ZMP
cops2
Ensembl ID:
ZFIN ID:
Description:
COP9 signalosome complex subunit 2 [Source:UniProtKB/Swiss-Prot;Acc:Q6IQT4]
Human Orthologue:
COPS2
Human Description:
COP9 constitutive photomorphogenic homolog subunit 2 (Arabidopsis) [Source:HGNC Symbol;Acc:30747]
Mouse Orthologue:
Cops2
Mouse Description:
COP9 (constitutive photomorphogenic) homolog, subunit 2 (Arabidopsis thaliana) Gene [Source:MGI Symb
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12873 | Essential Splice Site, Missense | Available for shipment | Available now |
sa38113 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa16281 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12873
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 > C
Consequence:
Essential Splice Site, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006124 | Essential Splice Site | 124 | 443 | None | 13 |
ENSDART00000133872 | Missense | 125 | 282 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 25 (position 33356491)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 31966893 |
GRCz11 | 25 | 32377850 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAGAAATCCATYAACTCCATTTTAGACTATATCTCAACCTCCAAACAGG[T/C]AATGGTATGTTTTACATTGCTGTGTGAGTTTGCATTKYATTCAGTTTCAT
Long Flanking Sequence:
ATAATGCTGCTGATATGATTTTAAAGCATAAATAACTGCATTTTAACTTAGAAAATGAATAATCACCTTCTTTTTGTTTTGCAGGTGCTGGAATTGGAGGGTGAGAAAGGAGAATGGGGATTCAAAGCACTGAAACAAATGATCAAGATCAACTTCAAACTGGTATGTAGTTATATAGTTTATTATAGTATAAAGTATTATTTGTTTGTTCGCCTAAAACATTATGAATATGAAATAAAATTGGGTAATGTCATAAAAAGATTCTATATCTGTTTGATAGTTTTTTTTTCATTTCTCAACCAATTATATATATAAGAATTATTGATCTGTTTGGAAATGACGTTGATTCATTTATTTTCTTCTGATTTCATAGACTAATTTTCCTGAAATGATGAACCGGTACAAACAGCTTTTGACTTATATTAGGAGCGCTGTCACCAGAAATTATTCTGAGAAATCCATCAACTCCATTTTAGACTATATCTCAACCTCCAAACAGG[T/C]AATGGTATGTTTTACATTGCTGTGTGAGTTTGCATTTCATTCAGTTTCATTACATTATCAACCCTCGTAATACATTCAAGTCCTGTAAGAAGTGCATTATAGTTTTAAACTAATAAAGAATCTAAAAGAATTATTATTATTATTATTAATATTATTATTATTAAGGAATTATTATTATAATAACAAGGTGATGCAGTGGCGCAGTAGGTATTGCTGCCGCCTCACAGCAAGAAGGTCGCTGGGTCGCTGGTTCGATCCTCGGCTCAGTAGGTGTTTCTGTGTGGAGTTTGCATGTTCTCCCTGCGTTCACGGGGGTTTCCTCCGGGTGCTCCGGTTTCCCCCACAACCCAAAGACATGCGGTACAGGTGAATTGTGTAGGCTAAATTGTCCGTAGTGTATGAGTGTGTGTGTGAATGTGTGTGTGTGGATGTTTCCCAGAGATGGGTTGCGGCTGGAAGGGCATCCGCTGCGTAAAAAATGTGCTGGATAAGTTGGCGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38113
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006124 | Essential Splice Site | 180 | 443 | 6 | 13 |
ENSDART00000133872 | Essential Splice Site | 182 | 282 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 25 (position 33353578)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 31963980 |
GRCz11 | 25 | 32374937 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTTGGAAAACTTCAGAAGATTCTCAGGCAATTACATCAGTCGTGTCAG[G/A]TATAGTAAATGATCTAAATAGAAAAATAGCATTCATAAAAGGTGCTGCAA
