ZMP
acot13
Ensembl ID:
ZFIN ID:
Description:
acyl-coenzyme A thioesterase 13 [Source:RefSeq peptide;Acc:NP_001074272]
Human Orthologue:
ACOT13
Human Description:
acyl-CoA thioesterase 13 [Source:HGNC Symbol;Acc:20999]
Mouse Orthologue:
Acot13
Mouse Description:
acyl-CoA thioesterase 13 Gene [Source:MGI Symbol;Acc:MGI:1914084]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa43305 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa31035 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43305
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000088401 | Nonsense | 26 | 144 | 1 | 3 |
| ENSDART00000134107 | Nonsense | 26 | 141 | 1 | 3 |
| ENSDART00000088401 | Nonsense | 26 | 144 | 1 | 3 |
| ENSDART00000134107 | Nonsense | 26 | 141 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 19 (position 32822407)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 31989696 |
| GRCz11 | 19 | 31577009 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAACAGATCTTCAGAGCGATGGCGGACAGTCCTGGGTTTGACCGGGTTT[T/A]AAGTAAGGTGAGTGTTTGTGGTTCTCCTTGAGGGTCCTGCCAGACCAGAC
Long Flanking Sequence:
ACCTACATGGAAAACGTTATTTAATTCAAGTGCCTTTGTCCGCGAACACCGTTACAATATTATCGATTTTCTATTTCACCGATTGATTCAGATCGTTTCGTAAACCGGTTCAGCGGGTTCGTTACAAAGATCCGACTCCGATGGATGAATAAAAAGATCCATTATTTCAAACTAAAAGCCGAATGTTCATCACATCTTACAAATCGCTTAGAAATTAGTTTGAGAAGAACGCAGGGCAATTTTAAAACACTTGTATACAAGCTTTATTTTCTATTATAAGATATATATATTTTTTTAATTAAGGGGTTCAAAGACGAAAAAATAACAAAACTCTTATTTTGTATAACTTGGGCCAGCTTTCAAGCGGTTTACAATAGTGAACTTGTCCTTCTCTGTGTTTTGTTACTTAATGCTAGAATCAGTAATGGCTTCATTAACGCTGAATACAGTCAAACAGATCTTCAGAGCGATGGCGGACAGTCCTGGGTTTGACCGGGTTT[T/A]AAGTAAGGTGAGTGTTTGTGGTTCTCCTTGAGGGTCCTGCCAGACCAGACACAGTGATATTGAGTTGATATTGTGAGCAGGTGGAGGTTCTGTCTGCGGCTCCCGGTAAGGTGGTGTGTGAGATGAAGGTGGAGGAGCAGCACACGAACAGAGGGGGAACTCTTCACGGAGGAATGACAGCCACGCTCGTGGACATGATCTCCACCATGGCCATCATGTACAGTGAGAGAGGAGCTCCTGGAGTCAGTGTGGACATGAACATAACGTGAGTCTGTCTCACTGTAAAGGAAAACTGCATCTCTGCTACCGTCACATGTGCAGGGATGTCTTGGGCAACATATTATTAGTTATACACTCACCAACAACGATCCAGAATTGGAATATAGCTTAATAATGTCAAGAAAGAGTATGTTTAAATACTATTGTTATATTAAAATTAAAAATAAATGTGGACTCATAGGTTTAAGAGTTGAAGTACTAATATTACTGTTCACACATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31035
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000088401 | Nonsense | 26 | 144 | 1 | 3 |
| ENSDART00000134107 | Nonsense | 26 | 141 | 1 | 3 |
| ENSDART00000088401 | Nonsense | 26 | 144 | 1 | 3 |
| ENSDART00000134107 | Nonsense | 26 | 141 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 19 (position 32822407)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 31989696 |
| GRCz11 | 19 | 31577009 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAACAGATCTTCAGAGCGATGGCGGACAGTCCTGGGTTTGACCGGGTTT[T/A]AAGTAAGGTGAGTGTTTGTGGTTCTCCTTGAGGGTCCTGCCAGACCAGAC
Long Flanking Sequence:
ACCTACATGGAAAACGTTATTTAATTCAAGTGCCTTTGTCCGCGAACACCGTTACAATATTATCGATTTTCTATTTCACCGATTGATTCAGATCGTTTCGTAAACCGGTTCAGCGGGTTCGTTACAAAGATCCGACTCCGATGGATGAATAAAAAGATCCATTATTTCAAACTAAAAGCCGAATGTTCATCACATCTTACAAATCGCTTAGAAATTAGTTTGAGAAGAACGCAGGGCAATTTTAAAACACTTGTATACAAGCTTTATTTTCTATTATAAGATATATATATTTTTTTAATTAAGGGGTTCAAAGACGAAAAAATAACAAAACTCTTATTTTGTATAACTTGGGCCAGCTTTCAAGCGGTTTACAATAGTGAACTTGTCCTTCTCTGTGTTTTGTTACTTAATGCTAGAATCAGTAATGGCTTCATTAACGCTGAATACAGTCAAACAGATCTTCAGAGCGATGGCGGACAGTCCTGGGTTTGACCGGGTTT[T/A]AAGTAAGGTGAGTGTTTGTGGTTCTCCTTGAGGGTCCTGCCAGACCAGACACAGTGATATTGAGTTGATATTGTGAGCAGGTGGAGGTTCTGTCTGCGGCTCCCGGTAAGGTGGTGTGTGAGATGAAGGTGGAGGAGCAGCACACGAACAGAGGGGGAACTCTTCACGGAGGAATGACAGCCACGCTCGTGGACATGATCTCCACCATGGCCATCATGTACAGTGAGAGAGGAGCTCCTGGAGTCAGTGTGGACATGAACATAACGTGAGTCTGTCTCACTGTAAAGGAAAACTGCATCTCTGCTACCGTCACATGTGCAGGGATGTCTTGGGCAACATATTATTAGTTATACACTCACCAACAACGATCCAGAATTGGAATATAGCTTAATAATGTCAAGAAAGAGTATGTTTAAATACTATTGTTATATTAAAATTAAAAATAAATGTGGACTCATAGGTTTAAGAGTTGAAGTACTAATATTACTGTTCACACATTC
Associated Phenotype:
Not determined