ZMP
si:dkeyp-89c11.3
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC557032 [Source:RefSeq peptide;Acc:NP_001020658]
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 |
---|---|---|---|
sa40304 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20290 | Nonsense | Available for shipment | Available now |
sa9080 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38443 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa40304
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041965 | Nonsense | 4 | 450 | 2 | 12 |
ENSDART00000066942 | None | None | 430 | None | 11 |
ENSDART00000133425 | Nonsense | 4 | 450 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 4 (position 24717731)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 25641400 |
GRCz11 | 4 | 25630598 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCTAGTTTGATTTACTGTAATCAATTTATTATCACAAATGAAACGCTG[G/A]TCTACTCTTATCGGACGTGTCATCATGCTAGCACCAGTTAGGTAATGTAC
Long Flanking Sequence:
TGCTAATTTATGCTAGAATCATGCCAACAACATGCTAAGTCATGCTAGAATCATGCTAGTAACATGCTAATTCATGCTAGAATCATGCTAACAACATGCTAATTCATGTAAGAATCATGCTACTAACATGCTAATTCATGCTAGAATTATCCTAGTAGCATGCTAATTCATGCTAGAATCATGCTAGTAACATGCTAATTCATGCTAGAATCACGCTAACAACATACTAATTCATGCTAGAATCATGCTAGTAACATGCTAATTCATGCTAGAATCATGCTAACAACATCCTAATTCATGTAAGAATCATGCTACTAACATGCTAATTCATGCTAGTAATATGTTAACTCAAGCTAAAATCATACTAACATTCTATTTACACTTTAAAACCACTTCAAACTTTGAGATTCGGCTTTTCAAGCCACCATAAAGTTTGTCCTCAAACTTTAATATCTAGTTTGATTTACTGTAATCAATTTATTATCACAAATGAAACGCTG[G/A]TCTACTCTTATCGGACGTGTCATCATGCTAGCACCAGTTAGGTAATGTACAAATATTTCTTTTATGTTTCTTACAAAGAGTAATAAAAATTCATTTTTTTCTGTTACAGAATCATAAATTGCCTTTCTGTCATTTAATTGTTATTGCCTTATTTATTTATTTATTTATTTATTTATTTTTTGATGACAGTTACCAGTATAGTTTGTGACTAACACAAAAAAATGTGCCATTTTGATGGAAAGCTTGTGGATTTTGCCTTTCAACTCCACGACATTGAAGACTAGACAGTAATGTGTAATAGCCACTGAATAGCTGTTAGTGTGTCAGCTTCAAAAAGAACACAAAAGGATAGCCACAGATGTTTCAGGAAAGTGGCCTGCCTTGCCTACATATGACTTCTGAAGCAAGGTTAGTGAGTGAAAAACAAATAAAAGTTGTTGATTTATTCAATGAAAATCCTTGTGTTGGCGTGCTCTTGGGTAGGCATGGGACGATAACTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20290
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041965 | Nonsense | 104 | 450 | 4 | 12 |
ENSDART00000066942 | Nonsense | 103 | 430 | 3 | 11 |
ENSDART00000133425 | Nonsense | 104 | 450 | 3 | 11 |
Genomic Location (Zv9):
Chromosome 4 (position 24720072)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 25643741 |
GRCz11 | 4 | 25632939 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAGATGAAAGTTTGGGAGGCACGTATGAAGGGACAGAGCAGATGGGTT[T/A]GCTGTGGAGCTTGAGGCCTGTACCAGGAAGTCGATCTGCACTCAGGTAAG
Long Flanking Sequence:
ACCTCATCCACTTACCACTCTATCTTAGATTGTTTCCATTCGTTGCTTATATAAAAATGGCTCATTTTGTACAGTTGGTACATAATTGGCTCATATTCTGCACAGCAGATGATAATAAAGAACTTGCTTTGACAAACTAAAGGTAATATTAACTTAATTTTAGCTGAATGTTTCAGCTGGGTACCAAAATGTACAATCCATCCGTCCATCCATTACTAAGAATCAAACATTAATAACCTAAAACGATGGTGCAGAATCCATGTATGACATCATGACTACATATTGTATCCATACTGTATCCTATTTAAATAATGGCACAAGCTTACATTATGAAAAATAACCGGTTTGACTAATTAAAGATCATATTAAAGTAACTTTAGATGGATTTTCCAGCTGGACACTTAAATGTATAATGAATGACATTTGTATGTATCCTGTTGTAATAGTGGCAAAAGATGAAAGTTTGGGAGGCACGTATGAAGGGACAGAGCAGATGGGTT[T/A]GCTGTGGAGCTTGAGGCCTGTACCAGGAAGTCGATCTGCACTCAGGTAAGTTACCGTAGTATTATGGTGTATTTACTGTAGTCTGTTTTACAAAATTTAAATACCTTCTTTTGCAAAAAGCGAGGTCATTATTTTTATTTATTCCTACACTTTTTTATTATTCAAGGTTGCGCAAGATGAATGTACTCACGCCAATGGTAGTTAACATATCAGTCTACAATGGGCATCTGTCTCAAGGATTCAGTCAGACCTCAGCGCTGGCCACGACTGTCACAGAGCGCTGGTACATGGCACCAGGTGTACAGAGGGTGGACATAAGAGAGAACGGAGTTCGAGGAACTTTATTTCTTCCCCCAGGTAAAATACAATTCATACATATATAAATGTAAACATGTCTCTTCTAAGACGTAAGATTTTTATTTTTTTGGTGATCGTCAAAAAAGGCAAAAATGTCAGAGTGAAAAATGTTGGTTGGGTTTTGAACCAAAACCCAGAATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9080
