ZMP

zgc:123262

Ensembl ID:

ENSDARG00000058390

ZFIN ID:

ZDB-GENE-051113-136

Description:

acyl-CoA thioesterase like [Source:RefSeq peptide;Acc:NP_001032476]

Human Orthologue:

ACOT9

Human Description:

acyl-CoA thioesterase 9 [Source:HGNC Symbol;Acc:17152]

Mouse Orthologues:

Acot10, Acot9

Mouse Descriptions:

acyl-CoA thioesterase 10 Gene [Source:MGI Symbol;Acc:MGI:1928940]
acyl-CoA thioesterase 9 Gene [Source:MGI Symbol;Acc:MGI:1928939]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa44135	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa37888	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa44135

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:

T > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000058948	Essential Splice Site	5	425	1	15

Genomic Location (Zv9):

Chromosome 24 (position 22559790)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	21806668
GRCz11	24	21951842

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCAGTTCCCCAAGCGGCAAGGGAAGAATAAAAAGATGTTTTGTCCACGG[T/G]GAGTGTTAAATAGACATTTTCCGATTTTGTTTTAATCTGTAAGGCTACTA

Long Flanking Sequence:

ATAAGTCCAGGGCACTCTAAAAGTAAATTAAAAAAAAATGTAAAACACTTACTTTTCGAATGGCTTGGACCTATGATTTCGTTTATCTTTTTCATTGTCAAGCTCTGTTGCGCCACCGAGTGACACACTCGTGAAACTGCAGTGTAATAAATAGACATGTACGTCATCACACTGTTATATTTGGTCACGTTGAGACTGTGAGTAAATGTTAATAGATTTTTTTGCTGCTAAATTTACCTAAATGGCTTAAACTACAATGTAACAACATGCCGTCCCAAGTTTAAGTATTTTCTCCATCGATCATTTATTGCTTTGGAAACATTCTAACGATATCTAAAGGTTCGTTTATTACGGTTAAAAGCGCGTTTATAGTAGTTTACACGGTGCGCGGATGATCGGAAACTGAAAACACAACTAATAACTGCAAGCTGTTGGTTTGAAGAAAGTTTCTGCAGTTCCCCAAGCGGCAAGGGAAGAATAAAAAGATGTTTTGTCCACGG[T/G]GAGTGTTAAATAGACATTTTCCGATTTTGTTTTAATCTGTAAGGCTACTAGTTCAACCGGTTTGCTAAATGTTTATTTATTTGCTAATGAACGGCTCCCTCATATCAGCTCCCTCATTTCGCACAGGTTCCTGAAGGCTGCCGTGTCCTTCACGTGCAGGAAGTTTTCCATGGGTCAAATATCTCGACAAGGAAAGACTCTTGATATGGCTGAAGGTAAATACAGGAATACGCTAATCATTCCTGTTATGCAATAGTGATTATGTTTCATAAAAAGTACAGTAGAAATAACCCTATATGCGGGTCAGGCTCGGGCGCTTACCTTTTTATACACAATGGCAAGAAAATGAACAGGATGTCTAACAGGATGGACATAATGAACTAAAGTTAGACATTCCTCTGTGAAGGGTTGGGGGTGTAAGTTGACATTATCAACCTGATCACTTGCATCTTTCGAAATTTATTGTTAAAACAATATTTCTGTAATTTTATCCAAAAGGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa37888

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
ENSDART00000058948	Nonsense	259	425	10	15

Genomic Location (Zv9):

Chromosome 24 (position 22550716)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	21797594
GRCz11	24	21942768

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTCTTCTGAAAGTGGCTCCTACAGCAGAGGAGAGGACACTCATTCACAAC[C/T]AGTTCCTCAACACTCTTGACACACGGTCCATTTATGAGCATTACACAGAT

Long Flanking Sequence:

CAAGGTCTTTATCAGGTCACCAGATGAAGGCCTTGTTGGTCAAACTGTTGTCCAATTCAATTGTGTTTTCAGAGCTAAAGTGGCAGTGTGCCATTTTGACCTTTTCTATTGTATTTGGCTTGATCAAGCACCTGCCTTCAATATTTTCTTAGATGTTTGCACACTGATAGTTTTTGTTTTAAATGAAAATTATATTTCCCAGGGATGGGTTGCAGCTGGAAGGGCATCCGCTGCGTAAAACATGTGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGTGACCCCGGATTAATAAAGGGACTAAGCTAAAAAGAAAATGAATAGATGAATAAGAATTATATTAAAAAATACATTAAAAAATAAAAGTCTGTGTTTGTATTGCTTTATTATTAATTATGAAATTTACATTGGTCAGTAAACAAGAAGAGGCGTGTGGAGCTGAGCACGGCGTCTCTTCTGAAAGTGGCTCCTACAGCAGAGGAGAGGACACTCATTCACAAC[C/T]AGTTCCTCAACACTCTTGACACACGGTCCATTTATGAGCATTACACAGATAGAAATACCTGCACCTTTTAAAAACCATTTTTAAAGAATAGTTATTTTTACCTGATAGGACTGTCAGCTTTCGCAGTCGGATTTTACCTCCAAATTCAGTGTGGATGGAAGATGCCAAATTGAAAGGGCTTGAGATTTGCCATCCACAGGTAAGAGGAAAAGAAGTTCAATCATTTTAATAAATAAATATTTTCTTTTTATATATATTAATGTAATGTGGGCTTTGTACAGGAAAGAAATATCTTCAATCGGATATTTGGTGGTTTTCTGATGAGAAAGGCTTATGAGCTTGGTCGAGCTAATGCCTGTGCATTTGCGTAAGAGGAAAATTAATCATTAAAAAATGTTCTTTTAAACAATGCTGTTCTTTCCTCTCATGGCCGTATTTGTGTCTTTCAGTGGATGTAGACCAACTGTTGTGGCAGTTGATGATATTTTATTTCGGAAGCC

Associated Phenotype:

Not determined