ZMP

opn1mw2

Ensembl ID:

ENSDARG00000094617

ZFIN ID:

ZDB-GENE-030728-5

Description:

Green-sensitive opsin-2 [Source:UniProtKB/Swiss-Prot;Acc:Q8AYM8]

Human Orthologue:

RHO

Human Description:

rhodopsin [Source:HGNC Symbol;Acc:10012]

Mouse Orthologue:

Rho

Mouse Description:

rhodopsin Gene [Source:MGI Symbol;Acc:MGI:97914]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa33930	Nonsense	Available for shipment	Available now
sa40768	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa33930

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC

Mutation:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000025241	Nonsense	66	349	1	5

Genomic Location (Zv9):

Chromosome 6 (position 41117445)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	41189045
GRCz11	6	41186581

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCTTCGGGCTGCCGATCAACGTGCTCACGCTGTTGGTCACAGCTCAGCAC[A/T]AAAAGCTGAGACAGCCTTTAAATTATATTTTGGTGAACTTGGCTTTCGCT

Long Flanking Sequence:

GAGGACTGTATGCAACCCATTCCACTGGATAATCTCTCAGCCTCCGACTTAGAACAAAGATTACAAGGTCAAAGATTTGAAACTTAATCCCCTACAGAGGGGATGGATATCATATGAGAGTTGGTAAGGAGCCAAGTAGATTCAATCCAGTAGGTTATGAAGCTCGGTGTCCGCCAAATCTTCTTAATGGTGACACCCCTTTTGACAAGGGACTCCGCTGAAGATATAAAAGCGGGCAGCTGGCAGTTTTGTGGAGTACAGTTTTGCTGGTGTCTTCTTGGCATACGTGCAACACCTCCAGCAGGATGAACGGCACCGAAGGAAACAACTTTTACATTCCTATGTCCAACAGGACTGGGCTAGTGAGGAGTCCTTACGAATACACACAGTATTACCTGGCAGATCCATGGCAGTTTAAGGCACTGGCTTTTTACATGTTTTTTCTGATTTGCTTCGGGCTGCCGATCAACGTGCTCACGCTGTTGGTCACAGCTCAGCAC[A/T]AAAAGCTGAGACAGCCTTTAAATTATATTTTGGTGAACTTGGCTTTCGCTGGAACAATTATGGCCTTTTTTGGATTCACGGTTACGTTCTATTGCTCCATTAATGGTTATATGGCTCTAGGTCCTACAGGTTGTGCCATTGAAGGCTTCTTTGCTACACTCGGAGGTAAGAATATTTCAGCAGGAATTCGTTTATTTTATTGTTTCATATTCCATATTGTGATCGTTTTATTTGTCCACAGGTCAGGTTGCTCTTTGGTCTCTTGTGGTTCTTGCCATTGAGAGATACATAGTGGTTTGCAAGCCAATGGGAAGCTTCAAATTCTCCTCAAACCATGCGATGGCCGGCATTGCCTTCACATGGGTCATGGCCTCTAGCTGTGCAGTCCCCCCACTTTTTGGCTGGTCCCGGTAAGTCATCCACGCTAATTAGAGACTTTTAATCAGCGCCAAAAGAGATTAAGGCTCAAATAATCACTAAGTTTAACCAATGGTTGCGCT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa40768

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000025241	Essential Splice Site	177	349	3	5

Genomic Location (Zv9):

Chromosome 6 (position 41118531)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	41190131
GRCz11	6	41187667

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GATAGGGTCTGAAAAGATGTGTGACAATCTTATTTTATTGTTTTGACACA[G/A]ATACATCCCAGAGGGAATGCAGACATCCTGCGGACCAGATTATTACACCC

Long Flanking Sequence:

GAGATTAATTAACTGTTTACTCACTATATCCAAATCTTGATGAGTTTCCCTTTTCTTTAAAAGACATTTTGGAAGTCATTGATATCTATAGTAGAACAAAATAACTGGAATTTAAAGCCTTTTGGTCTCAAACATACTGAAGAATCTCAGTTTTGTAACAAGTGTATAGGCAGTAAATGATGACAGTTTAAACTTAAAATAATCACCTTGGTAATGACGAAAAAGCATTATATGAGAAGTTTATTCAGACTAAAGTTGTTGTTCTACATGATAACACTTTAAATGTCTTTTACTGGATATGAGTATGCACATGTTACCTAGCCGTGGTAACACTTTATTTGAATAGTCTCTCAACAGACATTCTATTGACTAATTGTAACTCTGCAAGTATTTATTCAACTAACCCTAACTTCTAATTTACAGTCTACATATACTATTGATAATGCAAGAGATAGGGTCTGAAAAGATGTGTGACAATCTTATTTTATTGTTTTGACACA[G/A]ATACATCCCAGAGGGAATGCAGACATCCTGCGGACCAGATTATTACACCCTGAACCCAGAATACAACAATGAATCATATGTTTTGTACATGTTCAGCTGTCATTTCTGCGTTCCTGTTACAACCATCTTCTTCACTTATGGAAGCCTCGTTTGCACAGTCAAAGCTGTAAGTGAATATAATATTACAATAACATTCAGCATATTTAAATGCCGTAAAGTAATAATTTTTTTTTCTTTCAGGCTGCAGCTCAACAGCAGGAATCTGAGTCCACTCAAAAGGCTGAGAGGGAAGTAACACGCATGGTCATCCTAATGGTTTTGGGCTTCTTGGTGGCTTGGGTTCCCTATGCCAGCTTTGCGGCCTGGATCTTTTTTAACAGGGGAGCTGCTTTCTCCGCACAAGCCATGGCTATCCCAGCTTTTTTCTCAAAAGCCTCTGCCTTGTTTAACCCCATTATCTATGTGCTCCTAAACAAACAGGTGAGCCACTTTTTAATACA

Associated Phenotype:

Not determined