ZMP

ACOT12

Ensembl ID:

ENSDARG00000054534

Description:

acyl-CoA thioesterase 12 [Source:HGNC Symbol;Acc:24436]

Human Orthologue:

ACOT12

Human Description:

acyl-CoA thioesterase 12 [Source:HGNC Symbol;Acc:24436]

Mouse Orthologue:

Acot12

Mouse Description:

acyl-CoA thioesterase 12 Gene [Source:MGI Symbol;Acc:MGI:1921406]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa9440	Essential Splice Site	Available for shipment	Available now
sa34983	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa9440

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
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Mutation:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000076731	Essential Splice Site	236	570	6	15

Genomic Location (Zv9):

Chromosome 10 (position 44279026)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	43085052
GRCz11	10	42913432

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GGAGGRCAGATCATGGCCTGGATGGAGAATGTAGCTACAGTAGCAGCCAG[G/A]TATCAGATACACCTGCAARATGCATCATTAGCTGCACAACAACCCCATCG

Long Flanking Sequence:

TGTACCTAATAAAGTGGCCGGTAATATTGCATTATCAATTTGTAATATCAAGTTACCTTTCTCCCATCCTGTAAATAACAAATATGTAGGTTTTTAAACATGCTTATAAGGCCTCGTGCATGCATAATTATTGCATACTGCACATGTTGTATTTAAGCTTAAGCTGTTCCTGATTTTTTTTCCTACATTTAATTGTACAAATGTTTTTGATGAATCATGATTTATTCATGAAAAAAGTTGCATGTATGCATGCTTAGTAAATGTGACCCACTGTCTCTGGTGGAATGAACCAGTTGGTGCTGGTGGAGAGTGTGCTGAGCAGGATCTGTTGATGTTTCAGGATTGTACAGAGGGAAACCTGTGACACCTGCAGTGTCGACTGAGCTCACACGGGTCGAGAGCATCGAGTTGGTGCTGCCGCCACACGCTAATCACCATGGAAACACGTTTGGAGGGCAGATCATGGCCTGGATGGAGAATGTAGCTACAGTAGCAGCCAG[G/A]TATCAGATACACCTGCAAGATGCATCATTAGCTGCACAACAACCCCATCGCAAACCACACAAAACAACAATGCAACTTCCTGGGAAGCATTCAAAACATGCCATCAACTGCACAACAACACCTTTACAACACCCTAGAGACAAGTCAAAACATACTAGCAACCAAATACTAACCTCATGTCTATCTGTTGTTCTTGCTATCATACATGTGTTACATTTATTACAAAATAGCCAAGAAATACAACTGTTTATGATTGATTATTATAAATGATAATTCTGCAGGACTATGCAGTGTAGTTCTTAGCTCTTGGGTGTAATATATCTGCATTTTTTGTCTGTGTGTTTGTGTTCTCGCAGTCGTCTGTGTGGCTACTATCCTTCTCTCGGAGCTGTGGACATGTTTCGCTTCCGAGGGCCGTCATTTGTTGGTGACAGATTAGTGTTCAAAGCCATGGTCAATAACACCTTTCAGAACAGGTAAAGGAGCTACACACACCTGAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa34983

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
ENSDART00000076731	Essential Splice Site	439	570	12	15

Genomic Location (Zv9):

Chromosome 10 (position 44275341)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	43081367
GRCz11	10	42909747

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCATGCTCGCCGACCTGCAGCTACGGCCACAGTGGGACAAAAACTACCTG[T/C]AGGAGAACAAGAGATTGCGGTTTATGAGTGCAAAAACACTTCAAATTGAG

Long Flanking Sequence:

TTCCATAGCATTTGTTTTCCTACTATAGAAGTCAGTGGTTACAGGACTTCAGCTTTCTTCCAACTATCTTCATTTGTGTTCCACAGAATAAAATAAAGGTTTGGAAACACTTAAGAGTGTGTAAACTGAGTGCAAATTTACATTTTTGGGTGAACTATCCCTTTAAGCAGAACTAATGTTGTGTGTAACATCTCTGCCCTCTGCAGGTGTATTTGGGGTACAACAATGTGGCAGCTCTCACCGTGATAGCTGGACAACGGGACTGGGAGCCCAATAACATCACTGATAAGGTCATAACCATATAACATTTTATATATAAACTAAATTATATAATGTGCTGAATTAGCTGTGTGTGTGACTGGCAGATGGGACTCTATGTGCACGAGGAGGCAGATAAGCTGTGTTTAAAAGTCGAGATGCAGGCCAAAACCACGGCTTTTCATGCTTTCTCCATGCTCGCCGACCTGCAGCTACGGCCACAGTGGGACAAAAACTACCTG[T/C]AGGAGAACAAGAGATTGCGGTTTATGAGTGCAAAAACACTTCAAATTGAGTTTCTCACCATCTGAACTTTCTCCAGGAGCTGTGATGAGGTGGAGAAAGCAGACGAGGAGGAGACCATCTATCATGTTAAATGTGCTACAGTTAATGGAGGCAAATGTCGGGATTTTGTGTACCTGCTGTCTAAAAGGCAGCCCTGCAAAGATGGGTAGGTTTCACTAATGCACTTTTAACAATTTCTCAGTGCTTGCAGGGTTTCTGTGAGGTTTTAAAAAGTTTTAAATTCACTGAAATGTTGTCTTGTAGGTCTTAAATCCTTTTAAACATGTCTTAAGTTTCCTCTGTCCATAGCCCCTTTCACACATACAGACCTTTCCGGAAAATTACCGGCAATTTTTCGGAAAGGTTGTATGTGTGTACAGGCCCTTCTTGAAAATACTGGTAAATTCGTTCTGGCTATTTTCCGGAAAGAGAAGTTGTAATATTACCGGCAATTTGCCGGA

Associated Phenotype:

Not determined