ZMP
zgc:92453
Ensembl ID:
ZFIN ID:
Description:
ubiquinol-cytochrome c reductase core protein II [Source:RefSeq peptide;Acc:NP_001002657]
Human Orthologue:
UQCRC2
Human Description:
ubiquinol-cytochrome c reductase core protein II [Source:HGNC Symbol;Acc:12586]
Mouse Orthologue:
Uqcrc2
Mouse Description:
ubiquinol cytochrome c reductase core protein 2 Gene [Source:MGI Symbol;Acc:MGI:1914253]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa40184 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa17592 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa40184
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000010395 | Essential Splice Site | 96 | 459 | 4 | 14 |
Genomic Location (Zv9):
Chromosome 3 (position 59039774)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 58101449 |
| GRCz11 | 3 | 58171973 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGTTTAGATTAAATACTGGATGTGCTGTGAATAATGCCTGTGTGTTTC[A/T]GACCACTAAAGGTGCGTCAGCCTTCAAGATCTGTCGCAGTCTGGAGGCTC
Long Flanking Sequence:
ATATGTGTATATATATATATATATATATATATATATATATATATATATATATATATGTAAACATTTTGGATTTATAAAATGTAGAAACACTCTTCTCTATCAAAATAAAAAACAATTCAGTTCCTCTGTATAATAAGCACTTCTTGTGTGTATTGCCTTGTTGTATCACTGAATCCCTCCTCAAATCTAAATGTAATGCACTGGATCAGGGGTGTTTAAATGAGATTTCAAATCCTCCGCCCTTACCCATGATCAACACCACTTGTTTTAGGTGTCCAAGCTGCCCAGCGGTCTTGTGGTGGCCTCTCTGGAGAACTACTCCCCCGTCTCCAAAATCGGTGTGTTTGTGAAAGCCGGCAGCCGCTATGAGACTGCAGAAAACCTGGGCGTCACGCACATGCTCAGATTAGCAGCGAATATGGTGAGTGACAGCTCAGAATCAGAGGACTTGCAGTTTAGATTAAATACTGGATGTGCTGTGAATAATGCCTGTGTGTTTC[A/T]GACCACTAAAGGTGCGTCAGCCTTCAAGATCTGTCGCAGTCTGGAGGCTCTGGGTGCTAGTTTGAGGTCAGTTTCATGAGTGTGCATGAACACTTTCACTTTGCACTTTATCATTTCTCTCACGGTCGTGTTTTGTTTGGCTGTTTTTCAGTGTGACGTCTTCGAGGGAACACATGGTATATTCCCTGGACTTTCTTAGAGATGATTTGTGAGTATCATTGCTGTACATGAGCCATCAGCAACATCTAATAGACATGAAATATACTCTACAGATACAAGAAACACGGACACTGGAGTGTTTTAATGTAACGTCGATCAGCTGGTTTGTCTATAAGCTGACATACGAGCGATCCGCTGATGAAGCGTGGCTTTAAAACACTCCAGTGTCCCTGTATCTGTGTTTACACTCAGTAAACAGCGGTGAGTTCGGTGAACTGATGGCCAACCACAGCCATTTCTGTTGAGCACGTGAACACAATGGCAAATCCACGCTGTTTAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17592
Status:
Available for shipment
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:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000010395 | Nonsense | 198 | 459 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 3 (position 59042238)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 58103913 |
| GRCz11 | 3 | 58174437 |
KASP Assay ID:
2259-4215.1 (used for ordering genotyping assays)
KASP Sequence:
AAGCTGCATGAAGCTGCTTATAAAAACGCYTTGTCCAACTCGCTCTACTG[T/A]CCAGACATCATGCTGGGGAAGATCAGTGTTGATCATGTAAGAGGCGAACA
Long Flanking Sequence:
AAAGAGGGCCAGTGTCCAGGAGAGTTTAGCTCCAACCCTAATCAAACACACCTGAACAAGCTAATCAATCTCTTAGTAGGTATACTAGAAACTTCCAGGCAGGTGTGTTGAAGCAAGTTGGAGCTAAAGTCAGCAGGACACCGGCCCTCCAGGACTGAATGTGGACATCCCTGATGTAGACAGTCTGTCCTGTAGATTATATTTAAAAATTACTCTTGTGTGTGTTTTTGTGTGCAGTGACGGTGTGATCGAATACCTTGTGGATGTGACTACTGCTCCTGACTTCAGACCCTGGGAGTTGGCAGATCTCACCCCGAGGGTCAAGATCGACAAAGCCTTGGCTGAACAGAGCCCACAGATAGGTGCAGTACATGGTTTACTCCTAAATTAATGTAGAAAGTTGATTAAGTGATACTGAACAGCTGTTTTCTCCGCTCAGGTGTCCTGGAGAAGCTGCATGAAGCTGCTTATAAAAACGCCTTGTCCAACTCGCTCTACTG[T/A]CCAGACATCATGCTGGGGAAGATCAGTGTTGATCATGTAAGAGGCGAACAGCTTTCTGTACTGTTCCCCTACTGAAATGAGTACCAGTGTATACTAACACTGCCTTTCTGCTCTGAATCTGCAGCTTCAGCAGTTCTTTGACAATAATTACACCAGTGCAAGAATGGCTCTCGTTGGATTAGGTAAGTAATTTTTCTGCATAAAGTGTTCATTTCTTTTAAATAAGCTTATTTCAGGAAATTAACTCAGTAAATAGCAACAATTTAGGATTTATACACTTTTTGCTTATCGTTATAGTTCAGCTTAAAGGGATAGTTCACCCTTAAATCAATATTTACTACTGTTTATTCAACCCCTAAATGGTTTCAAAGCCTTTATGAGTTTCTTACTTCTGTTAAACACCAAGAAAGATATTATAAAACTATGGAGGTCAGTGGTTACAGGTTTCCAGAATTGTTCATATTTTCTTGTTTTGTGTTCAACTGAAGAAAGAAACTGAA
Associated Phenotype:
Not determined