ZMP
osr2
Ensembl ID:
ZFIN ID:
Description:
Protein odd-skipped-related 2 [Source:UniProtKB/Swiss-Prot;Acc:Q567J8]
Human Orthologue:
OSR2
Human Description:
odd-skipped related 2 (Drosophila) [Source:HGNC Symbol;Acc:15830]
Mouse Orthologue:
Osr2
Mouse Description:
odd-skipped related 2 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1930813]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22965 | Nonsense | Available for shipment | Available now |
sa19156 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10900 | Nonsense | Available for shipment | Available now |
sa36277 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22965
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 |
---|---|---|---|---|---|
ENSDART00000055395 | Nonsense | 46 | 238 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 16 (position 58052695)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 54701127 |
GRCz11 | 16 | 54404902 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCCGGTGGCGGTGGATCAGCTGTACGGCCTCAGCGCGCTCCACACCGTG[C/T]AGATGAACCGGTGGACGGTGGGCTTCCCGCAGCTGCAGGGCCTGGCGGAC
Long Flanking Sequence:
TGTTCTCTGCCTTCACTGCTCCAGAACAGTTCCTTTATTCTGTTCAGCACAAAAGGAGATGTTTTGAAGAATGTTGGAAACCTGTAACCATTGACTCCCATTGCAGGAAAAAAGGCAAATACTCTGGGAATCAATGGTGACAGGTTTCCAGCATTCTTCACACTGTTTATTTTGTGAACAGAGGATCTGCTCGGCCTGCTGTGAGTGTGTTTCTGACAGCTCCTCTAATAATCACATGACGGAAATCATTTCACAATTACAGTAAACCGCTCAAACTGTGTGTTTCATGGTAATGTGATCATTAACGGGGCCGTGCGGGACTGACCGGTGCGTGTGCTCGTGTTCCCGCAGGATCTGCACCGGGAATGGGCAGTAAGACTCTCCCGGCTCCGGTGCCTCTCCACCCGGCGCTGCAGCTCAACTACTCGCTCCTGCAGACACTGAACGCGTTCCCGGTGGCGGTGGATCAGCTGTACGGCCTCAGCGCGCTCCACACCGTG[C/T]AGATGAACCGGTGGACGGTGGGCTTCCCGCAGCTGCAGGGCCTGGCGGACCCGCGCTTCCCCGGCGCACTCCCGTTCCCCGCCGCCGCCGCGCATCTGTTGCCGCACAAACACCCGGTGCACCGGAAGGACAGGCCGCGCTTCGACTTCGCCAATCTGGCGGTGGCGGCGACGCAGGAGGACCCGCCGGTGACCGGACAGAGCAGACTGAGCCCGGAGCGCAGACCGGCGCGCGGCAGACTCCCGGCCAAGAGCAAGAAGGAGTTCATCTGCCGGTTCTGCGGGAGACACTTCACCAAATCCTACAACCTGCTGATCCACGAGCGCACACACACCGACGAGCGGCCCTACACCTGCGACATCTGCCACAAGGCCTTCCGGAGACAAGACCACCTGCGGGACCACCGGTGAGCGCGCGCGCGTGAAAGAGAGAGAGAGAGTGTGTGTGTGAGAGAGAGTGTGTCTGTCATATATTTGCGTGTGTGTGTGTTTATCTGTCGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19156
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055395 | Nonsense | 147 | 238 | 2 | 4 |
