ZMP

cox15

Ensembl ID:

ENSDARG00000075933

ZFIN IDs:

ZDB-GENE-040426-955, ZDB-GENE-040426-955

Description:

COX15 homolog [Source:RefSeq peptide;Acc:NP_957500]

Human Orthologue:

COX15

Human Description:

COX15 homolog, cytochrome c oxidase assembly protein (yeast) [Source:HGNC Symbol;Acc:2263]

Mouse Orthologue:

Cox15

Mouse Description:

COX15 homolog, cytochrome c oxidase assembly protein (yeast) Gene [Source:MGI Symbol;Acc:MGI:1920112

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa9235	Nonsense	Mutation detected in F1 DNA	Not yet available
sa42108	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa9235

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
ENSDART00000109737	Nonsense	158	399	4	10
ENSDART00000110737	Nonsense	158	399	4	9

Genomic Location (Zv9):

Chromosome 13 (position 589990)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	587973
GRCz11	13	718264

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CGCATGTGGGGTCGTCTGGTGGGATTAGCTTACATTCTCCCCGCTGCGTA[T/A]TTCTGGAGGAGAGGATACTTCAGCCGCTCCATGAAGACTCGGGTTTTGGG

Long Flanking Sequence:

TGTAAGAATAGCCAAAACTGCATTGTATGAATTAAAAATATAAATGTATAACCCTGTCCTTAGGACATTATGTATGCTGTTATGTTGTAATGTTCCATGAAGACATTTAGTAAATTTCCTACTGTAAATATAGCAGATGAATGTTTGACTAGTCATATGCATTGCTGAAATCTTTCGCTTACTCCAGTGTCAGATTCTTTTGCTTTTTTTAAGGAGAAACTGTCTTCATTTTGACTCATTATTTCTGAAAACAACACTATATTTGTTGATGGTCTAGAAAAAGCTTCTTGATTTAAGAGTTTGTAGATATTGAGACAAGAAACAAGACACAAACTCTCTGCAGTGTGTGTGGATGTTGAATTGACGCAGCGCTGCTGTGTTTCTGACAGCATGAATCACGACATGACGCTGACAGAGTTTAAGTTCATCTTCTACATGGAGTGGGGTCACCGCATGTGGGGTCGTCTGGTGGGATTAGCTTACATTCTCCCCGCTGCGTA[T/A]TTCTGGAGGAGAGGATACTTCAGCCGCTCCATGAAGACTCGGGTTTTGGGCCTGTGTGGCTTTGTTGTCTTTCAGGTAAACACACACACACACACACACACACACACACACACACACACACACAATCTGTGCATTTACTTTTCTAAACAAATGCTTCTTGATTTAAGAATTTGTTGATATATGGACTAGAAACAAGACAGAAACTGCATGCATGCCTCAATAATGGTACGATACGGCTTAGTTTGGTACACTTTTATGGCTGTTTCCACTGTCAAAAGGTACCTACAAGTGAACCTTACCATACTATTTGGACACCCTTTGCAAAGGGTACCTAGTATGCTAACAGTACCAAAAGGCGGAGCTAGATGTGCAGCTGAACGCTATTGCTTTACAGAGCAAACATTGTTATACTATATGCATATAATAATGAGCCATAGTCGACCCAAACTCAAACAAACCTTGTCGTTGTCTTGATGTACAGCCAATAAGCCAAGAACAAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42108

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109737	Nonsense	354	399	8	10
ENSDART00000110737	Nonsense	354	399	8	9

Genomic Location (Zv9):

Chromosome 13 (position 593433)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	591416
GRCz11	13	721707

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTCCCCAGAAGAGCCAAGATGGCCATCAGCCTCCTCACCGCCATGGCCTA[C/A]ACACAGGTGAGACGCTGACCATAGACACTCACTAGAGGTCCAGAGCAAAT

Long Flanking Sequence:

ATAAGCGTGGGATTGTGTTGTCTGTGTTCTTCTTCTCTCTCAGGGGCTTTTGTGGCTGGTCTGGATGCAGGTTTGGTTTATAACTCCTTCCCGAAGATGGGCGAGCGCTGGATCCCAGATGACCTGTTAGCTTTTTCTCCAGCGCTCAAGAACGTCTTTGAAAACCCCACAACAGTGCAGTTTGACCACCGCATTCTGGTGAGCGGTCTGAAACATGTCTGTAGCTGTGTTTCCATCTAAAGATGTCAATTAGATTTATTCTCAAACTGTGATATCACATAAACATCAGTGAATAAAGCAGAGTTTACTGTCATTGAGAAACAAAAGAGAATAAACCGTGTGTCTGTGTGTGTGTGTGTGTGCGTGCATGCGTGTGTGCGTGTGTGTCTGCAGGGCATCGGCTCTCTGACCGCCATCACTGGACTCTACCTGTTCTCCAGGCGCATGATCCTCCCCAGAAGAGCCAAGATGGCCATCAGCCTCCTCACCGCCATGGCCTA[C/A]ACACAGGTGAGACGCTGACCATAGACACTCACTAGAGGTCCAGAGCAAATTAAAATGATTTGCCTCCTTTGCACTAGAAGACTCGACTTTCCGCACCGCATCTGTTTTCTCAGTCAGAACGTGAAACCAGAACTTCCGATGTGCACTGACAAAGCGTAAACAAAGCAGTGTTCAGCTCCATTATCACAGGTTGCATTCACATCAGAAGTGAACCGGACCAGAGTTCGCATGAGCCGTACCCCAGATCACCTCTTTCAGGTGGACTCGGGTACGGTAAACGAGTGTGCACTAGAGTTCAGAAGACACGTTCACACTAGCTAAACGTACCATACTATGCATCAAATGAACCTGGGTGCGGACCAAAAGTGCTAGTGTGAAAGCACCCTTAATCACAGATCGGACCATTTTTTGATCAGCCAAAAAGGGAAGGAGACAAATGTCGTTTGCTTTCCATTTATTACAAAAACATATAAACAATTAAAAAGTAATATGAAGAAATA

Associated Phenotype:

Not determined