ZMP
si:ch211-37p17.5
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens OPN5, opsin 5 (OPN5) [Source:UniProtKB/TrEMBL;Acc:B0S8K9]
Human Orthologue:
OPN5
Human Description:
opsin 5 [Source:HGNC Symbol;Acc:19992]
Mouse Orthologue:
Opn5
Mouse Description:
opsin 5 Gene [Source:MGI Symbol;Acc:MGI:2662912]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa5778 | Essential Splice Site | F2 line generated | Not yet available |
| sa2443 | Essential Splice Site | F2 line generated | Not yet available |
| sa8471 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa5778
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000098326 | Essential Splice Site | 127 | 365 | 3 | 6 |
| ENSDART00000141691 | Essential Splice Site | 98 | 374 | 2 | 5 |
| ENSDART00000098326 | Essential Splice Site | 127 | 365 | 3 | 6 |
| ENSDART00000141691 | Essential Splice Site | 98 | 374 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 8 (position 51752886)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 49503273 |
| GRCz11 | 8 | 49492042 |
KASP Assay ID:
554-3049.1 (used for ordering genotyping assays)
KASP Sequence:
ACGGCTCTGTCGTCCGTCTGCTGCCTCAAAGTCTGCTTCCCAAACTACGG[T/C]AATYTTCCTTTGACAACATTCAAGTCAAGATGRCATTTGTRAACGTACAC
Long Flanking Sequence:
TTCCTCCGGGTGGTCCGGTTTCCCCAACAGTCCAAAGACGTGCGGTAGGTAAACTGGGTAGGCCAAATTGTTTGTTGTGTATGTGAATGAATGTATGTATGTATGTGAGTGAATGAATGTGTATGGATGTTTCCAAGAGATGGGTTGCAGCAGGAAGGGCATCCGCTATGTAAAACATATGCTGGATAAGTTGGCGGTTCATTCTGCTGTGGCGACCCTGGATTAATAAATGGACTAAGCTGAAAAGAAAATGAATGAATGAATGAATGTAATGCATAAATCTAAAAAACGCAGATCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTTTCTCTCTTTCTGTCTGGTTTTCTCAGGTGGTTGTTTGGAGAGCTGACGTGTTTATGCTATGCTGTATGCGGCGTCCTCTTCGGATTATCCAGCTTGACAAACCTCACGGCTCTGTCGTCCGTCTGCTGCCTCAAAGTCTGCTTCCCAAACTACGG[T/C]AATTTTCCTTTGACAACATTCAAGTCAAGATGACATTTGTGAACGTACACTTGAACGAAACGTCATGTCTCGCAGGACAACAGTGCTACATGAATAAACATAATCGTAAATAAGAACACAACACTGGACTTAAGTGCTGATTTTAAATCTATACGTAACTAACACATCAGAGCTGTAATCTAACTAATAACTATACATAAACTATACGTACTTAGCTATACACAAAATTTAAACCCAAATAAAAAAAGAAAGTAGTGATTTCTATATTTATTTTGACTTGTATTTCACTGGGTGAGGCAGGGGCGCAGTAGGTAGTGCTGTCTCCTCACAGCAAGAAGGTCGCTGGGTCGAACCTCGGCTCAGTTGGCATTTCTGTGTTTTCCCTGCCTTCGCGTGGGTTTCCTTCAGGTGCTCCGGTTTCTCCCACAGTCCAAAGACATGTGGTACAGGTGAATCGAGCAGGCTAAATTGTCTGTAGTGTATGAGTGTGTGTGTGAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2443
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000098326 | Essential Splice Site | 127 | 365 | 3 | 6 |
| ENSDART00000141691 | Essential Splice Site | 98 | 374 | 2 | 5 |
| ENSDART00000098326 | Essential Splice Site | 127 | 365 | 3 | 6 |
| ENSDART00000141691 | Essential Splice Site | 98 | 374 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 8 (position 51752886)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 49503273 |
| GRCz11 | 8 | 49492042 |
KASP Assay ID:
