ZMP
coq10b
Ensembl ID:
ZFIN ID:
Description:
Coenzyme Q-binding protein COQ10 homolog B, mitochondrial [Source:UniProtKB/Swiss-Prot;Acc:Q567E6]
Human Orthologue:
COQ10B
Human Description:
coenzyme Q10 homolog B (S. cerevisiae) [Source:HGNC Symbol;Acc:25819]
Mouse Orthologue:
Coq10b
Mouse Description:
coenzyme Q10 homolog B (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:1915126]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34679 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa41456 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa34680 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34679
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
|---|---|---|---|---|---|
| ENSDART00000078576 | Nonsense | 8 | 238 | 1 | 5 |
The following transcripts of ENSDARG00000056141 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 33211945)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 32367891 |
| GRCz11 | 9 | 32178637 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGAGGCGAAAGAGAGGTGAAGTGAAGATGGCGAGAGGCTCCCGGTGTT[T/A]GAGGAGAGCGGTAGCGGAGTGTATCAGAAACTTACCGTCCACAGCCGGTC
Long Flanking Sequence:
ATTGACTTAGGACTAACTTATATTACTATCAAATTCTGTGACGATAACAGTAATGGCAACAGTAGTTTAGTAGCAATTTCATTGTAACTTAACTGGACAGATATGCATAAATATTATTTAATTTACATATTTGTTAATTATAATACTTTATAGTAAGCAAAACTTATTAATTCGTTTACACTGACTGTGTCCTCAAACAAATTTAGCAGTAACCTTTACTAACTATGCACTGTAGGTCGCGCAGTCTGGGCAACCCTATCCTGCATCCCGTGACAATTCTGCGCACGCAAACCCTCTGCACAATTAAAACACTTACGTCAGTGAGTGTCATCGATGACGGACGGACGACTCAACGAATCAGAGGCCGTGAAAAACAGCCTCGGCCAATGACATTGTAGGACGGGTCTTCGAGAGGGCTGGTCTTCGAGACGGGAAAAGAGTTCTCGACGGGAGGAGGCGAAAGAGAGGTGAAGTGAAGATGGCGAGAGGCTCCCGGTGTT[T/A]GAGGAGAGCGGTAGCGGAGTGTATCAGAAACTTACCGTCCACAGCCGGTCGAGAAACACCAGGGAAGAGTGGAGTGAGGTAATTAAAGACGGTTTAATGTTTCGCACTGTCTCTGTGCGGTTATCTGAAGACTAAACTGAGTAACGCAGTGAAGTAAGTCGCGAGCTTCTGACGATATTTGGACGGTTAGTTTCGCTCTTACAAGTGGATCCTGTTTAAGGCCAACTTGACAAGTTTATGTAAATGAAGACCTTATTAATAGTTCAACAATGGTTTAAACATTCTGACGTGCTCTAATAAGTGTTTAAAAAACTTTAGAGGGAGGGTTGGGTGGGTGGGAGTCACATATCTGGTTGCCAGATAAAGTGTCAGTAGCAAGGTTAAGATATTATGTAATTGTCCAGGTGTATCTAGCAAGCGCTTTTCTCATTTTTGCAATGACCGTTAATGAGCTGTATACAGCTAGTGTTTATTTAATACAGCTCTGAAATCACATACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41456
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
|---|---|---|---|---|---|
| ENSDART00000078576 | Nonsense | 35 | 238 | 2 | 5 |
The following transcripts of ENSDARG00000056141 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 33215119)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 32371065 |
| GRCz11 | 9 | 32181811 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTATGCTGTGTCTGAATGACAGACTTTCACCCTGTTTTGTCAACAGATA[T/A]CTGTCTTCATGTGGGATCTTGATGACCAGGGCGCCGCCCCTCTTCAGGGC
