAATGGATGGACTGCACAGCATGTCTGTCTGGTGAGTTTGCACAATGACTGACGCCACTCACCTTTAACCTGCATTGTAAAGGCTCCAGAACTTCTCTATATAAGCTTATCAGTTGTAGTATAATGACGTTCATACTGACAAACAAACCTAGAGCAAATAAAATCTAGATCTATGTGTGTTTGTGAGTGTTCTTCAGGGTTCTTACAGGTGCTGTAATCCTGGAAAATGCTTGGATTTATTCTAGTGTTTTCAAGATTTAAAAAGTGCTTTGATTTTCCAATAAAGTGCTTAGAACTGCTTGAAAATCTAATTGTGTTGCTTTCATAAGAATTCATTCATTCATTCATTCATTTTCTTTTCCGCTTAGTCCCTTTATTAATTCGGGGTCACCACAGCGGAATAACCCACCAACTTATCCAGCACATTTATTACACGGCGGATGCCCTTCCAGCCGCAACCCATCTCTGGGAAACATCCACACACACTCATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12500
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000076725 Nonsense 50 579 1 15
ENSDART00000081058 Nonsense 50 577 2 16
ENSDART00000145093 Nonsense 50 154 1 5
ENSDART00000076725 Nonsense 50 579 1 15
ENSDART00000081058 Nonsense 50 577 2 16
ENSDART00000145093 Nonsense 50 154 1 5
ENSDART00000076725 Nonsense 50 579 1 15
ENSDART00000081058 Nonsense 50 577 2 16
ENSDART00000145093 Nonsense 50 154 1 5

The following transcripts of ENSDARG00000058229 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 10822815)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 11247911
GRCz11 2 11031510
KASP Assay ID:
2259-1648.1 (used for ordering genotyping assays)
KASP Sequence:
AGATCGTGTTGCCCTGCYATGCCAACCACTGCGGAGAGCTGAGCGTCGGG[C/T]AGCTGCTCAAATGGATGGACTGCACAGCATGTCTGTCTGGTGAGTTTGCA
Long Flanking Sequence:
AATCCTGTCTAGGAGGTCTACAGATAATTCCTTTGTCTTCATGCTTGGTTTGTGCTTTGACATGCACTGTCCCCTTTGACCTTATATAGACAGGTGAATGCCTTTTCATTAAATGATGATCAATGAAAACAGAATGCACCTGAGCTCAATTTAGAGCTTCACGGCAAAGGCTGTAAATATGTGGTAGTCATTATTATGTTGTTCTGAAAAAAAATAAGGTCAGTATGCATTCTACTGAACAGAAAAAAAGAAAGCAACACATCTCCATGCCGTATTGCACTTTTATTCTTTTGATGCTTATAAACCACATGCGTGATTGTATTGAAGATTTCCGGTGTCCTCAACAGCTCATCATGGCATCATTAGAGTCCAGGCTAAAGGAGGATCTGCATGACCTTCATCTGGAGGATGGAGCTCAGCATCGCAACCCTTCAGAAGTGAAGATGAGCCAGATCGTGTTGCCCTGCCATGCCAACCACTGCGGAGAGCTGAGCGTCGGG[C/T]AGCTGCTCAAATGGATGGACTGCACAGCATGTCTGTCTGGTGAGTTTGCACAATGACTGACGCCACTCACCTTTAACCTGCATTGTAAAGGCTCCAGAACTTCTCTATATAAGCTTATCAGTTGTAGTATAATGACGTTCATACTGACAAACAAACCTAGAGCAAATAAAATCTAGATCTATGTGTGTTTGTGAGTGTTCTTCAGGGTTCTTACAGGTGCTGTAATCCTGGAAAATGCTTGGATTTATTCTAGTGTTTTCAAGATTTAAAAAGTGCTTTGATTTTCCAATAAAGTGCTTAGAACTGCTTGAAAATCTAATTGTGTTGCTTTCATAAGAATTCATTCATTCATTCATTCATTTTCTTTTCCGCTTAGTCCCTTTATTAATTCGGGGTCACCACAGCGGAATAACCCACCAACTTATCCAGCACATTTATTACACGGCGGATGCCCTTCCAGCCGCAACCCATCTCTGGGAAACATCCACACACACTCATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12913
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000076725 Nonsense 50 579 1 15
ENSDART00000081058 Nonsense 50 577 2 16
ENSDART00000145093 Nonsense 50 154 1 5
ENSDART00000076725 Nonsense 50 579 1 15
ENSDART00000081058 Nonsense 50 577 2 16
ENSDART00000145093 Nonsense 50 154 1 5
ENSDART00000076725 Nonsense 50 579 1 15
ENSDART00000081058 Nonsense 50 577 2 16
ENSDART00000145093 Nonsense 50 154 1 5