554-3049.1 (used for ordering genotyping assays)
KASP Sequence:
ACGGCTCTGTCGTCCGTCTGCTGCCTCAAAGTCTGCTTCCCAAACTACGG[T/C]AATYTTCCTTTGACAACATTCAAGTCAAGATGRCATTTGTGAACGTACAC
Long Flanking Sequence:
TTCCTCCGGGTGGTCCGGTTTCCCCAACAGTCCAAAGACGTGCGGTAGGTAAACTGGGTAGGCCAAATTGTTTGTTGTGTATGTGAATGAATGTATGTATGTATGTGAGTGAATGAATGTGTATGGATGTTTCCAAGAGATGGGTTGCAGCAGGAAGGGCATCCGCTATGTAAAACATATGCTGGATAAGTTGGCGGTTCATTCTGCTGTGGCGACCCTGGATTAATAAATGGACTAAGCTGAAAAGAAAATGAATGAATGAATGAATGTAATGCATAAATCTAAAAAACGCAGATCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTTTCTCTCTTTCTGTCTGGTTTTCTCAGGTGGTTGTTTGGAGAGCTGACGTGTTTATGCTATGCTGTATGCGGCGTCCTCTTCGGATTATCCAGCTTGACAAACCTCACGGCTCTGTCGTCCGTCTGCTGCCTCAAAGTCTGCTTCCCAAACTACGG[T/C]AATTTTCCTTTGACAACATTCAAGTCAAGATGACATTTGTGAACGTACACTTGAACGAAACGTCATGTCTCGCAGGACAACAGTGCTACATGAATAAACATAATCGTAAATAAGAACACAACACTGGACTTAAGTGCTGATTTTAAATCTATACGTAACTAACACATCAGAGCTGTAATCTAACTAATAACTATACATAAACTATACGTACTTAGCTATACACAAAATTTAAACCCAAATAAAAAAAGAAAGTAGTGATTTCTATATTTATTTTGACTTGTATTTCACTGGGTGAGGCAGGGGCGCAGTAGGTAGTGCTGTCTCCTCACAGCAAGAAGGTCGCTGGGTCGAACCTCGGCTCAGTTGGCATTTCTGTGTTTTCCCTGCCTTCGCGTGGGTTTCCTTCAGGTGCTCCGGTTTCTCCCACAGTCCAAAGACATGTGGTACAGGTGAATCGAGCAGGCTAAATTGTCTGTAGTGTATGAGTGTGTGTGTGAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8471
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000098326 | Nonsense | 282 | 365 | 6 | 6 |
| ENSDART00000141691 | Nonsense | 253 | 374 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 8 (position 51739238)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 49489625 |
| GRCz11 | 8 | 49478394 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCCTGACAATGTCCCACCAATGGCCTTTGCRTTAGCAGCTATATTYGCC[A/T]AATCCTCCACCATCTACAAYCCTGTGGTCTACCTGGTATTCAAGCCCAAC
Long Flanking Sequence:
ACGTATGTAATTGAGTTGCAGAGAGGAGTTGACCATGACAATGGGGTTCAAGTCCGGCGAAGAACGGTTTCAGAAAGCAGGTAAAACAAAAACAGTGGCCTCTGGTGGATTTACATGAGAGGAGCAGGCACAAATGGCACTTGTGAGAGAAATTTGAGATCTGAAAAAGAGTACACAGTGGCCTCACAGTGGATTTGCGAAAACAAAAACGGCAAAAAAAGTACCCTCCTTGGGTGTATTTCGCTATCCAGAAATGTATACAGGGGTACATATCCATAATGAGCCTGAGTTGATAAACTCCAATGTGGGCTGTTTAAATCCCCCAGAGCATAAAAAAATGTTCTTAAGAGCTATTTTTGGTTCTCTTACAGCTCTCGGTGGCAGTGTGCATCGGTTTTCTGACCGCCTGGAGCCCTTATGCGGTTGTGGCAATGTGGGCTGCGTTTGGAGAGCCTGACAATGTCCCACCAATGGCCTTTGCGTTAGCAGCTATATTCGCC[A/T]AATCCTCCACCATCTACAACCCTGTGGTCTACCTGGTATTCAAGCCCAACTTTCGCAAATCTTTGAGCAGGGACACGGCTCAGATTCGCAGACGGATATGTTCCAGCCCTTGCAAGGGAAGCCCTGTGCCTGGAGAGAAGGATCTTCAACGGCAAACCTCTTTACGCTGCAACAAGGACGCTAGTAACTCGACGCGTCTCTCCAACGGCCTAGCAGACAGCCACGGGGCTTGTCTCCATTGCACCGAGACAGACCCTCATTGTCAACAGACCCCGACTCAAAGGACTGCCTGTGTGCTGGTCGGGACATCCTACAGCGAGGTGACTGTGAGTCAGCTGCCAGAGAAGATGCAAGCTGACTTCTTGTGAAGGCCCTGCAGGCTTTCCCAGGACAAATGTGGGTAAACGATGGATGGGCAGCCTTAAAATGCGACTTCTGGCCACTAGAGATAAGCTTGACGTGTCAAAAACAGGCTGTGTCTGAAAACACTACAGATACAG
Associated Phenotype:
Not determined