ZMP
opn1lw2
Ensembl ID:
ZFIN ID:
Description:
Red-sensitive opsin-2 [Source:UniProtKB/Swiss-Prot;Acc:Q8AYN0]
Human Orthologues:
OPN1LW, OPN1MW, OPN1MW2
Human Descriptions:
opsin 1 (cone pigments), long-wave-sensitive [Source:HGNC Symbol;Acc:9936]
opsin 1 (cone pigments), medium-wave-sensitive 2 [Source:HGNC Symbol;Acc:26952]
opsin 1 (cone pigments), medium-wave-sensitive [Source:HGNC Symbol;Acc:4206]
opsin 1 (cone pigments), medium-wave-sensitive 2 [Source:HGNC Symbol;Acc:26952]
opsin 1 (cone pigments), medium-wave-sensitive [Source:HGNC Symbol;Acc:4206]
Mouse Orthologue:
Opn1mw
Mouse Description:
opsin 1 (cone pigments), medium-wave-sensitive (color blindness, deutan) Gene [Source:MGI Symbol;Acc
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31832 | Essential Splice Site | Available for shipment | Available now |
sa21914 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31832
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065940 | Essential Splice Site | 132 | 356 | 3 | 7 |
The following transcripts of ENSDARG00000044861 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 26415340)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 25244165 |
GRCz11 | 11 | 25481781 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCGGACATCCCATGTGTATTTTTGAAGGCTACACTGTGTCAGTATGTG[G/A]TAAGTTACTACACACAGAAAGCAAACTGAATAGTGTGCTGGACTGAAGAT
Long Flanking Sequence:
CAAAATGGCAGAGTGGGCCAATGCGGCATTTGCCGCGAGACGGCGAGGGGACGAAACAACAAGGGACAACGCTTTCTCATATACCAACAGCAATAACACAAGGGGTAAAATACTAACTTAATCTTCAGGAACAGCTGGATAAATCATGTGCTTTATGATTGATTAGAATTGTAAAAGTTTTTAATAATGATCTCTTTTCACAGATCCCTTTGAGGGTCCCAATTACCACATTGCCCCTCGATGGGTGTACAATGTTGCAACAGTCTGGATGTTCTTTGTGGTTGTCGCCTCAACCTTCACCAATGGCCTGGTACTGGTGGCCACGGCCAAATTCAAGAAGCTCCGTCACCCTCTCAACTGGATCTTGGTCAACCTTGCTATAGCTGATCTGGGAGAGACTCTGTTTGCCAGCACAATCAGCGTCATCAATCAGGTTTTCGGCTACTTTATACTCGGACATCCCATGTGTATTTTTGAAGGCTACACTGTGTCAGTATGTG[G/A]TAAGTTACTACACACAGAAAGCAAACTGAATAGTGTGCTGGACTGAAGATTTAGGAGGTTTTTAATGATATTTACCAACACAGGTATTGCTGGACTGTGGTCGTTGACTGTCATCTCTTGGGAAAGATGGGTGGTTGTCTGTAAACCATTTGGAAATGTCAAGTTTGATGGTAAATGGGCATCTGCTGGCATTATCTTCTCCTGGGTTTGGGCTGCTGTTTGGTGTGCACCTCCCATCTTTGGCTGGAGCAGGTAAGGAATGAAATAGTCCAGTTTTGCACTCTAAATGATTTGATAATGTCATACATGTATGTGAGAGCTGTTATCCCTGCTCTATAGGTATTGGCCTCATGGTCTGAAGACCTCCTGTGGACCTGATGTGTTTGGAGGAAACGAGGACCCCGGAGTCCAGTCCTACATGCTGGTCCTAATGATCACCTGTTGCATCCTTCCTCTTGCTATCATCATTCTCTGCTACATTGCTGTGTTCCTGGCCATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21914
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 |
---|---|---|---|---|---|
ENSDART00000065940 | Nonsense | 136 | 356 | 4 | 7 |
The following transcripts of ENSDARG00000044861 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 26415432)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 25244257 |
GRCz11 | 11 | 25481873 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGAAGATTTAGGAGGTTTTTAATGATATTTACCAACACAGGTATTGCT[G/T]GACTGTGGTCGTTGACTGTCATCTCTTGGGAAAGATGGGTGGTTGTCTGT
Long Flanking Sequence:
ATAACACAAGGGGTAAAATACTAACTTAATCTTCAGGAACAGCTGGATAAATCATGTGCTTTATGATTGATTAGAATTGTAAAAGTTTTTAATAATGATCTCTTTTCACAGATCCCTTTGAGGGTCCCAATTACCACATTGCCCCTCGATGGGTGTACAATGTTGCAACAGTCTGGATGTTCTTTGTGGTTGTCGCCTCAACCTTCACCAATGGCCTGGTACTGGTGGCCACGGCCAAATTCAAGAAGCTCCGTCACCCTCTCAACTGGATCTTGGTCAACCTTGCTATAGCTGATCTGGGAGAGACTCTGTTTGCCAGCACAATCAGCGTCATCAATCAGGTTTTCGGCTACTTTATACTCGGACATCCCATGTGTATTTTTGAAGGCTACACTGTGTCAGTATGTGGTAAGTTACTACACACAGAAAGCAAACTGAATAGTGTGCTGGACTGAAGATTTAGGAGGTTTTTAATGATATTTACCAACACAGGTATTGCT[G/T]GACTGTGGTCGTTGACTGTCATCTCTTGGGAAAGATGGGTGGTTGTCTGTAAACCATTTGGAAATGTCAAGTTTGATGGTAAATGGGCATCTGCTGGCATTATCTTCTCCTGGGTTTGGGCTGCTGTTTGGTGTGCACCTCCCATCTTTGGCTGGAGCAGGTAAGGAATGAAATAGTCCAGTTTTGCACTCTAAATGATTTGATAATGTCATACATGTATGTGAGAGCTGTTATCCCTGCTCTATAGGTATTGGCCTCATGGTCTGAAGACCTCCTGTGGACCTGATGTGTTTGGAGGAAACGAGGACCCCGGAGTCCAGTCCTACATGCTGGTCCTAATGATCACCTGTTGCATCCTTCCTCTTGCTATCATCATTCTCTGCTACATTGCTGTGTTCCTGGCCATCCATGCTGTATGTTAACCTTTTGAGAGGAAACTTTTTAAAGAAAAATGTTCTGCTATGGAGAACTGAGTGTGTTTTCAATCATCTTCAACAGGT
Associated Phenotype:
Not determined