Long Flanking Sequence:
TTGATTAAAAACATATGCTATTGTGCTGTGAAAATGACGTATGGGAATGTTATTGCTCTAGTAACTTCTAAATTGGTGAGACTTTGTGAGTTAATATTGTGTGTTTAGCCTGAAAAGACGACAGTATAAACATGTCAATTTTCCAGTCATCTAGTCTAGATTTATGTTTGTTTTTTCAGGTCAGAAAACATTTTTTTGGGATTTAGATTAAGGTCAGAAAGTAATTGTTTTCACTAATTCTCAGGAGAAAGGGCTCTGTATTGATTAAGAGTTGTAATCTTGTTAATTGCACACAGCCATCTTTGTGGTTGATAGGTTTTCTCAACTCTTATCTGACTCAGGAGACGTCTGCTATGTTAAGGCATTCAACAAGCAAACAGGGCCTAAATCATCATACTTATCATTGCATGTACACAAAGTCTTGTACAATGCCGCTACGTGTCTTTATTGAGTATGCTGTGTCTGAATGACAGACTTTCACCCTGTTTTGTCAACAGATA[T/A]CTGTCTTCATGTGGGATCTTGATGACCAGGGCGCCGCCCCTCTTCAGGGCTGTATCAAGTCGTGCAGTGGTGGCTCCAGCCAGGAGCTTCTTCAACTTTGCAGAGTCATTCAACAAGAGGAAGGAGTACTCTGAAAGACGCATTATTGGGTATGTTCCCAACCATGTTGGACGTGATGCATGATCTAATGCTAATTTTAGTTTTTATTGAGGTCTGTCATTACTCTGACCCTTATGTAACAGGGCATGGGAATATTTATGGTGTCAGCTTTTTAGGTATCTGCCTGGAACATTTATCTCCAGCAATAATGCAGAAAATGTACGGCTAAAGCAGTGGTCACCAAACTTGTTCCTGGAGGGCCGGTGTCCTGCAGATTTTAGCTCCAACCCTAATCAAACACACCTAACCAAGCTAATCAAGGTGTTACTAGGTATACTTGAAACATCCAGGCAGGTGTGTTAAGGCAAGTTGGAGCTAAACCCTGCAGGGACACCGGCCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34680
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000078576 | Nonsense | 99 | 238 | 3 | 5 |
The following transcripts of ENSDARG00000056141 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 33217365)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 32373311 |
| GRCz11 | 9 | 32184057 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACACGCAGGTACTCAATGCAGGAAATGTATGAGGTTGTGGCCAAAGTT[G/T]AAGACTACCTGCTATTCGTGCCCTGGTGTAAGAAATCAGATGTTATTTTC
Long Flanking Sequence:
AAATAATATTTCAAAACTCTTCCATCGTTTATTGTTTTTAAGAAAATATCTAAAATCTTTGTGAAATGAAAGTTTAAAATGGCTTAAGGGTTTAATTTATGTATTGTATTTACCTACATTGTTATAGCATTTGTTTGTTTTATATTGGTTTATTAATTTAATGTAATTTTATTATAACGGATATTTGTAATTCTTTAAATGATTTCAACTTGGGCGATTTTTATCTTGATTTGACACTATTGTGTTGAGCCTACAAAAGTAAAACACATAATTTGTAAAGTTTTATGTCTTTCTGCTGTATTCATATTTTGTATTATCTCCAAAATAAAGAAAGAAAGAAACCCTGCTGCTCGCAGCATCAACAGAGCTGTCAAGCAAGCGCTCTTTTGCCCTGTCTCTCACACACATACAGGCATCTATTCTTTCATCAATTCATCAATCTATTCTTTGTGACACGCAGGTACTCAATGCAGGAAATGTATGAGGTTGTGGCCAAAGTT[G/T]AAGACTACCTGCTATTCGTGCCCTGGTGTAAGAAATCAGATGTTATTTTCCGCCGCTCAGGCTTTTGCAAAGCTAAACTGACTGTAGGCTTCCCTCCTGTGGTAGAAAACTACACCTCTCTCGTTTCTACAGTTCGCCCTCATTTGGTCAAGGTATGTGCAGCGTTTCATTGCATAATAAAGATCTGATATGTTTAATACATGGCAGTGGTTAAGTGGCAAACACAATATTAAACAATATGTTGTTAATCCAGTGTATGTGCTACAGTTCATTTGTAACTTCTGTTCTTAAGGCGTCTTGCTCTGATGGAAAACTCTTCAATCACCTGGAGACAGTGTGGCGCTTCAGTCCTGGCCTTCCTGGCTACCCACGTACATGCACACTCGACTTCGCTGTGAGTTTTACAAACACAATCCAGTTTCTAACCTACTGAGACTGCTTTTGATTATTAAATACACTCACTGACCACTTTAAAAGGTACACCATACTAGTACCGGGTT
Associated Phenotype:
Not determined