ENSDART00000055395 | Nonsense | 147 | 238 | 2 | 4 |
ENSDART00000055395 | Nonsense | 147 | 238 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 16 (position 58052390)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 54700822 |
GRCz11 | 16 | 54404597 |
KASP Assay ID:
2261-0415.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAAGGAGTTCATCTGCCGGTTCTGCGGGAGACACTTCACCAAATCCTA[C/A]AACCTGCTGATCCACGAGCGCACACACACCGACGAGCGGCCCTACACCTG
Long Flanking Sequence:
CGGGGCCGTGCGGGACTGACCGGTGCGTGTGCTCGTGTTCCCGCAGGATCTGCACCGGGAATGGGCAGTAAGACTCTCCCGGCTCCGGTGCCTCTCCACCCGGCGCTGCAGCTCAACTACTCGCTCCTGCAGACACTGAACGCGTTCCCGGTGGCGGTGGATCAGCTGTACGGCCTCAGCGCGCTCCACACCGTGCAGATGAACCGGTGGACGGTGGGCTTCCCGCAGCTGCAGGGCCTGGCGGACCCGCGCTTCCCCGGCGCACTCCCGTTCCCCGCCGCCGCCGCGCATCTGTTGCCGCACAAACACCCGGTGCACCGGAAGGACAGGCCGCGCTTCGACTTCGCCAATCTGGCGGTGGCGGCGACGCAGGAGGACCCGCCGGTGACCGGACAGAGCAGACTGAGCCCGGAGCGCAGACCGGCGCGCGGCAGACTCCCGGCCAAGAGCAAGAAGGAGTTCATCTGCCGGTTCTGCGGGAGACACTTCACCAAATCCTA[C/A]AACCTGCTGATCCACGAGCGCACACACACCGACGAGCGGCCCTACACCTGCGACATCTGCCACAAGGCCTTCCGGAGACAAGACCACCTGCGGGACCACCGGTGAGCGCGCGCGCGTGAAAGAGAGAGAGAGAGTGTGTGTGTGAGAGAGAGTGTGTCTGTCATATATTTGCGTGTGTGTGTGTTTATCTGTCGTATGCGTTTGTATAAAGAGTGTGTGCGCGCGTGTGTGTGTTACAGAATGCTGTGTTGCTGTAACCCCGCGCTGGGTCAAACGCTGATATATTCTTTAATTAAACCTAAAGACTAAAATCGCCTGAAGATGATGATGAAGAATGTTCTCGCTATTCTACACCTCTGAGTGTGTTGATTATTCTGAACATGAGCAAGTGGAGAGAGCTGAACACCGGTCACCGCTGACCCACAGCGGAGAGGAATACACACGAGTGAACGGTGACCGGTGTTCCTCTGCTCAACAAGAAAAACTCAAACATGTTTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10900
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055395 | Nonsense | 147 | 238 | 2 | 4 |
ENSDART00000055395 | Nonsense | 147 | 238 | 2 | 4 |
ENSDART00000055395 | Nonsense | 147 | 238 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 16 (position 58052390)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 54700822 |
GRCz11 | 16 | 54404597 |
KASP Assay ID:
2261-0415.1 (used for ordering genotyping assays)
KASP Sequence:
AAGAAGGAGTTCATCTGCCGGTTCTGCGGGAGACACTTCACCAAATCCTA[C/A]AACCTGCTGATCCACGAGCGCACACACACCGACGAGCGGCCCTACACCTG
Long Flanking Sequence:
