ZMP
si:dkey-183c16.7
Ensembl ID:
ZFIN ID:
Description:
Si:dkey-183c16.7 protein [Source:UniProtKB/TrEMBL;Acc:A8WG99]
Human Orthologues:
ACOT1, ACOT2, ACOT4, ACOT6, BAAT
Human Descriptions:
acyl-CoA thioesterase 1 [Source:HGNC Symbol;Acc:33128]
acyl-CoA thioesterase 2 [Source:HGNC Symbol;Acc:18431]
acyl-CoA thioesterase 4 [Source:HGNC Symbol;Acc:19748]
acyl-CoA thioesterase 6 [Source:HGNC Symbol;Acc:33159]
bile acid CoA: amino acid N-acyltransferase (glycine N-choloyltransferase) [Source:HGNC Symbol;Acc:9
acyl-CoA thioesterase 2 [Source:HGNC Symbol;Acc:18431]
acyl-CoA thioesterase 4 [Source:HGNC Symbol;Acc:19748]
acyl-CoA thioesterase 6 [Source:HGNC Symbol;Acc:33159]
bile acid CoA: amino acid N-acyltransferase (glycine N-choloyltransferase) [Source:HGNC Symbol;Acc:9
Mouse Orthologues:
Acnat1, Acnat2, Acot1, Acot2, Acot3, Acot4, Acot5, Acot6, Baat
Mouse Descriptions:
acyl-CoA thioesterase 1 Gene [Source:MGI Symbol;Acc:MGI:1349396]
acyl-CoA thioesterase 2 Gene [Source:MGI Symbol;Acc:MGI:2159605]
acyl-CoA thioesterase 3 Gene [Source:MGI Symbol;Acc:MGI:2159619]
acyl-CoA thioesterase 4 Gene [Source:MGI Symbol;Acc:MGI:2159621]
acyl-CoA thioesterase 5 Gene [Source:MGI Symbol;Acc:MGI:2384969]
acyl-CoA thioesterase 6 Gene [Source:MGI Symbol;Acc:MGI:1921287]
acyl-coenzyme A amino acid N-acyltransferase 1 Gene [Source:MGI Symbol;Acc:MGI:2140197]
acyl-coenzyme A amino acid N-acyltransferase 2 Gene [Source:MGI Symbol;Acc:MGI:2444345]
bile acid-Coenzyme A: amino acid N-acyltransferase Gene [Source:MGI Symbol;Acc:MGI:106642]
acyl-CoA thioesterase 2 Gene [Source:MGI Symbol;Acc:MGI:2159605]
acyl-CoA thioesterase 3 Gene [Source:MGI Symbol;Acc:MGI:2159619]
acyl-CoA thioesterase 4 Gene [Source:MGI Symbol;Acc:MGI:2159621]
acyl-CoA thioesterase 5 Gene [Source:MGI Symbol;Acc:MGI:2384969]
acyl-CoA thioesterase 6 Gene [Source:MGI Symbol;Acc:MGI:1921287]
acyl-coenzyme A amino acid N-acyltransferase 1 Gene [Source:MGI Symbol;Acc:MGI:2140197]
acyl-coenzyme A amino acid N-acyltransferase 2 Gene [Source:MGI Symbol;Acc:MGI:2444345]
bile acid-Coenzyme A: amino acid N-acyltransferase Gene [Source:MGI Symbol;Acc:MGI:106642]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44591 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa33473 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa26305 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa40305 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44591
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047113 | Essential Splice Site | 6 | 438 | None | 11 |
ENSDART00000066944 | Essential Splice Site | 6 | 289 | None | 8 |
ENSDART00000132864 | None | None | 437 | None | 10 |
ENSDART00000139053 | Essential Splice Site | 40 | 472 | None | 12 |
Genomic Location (Zv9):
Chromosome 4 (position 24779492)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 25703161 |
GRCz11 | 4 | 25692359 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGAAGAAAGAAACGTCTATTATCGGACTACCATGTTGGCACCTGTTAGG[T/C]AACGTACATATATTTCTTGTCATCAACAAAGGTTTTAACAAAATACTGTA
Long Flanking Sequence:
TGACATGCTAATTTAGAGTTTCAGTGTCGGAATTTACAGTATTTGCATTAAAAAGGTATGCCCTGGCTTTAGAATGTTATAAAGGACATTTGCTGCTGTGATGACATTCTGTGTCAAAGGTAACATTTCGTCATCAGCATTAGTCCATGCTGAACTTCAGAACGTCATCACTACAGGTAGTTATTTGAACGATAAGTTAAATTATCTAACGTTATACTAACGTTACGTCTACAATTTGTAGTTATAACGTTCATTTCCTGTAGGTAAATTAAAATAGATTGGATTTAAATTAGATGGATATCGTTCTTTAAAACTTCCTTCTGCCTGGGTCTTTCACTTACGCAAGCTTACACGTTAAACAAGTTGTAAACTTTTTGAGAAGTGAAGTAATACATAATTTATTTATCTTTTGCCTTTGTAGGAATATTGTGACTGACTCTAATCAGTTTATAGAAGAAAGAAACGTCTATTATCGGACTACCATGTTGGCACCTGTTAGG[T/C]AACGTACATATATTTCTTGTCATCAACAAAGGTTTTAACAAAATACTGTATGTATTTTTTACAGCTACAGAATCATGACTTCGTAATTTAATTAATTCGTTTATTTTTTTGTCTGTGATTGTGATTAAGTTAACATTATCATAATTTGTGACATTGCGGCAGGTAATTGTTGATTTTACTAGCGTTTATTAGGCAACATGATTGCAACTCACTTACCCTGATTGTTCCAAAGTCATGTAGGCTAACTGTGTAGTGTGTAGCAAATGGGGAATTTTGCCTTTTCCCCTCCATGACATTGATGAATAGTAACTGACTAACGTTAGTGTAGTGTAAAAATAAATGTAAAAGCACCACATTTCATAAAAATGGTCAGAGTCTTGTCTTAAATGTGTCTTCAGGAAAAAAAATATAACATTTTCAGAACAATTCTTCTCCTGAGATAGTAATGCCTGGTTTATTAATCAAAGTCAGCTTTGTTGTTGTCTATTAAATGATATGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33473
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047113 | Nonsense | 101 | 438 | 3 | 11 |
ENSDART00000066944 | Nonsense | 101 | 289 | 4 | 8 |
ENSDART00000132864 | Nonsense | 100 | 437 | 2 | 10 |
ENSDART00000139053 | Nonsense | 135 | 472 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 4 (position 24781824)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 25705493 |
GRCz11 | 4 | 25694691 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAAGGCACAGAGCAGATGGGTTTGCTGTGGAGCCTGAGGCCTGTACCA[G/T]GAAGTCGATCAGCTCTCAGGTAATGAATGATAGTGTACTAAGTTTAAAAA
Long Flanking Sequence:
TGAATGTCACAATCTTTCCTAAGTCATTACATTATATTGATATTGTACTCAAGAAAAATGTAATATTATTTAACTATTATTATCATCATCATCATCTGTTAAAAATGAATGTGCTGCTTATAATTTTTATGCAAACCAAGATACATTTTTCAAGAATCTTTGATGAATAGAAAGTTAAATGTTTAATTTCTTCTTTTACAACTAATATTACAGGTTTTTTAAACTTTTAAAAAGTTTATATTTTAACAGCCTCAAACTTTAAACAGTAGTGTATAATCTGCAAAGACTGTTTATTCCATTTGTTATTTGTTTTGTTAAGTACTTAAATTACCTCACATTATGATAAATAACCTGCTTCGACTAATTGAAGATCAGTCACTTTAGCAATGAATGACATTTGTATGTATCCTGTTGAAATAGTGGCAAAAGATGAAAGTTTGGGAGGTACATATGAAGGCACAGAGCAGATGGGTTTGCTGTGGAGCCTGAGGCCTGTACCA[G/T]GAAGTCGATCAGCTCTCAGGTAATGAATGATAGTGTACTAAGTTTAAAAATACATTTTGATCCTAATGAATCCAAATTGTGAGATTTAAGTTTATTTATTTTATTGCATATTCATTCACTAATTTTTCAGGTCTCTTTTCATTTAAGGTTGCGCAAGACAAATGTACTCACACCGATGGTAGTTAACATTTCAGTCTACAATGGGCATCTGTCTCAAGGATTCAGTAAGACCTCAGTGCTGGCCACAACTGTCACAGAGCGCTGGTACATGGCACCAGGTGTCCAAAGGGTGAACATAAGAGAGAATGGAGTTCGAGGAACTTTATTTCTACCCCCAGGTACACACACACAGGAGAGGTGGTACACTTGTGGTAATACAAGAAAAAAATGATTCTGTGCAATTTTCCAACCAACGTTTTAAAACATTTGAATGAGTAAATGCACAATATGTACTTGCTTTTAATGTTCAGGTTATTTTAGTGTACAGATTTTTGTTTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26305
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047113 | Essential Splice Site | 171 | 438 | 4 | 11 |
ENSDART00000066944 | Essential Splice Site | 171 | 289 | 5 | 8 |
ENSDART00000132864 | Essential Splice Site | 170 | 437 | 3 | 10 |
