ZMP
LOC566133
Ensembl ID:
Human Orthologue:
OPN4
Human Description:
opsin 4 [Source:HGNC Symbol;Acc:14449]
Mouse Orthologue:
Opn4
Mouse Description:
opsin 4 (melanopsin) Gene [Source:MGI Symbol;Acc:MGI:1353425]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22105 | Essential Splice Site | Available for shipment | Available now |
sa7361 | Missense | Mutation detected in F1 DNA | Not yet available |
sa22104 | Nonsense | Available for shipment | Available now |
sa35304 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22105
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 |
---|---|---|---|---|---|
ENSDART00000076051 | Essential Splice Site | 91 | 516 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 12 (position 27689838)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 26026647 |
GRCz11 | 12 | 26118007 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTTCTTCACCACCAGTTTGCACAAGCGATGGATCTTTGGAGAAAAAGG[T/C]AATCCAGCTGTTAGAAAATCACGACTTGATAAAACAAATCTTTTGAAGGC
Long Flanking Sequence:
TTCTAGATTTTCTAAAATGTTCATAAAAATAGGTGGATGGAAATATACTGATAAACCAACGCAATTCGTAACTTTTTGATTTAGTGGTTAATTCGTATGAATTCGTACGATCTAATTTGTACAATTTAGTATGATTTGCTTATTACTTAATGAATTTTGGGGTTAGGGGTTGGGTACCATGCCTCCTTTTTAAAATCGCACATTTTCGTACGACTGAACTTGTGAGAATTCATACGAATTAGTCACTAAACTGACAAAATGTAAAATATTTACATTTCCTTGTGAGATCAGGCTGGATAAACTGATGTTCTCTTTTTTAAATTCAGAACTTTATAATTTGTCTTTTGTTTTGTTTATGTTTTCAGGAGCCGGAGTTTGAGAACACCTGCCAACATGTTCATCATCAATCTTGCTGTCACTGATTTCCTGATGTGTGTCACTCAAACACCAATCTTCTTCACCACCAGTTTGCACAAGCGATGGATCTTTGGAGAAAAAGG[T/C]AATCCAGCTGTTAGAAAATCACGACTTGATAAAACAAATCTTTTGAAGGCATTCAAGATTTCTTGTACAGATGTTAAGAAAGAGCTGGACGTCAGGGGAACTGCATTTTTTTTTTATAGCAGATTATCTTCATGATTCACCGATTGTAGTACAGATGAGAGGAAAGTACAGAACAGATAATGCTAGAGGATCACATTTGGAGAGGGATTATTCATTGATGCATAACTGCATCCTGGTCAAGGAGAAGAAACACCTCAGTGTCCTCAGAGGTCATAGCGGAAGAATCAGTGTTTTGATGACAATGCAAAGAGGCTTCTTTAAATCAACCATCATTATGTGCAATGGAAATGTTTTTGGTACATCAAGCAGAACGAACATAATTGGGGATACATTTATCAGTCTTTTTTCAGGGTGTTATTATTGAGGAGAATAACTGTGGTAATTATGTTTTCATCATCCTAGAACAACAATAAACATAAATATATTAAAAACAAATATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7361
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 > T
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000076051 | Missense | 236 | 516 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 12 (position 27676956)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 26013765 |
GRCz11 | 12 | 26105125 |
KASP Assay ID:
554-4368.1 (used for ordering genotyping assays)
KASP Sequence:
GGAAAATCAATGRAGAAGGAGGACCCAGAGATTCTATCAAAAAGATCCAC[C/T]GGATGAAAAACGAATGGAAGATGGCAAAGATAGCGCTCATAGTGATCCTG
Long Flanking Sequence:
ACAATATGTAATTATATTTTCTCCTGTCAGGTGCATATGTTCCTGAAGGTCTGCTGACGTCCTGTTCGTGGGACTACATGACCTTCAGTCCTTCTGTTCGAGCCTACACAATGCTGCTCTTCACTTTTGTATTCTTCATTCCCCTCTTCGTCATCATTTATTGCTACTTCTTTATCTTCAAGGCCATCCGTGAAACCAACAGGTAAACTGGTTAAGTACGTCATACTGGAGAAAAAAAAAATCTGTAAAAGAGAGGTTCATTATTTATCAAAAAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAGAGATCCATTTTAGATTAGTGCTTTGTTGTGTTCTTTACGTGGTTGATTAAATATGTCACTGCGTAAACTGATGTGCATTGTATTTATCTGTTTGTTTTCACATCTGTATGATGGGAATAATAGAGCTGTGGGGAAAATCAATGGAGAAGGAGGACCCAGAGATTCTATCAAAAAGATCCAC[C/T]GGATGAAAAACGAATGGAAGATGGCAAAGATAGCGCTCATAGTGATCCTGTTGTATGTCATCTCCTGGTCTCCATACTCCTGTGTGGCTCTCACTGCTTTTGCTGGGTGAGAATCAGCATGTTTTACAATTACCATCCAGAACTTTTGATTGCAATTTACAATGTACTTAAAGTTTAAAAAGCAATTACTTCACTTTAGTTTAAAAAGTGAGTAAACCAGTTGGTCTCAAAGCAATAAATTGACTTTACTTAAAAAGATAAGGAAACTCATTGCCTTAAAAGTATTAAATCAATTAATAAAGTGCCTAATTTTAAAAATTAAGTCCTCTAAAACAATTCCACCACTCCAAAAAATAACTTTTGCTGCTTGTATAAAGTGCATTGGAACAATACAATTCTTAATTTATTTTTTTTTTGGGGGGGACAGCCTATTTGTTTTATGTTCAATCCACTTAAGTTTGTAACAATGATTAAGTTAACTTAATGGATTTGTATTGGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22104
