ZMP

acad11

Ensembl ID:

ENSDARG00000045411

ZFIN ID:

ZDB-GENE-040426-814

Description:

acyl-CoA dehydrogenase family member 11 [Source:RefSeq peptide;Acc:NP_956472]

Human Orthologue:

ACAD11

Human Description:

acyl-CoA dehydrogenase family, member 11 [Source:HGNC Symbol;Acc:30211]

Mouse Orthologue:

Acad11

Mouse Description:

acyl-Coenzyme A dehydrogenase family, member 11 Gene [Source:MGI Symbol;Acc:MGI:2143169]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa11388	Nonsense	Available for shipment	Available now
sa6759	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa11388

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000066778	Nonsense	78	769	3	20
ENSDART00000143921	Nonsense	78	277	3	7

Genomic Location (Zv9):

Chromosome 24 (position 11217038)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	11304441
GRCz11	24	11444808

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TNNNNNNAAATTCATGTATTGTGTGACTTTTTTNGTTTACAGATAGATAGAGAGTA[T/A]GCTGTTCAAAAGTCTTTACATTCYGTTGGCTTTCCTGTTCCYTGYCCTGT

Long Flanking Sequence:

TTAATGTTTTTTCTTTAAATATGTTTTGCTATGGTTTAAAAAAATAATAATTATACACTACATCAATTCAGTGGCCAACATATAAATGTTGAAACAACACTAACTTCTTTCGTTATTTTTTTTAGTAAGTTAGTGTTTAATTGGAGCAAAAATAGTATAGCTCAATATTTTTACACTTTTTTGACGCATATTACATATAAACTACATCTAACTAAGCCAATGGTAATAAAAATATGCCAGGTATAGTTTTTTTAATTTTTTATCATTTTGTTGAATATTTTATTTCTTTATTATTATTATTATTATTATTATTATTATTATTATTAATGAGGAATAAGGAGCACAAATAAAGAAGGTATGTACATGACACAGGACCTTGGACTATTTCTCATTTTGTGAAAACATGATTGAGCTCTGATTCCCAGCTCTGCTTTATTTTAAAGAAATACTTAAATTCATGTATTGTGTGACTTTTTTTGTTTACAGATAGATAGAGAGTA[T/A]GCTGTTCAAAAGTCTTTACATTCCGTTGGCTTTCCTGTTCCCTGCCCTGTGTTATACTGCGCAGATACTGGTGTCATTGGCACAGAGTTTTACATCATGGAGCATGTACAGGTATGTACAATCTGTAGTTATTTTTTATCTCTTTCCATTCAAAGGAGCAACAAGGATGCACATTTAATGCCCTTTTTTACTTGGGAAGCAGAAAGCGATGCCTTCTGTTTCTCCTAAAGTGAAAGCATTTTGTCCGATCGAGCGTGGTGTATGCATTGGGGTTTTCGATGTTGCAATAGTTACGGTCAACAATGTGACATTGTATTTGCTCATATCTAACACAGATGTTACACAGGAGTGCAACCAAACTTAAATAGGTACTACCAAAAAGTCTGTCCTGCACAGGTCTAGTCTGAATACACTCTTCCTAATAGATCTGCAGACAGTTTACCAGCTTTTGGCATCTGCCAGGAAATTGTTTTTCCTTTTTTTTTTTTACAACAGATAAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa6759

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
ENSDART00000066778	Nonsense	642	769	17	20
ENSDART00000143921	None	None	277	None	7

Genomic Location (Zv9):

Chromosome 24 (position 11128971)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	11216374
GRCz11	24	11356741

KASP Assay ID:

554-4384.1 (used for ordering genotyping assays)

KASP Sequence:

GCATGAGGGCAGTAGGGCTGGCAGAATGTGCACTGGAGCTGCTCTGCCAT[C/T]GATCAGCCCAAAGACAAACCTTTGGAAAAAGACTGTACCAACATGTACGT

Long Flanking Sequence:

ATGTTTTACTAGATGTTTTTCAAGACACTTCTATACAGCTTAAAGTGACATTTAAAGGCTGGTTAGGGTAATTAGGCATGTTATTGTATAATGATGATTTGCTCTGTAGACTATCGAAAAAAATATACCTTAAAGGGGCTAATAATTTTTTCCTTAAAACGTTTTTTTTTTTAATTTTAAACTGCTTTTATTTTAGCCAAAATAAAACGCATAAGACTTTCTCCAGAAGAAAAAATATTATCAGACATACTGGGAATATGTCCTTGCTCTGTTAAACATCATTTGGGAAGTATTTAAAAAATAAATAAAATCAAAGGGGGTTTAATAATTCTGATTGCAACTGTATATTTGATTTACAGTATTGTTTCTTCTTTGATTGGCTGTTTAAAGGTGAGGGGCGGGGTTTTGAGATAGCTCAGAAACGGCTGGGGCCTGGTAGACTTCACCACTGCATGAGGGCAGTAGGGCTGGCAGAATGTGCACTGGAGCTGCTCTGCCAT[C/T]GATCAGCCCAAAGACAAACCTTTGGAAAAAGACTGTACCAACATGTACGTATGTGATGTTTTTGAATGTAGTTTATAATTTAAATTTCACTGCTTGTTAAATATGTTCTGTTTAACTGTGCATGTGACAAATAATAATCATTCATTTAGATTCTTGAATCTATATATTACAGTTACTCAGCTTAAGATATATTTTAGCTTGCCATTTATGTTGCAGTACTCAATAACTTCATTTCAAAAACAATAGAAAGAATTGTGTAAATATATAAAACTTGCTGCTTATTTAGATTTTTTTGAAAATGCCCTGCTCTTTCCTGTTTTTTTTGTGATCCATTTGTTTGGTGTCCCACCACATATTAGTTTCCACTGACATTTTTTTTTTTTTTATCCTACTTAATTTATTTGCCCTTATGCATTTAAATCCTTCCTCCCCTTTAAGTTTCTCTCTTTTTTCAGTCTCGTTGAAAGAGTTAATCATCATCATTGTTGTGTCATGCAGTT

Associated Phenotype:

Not determined