ZMP

opn1mw3

Ensembl ID:

ENSDARG00000044279

ZFIN ID:

ZDB-GENE-030728-6

Description:

Green-sensitive opsin-3 [Source:UniProtKB/Swiss-Prot;Acc:Q8AYM7]

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
sa7586	Missense	Mutation detected in F1 DNA	Not yet available
sa33931	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa7586

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:

T > A

Consequence:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000000877	Missense	61	349	1	5

Genomic Location (Zv9):

Chromosome 6 (position 41122578)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	41194178
GRCz11	6	41191714

KASP Assay ID:

554-4211.1 (used for ordering genotyping assays)

KASP Sequence:

GTTCTTCCTCATGTGCTTTGGGTTTCCCATCAATGGCCTTACATTGGTGG[T/A]AACAGCTCAACACAAAAAGCTGAGGCAACCTCTCAACTTCATTCTGGTCA

Long Flanking Sequence:

TCCCATTTTTCAATGAAGCACAGTGTTGCGTATACTCACTCTGCACTCAAAAACCGACACTGTCTTTTATATATAAGAATCTCAGATGTCAAAAAAGATCCAAAGCTTCACTGACTGATTAGTCCAAAAGTGATTATGTCTGCTCTTATCATTCAAATCCCACATAGTAACACCCTCCCTTTCTTGCGCTCCTGGATTTATCCCTTATAAGGATCCCCACAGGGATATATAACCACAGCTGATGCATCTATGCAATAAAGAGCAGGTCCACTGCAACAGATTGCATCCTCCTCGTGTTCTGGATCACTAGCAGGCAGAGATGAACGGCACTGAAGGAAACAACTTCTACATCCCCATGTCCAACAGGACAGGGCTTGTGAGGAGTCCGTACGAATATCCTCAGTATTATCTTGCTGAGCCATGGCAGTTTAAACTGCTCGCCGTCTACATGTTCTTCCTCATGTGCTTTGGGTTTCCCATCAATGGCCTTACATTGGTGG[T/A]AACAGCTCAACACAAAAAGCTGAGGCAACCTCTCAACTTCATTCTGGTCAATCTGGCTGTGGCTGGCACCATCATGGTTTGTTTTGGATTCACGGTCACTTTCTACACAGCCATTAATGGATACTTTGTTCTGGGACCAACTGGCTGTGCGATTGAGGGATTCATGGCCACACTGGGAGGTGAGGATAATTGTTCTGCAGTTTACCTTTTGGATTTATTTGATTTGTGATTTGATTGTTTTATTTGCTACACAGGGCAAATTTCCCTTTGGTCACTCGTGGTGCTGGCCATTGAGAGATACATTGTGGTTTGCAAGCCAATGGGGAGTTTCAAATTTTCATCCAACCATGCTTTCGCTGGGATTGGATTTACATGGATAATGGCCTTGTCTTGCGCAGCTCCTCCTCTGGTTGGCTGGTCAAGGTCAGTGTAATGATAAATACAATATAAAGCAATTCATTTGCTCTATATTTTGATGGACAAGTGATTAAAACTAAAAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa33931

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:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000000877	Nonsense	149	349	2	5

Genomic Location (Zv9):

Chromosome 6 (position 41122917)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	41194517
GRCz11	6	41192053

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CATTGAGAGATACATTGTGGTTTGCAAGCCAATGGGGAGTTTCAAATTTT[C/A]ATCCAACCATGCTTTCGCTGGGATTGGATTTACATGGATAATGGCCTTGT

Long Flanking Sequence:

CAACTTCTACATCCCCATGTCCAACAGGACAGGGCTTGTGAGGAGTCCGTACGAATATCCTCAGTATTATCTTGCTGAGCCATGGCAGTTTAAACTGCTCGCCGTCTACATGTTCTTCCTCATGTGCTTTGGGTTTCCCATCAATGGCCTTACATTGGTGGTAACAGCTCAACACAAAAAGCTGAGGCAACCTCTCAACTTCATTCTGGTCAATCTGGCTGTGGCTGGCACCATCATGGTTTGTTTTGGATTCACGGTCACTTTCTACACAGCCATTAATGGATACTTTGTTCTGGGACCAACTGGCTGTGCGATTGAGGGATTCATGGCCACACTGGGAGGTGAGGATAATTGTTCTGCAGTTTACCTTTTGGATTTATTTGATTTGTGATTTGATTGTTTTATTTGCTACACAGGGCAAATTTCCCTTTGGTCACTCGTGGTGCTGGCCATTGAGAGATACATTGTGGTTTGCAAGCCAATGGGGAGTTTCAAATTTT[C/A]ATCCAACCATGCTTTCGCTGGGATTGGATTTACATGGATAATGGCCTTGTCTTGCGCAGCTCCTCCTCTGGTTGGCTGGTCAAGGTCAGTGTAATGATAAATACAATATAAAGCAATTCATTTGCTCTATATTTTGATGGACAAGTGATTAAAACTAAAAATAGTTCAGTCATATATATGAGGGAATTTCTTTTTTATTTGATCAGTACTAAAAAGTTACAATGTAAGGATGTCATTTTGACTCTTCAGAGTCAAACACATTACCTTAATTATAATAACTGTAGTAATATGTTAGATTGAACTGAATAGATTGTACATATGTTTTTTAAATGAAGAATAGGAAGAAGACAGTCAAAAATGTATTAACCTCTGGTGATTTCCTATCAGGTATATTCCAGAGGGAATGCAGTGTTCATGTGGACCAGACTACTACACCTTGAACCCTGACTACAATAATGAATCATATGTCCTCTACATGTTCTGCTGCCACTTTATATTTC

Associated Phenotype:

Not determined