Long Flanking Sequence:
TTCTGTTGATTCCTAATAATTATAGTAATACAAGCAAATGTTACCGCTCCATTCACACGGGGCTTCAGCGTCAACGATTGACTGAAGGCGTGTCTGAAGTTGGGGCTGAAGCAATCGTCATAGAAGCGTCAGCCAATGAAATTCAGCAATAGGCCACTGTCTAGCTGGTGTATTTGCATACAGCGATCTGATTGGCTGACGCTTCCGTTGGAGCTTGAAAAGTTGAGCTAGTCGCAACTTCTGCAGCGAGCAACCCCTCTGAAGCGGCGCCGATGGATCCCCAATGCAGTTCGGCAACGCCTGACGTCACCCATTCAAAGTGAATGAGAAGCGTTGATGCTGACGCCCCTTGTGAATGGGGCGTAAGAGTCTGTGTCAATACTCACTTTTAAGACTATTGCAAACCTCTCTGTTTCATGCAGCTGGGAAAGTTGTACCTGGAAAGAGAAGAATTTGGAAAACTTCAGAAGATTCTCAGGCAATTACATCAGTCGTGTCAG[G/A]TATAGTAAATGATCTAAATAGAAAAATAGCATTCATAAAAGGTGCTGCAAATATCTGAAAGTGGTCGATGTTGTTGGTTTAGACGGATGACGGAGAGGATGACTTGAAGAAGGGCACTCAGCTTTTGGAGATTTACGCTTTGGAGATCCAGATGTACACGGCACAGAAAAACAACAAGAAGCTCAAAGCCCTTTATGAGCAGTCATTACACATCAAATCAGCCATCCCACATCCACTCATCATGGGAGTCATCAGAGGTGTGTTGCATGTTTTTAGTCTAAATTGTTTAATTGCTTCTCAAAGGTTTATTTGTTTTTTTGTTTAATTTTCTTTTGTAATTCAGATTTGTGTCTGCGTGTCTCAGATTTGGTTTGTCTTGTTTTGTGCACGATTAACAAGTCCTCTAATTCTGCTTGGTTTTGTTTTTTGTTTTTTTGCATGATTAGAATGTGATTTAGTTTTGTTTTTGTTTATTTTTTGATTTGTTTAATTTTAGTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16281
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 |
---|---|---|---|---|---|
ENSDART00000006124 | Nonsense | 273 | 443 | 8 | 13 |
ENSDART00000133872 | Nonsense | 275 | 282 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 25 (position 33351129)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 31961531 |
GRCz11 | 25 | 32372488 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGACTTTTTTGAAGCGTTCAAAAACTAYGATGAGTCYGGAARCCCCAGA[C/T]GAACCACTTGTCTGAAGTACCTGGTCCTGGCCAACATGYTRATGAAGTCT
Long Flanking Sequence:
TGGTTTGTTTTGTGCACCCTTGCAAAGTTGTTTTTCTTTAGTTTGTTTGTTTTTGTACAGTTGTTTTGTTTTATTTTTTAGTGTGTTTTTATTTGGTTTTTGTGGGCGTGTAATTGGAAAAGTGTTTTTTGTTTTAGTTATTCTTGTGCATTTAGTTGTTTTTTGCTAAAATTGAAAGTTTGCTTTCGGGTTTTGTTTTTGCTTTTTGGCTTGGTTTGTGTACAGTTGTAATATCTTTATTTCTATCAGAAAGTTTGTTTGCTTTTTTTTTTATTTACAATTTATTGACAGTTGTTGTTTTTTTCATTGGTGCGGTTTAGTCGCAAAGTTGGCTCATTATTTTATTTTTTATACAGCTTGTCTACTAATCATCTTTAACTTGTGGCTTGTTCTCTACAGAGTGCGGCGGTAAAATGCACCTGAGAGAAGGAGAGTTCGAGAAGGCACATACAGACTTTTTTGAAGCGTTCAAAAACTACGATGAGTCCGGAAGCCCCAGA[C/T]GAACCACTTGTCTGAAGTACCTGGTCCTGGCCAACATGCTGATGAAGTCTGGAATCAACCCGTTTGATTCTCAAGAGGTACGGCTGCACAAAATATCGTTTCTGCATCGATATCGCAATGTTCACACCCATAAAGTCATATAGCAGGATGTGCAATGTTGAGTTGGGATTATATTTGGTCAGCACTGCAGTTCAGAACACATGAGATTTGTGGAGTCACTGTAGAGTTTATCCATAATATACAGGGCTTGGACAATGAAACTGAAATGTCTGGTTTTAGACCACAATAATTCATTAGTATGATGTAGGGGCTCCTTTTGCGGCCAGTACAGCATCAGTTCTTCGATTTTGAGCCATTGTTCTTGCAGAATAGTGGCCAGGTCACTATGTGATGCTAATGGAGAAAAATGTTTCCTGACTCGCTCCTCCAAAACACCCCAAAGTCACTCAATAATATATAGATCTGGTGACTGTGCAGGCCATGGGAGATGCTCAACTTCA
Associated Phenotype:
Not determined