ZMP
cpox
Ensembl ID:
ZFIN IDs:
Description:
coproporphyrinogen-III oxidase, mitochondrial [Source:RefSeq peptide;Acc:NP_001035183]
Human Orthologue:
CPOX
Human Description:
coproporphyrinogen oxidase [Source:HGNC Symbol;Acc:2321]
Mouse Orthologue:
Cpox
Mouse Description:
coproporphyrinogen oxidase Gene [Source:MGI Symbol;Acc:MGI:104841]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21253 | Nonsense | Available for shipment | Available now |
| sa6095 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa21253
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089172 | Nonsense | 157 | 449 | 1 | 7 |
| ENSDART00000127364 | Nonsense | 157 | 449 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 8 (position 19137431)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 18582319 |
| GRCz11 | 8 | 18613480 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGGAAAGACGAGATGTCGACAAGGATGGAGATGCTCATCATGGAGACA[C/T]AGTCGGCTTTCTGCAGAGCCCTGGAGCAGGTGGATGGAGGCTCATTCAGG
Long Flanking Sequence:
ACAGACTGCGTCGTGTTCGCTCAGCAGACAGCATGACTTCGTTAGCTTTGTGCACAATTAACAGCTCAACGAGATCAATAGCAAGACTGTGCCGAGTGTCCCACTCTGCGCATGGCACAGCTGATGTACACTCTTTCGTAGCCCGTTACTCAACCCTGCGTAATTGTAGTGCTTCTCTTCCGAGAGGAAAATGCTCATTCATAAAAACGGTAACCAGGCAGATGTGCCAGTCGTCGCCGAGGAGGATCTCTCTCGGACGGTACGGTAAAGGCGTGTTTCTGGCTGCAGGAGCCGCGGCTGTCACCGGTGTTCTGGCGGCTGGTGTAAGTCACTTCCAGCGGGCAGAAATGGCAACGAAGATCTCCAGAGTTGAGGAGGAGGACGGAGACATTCGGGAGAGGTGCAAGTCGTTCATGTCTCCACCAGTCACTGACATCAAGCTCCTAGAGCAGAGGAAAGACGAGATGTCGACAAGGATGGAGATGCTCATCATGGAGACA[C/T]AGTCGGCTTTCTGCAGAGCCCTGGAGCAGGTGGATGGAGGCTCATTCAGGGTGGATAGGTGGAGCAGAAAGGAAGGTTGGCTCTTTAATGTATATATATTTTTTAATTTCATCATGAAGCTTTCACTGTAAACTGTATTTTTTTAATATAATTTTTCTTAGTGTGTTTTGTTGTTAAAACAAGTTAGTTTGGATGAAACAATAAATGTGTAGTACATAACTTTTGGCACACAACAGGTTGAAAGTAGAACAAACAGTGTGGGCTAAAGTCCTGATTTCTGTTTAAGATATTTCCACATAAAGAGCACAGGGGTGTAATAATTATGTTACCACCTTTTAATTATATTAAGAATCAAAATTTTGGAGATTAAAAAAAATTAAAGTTGGTCACACTTAAGGTTCCACTGGTTTATTTATTTAATGTGTTTGAGGAATTTCAGCGTTATGGATGTGACATTTGCAGTAAAAACTCAAAACTTAAATTCACTAGAAAGTATATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6095
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089172 | Essential Splice Site | 267 | 449 | 3 | 7 |
| ENSDART00000127364 | Essential Splice Site | 267 | 449 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 8 (position 19135154)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 18580042 |
| GRCz11 | 8 | 18611203 |
KASP Assay ID:
554-3765.1 (used for ordering genotyping assays)
KASP Sequence:
CCCACAGTGCACTTCAACTACAGATACTTTGAGATTGARGAAGCAGATGG[T/C]GAGTGCTTTYACAGTCGTGTGAGGAGAGATGTTGTTATCTGCRAGCACCA
Long Flanking Sequence:
TCTGTTTCTCTTGTTTTTTACTAAAGGTGGTGGCGGCATCAGCTGTGTGATGCAGGATGGCAAGATCTTTGAAAAAGCAGGTGTGAATGTGTCTGTGGTGTATGGGAATCTTACTGAGGAGGCCGCCAGGCAGATGCGCAGCCGTGGAAAAATCCTGAAAGGAAAAGATGGTGAGACGCCGACTTCCCGTTTCAAAGTGAACCCAGAGAGTGACTGAAACCAGATCTTTGTGTCTTCAGTTCTGCTTCTAGATTTATTTCTGAACTCCGTCTGAACTATCAGTGGTCTCAAGGCTGTTTCCCTGATAGTTTGTCATACTAGCTCATAAATTTGACAGGAAGTTACGTCGTATATACTGTTTTACAATATCATTATCTCTGCGTTCCAGGAAAGCTGCCATTTCGTGCAATGGGTGTGAGTTCTGTCATACACCCCAAAAACCCCCACATTCCCACAGTGCACTTCAACTACAGATACTTTGAGATTGAAGAAGCAGATGG[T/C]GAGTGCTTTTACAGTCGTGTGAGGAGAGATGTTGTTATCTGCAAGCACCACTCATCTCTGTCTCCATCTCCCTTCTTTCTATAGGCACAAAGCAGTGGTGGTTTGGTGGAGGAACGGATCTCACTCCTGTTTACATTGATTTGGAAGATGCCACCCATTTCCACAAGACTCTGAAGGAAGCCTGTGACAAGCATCATCCTAAATATTACCCAGACTTCAAGAAGTGGTATGTAGTCTTATTCAGTGTGTGAATTATACATTGACAATTGGGGGGGATGTGATGATTAAAAGGCTTAACTAGGTTAATTAGGTTAACTAGGCAGTTTAGGGTAATTAGGCAAGTTGTTGTATAACGATGGTTTGTTTTGTAGATTATTGAAAAAAATTTGCTTAAAGGGGCTGATAATTCTGACCTTAACATTCTTTTTAAAAACTGCTTTTATTCTAGCCGAAATAAAACAAATAAGATCTTCTCCAGAAGAAAAAATAGTATCAGACAT
Associated Phenotype:
Not determined