ZMP

LOC558443

Ensembl ID:

ENSDARG00000036460

Human Orthologue:

OPN3

Human Description:

opsin 3 [Source:HGNC Symbol;Acc:14007]

Mouse Orthologue:

Opn3

Mouse Description:

opsin 3 Gene [Source:MGI Symbol;Acc:MGI:1338022]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa45519	Nonsense	Mutation detected in F1 DNA	Not yet available
sa9212	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa45519

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000075676	Nonsense	98	320	1	4

Genomic Location (Zv9):

Chromosome 14 (position 32636343)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	31426150
GRCz11	14	31766464

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATACTGGTCTGCTTGTTTGGGACTCCCTTTAGCTTCGCGTCCAGTCTCTA[T/A]GGGAAATGGCTTTTGGGACATCACGGCTGCAAATGGTACGGTTTCGCCAA

Long Flanking Sequence:

CCCCACACAGCTCATAATTCGCACCCTGGTCATCTGTGATCAGAGAGCGGGGGTCAGCGGCGCAGAGGCAGAGTGTCGATGGTGGGCAGCGCGTCAGTGAGGTGGAGACATGAAAACTGTGAATCTTTCCGTCAGGAAAGTCATAGTGTCAACATCATTTCCCCGTGCAGGGAGGCTGCTATGGTCGTCTACATCTGGAGTTTGAACATCAGCAGCAAAGACACTTCTGCGCTTAACCAAAGTGGCAATGTGAGTTCAGGGGATCCTCTGGAGCCCCATGACAGCCCACCCGGCCTGAGCAGGACCGGCCACACGGTGACCGCCGTCTGCCTCGGAGCCATCCTGCTGTTGGGATGCCTGAACAACCTCTTTGTCCTGCTCGTCTTCGCGAGGTTTCGCACACTGTGGACTCCTATAAACCTGATCCTGCTGAACATCAGCGTCAGTGACATACTGGTCTGCTTGTTTGGGACTCCCTTTAGCTTCGCGTCCAGTCTCTA[T/A]GGGAAATGGCTTTTGGGACATCACGGCTGCAAATGGTACGGTTTCGCCAATTCGCTTTTTGGTAAGTTTTGCTGAAGTTCATTCAACAGGGAACTTCCGTTTACGAGCCCTCAGAGAATTTAGACGAACTTTTTCTCGCTATTGCTTTGCTGATATCAGGATTTTAACTGTACTCTTTCAAATGCTTGAGAATCTTAATATTTTAGTATCTAAAAAATTTGGGATTGCAGTTTATTGAAACTGTTTAGACGGAGAATCAAAATAGAGCTGCGCAAATAGGAAAACTATTAAGGACATACATTTTACAACAACAACAAATATATAAGACTTTATCATACATTAAACATTAGCTAGAACACATTAGACCAATATATTTCACAAAATGTATTAATCACTGAGGATGTTAATTGATAAGTATGCTGTATTGACAAATTCAGAACAAATTATATTGCTTTATAATTAATTGAAATTTTGTTGAAATTAATTTGATCAAAGATTAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa9212

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 > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000075676	Essential Splice Site	119	320	1	4

Genomic Location (Zv9):

Chromosome 14 (position 32636406)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	31426213
GRCz11	14	31766527

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TTGGGACATCACGGCTGCAAATGGTACGGTTTCGCCAATTCGCTTTTTGG[T/G]AAGTTTTGCTGAAGTTCATTCAACAGRGNACTTYCGTTTRCGAGCCYTCA

Long Flanking Sequence:

AGAGGCAGAGTGTCGATGGTGGGCAGCGCGTCAGTGAGGTGGAGACATGAAAACTGTGAATCTTTCCGTCAGGAAAGTCATAGTGTCAACATCATTTCCCCGTGCAGGGAGGCTGCTATGGTCGTCTACATCTGGAGTTTGAACATCAGCAGCAAAGACACTTCTGCGCTTAACCAAAGTGGCAATGTGAGTTCAGGGGATCCTCTGGAGCCCCATGACAGCCCACCCGGCCTGAGCAGGACCGGCCACACGGTGACCGCCGTCTGCCTCGGAGCCATCCTGCTGTTGGGATGCCTGAACAACCTCTTTGTCCTGCTCGTCTTCGCGAGGTTTCGCACACTGTGGACTCCTATAAACCTGATCCTGCTGAACATCAGCGTCAGTGACATACTGGTCTGCTTGTTTGGGACTCCCTTTAGCTTCGCGTCCAGTCTCTATGGGAAATGGCTTTTGGGACATCACGGCTGCAAATGGTACGGTTTCGCCAATTCGCTTTTTGG[T/G]AAGTTTTGCTGAAGTTCATTCAACAGGGAACTTCCGTTTACGAGCCCTCAGAGAATTTAGACGAACTTTTTCTCGCTATTGCTTTGCTGATATCAGGATTTTAACTGTACTCTTTCAAATGCTTGAGAATCTTAATATTTTAGTATCTAAAAAATTTGGGATTGCAGTTTATTGAAACTGTTTAGACGGAGAATCAAAATAGAGCTGCGCAAATAGGAAAACTATTAAGGACATACATTTTACAACAACAACAAATATATAAGACTTTATCATACATTAAACATTAGCTAGAACACATTAGACCAATATATTTCACAAAATGTATTAATCACTGAGGATGTTAATTGATAAGTATGCTGTATTGACAAATTCAGAACAAATTATATTGCTTTATAATTAATTGAAATTTTGTTGAAATTAATTTGATCAAAGATTAATAAATGCTGTAAAATATTGTTTTGATTGTTCATAATAATGAACTTAGTTAATTAATGTTTAAT

Associated Phenotype:

Not determined