ZMP

acsl5

Ensembl ID:

ENSDARG00000075931

ZFIN ID:

ZDB-GENE-040912-169

Description:

long-chain-fatty-acid--CoA ligase 5 [Source:RefSeq peptide;Acc:NP_001004599]

Human Orthologue:

ACSL5

Human Description:

acyl-CoA synthetase long-chain family member 5 [Source:HGNC Symbol;Acc:16526]

Mouse Orthologue:

Acsl5

Mouse Description:

acyl-CoA synthetase long-chain family member 5 Gene [Source:MGI Symbol;Acc:MGI:1919129]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa6263	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa42064	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa6263

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000043887	Essential Splice Site	None	681	1	22

Genomic Location (Zv9):

Chromosome 12 (position 33144330)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	31342327
GRCz11	12	31457229

KASP Assay ID:

554-4693.1 (used for ordering genotyping assays)

KASP Sequence:

ACGTACACACTGGACACCTGCAGGTTACAAAGCTTTTAGCATCCTGAAAG[G/A]TACTAGCTTTCATTCTGAATTTCATATACATGGCATTGTGCAAAACACTA

Long Flanking Sequence:

CCAGAGTAATTAGCGATTGTAATGAAAACTTGAGTATGTGAGTGGGAACAGAAGCTGTATACAATATTTTAACCTGATCTATGCAACTTTCTACCCAATTCCATGTCACACTGACCAGCAAAGGCAAATGTCATAGTCCACATTTCAAACTAATGCTGTGCTGTTTTACATTCGCATGTCCTTTGGTGCATCCAGACTTTAAAAGCACAGTCTTGTGAATCTTGAGCAACATGCAATTACTTCACTGGACTCACTATATAGCCGCGATTCTGTTATTGTTCAGTCATTTGTATTATCAGGACACAGATAGCAGCATTTAGTTCAAAGGTCACTTATGTGCTTGTTTTATTGGACCCGGGACTATGCCTTTCTCCTCAGTCTTCTTGTGGCTGTTGCAAACCTCTACAAGGGACTCTCTCTCAGGATATTTTCTCCCAGTTTCAACTCTCGACGTACACACTGGACACCTGCAGGTTACAAAGCTTTTAGCATCCTGAAAG[G/A]TACTAGCTTTCATTCTGAATTTCATATACATGGCATTGTGCAAAACACTATTGTTCAGTTGCTGTGAAGGTATCAATTTGCGTTTAGTTTTATGCATGTTTACAATAGAAATGATTGTAATTTGATTTACGGTATATGTTCTTAGAGTTTAGTTGTCTATGAACATAATATGAAGTAGCTACATAGGTTTGGTTATTGCATAGTGCCTAGTTGTTATCCGATTTACAGTATGATAAGCCTGTGCATGGTATGTGCTGTACATGCTAAAAAGGACTGTTAAATAAAGTGTTACCACACAATCTGCACAGAAAAGGGTCACTTAAAAAAAGAGGACTTGTGTCTGTTGCATTTTGCACAATATAGAAGTAGTTTTGTATCCATAGATGATGGTATCAATTGTTCTTGTTGTGATAAACTGCTGAAGCGTTCATCAAGATATTTAGTATTGTCACATTATTGATGTAAGCTCCAAAAAAGGGTTATTTTAAAAACAAAAATAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42064

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000043887	Nonsense	471	681	16	22

Genomic Location (Zv9):

Chromosome 12 (position 33129500)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	31327497
GRCz11	12	31442399

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCTGATTTTCATTTTCTGACTTTAGGGCATGTTGGAGCTCCTATTCCATG[T/A]AACACTATCAAACTTGTTGATGTTGAGGAAATGGACTACTTTGCATCCAA

Long Flanking Sequence:

AATTCCATAATCAGGAAAGGAAAACTAGAAAAAGCAACACATCCTTTTACATGATCTTCCATTAATACAAAAACTATTTACAGACGTAACCAGCCCATTAGAAAAAATCTTTAATATTTAGCCCTGTATAAGTCTAAAACTTCATTCATAATGGTCTTAAAACGTTTTACAATTGACTCAAAAAAAACCTGCAGAAACCCTGAAAAATGAAAATAAACAGGTCTGAATATGTGCCCCTTTTTGTTATTTTAGGCAAACAAATGCACTAAATGCCATTTTTATTCTGTATTTGGAAGAAATGTGAAGAGTAGTTTGCAGAATAAAGCAGAAATCACACTTTAATCAGACACCTAACGTAAATACAGATTAACTGATCATTTTCAAGAGGATCATTTTCCATATCTTTGTTTGAATAAATAATAAATATAATATCATATTTATATATAGAATGCTGATTTTCATTTTCTGACTTTAGGGCATGTTGGAGCTCCTATTCCATG[T/A]AACACTATCAAACTTGTTGATGTTGAGGAAATGGACTACTTTGCATCCAATGGTGAAGGAGAGGTAATGGAACACAATTTTAGAAACCATCAACCGATATGTCATTGAAACATCTTATAGCTTTGTTTTTTCATTTCAGATTTGCGTCAAAGGGACAAATGTTTTCCGTGGGTATCTCGGTGATCCAGAAAAAACAGCAGAGGCTTTGGACAAAGATGGGTGGCTTCACACTGGCGATATTGGCAAATGGCTTCCTGTGAGATTTCAATTTAAGAGTCATACATAACTATATATATATATTTTTTTTTTTTTTCTTTTTTTCTTTTTTACAAATACATCAAACTTCATTAGCCAAGGTCACAAAACTAAAGAAAAATGTAAAACTGGATGTGATGGATGCTGAGCTTTGACTTCTAAATTATATATACAAGTCAATATTATAATAAGTACATGATTAGTCTAGTTGGCTAGTTAATCTTTAAAGATTAAAATGTTGTTGC

Associated Phenotype:

Not determined