ZMP

acaa1

Ensembl ID:

ENSDARG00000004687

ZFIN ID:

ZDB-GENE-040704-48

Description:

3-ketoacyl-CoA thiolase B, peroxisomal [Source:RefSeq peptide;Acc:NP_001002207]

Human Orthologue:

ACAA1

Human Description:

acetyl-CoA acyltransferase 1 [Source:HGNC Symbol;Acc:82]

Mouse Orthologues:

Acaa1a, Acaa1b

Mouse Descriptions:

acetyl-Coenzyme A acyltransferase 1A Gene [Source:MGI Symbol;Acc:MGI:2148491]
acetyl-Coenzyme A acyltransferase 1B Gene [Source:MGI Symbol;Acc:MGI:3605455]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa11166	Essential Splice Site	Available for shipment	Available now
sa30748	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa11166

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC
Order Allele From EZRC

Mutation:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000007997	Essential Splice Site	128	418	4	12

Genomic Location (Zv9):

Chromosome 24 (position 20935292)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	20182421
GRCz11	24	20326840

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TGTAAACAGGCAGTGCTCCTCTGGACTACAGGCACTTTTTAATATTGCAG[G/A]TAASAATGACATTAAAGCTGTAAAAYGGCYCACTCYTAATAGGGTACAAG

Long Flanking Sequence:

CAGACTATTTTTATGAAGTGTAATTATAAAACTAGAAATTATTTTTACCATTAGAGACTGGCTATACACACTGTTGACACGATAATGTTAAAACTCCTTATAAAAGTGATTTTTGCATAATTGGTCTCCTTTAAAATATCCCAACATACTAGCAATACAAATGACAGTCATATATTTATATTTATATATATTTTTTCAGGTAATGTTCTACAACCTGGGGCAGGTGCACTGATGGCTCGAGTTGCACATTTTTTTAGGTGAAATTAATTTACAGTATATATAATAAATGAGTAATCAATTGAATATATGTGTAGTATCTATAGTATTTGTAGTGTCTAAAGTGAGTTAAGTAATTGATATTACTATAGAATAATAAATCAATGATGTTGAATATATGAATTGGCTGACTTTATATTTCAGTGGCTTTCCAGAGTCCGTACCAGTCTATACTGTAAACAGGCAGTGCTCCTCTGGACTACAGGCACTTTTTAATATTGCAG[G/A]TAAGAATGACATTAAAGCTGTAAAATGGCTCACTCTTAATAGGGTACAAGATTACAGTTGTCACAGGATATTTTCTTTGTTTTAAGGTGGAATCAGAGGAGGTTCCTATGACCTGGGACTTGCTTGTGGGTTAGTACAGTATGGCAAATCTGTAGTGAAAGATATGTAGTATTAAAAATTTGATATTATCTGTTTAAACCGTTTGCCAGCAATACAATATTTTCTTGAATAACCCCTGAGACTTTAAGTTAGGATTTAAATAATGTAACAGATTCGCAAATTCCTGGTTCTCTTAAGCTTTTACACCGTAAACATTTTTGCGTTTCACAGGATTGATTAGATTTAATTTGATGATTTATGCTGACATCTGAACTTAGCTCTGCACCAAACAAGTGGACCAAGTTCTCTTGAAAAAATGGGTCTTAGTCTGCTTTCAAATAAACTTTATTCATAATAAAACCCCCTTTTTTAAGTTTTCAGTGTGAATTCTAAATAAGCAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa30748

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000007997	Essential Splice Site	143	418	5	12

Genomic Location (Zv9):

Chromosome 24 (position 20935423)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	20182552
GRCz11	24	20326971

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTTAAGGTGGAATCAGAGGAGGTTCCTATGACCTGGGACTTGCTTGTGGG[T/C]TAGTACAGTATGGCAAATCTGTAGTGAAAGATATGTAGTATTAAAAATTT

Long Flanking Sequence:

TAAAATATCCCAACATACTAGCAATACAAATGACAGTCATATATTTATATTTATATATATTTTTTCAGGTAATGTTCTACAACCTGGGGCAGGTGCACTGATGGCTCGAGTTGCACATTTTTTTAGGTGAAATTAATTTACAGTATATATAATAAATGAGTAATCAATTGAATATATGTGTAGTATCTATAGTATTTGTAGTGTCTAAAGTGAGTTAAGTAATTGATATTACTATAGAATAATAAATCAATGATGTTGAATATATGAATTGGCTGACTTTATATTTCAGTGGCTTTCCAGAGTCCGTACCAGTCTATACTGTAAACAGGCAGTGCTCCTCTGGACTACAGGCACTTTTTAATATTGCAGGTAAGAATGACATTAAAGCTGTAAAATGGCTCACTCTTAATAGGGTACAAGATTACAGTTGTCACAGGATATTTTCTTTGTTTTAAGGTGGAATCAGAGGAGGTTCCTATGACCTGGGACTTGCTTGTGGG[T/C]TAGTACAGTATGGCAAATCTGTAGTGAAAGATATGTAGTATTAAAAATTTGATATTATCTGTTTAAACCGTTTGCCAGCAATACAATATTTTCTTGAATAACCCCTGAGACTTTAAGTTAGGATTTAAATAATGTAACAGATTCGCAAATTCCTGGTTCTCTTAAGCTTTTACACCGTAAACATTTTTGCGTTTCACAGGATTGATTAGATTTAATTTGATGATTTATGCTGACATCTGAACTTAGCTCTGCACCAAACAAGTGGACCAAGTTCTCTTGAAAAAATGGGTCTTAGTCTGCTTTCAAATAAACTTTATTCATAATAAAACCCCCTTTTTTAAGTTTTCAGTGTGAATTCTAAATAAGCAAGGACTAAATTGATAATTTTTCTGGTCCATATCAAACTTTATGTATATGGATTTTACTTTAACTAGATAAAAATCCATTGAGATCAAGATCTCTTTTACAAGGGTGACCTGGCCAAGAGGTCTGCAACACAC

Associated Phenotype:

Not determined