ZMP
si:dkeyp-89c11.2
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC557184 [Source:RefSeq peptide;Acc:NP_001025281]
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 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18000 | Nonsense | Available for shipment | Available now |
sa6948 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18000
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028297 | Nonsense | 36 | 449 | 2 | 12 |
ENSDART00000044739 | Nonsense | 36 | 439 | 2 | 11 |
ENSDART00000133929 | Nonsense | 36 | 439 | 3 | 12 |
The following transcripts of ENSDARG00000089159 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 24695977)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 25619646 |
GRCz11 | 4 | 25608844 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTGAGCACTGAGAGTAGGAGATGTCCTCTGTTAACTGTTCAGCCAYGT[C/T]GAGGAATGGTGGACGAGAAAATTCAGATTATCATAAGGAATTTACTGCCC
Long Flanking Sequence:
ATTTATCCTGAAATGTTTACTGTTCCTAAATAGTTTAAAGGTTTCTCAAAACAAAATATTATGTGTTCAAAGCTGAAAATAGTTTTATTTTTTTACTCCGATTTAAAAATAATATATTTCAGAGCAATAATCACAATACCGTAAAATCGTAATATTTTTATCCAGGGTTATCAGGCCATCAGAATCGTATACTGGCCCATGCCTACTCCATAGAAAATGTCTGAACTTTTCACTGAATTGTTTTGTATGTAAATCAATGACTCAGTCACAAATATTTTTTTTACTTTTTAGCTTTTTAAATAATTTTTAATGTCTTAAAGTTAGTTTTAATTTATATTATTAAACATATCAGCCACTAATAGAAACCAATATGTGAATGGAAGTGTATTCTTAACAGAAACAAGACTTGCAAACAAGACGTTGCTGCCTTTCATTTATTTATCTCTAGAACTGTGAGCACTGAGAGTAGGAGATGTCCTCTGTTAACTGTTCAGCCATGT[C/T]GAGGAATGGTGGACGAGAAAATTCAGATTATCATAAGGAATTTACTGCCCAATCAAGAGGTAACGCTACACTCTCTACATCAGTCTGAAGATAAGGACTTCTGGGAGGCTTTTGGACACTATATCAGTGATAAACATGGAAAAGTAACAGGTGTGTACAACAATCTGATGCATGATTCTTTAAAATTTGAACACATGTAAACATACTCCATGAAAAAAATGACCCATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCCATCTATCCATCTATCCATCCATCCATCTACCTAATAAGAATTGAACATTAATAACCTAAAACAACGGTCCAGAATCCATGTATGACATTATGACTACATATATCCTGTTAAAATAGTGGCACAAACTTATGTTATGATAAATAACCTGTTTGACTATTTAAAGATCATATTAAAGTAAGGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6948
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 |
---|---|---|---|---|---|
ENSDART00000028297 | Nonsense | 54 | 449 | 2 | 12 |
ENSDART00000044739 | Nonsense | 54 | 439 | 2 | 11 |
ENSDART00000133929 | Nonsense | 54 | 439 | 3 | 12 |
The following transcripts of ENSDARG00000089159 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 24696031)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 25619700 |
GRCz11 | 4 | 25608898 |
KASP Assay ID:
554-4585.1 (used for ordering genotyping assays)
KASP Sequence:
GAATGGTGGACGAGAAAATTCAGATTATCATAAGGAATTTACTGCCCAAT[C/T]AAGAGGTAACGSTACACTCTCTACATCAGTCTGAAGATAAGGACTTCTGG
Long Flanking Sequence:
AATATTATGTGTTCAAAGCTGAAAATAGTTTTATTTTTTTACTCCGATTTAAAAATAATATATTTCAGAGCAATAATCACAATACCGTAAAATCGTAATATTTTTATCCAGGGTTATCAGGCCATCAGAATCGTATACTGGCCCATGCCTACTCCATAGAAAATGTCTGAACTTTTCACTGAATTGTTTTGTATGTAAATCAATGACTCAGTCACAAATATTTTTTTTACTTTTTAGCTTTTTAAATAATTTTTAATGTCTTAAAGTTAGTTTTAATTTATATTATTAAACATATCAGCCACTAATAGAAACCAATATGTGAATGGAAGTGTATTCTTAACAGAAACAAGACTTGCAAACAAGACGTTGCTGCCTTTCATTTATTTATCTCTAGAACTGTGAGCACTGAGAGTAGGAGATGTCCTCTGTTAACTGTTCAGCCATGTCGAGGAATGGTGGACGAGAAAATTCAGATTATCATAAGGAATTTACTGCCCAAT[C/T]AAGAGGTAACGCTACACTCTCTACATCAGTCTGAAGATAAGGACTTCTGGGAGGCTTTTGGACACTATATCAGTGATAAACATGGAAAAGTAACAGGTGTGTACAACAATCTGATGCATGATTCTTTAAAATTTGAACACATGTAAACATACTCCATGAAAAAAATGACCCATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCCATCTATCCATCTATCCATCCATCCATCTACCTAATAAGAATTGAACATTAATAACCTAAAACAACGGTCCAGAATCCATGTATGACATTATGACTACATATATCCTGTTAAAATAGTGGCACAAACTTATGTTATGATAAATAACCTGTTTGACTATTTAAAGATCATATTAAAGTAAGGATTTAGTTTTAGATTTTCATTTAATTTAATTTAGATTTTCCAGCTGGACACCAAAAA
Associated Phenotype:
Not determined