ZMP
cog2
Ensembl ID:
ZFIN ID:
Description:
conserved oligomeric Golgi complex subunit 2 [Source:RefSeq peptide;Acc:NP_998519]
Human Orthologue:
COG2
Human Description:
component of oligomeric golgi complex 2 [Source:HGNC Symbol;Acc:6546]
Mouse Orthologue:
Cog2
Mouse Description:
component of oligomeric golgi complex 2 Gene [Source:MGI Symbol;Acc:MGI:1923582]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12307 | Essential Splice Site | Available for shipment | Available now |
sa8649 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa18123 | Essential Splice Site | Available for shipment | Available now |
sa12578 | Essential Splice Site | Available for shipment | Available now |
sa8564 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12307
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000026189 | Essential Splice Site | 74 | 730 | 2 | 18 |
ENSDART00000026189 | Essential Splice Site | 74 | 730 | 2 | 18 |
ENSDART00000026189 | Essential Splice Site | 74 | 730 | 2 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 24240587)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 23886247 |
GRCz11 | 13 | 24016697 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTTATTAATAAAGACTATGCAGATTTCGTYAAYCTCTCCACCAATCTTG[T/A]AAGTSTTTGGTCTTTATTAACATTACTTTATCAGCAGAATTGTGTGCTAC
Long Flanking Sequence:
ATTGTGCACAGAACCAGAAATCCTCATCATCTCAAATCTCGGAAATCTTCAAACATGCCAAATATAAAAATTCTACTGAGTATAGCTGAAATATGTTATCAAGTTGAAATTCATGTTTAATAAGTTCTCTTGTGGTTATGAAGAGTCCTGAAATATTAACTTGATACTTAAATATATTTTAACACGGTTGACTGTTCTCTTAAACCCCAAACAGAATTGAAACTAATTAATTGAAACTCAGATTGTTTATAAATAAATTTTTTAAGCATTTCTGACATTATTTAGCATCATATTTCTACTTGATTTTTTGAATATTTATTTGTATGTTTCCATGCAGGATGACTTCGACGTGGACAAATTTGTGGCTGACTGCCGAAAGCGTGTCCAGTTGGAGGAGATGCGTGAAGATCTGGAGCAATATTACAGACTCCTCAAAACAGCCATGGTTGAGCTTATTAATAAAGACTATGCAGATTTCGTTAACCTCTCCACCAATCTTG[T/A]AAGTCTTTGGTCTTTATTAACATTACTTTATCAGCAGAATTGTGTGCTACTGTAAAGTGTGCTTTATGTCTTATTTCTAGTGCAAGATTATGTCATTTTTGCTATGTAAGCATGTATTTGTGTTTTAGGTTGGGATGGATAAAGCCCTCAATCAGCTGTCTGTTCCACTCGGCCAGTTACGTGAAGAGGTGCTGGTAAGTGCTTAACACATCCCTGAATATTTATGGATTGGCCATATTTCATCAAGTCAATATCTAAGTATGTTCCTGTCATCAACAGAGTTTACGATCCGCTGTGAATGAAGTTATTGAAGCTATAGACACCCAGTTGTCCAAGCAGGATGACATTCAGAAAAAGAAGGTAGGGCATGATGCGAAAACTTCATTTATTTTATTTTGAAATATGATTTTACCACTTTACACATGTTGATCAATAATATTGTGTCCCGTGCAGCTCTGTGTGTTAAGACTGATTCAAGTTGTGAGATCAGTAGAGAAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8649
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 |
---|---|---|---|---|---|
ENSDART00000026189 | Essential Splice Site | 74 | 730 | 2 | 18 |
ENSDART00000026189 | Essential Splice Site | 74 | 730 | 2 | 18 |
ENSDART00000026189 | Essential Splice Site | 74 | 730 | 2 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 24240587)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 23886247 |
GRCz11 | 13 | 24016697 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTTATTAATAAAGACTATGCAGATTTCGTTAAYCTCTCCACCAATCTTG[T/C]AAGTSTTTGGTCTTTATTAACATTACTTTATCAGCAGAATTGTGTGCTAC
