Busch Lab

ZMP

zgc:123115

Ensembl ID:
ENSDARG00000042122
ZFIN ID:
ZDB-GENE-051127-37
Description:
thioesterase, adipose associated [Source:RefSeq peptide;Acc:NP_001032661]
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 2 alleles of this gene:

Allele Name Consequence Status Availability
sa41171 Nonsense Mutation detected in F1 DNA Not yet available
sa11419 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa41171
Status:
Mutation detected in F1 DNA
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
ENSDART00000080026 Nonsense 123 340 6 11
ENSDART00000121660 Nonsense 123 585 4 15
ENSDART00000122730 Nonsense 123 253 5 7
ENSDART00000125014 Nonsense 123 575 6 17
ENSDART00000133666 Nonsense 123 138 5 5

The following transcripts of ENSDARG00000042122 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 18523037)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 17967925
GRCz11 8 18003637
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCTCAGGTTGGGATTTCAGTGAGTTGTGAGGATCTCTTCAGTGACAGA[C/T]AGTGGAAAGTCTGCCATGCTTTTGCCACCTTCGTTGCTCGTCGTACAGAA
Long Flanking Sequence:
ATGGAATTCAATAAGGGCAAAAACAGCCACCAATAGTAAATTAGGGAGAAAAAAAAATCTAACAATCCATCAAAGACAATGTTGTTACTAATCGTTTACATGTCCAAGACATGTAATTAAAAAATCCAGAGTCCACAACTACTTCATATATTAAAAATACGTCATTTTGTGTGATTTTATTTTACCAAATTAGTAACATCATTTGTGAACTTGGCAATTAAAGTGTTAAAATCCTGTACTTTTCTAAGCAATTAAGTAGTTTTTATCAGGACTGAGGTTGATTAGTAGATTTATGCAAAAAAAAATTGAAAAAAATAAAATAAATACATCTGATGCATTTTTATAGCATTTTAGTTCAGTTTATGTTTTCATCGCAAACATACCTAAAGAACAGTAAATTTGAACAGTGCAATTAAGTTCAGTTGTAGTAAAGCTAAATGTGTGACTATGATTCTCAGGTTGGGATTTCAGTGAGTTGTGAGGATCTCTTCAGTGACAGA[C/T]AGTGGAAAGTCTGCCATGCTTTTGCCACCTTCGTTGCTCGTCGTACAGAAGCAGGAAAAGTAAAAAGCATCCAGTCCAACCAGTTCACAACAAATCCTTTTTACAACATCAAATCAGATCTTTAAAAAAAAACTTGGATTTGGTCCATGTCTTGTTAGAGCTGTGATTTGGGTTTGCGCAGGTACAGCTGAAGCAGGTGATTCCACACACGCAGGCAGAGCAGATGGAGTACAGCCTTGCCGCCGAGCGCAGGAGGATGAGACTAATCCATGCAGAGATAATTAACGATCTTCTTAGCAGCTGCTGCTCTCAGACAGGTGAGCAGAGACACTCACTTTCTCCAGGTGTGTTTGTTTACTTCCAAGACTTTGAAGAGAGAGGGCTCAGAAATGCTTGCCACGTGAAATGAGTCATGAATCAGAAGTTGAGCTCTGATTAAAGGTGTCTTTCGGTTTGTTTGGTGTCTCATCACGAGCATTCTGCCAACACTCATTTAAGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11419
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000080026 None None 340 None 11
ENSDART00000121660 Essential Splice Site 440 585 12 15
ENSDART00000122730 None None 253 None 7
ENSDART00000125014 Essential Splice Site 440 575 14 17
ENSDART00000133666 None None 138 None 5

The following transcripts of ENSDARG00000042122 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 18515146)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 17960034
GRCz11 8 17995746
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCCTACTGTCTGATYTAAGGCGAAGGAAGGYGTGGGACCACCACTACCA[G/A]TATGTAAAATGTATTTTTTCTGMAAGCTGKAGAATAATWATAATTTCAAC
Long Flanking Sequence:
ACATTGTCTTAACTGATGCCCAACACACACAAATCTGGTAAAAAAAATAAATAAAAAGTACTCGAGATTGTCTTTAAACATTAAGAGCTACAAATGTCATAGACAAGCTCAAACATTTAACTGAACCATGTGATTATTCCATATCTTGGCAGATGTATCTCAGTTACAATAATGTTTCGGCACTTAAGATGTTGGCTGCCCGAACCAACTGGGTCTTGACCTCTGAGAAAAATAAGGTAGGTATAGGTATAATAATTAAATTTGAAGTTTTGCTTTCTGTCCTCTTGAGATTATATAGGTAACTTGAGTGTACAAAAATGGTGTGTACACTTGAGAGAAATTTATGGAGTGAAATTTTGCACACAGGTGAGTTTATACACTCTGGAGGAGAACCAGGTGTTGTGCTTTAAGGTGGAGACCCATGTGGCTGTTGCAGCTGAGCAGGTGTTTCTCCTACTGTCTGATCTAAGGCGAAGGAAGGCGTGGGACCACCACTACCA[G/A]TATGTAAAATGTATTTTTTCTGCAAGCTGGAGAATAATAATAATTTCAACTATATTGACACGCCTGGGGGAATCTACTTTGCTTATTAAGCATTTGCAGATGTTTGTTATTCCCAAACAATCAATCTAACCAGAAATTGATCAAATCAAGTCATGTTTTATCTAAGGAAATTATATCCCTCTTTTGAAACTATATCCAGCCCACACACTGTTTTAAAACATTAATACAATCCAAGTCTGAAGAGAATTTCAGCACATGAACTTGCAGAAAATAAACATTGCTTTATGATTTCTTATGCTTTAGCAGTATTCAGGTACAGAAATGGTTTGTTCTTATGTCAAGCAGGTTTGGTTGAGCTTTTGTTTATATTTGCTAATCGCTGTGTACATTTGAACAAAAAGCCTAAGTGATCATGTTTCTTCAAAAGATTTGCACTAATTCACCTTCCTTGATATGTATTTGTTTTTTTAACTCCACTGATTTTTAGGTACCAGAGTCTT
Associated Phenotype:
Not determined