The following transcripts of ENSDARG00000058229 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 10822815)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 11247911
GRCz11 2 11031510
KASP Assay ID:
2259-1648.1 (used for ordering genotyping assays)
KASP Sequence:
AGATCGTGTTGCCCTGCYATGCCAACCACTGCGGAGAGCTGAGCGTCGGG[C/T]AGCTGCTCAAATGGATGGACTGCACAGCATGTCTGTCTGGTGAGTTTGCA
Long Flanking Sequence:
AATCCTGTCTAGGAGGTCTACAGATAATTCCTTTGTCTTCATGCTTGGTTTGTGCTTTGACATGCACTGTCCCCTTTGACCTTATATAGACAGGTGAATGCCTTTTCATTAAATGATGATCAATGAAAACAGAATGCACCTGAGCTCAATTTAGAGCTTCACGGCAAAGGCTGTAAATATGTGGTAGTCATTATTATGTTGTTCTGAAAAAAAATAAGGTCAGTATGCATTCTACTGAACAGAAAAAAAGAAAGCAACACATCTCCATGCCGTATTGCACTTTTATTCTTTTGATGCTTATAAACCACATGCGTGATTGTATTGAAGATTTCCGGTGTCCTCAACAGCTCATCATGGCATCATTAGAGTCCAGGCTAAAGGAGGATCTGCATGACCTTCATCTGGAGGATGGAGCTCAGCATCGCAACCCTTCAGAAGTGAAGATGAGCCAGATCGTGTTGCCCTGCCATGCCAACCACTGCGGAGAGCTGAGCGTCGGG[C/T]AGCTGCTCAAATGGATGGACTGCACAGCATGTCTGTCTGGTGAGTTTGCACAATGACTGACGCCACTCACCTTTAACCTGCATTGTAAAGGCTCCAGAACTTCTCTATATAAGCTTATCAGTTGTAGTATAATGACGTTCATACTGACAAACAAACCTAGAGCAAATAAAATCTAGATCTATGTGTGTTTGTGAGTGTTCTTCAGGGTTCTTACAGGTGCTGTAATCCTGGAAAATGCTTGGATTTATTCTAGTGTTTTCAAGATTTAAAAAGTGCTTTGATTTTCCAATAAAGTGCTTAGAACTGCTTGAAAATCTAATTGTGTTGCTTTCATAAGAATTCATTCATTCATTCATTCATTTTCTTTTCCGCTTAGTCCCTTTATTAATTCGGGGTCACCACAGCGGAATAACCCACCAACTTATCCAGCACATTTATTACACGGCGGATGCCCTTCCAGCCGCAACCCATCTCTGGGAAACATCCACACACACTCATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19688
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000076725 Nonsense 290 579 8 15
ENSDART00000081058 Nonsense 288 577 9 16
ENSDART00000145093 None None 154 None 5

The following transcripts of ENSDARG00000058229 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 10839582)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 11264678
GRCz11 2 11048277
KASP Assay ID:
2259-1649.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTATCTGTGGATTTGCAGTATGGAGGTTGGCGTCTGTGCAGAGGCGTA[T/A]ATTGGAGAGGAGCCTCTGAGGCACATTAACAGCGCCTTCATGACATTTGA
Long Flanking Sequence:
CTTGTAGTTGCTGACTAGTCTATTTTTGAACTACTGTCTCTAGATTTTTACTGACAGCCCAAATTTAGCCATTTTTTCAATCCAAAATGTGGTCCATATGTTCTCTATGTTTAGACTTCTTTTAAAACATACAAAAAGAACTGTGGCACCAAATGTTTTTCCTTTTATAGTCAGAACGTCAGCACAAGAAAAAAAATCTGACAGGTCTAATACTAAATATGTTAAAGAGTAAATATTTATTTGCTTTCTCTTTTTAACAGTCGTTTATGCAATGCTCATCCTACTCTGAGGGCCATAGACATGTTTCACTTCAGAGGCCCTTCTCAGGTCGGAGATCGGTTGATTCTGAAAGCCATTGTCAACAACACCTTCAAGAACAGGTGGGCTTGTATTAATACGCACCCGAGAGCTGTGTTTAGATTTAAAGGAGTAATGTGCCACTGCTCATTGTGTTATCTGTGGATTTGCAGTATGGAGGTTGGCGTCTGTGCAGAGGCGTA[T/A]ATTGGAGAGGAGCCTCTGAGGCACATTAACAGCGCCTTCATGACATTTGAGGTGCTGGATGACAAAGGAAGGCCACGTCCGCTGCCTTTGATAAAACCTGAACCTAAGGTGAGGAGTTTAAATCTGAAATCACATTGAGTTTATTGTATAATAATTAAAAAATCCTCATTTATGTCATTAAGATTCAAAGGGAAATGAGACTAAGGGTGTTTATTATTGCATTCTAAATTAAGTTGATTACGTTAACCTAATTGTTTTTACAAATTAAAGTGTATTTAAGCTGCAACCCCCCCCCCCCCCCCAAACAATAAATAAATAAAAAATAAATAAAAAACTGACGGACTGTGTTATTTCAGCGCATTATAAATAAGTAGTCTGAACAAGCAGCACATTTTTTTTTTTAATTTTATTTACTAGTTTACTAAGCAACAAAAACTGCTCAATTGAATGTAACTACCTACTTTGTATGTATAAATATATAAGATAAATGATCAAATAAG
Associated Phenotype:
Not determined