ZMP

nr2e3

Ensembl ID:

ENSDARG00000045904

ZFIN ID:

ZDB-GENE-041114-63

Description:

photoreceptor-specific nuclear receptor [Source:RefSeq peptide;Acc:NP_001007369]

Human Orthologue:

NR2E3

Human Description:

nuclear receptor subfamily 2, group E, member 3 [Source:HGNC Symbol;Acc:7974]

Mouse Orthologue:

Nr2e3

Mouse Description:

nuclear receptor subfamily 2, group E, member 3 Gene [Source:MGI Symbol;Acc:MGI:1346317]

Alleles

There are 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa15662	Nonsense	Available for shipment	Available now
sa30255	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa15662

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
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Mutation:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000067474	Nonsense	339	419	6	8
ENSDART00000127099	Nonsense	346	426	6	8

Genomic Location (Zv9):

Chromosome 25 (position 23001063)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	22180176
GRCz11	25	22277724

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TGCAAGTGGATCCAACYGAGTTTGCCTGCTTGAAAGCCATTGTTTTGTTC[A/T]AACCAGGTACATTTTGGCTTCTTTTTACCACAAGGGGGCATAAGTGATGG

Long Flanking Sequence:

TCTTCTCTTTATGTCTGTTAAATGGGCCAAGAACCTGCCAGTATTTTCACATCTACCTTTCAGAGACCAGGTGAGAGACTCAGATGTACTAACATCCCCTACTCTGCTAACATCCCCTACACTGTTAAACTCCGGATGAGTGTCTAAATATGCAGTATAGAATAGACAAAGAAAGTATTGTTTTTGGCTGTTTTGCTGTTTAAAAATATGAAATATTGTTGTAATGGTCTTAGCAATTTTTAACCCGACGTCCTTTATGATTATAGGTGATTCTGCTTGAGGAAGCATGGAGCGAGCTGTTTCTTCTATGTGCAATTCAGTGGTCTCTACCTCTGGACAACTGCCCTCTGCTGTCTCTGCCTGACCTCTCACCCACAGGACAGGGAAAGGGAAGCCCCTCTGCCTCAGATGTGAGGGTTCTGCAAGAGGTGTTTAGCCGGTTCAAGCCCTTGCAAGTGGATCCAACCGAGTTTGCCTGCTTGAAAGCCATTGTTTTGTTC[A/T]AACCAGGTACATTTTGGCTTCTTTTTACCACAAGGGGGCATAAGTGATGGCATCCAGTACATGGCTAAACTAGCCTGGAATAGATATTATTTTAATTAAGTTATTCTGTTACAGAAACACGAGGACTTAAAGACCCCGAACAGGTAGAGAACCTACAAGATCAGTCCCAAGTACTGCTTGCTCAACATATTCACACACTTTACCCCAGTCAAGTTGCCAGGTGAGTGAATATACACACATTTGCATTAGGAAGTCAACACTATTCATGAGAGAAGGTTGAACTAACACAGATTATGTTTTTCTTAGGTTTGGGAGACTATTACTTCTCCTTCCCTCCCTTCACTTTGTGAGCTCAGAGCGAATCGAGCATCTTTTTTTCCAGAGAACAATCGGGAACACACCCATGGAGAAACTCTTGTGTGACATGTTCAAAAACTGAGGAGCTTTTTCTGAAAGACTTGTTTAGAGGAATGAAAACCTCTTGAATTCAGGGGCTTTGC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa30255

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:

A > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000067474	Essential Splice Site	376	419	None	8
ENSDART00000127099	Essential Splice Site	383	426	None	8

Genomic Location (Zv9):

Chromosome 25 (position 23001368)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	22180481
GRCz11	25	22278029

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAACACTATTCATGAGAGAAGGTTGAACTAACACAGATTATGTTTTTCTT[A/G]GGTTTGGGAGACTATTACTTCTCCTTCCCTCCCTTCACTTTGTGAGCTCA

Long Flanking Sequence:

CTATGTGCAATTCAGTGGTCTCTACCTCTGGACAACTGCCCTCTGCTGTCTCTGCCTGACCTCTCACCCACAGGACAGGGAAAGGGAAGCCCCTCTGCCTCAGATGTGAGGGTTCTGCAAGAGGTGTTTAGCCGGTTCAAGCCCTTGCAAGTGGATCCAACCGAGTTTGCCTGCTTGAAAGCCATTGTTTTGTTCAAACCAGGTACATTTTGGCTTCTTTTTACCACAAGGGGGCATAAGTGATGGCATCCAGTACATGGCTAAACTAGCCTGGAATAGATATTATTTTAATTAAGTTATTCTGTTACAGAAACACGAGGACTTAAAGACCCCGAACAGGTAGAGAACCTACAAGATCAGTCCCAAGTACTGCTTGCTCAACATATTCACACACTTTACCCCAGTCAAGTTGCCAGGTGAGTGAATATACACACATTTGCATTAGGAAGTCAACACTATTCATGAGAGAAGGTTGAACTAACACAGATTATGTTTTTCTT[A/G]GGTTTGGGAGACTATTACTTCTCCTTCCCTCCCTTCACTTTGTGAGCTCAGAGCGAATCGAGCATCTTTTTTTCCAGAGAACAATCGGGAACACACCCATGGAGAAACTCTTGTGTGACATGTTCAAAAACTGAGGAGCTTTTTCTGAAAGACTTGTTTAGAGGAATGAAAACCTCTTGAATTCAGGGGCTTTGCTTTACTGCCATGCTAGTTGCTATGCTTTTTATCTGTGTGAATGCTACGATAAACACACATGTATATATGCTTTTTTATTATTTTTGCATAGGTTGCTTATTTTGTCTCATTATGTGTCATCTATTTTTATTTGTCCTACTGTAGAGATTTTTTTTAATATCTGTAATATTGCCCATAAGTCTATGCATCTCCATTATGTGGAATCTCAGATACTTGGCACAGCCTGTTTATGTATTTCATTTTGAGAAAAATGCCTTCCAAGCGCATTATAATGCAAGTTTACTTAGAATATGTTTGATGATCAG

Associated Phenotype:

Not determined