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041965 | Splice Site, Nonsense | 120 | 450 | 5 | 12 |
ENSDART00000066942 | Splice Site, Nonsense | 119 | 430 | 4 | 11 |
ENSDART00000133425 | Splice Site, Nonsense | 120 | 450 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 4 (position 24720241)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 25643910 |
GRCz11 | 4 | 25633108 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ASCGAGGTCATTAKTTTTATTTATTCCTAYACNTTTTTTATTATTCAAGRT[T/A]RCGCAAGATGAATGTACTCACGCCRATGGTAGTTAASATATCAGTCTACA
Long Flanking Sequence:
GTTTCAGCTGGGTACCAAAATGTACAATCCATCCGTCCATCCATTACTAAGAATCAAACATTAATAACCTAAAACGATGGTGCAGAATCCATGTATGACATCATGACTACATATTGTATCCATACTGTATCCTATTTAAATAATGGCACAAGCTTACATTATGAAAAATAACCGGTTTGACTAATTAAAGATCATATTAAAGTAACTTTAGATGGATTTTCCAGCTGGACACTTAAATGTATAATGAATGACATTTGTATGTATCCTGTTGTAATAGTGGCAAAAGATGAAAGTTTGGGAGGCACGTATGAAGGGACAGAGCAGATGGGTTTGCTGTGGAGCTTGAGGCCTGTACCAGGAAGTCGATCTGCACTCAGGTAAGTTACCGTAGTATTATGGTGTATTTACTGTAGTCTGTTTTACAAAATTTAAATACCTTCTTTTGCAAAAAGCGAGGTCATTATTTTTATTTATTCCTACACTTTTTTATTATTCAAGGT[T/A]GCGCAAGATGAATGTACTCACGCCAATGGTAGTTAACATATCAGTCTACAATGGGCATCTGTCTCAAGGATTCAGTCAGACCTCAGCGCTGGCCACGACTGTCACAGAGCGCTGGTACATGGCACCAGGTGTACAGAGGGTGGACATAAGAGAGAACGGAGTTCGAGGAACTTTATTTCTTCCCCCAGGTAAAATACAATTCATACATATATAAATGTAAACATGTCTCTTCTAAGACGTAAGATTTTTATTTTTTTGGTGATCGTCAAAAAAGGCAAAAATGTCAGAGTGAAAAATGTTGGTTGGGTTTTGAACCAAAACCCAGAATTTTTTTTTTGTGCCACTTAAATGATGAAGAGCTGTCAATTGATAGAAGAGGTGTGTGGTTTTTTTTAAGGATTGGTTCATTATTTCAGTGAATTTTTTTGCATGATAAACAGTGACTTGAAATTGCAAAATAACTTTTTATATAAGTGCAATTTTTTTATTTTATATATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38443
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041965 | Essential Splice Site | 336 | 450 | 9 | 12 |
ENSDART00000066942 | Essential Splice Site | 335 | 430 | 8 | 11 |
ENSDART00000133425 | Essential Splice Site | 336 | 450 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 4 (position 24727378)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 25651047 |
GRCz11 | 4 | 25640245 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAGAAATTATCTTGCCGATTCCCTCAGACCCGGCTCTCAAAGCAGACG[T/A]ATGTATGACTTTAGTATGTTTTTCTTTTCAGTGTGTTTTCATTTTTTTAA
Long Flanking Sequence:
TAGTGAGAGTAAATCATTTGAGACGCTTTCCGAAATTAGTTGAGGCCACATAGTCTATGAGAAAACAAAATGTTTGTTTTAAACATTGAATGCATGTATATCTTTTTAGCAGACCTACAAAACAAAATTAACATTTTTAAAATTATAGCAACAGGCATTTTTAACAATAAGATTTTTGCAATATTTTTACAAAATATAAATAATATTTTGTAATATTTGACTTTATCCACTGTATTAAAATAATGATATCATATGAGTATTTGGGTTGGTACATATTTGCATATTTTGCTAATGCAATTGAATGTTTTTGTCATGTGTCTTTCACAAAGTAAAAAATCATTTCATATCAGTGAATGACTGGTCCTAATGATAAACAGTCACACATTTTGTGAATGTTCATTGCAGGCTTATGGGTAAAGTACAAGAGAATGAGGACAAACATATAGTGACCAGAGAAATTATCTTGCCGATTCCCTCAGACCCGGCTCTCAAAGCAGACG[T/A]ATGTATGACTTTAGTATGTTTTTCTTTTCAGTGTGTTTTCATTTTTTTAAATATCAGTTGTGATTTATTTTTTCAGGTTGGGAGAATAAAGTGTCCTCTTTTGTTGGTGAATGGTACTGATGATCAGAATTGGGCTACTAATGAATCTGCTGAAGACGTGAGTTATTTGTATGCTTGTATGAATGTTTGTATGCATGATTTCAGGGTTACCACTTTAAGTCATTTCAAATTCTTTCACTGACTAAAAAGCTGATTTTCCATAAGCTATAATGTTGAGCAGTGCCTCCAGAATTTTTTGATTCTGTGAATGCTAAATGCTGCAATAATTAGAGGACCTTGCAATTTTTATTGATGCAAATTTTGGTCACACTATAGGAAATATCCATTACTAATATTTTTTGTATTTTGTGATTTGTCTAATGCCCGAAATGCTCAATCGTGTTAAATGCTGTTTTATGTTCAATCAACTTAAATTCATAAAAATGAATAAGTTGACTTAA
Associated Phenotype:
Not determined