Long Flanking Sequence:
ATTGTGCACAGAACCAGAAATCCTCATCATCTCAAATCTCGGAAATCTTCAAACATGCCAAATATAAAAATTCTACTGAGTATAGCTGAAATATGTTATCAAGTTGAAATTCATGTTTAATAAGTTCTCTTGTGGTTATGAAGAGTCCTGAAATATTAACTTGATACTTAAATATATTTTAACACGGTTGACTGTTCTCTTAAACCCCAAACAGAATTGAAACTAATTAATTGAAACTCAGATTGTTTATAAATAAATTTTTTAAGCATTTCTGACATTATTTAGCATCATATTTCTACTTGATTTTTTGAATATTTATTTGTATGTTTCCATGCAGGATGACTTCGACGTGGACAAATTTGTGGCTGACTGCCGAAAGCGTGTCCAGTTGGAGGAGATGCGTGAAGATCTGGAGCAATATTACAGACTCCTCAAAACAGCCATGGTTGAGCTTATTAATAAAGACTATGCAGATTTCGTTAACCTCTCCACCAATCTTG[T/C]AAGTCTTTGGTCTTTATTAACATTACTTTATCAGCAGAATTGTGTGCTACTGTAAAGTGTGCTTTATGTCTTATTTCTAGTGCAAGATTATGTCATTTTTGCTATGTAAGCATGTATTTGTGTTTTAGGTTGGGATGGATAAAGCCCTCAATCAGCTGTCTGTTCCACTCGGCCAGTTACGTGAAGAGGTGCTGGTAAGTGCTTAACACATCCCTGAATATTTATGGATTGGCCATATTTCATCAAGTCAATATCTAAGTATGTTCCTGTCATCAACAGAGTTTACGATCCGCTGTGAATGAAGTTATTGAAGCTATAGACACCCAGTTGTCCAAGCAGGATGACATTCAGAAAAAGAAGGTAGGGCATGATGCGAAAACTTCATTTATTTTATTTTGAAATATGATTTTACCACTTTACACATGTTGATCAATAATATTGTGTCCCGTGCAGCTCTGTGTGTTAAGACTGATTCAAGTTGTGAGATCAGTAGAGAAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18123
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
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000026189 | Essential Splice Site | 74 | 730 | 2 | 18 |
ENSDART00000026189 | Essential Splice Site | 74 | 730 | 2 | 18 |
ENSDART00000026189 | Essential Splice Site | 74 | 730 | 2 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 24240587)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 23886247 |
GRCz11 | 13 | 24016697 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTTATTAATAAAGACTATGCAGATTTCGTYAAYCTCTCCACCAATCTTG[T/C]AAGTSTTTGGTCTTTATTAACATTACTTTATCAGCAGAATTGTGTGCTAC
Long Flanking Sequence:
ATTGTGCACAGAACCAGAAATCCTCATCATCTCAAATCTCGGAAATCTTCAAACATGCCAAATATAAAAATTCTACTGAGTATAGCTGAAATATGTTATCAAGTTGAAATTCATGTTTAATAAGTTCTCTTGTGGTTATGAAGAGTCCTGAAATATTAACTTGATACTTAAATATATTTTAACACGGTTGACTGTTCTCTTAAACCCCAAACAGAATTGAAACTAATTAATTGAAACTCAGATTGTTTATAAATAAATTTTTTAAGCATTTCTGACATTATTTAGCATCATATTTCTACTTGATTTTTTGAATATTTATTTGTATGTTTCCATGCAGGATGACTTCGACGTGGACAAATTTGTGGCTGACTGCCGAAAGCGTGTCCAGTTGGAGGAGATGCGTGAAGATCTGGAGCAATATTACAGACTCCTCAAAACAGCCATGGTTGAGCTTATTAATAAAGACTATGCAGATTTCGTTAACCTCTCCACCAATCTTG[T/C]AAGTCTTTGGTCTTTATTAACATTACTTTATCAGCAGAATTGTGTGCTACTGTAAAGTGTGCTTTATGTCTTATTTCTAGTGCAAGATTATGTCATTTTTGCTATGTAAGCATGTATTTGTGTTTTAGGTTGGGATGGATAAAGCCCTCAATCAGCTGTCTGTTCCACTCGGCCAGTTACGTGAAGAGGTGCTGGTAAGTGCTTAACACATCCCTGAATATTTATGGATTGGCCATATTTCATCAAGTCAATATCTAAGTATGTTCCTGTCATCAACAGAGTTTACGATCCGCTGTGAATGAAGTTATTGAAGCTATAGACACCCAGTTGTCCAAGCAGGATGACATTCAGAAAAAGAAGGTAGGGCATGATGCGAAAACTTCATTTATTTTATTTTGAAATATGATTTTACCACTTTACACATGTTGATCAATAATATTGTGTCCCGTGCAGCTCTGTGTGTTAAGACTGATTCAAGTTGTGAGATCAGTAGAGAAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12578
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