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 |
---|---|---|---|---|---|
ENSDART00000076051 | Nonsense | 355 | 516 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 12 (position 27668126)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 26004935 |
GRCz11 | 12 | 26096295 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACGCTCCACATTGACCAGCCAGTCCTCTGAGACCAGCAGCAACTTGCAT[C/T]GAGCCGGAAAGGCACGCTTGTCCTCTGTATCTGACAGCGAATCAGTAAGA
Long Flanking Sequence:
ATTGTATTATTTGAATAATATTTCAGAATAGCACTTAACCTAAAAAATAAAAAGCATTTGCTAAAGAAATCATGTGATTTAATCTTTTTTCTGTATGTTTGTCCTACATAAAAATGTAAAATGCAACAATCTACCGGGTGGACTTCCAAGCAAGTTTACCAGAAAAGCTATGCAAATTTGCATTTACATGTATTTGTTAATAAATCATCCACTAATCATTTTTCTTTCTTTTTTAAAATTGTACAGATAAGCCTGTATCCAACAGTTTTCTCTGCAGTCCTTATTTGTGTAAAAAGAAGCAGATGTCATTGGTGTTTTACTGCCTCACATTTATATTTTCTCCCTTTTGCTCTGGCAGGTCTGCCATTGCCAAGTACATCCCTTGTCTTGGAGTGCTGCTCTGTGTTCCTCGTAGAGACCGCTTCAGCAGCAGTAGCTTTATATCCACACGACGCTCCACATTGACCAGCCAGTCCTCTGAGACCAGCAGCAACTTGCAT[C/T]GAGCCGGAAAGGCACGCTTGTCCTCTGTATCTGACAGCGAATCAGTAAGAAAGCACCTCCAGGCCAGAAACATTGAACCCATATATTTGTAGCCACATACTTCTGATTTCATGTGTGTAGTTTCAAATTCCCTTAAAATCACTGTTAGAAATTAACTTGATAGTTTTTAATCATTTTCAAGGTTTTTTTTTTATTCTACAAATGACTACTAATAGAACATTGTTACTATTATCCCCTATGTTAAGCTGCTTTGACTCAATCTACATTGTAAAAGCGCTATAGAAATAAAGATAAATTAAATTGAATTGAACATTGTACTTACACTTTTAAAAATGAAAGTGCGGGATTTTCTTTTTGTCGAAAGCTCTTCAAAGAAATGTTTTTGGTGTCAGGAACATTTTCATAGTCTTCCACTATATATATATATATATATATATATATATATATATATATATATATATATATATGTGTGTGTGTGTGTGTGTGTATAAACAAATCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35304
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 |
---|---|---|---|---|---|
ENSDART00000076051 | Nonsense | 399 | 516 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 12 (position 27665834)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 26002643 |
GRCz11 | 12 | 26094003 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACGGCCTGCTAGTCGCCAGGTCTCATCGGAAATCCGCAAAGATCTATG[C/A]GATATCAAGCACAGCAGCTCTCTGAGGCTGAAGGTCAAAAGCAGAGACTC
Long Flanking Sequence:
CATCCCAGTCTGTCTATCACTGACTGCTGTTTATCTGATGTAATGCAGGAGAAGCAGACACACATGTCAGAGCGGTGGGCAGGGAGAACCAGGTCATATGGATTTAAAACCACAGGCTACAACAACAGCTACAGTGTACTCAGACACCAAAATGGACAAATTCTATATTACATGTTAAATAATCTGATGAGTATTTTTTAGAGCTGAAACTTCACATACACATTCTAGAGACACCAAAGGTTTATCTTACATCTTAAAAGGATTTGCCCTTTAAACAGAATAAAGAAACTCAAAAGTTTAGATCCACTTGAGTGTGAGTAAATAGTGAGTACATTTTTGGTGGGTGAACTGTCCCTTTTTTAGCAAAGCTCTTTCTGTTGTAACTGCTTAATGTGTGTTGTGTATGGACAGGGCTGGACAGACACAGAGGCAGATCTCTCCACCGCAAGTTCACGGCCTGCTAGTCGCCAGGTCTCATCGGAAATCCGCAAAGATCTATG[C/A]GATATCAAGCACAGCAGCTCTCTGAGGCTGAAGGTCAAAAGCAGAGACTCTGGAATCTTCGACAGGACATCAGCCCAGAGTCTAGCCGACCCGAGCACCAACCGGCCCTGTGCGTACATCAGCGTAAGTGAGAGACTTCATTTAGTGTCATATCTACCTCATTTATCACCAGCTCCACAGCTCACCCGGCGCTCTTTGATTTATGAAATTAGGAAGTCCCACATTCATTTTAAGAGAGGAAACGACTCCATCAGATTTAAAAAATTAATTTGGAAATTTCATTCCATCCTTCATATCTCGACGACAGTTCGCTGCCCTGGTTTTAGCCAGCGCTGTACTTTGACAAATGACAAGAGTGCTCAAGAGTCTGCATGCTTATGTGTGCTAATGATGCACTTTCTGGGATTTCTTATGACTGTACGCTAATTAAGTTTGAGAGAAATTGGTGCCTCCTTCACCAACTTTTTCTTTTAAATGTAGTGAAGCTATTGCTGTCTGAC
Associated Phenotype:
Not determined