CGGGGCCGTGCGGGACTGACCGGTGCGTGTGCTCGTGTTCCCGCAGGATCTGCACCGGGAATGGGCAGTAAGACTCTCCCGGCTCCGGTGCCTCTCCACCCGGCGCTGCAGCTCAACTACTCGCTCCTGCAGACACTGAACGCGTTCCCGGTGGCGGTGGATCAGCTGTACGGCCTCAGCGCGCTCCACACCGTGCAGATGAACCGGTGGACGGTGGGCTTCCCGCAGCTGCAGGGCCTGGCGGACCCGCGCTTCCCCGGCGCACTCCCGTTCCCCGCCGCCGCCGCGCATCTGTTGCCGCACAAACACCCGGTGCACCGGAAGGACAGGCCGCGCTTCGACTTCGCCAATCTGGCGGTGGCGGCGACGCAGGAGGACCCGCCGGTGACCGGACAGAGCAGACTGAGCCCGGAGCGCAGACCGGCGCGCGGCAGACTCCCGGCCAAGAGCAAGAAGGAGTTCATCTGCCGGTTCTGCGGGAGACACTTCACCAAATCCTA[C/A]AACCTGCTGATCCACGAGCGCACACACACCGACGAGCGGCCCTACACCTGCGACATCTGCCACAAGGCCTTCCGGAGACAAGACCACCTGCGGGACCACCGGTGAGCGCGCGCGCGTGAAAGAGAGAGAGAGAGTGTGTGTGTGAGAGAGAGTGTGTCTGTCATATATTTGCGTGTGTGTGTGTTTATCTGTCGTATGCGTTTGTATAAAGAGTGTGTGCGCGCGTGTGTGTGTTACAGAATGCTGTGTTGCTGTAACCCCGCGCTGGGTCAAACGCTGATATATTCTTTAATTAAACCTAAAGACTAAAATCGCCTGAAGATGATGATGAAGAATGTTCTCGCTATTCTACACCTCTGAGTGTGTTGATTATTCTGAACATGAGCAAGTGGAGAGAGCTGAACACCGGTCACCGCTGACCCACAGCGGAGAGGAATACACACGAGTGAACGGTGACCGGTGTTCCTCTGCTCAACAAGAAAAACTCAAACATGTTTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36277
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055395 | Nonsense | 159 | 238 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 16 (position 58052356)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 54700788 |
GRCz11 | 16 | 54404563 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTCACCAAATCCTACAACCTGCTGATCCACGAGCGCACACACACCGAC[G/T]AGCGGCCCTACACCTGCGACATCTGCCACAAGGCCTTCCGGAGACAAGAC
Long Flanking Sequence:
GTGTTCCCGCAGGATCTGCACCGGGAATGGGCAGTAAGACTCTCCCGGCTCCGGTGCCTCTCCACCCGGCGCTGCAGCTCAACTACTCGCTCCTGCAGACACTGAACGCGTTCCCGGTGGCGGTGGATCAGCTGTACGGCCTCAGCGCGCTCCACACCGTGCAGATGAACCGGTGGACGGTGGGCTTCCCGCAGCTGCAGGGCCTGGCGGACCCGCGCTTCCCCGGCGCACTCCCGTTCCCCGCCGCCGCCGCGCATCTGTTGCCGCACAAACACCCGGTGCACCGGAAGGACAGGCCGCGCTTCGACTTCGCCAATCTGGCGGTGGCGGCGACGCAGGAGGACCCGCCGGTGACCGGACAGAGCAGACTGAGCCCGGAGCGCAGACCGGCGCGCGGCAGACTCCCGGCCAAGAGCAAGAAGGAGTTCATCTGCCGGTTCTGCGGGAGACACTTCACCAAATCCTACAACCTGCTGATCCACGAGCGCACACACACCGAC[G/T]AGCGGCCCTACACCTGCGACATCTGCCACAAGGCCTTCCGGAGACAAGACCACCTGCGGGACCACCGGTGAGCGCGCGCGCGTGAAAGAGAGAGAGAGAGTGTGTGTGTGAGAGAGAGTGTGTCTGTCATATATTTGCGTGTGTGTGTGTTTATCTGTCGTATGCGTTTGTATAAAGAGTGTGTGCGCGCGTGTGTGTGTTACAGAATGCTGTGTTGCTGTAACCCCGCGCTGGGTCAAACGCTGATATATTCTTTAATTAAACCTAAAGACTAAAATCGCCTGAAGATGATGATGAAGAATGTTCTCGCTATTCTACACCTCTGAGTGTGTTGATTATTCTGAACATGAGCAAGTGGAGAGAGCTGAACACCGGTCACCGCTGACCCACAGCGGAGAGGAATACACACGAGTGAACGGTGACCGGTGTTCCTCTGCTCAACAAGAAAAACTCAAACATGTTTGGATCTTTACATCACACTTTTACCCCGGGGTTGGGTT
Associated Phenotype:
Not determined