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000026189 | Essential Splice Site | 295 | 730 | 8 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 24234453)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 23880113 |
GRCz11 | 13 | 24010563 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCATCACTGCAGACTTCTGCGAGAGGTGACCGGTGGCGCAATCTCTAGG[T/C]ATGTTTGCCACTCACATAAAACTTTTACAGCATTGAGCCATTGTWGTCAR
Long Flanking Sequence:
GATCAGCGGATCAAAAGTTATTAAACATTTAAGAGCAATACTTATTTTTAGCCGCGGGCGGCTGTCTCGGTCTTTAAGGGTTAAAACCGTTGATATGCAATTGTTCATGGTATGATAATCGTGCACGTTCAAATCGTGGTAAACCGTCATACCGGTATATTGTTACAACCCTAGTGTGAACATAACTGAGAAGGTGGCAAGCGGGGACACTGGAACTTAGGTTTTGGTCCAGACAATTGAACCAAGTGTGAAAGCACCCTATAAGTGCTTTGTACCAATTCATCAATTTAAATGTACATGCATAGTAGTTAAGTCCACATAATATGAAGGAGAACCTTGCAATCTTCTAACCACAACTGTTCTTTTTTTGTCAGGTTATAGTTGAACAGTTTGTCAAGTCTAGCCCTAATGGTCTTAAGGTGATGTACGCAAAGCTGTTAGAGTTTGTGCCTCATCACTGCAGACTTCTGCGAGAGGTGACCGGTGGCGCAATCTCTAGG[T/C]ATGTTTGCCACTCACATAAAACTTTTACAGCATTGAGCCATTGTAGTCAGATCATACACAATATATTTTAATGAGCTTCCCTTTATGCACATCTAGTGATAAAGCTGACATTGTTCCCGGATACGACTTCCTAGTGAACTCCGTTTGGCCTGAAATCATTAGAGGTGTTGAGGAAAGAGTCCCTTCTCTTTTTAATCCCGGAAACCCAGATGTGTTTTATGAGGTGAACAAAGCAAAAAAAAAAAAAGTGCATTCATATTTTCTATAAAGTTTGGAGGATACATATAAAACTTTTTTTGCAGTTTTGACTGAAGTTAAAATTTGTCTTAATTTTTTTTATTTGTCTTTAAATTTATGTCTTGTATTCGTGCAGAGATACACTGTCAGCATGGATTTTGTGCGTAAGTTTGAGAGGCAGTGTGGTTCTCAGGCCAGTGTGAAGAGGTTGCGAGCACATCCAAGCTACCAGAGCTTTCACAACAAATGGAACCTGCCAGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8564
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 |
---|---|---|---|---|---|
ENSDART00000026189 | Essential Splice Site | 455 | 730 | 12 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 24226996)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 23872656 |
GRCz11 | 13 | 24003106 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAACTCAYTCTGCAGCTCATCTCCAGATACTCCACCTTTCTTACCGAGG[T/C]AATGCATTYCAGCTGAGAGGAATTTGAATCATAATAATAGAGTTATTGTT
Long Flanking Sequence:
AGCTTGATTCCGTTATGCTCAAAATACACCCATAACTCGTTAAGAGAATAAGCACAACCCTGTTAGACCATGTGCCAGGATGCATAGATAATTTTTCTATTTTTAAAATAGCAGAAGTGGATAAGGACACGCGCAATGTGCTTTAGACTTTGCGCCTAGATCGTTAAAATAGAGCCCAATGTGTTTTTTGTTAATGTGACAATGAATGCATCATAAAGATGTGTGGTCTATCCTTCTCTGTACACCTGTTGACCTGCCTTTTATGATAAATATAAAGCTGTCACTTTTAAGAGAGTGTAACAGATCAGCACTGACATCCAGTCTGCTCTGTGTATTTGTGAACGCAGTGGGCAGCAGCTTCCACCTGCAGGTGACCGAGGTGTTGTGGAGCTGTGTGTGCAGGTGCTGGACTGACCAGGTGTACTTGCCACCCCTCGCTCATCGGTTCTGGAAACTCACTCTGCAGCTCATCTCCAGATACTCCACCTTTCTTACCGAGG[T/C]AATGCATTCCAGCTGAGAGGAATTTGAATCATAATAATAGAGTTATTGTTCATGTCTTCCTTTTTTTGTCTCACAGGTTCTAACAAAAACATCATCTACAGAGGCAAGCAAAGATTCAGTAAGGCCGCTTCCCAGCTCTGCATCTTCCACATCCAGCCGCACATCACAGGATGCAGACAGTGAAACTGGCGGTCCCACTGTTTTATCTACTAAACAGCTTTTCTTCATTGCAGCTGATGTTGATAAGTTACAAGGAAAGGTAATTCAAATGTTCATTTAAAATAGTTTACAGAGTCCTCGTGCTTTTTTTTTTTCCTTTTTCTTTTTTTCAAAACAGTTTAGAACAAAAAACATTTTCAAAGGAACATGGAAATAGAAAAGACATATAATACAGGTGCCAAAGGTCACCCAATACAATGTTATTTACATTCGTATTTATGGTTGTTAAAATGTTGCTATATAAAATTTTGTTAAGGGTTACATATCAGGCTCCAGAAATA
Associated Phenotype:
Not determined