ENSDART00000139053 | Essential Splice Site | 205 | 472 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 4 (position 24782164)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 25705833 |
GRCz11 | 4 | 25695031 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGAACATAAGAGAGAATGGAGTTCGAGGAACTTTATTTCTACCCCCAGG[T/C]ACACACACACAGGAGAGGTGGTACACTTGTGGTAATACAAGAAAAAAATG
Long Flanking Sequence:
TGATAAATAACCTGCTTCGACTAATTGAAGATCAGTCACTTTAGCAATGAATGACATTTGTATGTATCCTGTTGAAATAGTGGCAAAAGATGAAAGTTTGGGAGGTACATATGAAGGCACAGAGCAGATGGGTTTGCTGTGGAGCCTGAGGCCTGTACCAGGAAGTCGATCAGCTCTCAGGTAATGAATGATAGTGTACTAAGTTTAAAAATACATTTTGATCCTAATGAATCCAAATTGTGAGATTTAAGTTTATTTATTTTATTGCATATTCATTCACTAATTTTTCAGGTCTCTTTTCATTTAAGGTTGCGCAAGACAAATGTACTCACACCGATGGTAGTTAACATTTCAGTCTACAATGGGCATCTGTCTCAAGGATTCAGTAAGACCTCAGTGCTGGCCACAACTGTCACAGAGCGCTGGTACATGGCACCAGGTGTCCAAAGGGTGAACATAAGAGAGAATGGAGTTCGAGGAACTTTATTTCTACCCCCAGG[T/C]ACACACACACAGGAGAGGTGGTACACTTGTGGTAATACAAGAAAAAAATGATTCTGTGCAATTTTCCAACCAACGTTTTAAAACATTTGAATGAGTAAATGCACAATATGTACTTGCTTTTAATGTTCAGGTTATTTTAGTGTACAGATTTTTGTTTGTTATCAGCACTAGCTACTAGTGTACGCGAAAAATCGCATTAGGAGTTTAGGGATATGGCACAAGACATAAACGTGTATTCAACACTTATATTCAGCAGTCTACATATGTTTGTTGCTTTACAAACATGCACAGCAAGTTTTAATAAATACAATTAAACATACCTTATGCCTTCTTGGGGTGGCGCTGAATAAATTTATAATCCATATATCCATCATTTTGGATTGCGAGAACTGCAGTGCATTGGTGTCAGTTGCTTAGCAACAGAAAACAACCGCAAAACCATTGTGCACCTGGCTTTATTGCTCTACCTGCATCTCCTGTTTTTAAAATCAGAGTCCTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40305
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047113 | Nonsense | 329 | 438 | 9 | 11 |
ENSDART00000066944 | None | None | 289 | None | 8 |
ENSDART00000132864 | Nonsense | 328 | 437 | 8 | 10 |
ENSDART00000139053 | Nonsense | 363 | 472 | 10 | 12 |
Genomic Location (Zv9):
Chromosome 4 (position 24785973)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 25709642 |
GRCz11 | 4 | 25698840 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGGCTCTTTATAAATATTACATCTATTTTTAACGCAGGTTGGGAGAATA[A/T]AGTGTCCTGTTATGTTGGTGAATGGTGGTGATGATCAGAACTGGGCTTCT
Long Flanking Sequence:
CCCCGCATTATTTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTTGGCTAGAATAAAAGCAAATTTAAAGGTCAATTTTAAAGTCAATATTATTAGCCTCTTTAAGCAATTTTTTTGGCATTGCCTACAGAACAATCCATCATTATACAAAGAATTGTCTTATTACCATAACTTGCCTTATTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGCTAGTAAATACTAGTATCTCGAAAAATAACTAGTAAAATATTATGTACTGTCATTATGGCAAAGATAAAAGAAATTAGTTTTTATAAATGAATTATTTAAACTATTATGTATAGAAATGTGTTAAAAAAATCTGCTCTCCGTGAAACAATTAGGAAAAAATATAAGCGGGCCAATAATTCAGAAGAGCTAATAAATCTGACTTCAACTGTATATAGAGATATTTCAGTTTTTTTAGGCTCTTTATAAATATTACATCTATTTTTAACGCAGGTTGGGAGAATA[A/T]AGTGTCCTGTTATGTTGGTGAATGGTGGTGATGATCAGAACTGGGCTTCTGTTGAATCTGCTCAAGATGTGAGTCATAATATACATCTTCAGTTATATTGAACAGTATATAACTGTTCAGTGCACAGTATAAATGAGAATTTTGAAAATAATTATTTTGATTATTTCTCATTGCATATAAACAATATATTTTGATGCATTTTAAAAAAACTATATCATTATATCAATTAACTGAGTGGTCATCTAACATCTTCAGGAATAGAAAAATAATACATTTAAATTCAAATGAGTTTTTTTTTTCTGGCTGGGTGTCGATGTAACAATTTTGTATTGCATTACATCTACATGTTTTGAATGACAAAATAAAGGAAACTAAGTTTATTTAGTTCTCTTGAGTTTTTCTCTATTACATTTTTATTTAATACGTTTTTCTAACATATTCATTGGGGTGTACTAATTTTTTCACCATGATCATTTATTTTGTTAAATTTGTGACAGTTT
Associated Phenotype:
Not determined