ZMP

nr1i2

Ensembl ID:

ENSDARG00000029766

ZFIN ID:

ZDB-GENE-030903-3

Description:

nuclear receptor subfamily 1 group I member 2 [Source:RefSeq peptide;Acc:NP_001092087]

Human Orthologue:

NR1I2

Human Description:

nuclear receptor subfamily 1, group I, member 2 [Source:HGNC Symbol;Acc:7968]

Mouse Orthologue:

Nr1i2

Mouse Description:

nuclear receptor subfamily 1, group I, member 2 Gene [Source:MGI Symbol;Acc:MGI:1337040]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa1903	Essential Splice Site	F2 line generated	Not yet available

Mutation Details

Allele Name:

sa1903

Status:

F2 line generated
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
ENSDART00000017326	None	None	430	None	9
ENSDART00000061525	Essential Splice Site	None	430	10	10
ENSDART00000123247	None	None	430	None	10
ENSDART00000125174	None	None	430	9	9
ENSDART00000126964	None	None	327	None	8

Genomic Location (Zv9):

Chromosome 9 (position 9783633)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	9584184
GRCz11	9	9562221

KASP Assay ID:

554-1893.1 (used for ordering genotyping assays)

KASP Sequence:

TAYAGTGAACTTAATCCATTTGAGTAAACAAAGCAATTTGAGCACAGTGA[G/A]GCCCAATAAATGAAGAGAACTCAAACCTACTGAGTACTGTAATACCCAAG

Long Flanking Sequence:

ACTCTACTTATTCCCAACTACAACACTATTGCTGACCTTCATCCGAGGACATTCAAAACCGAAAGACTAGCAATGGCAGGGACTGTACCTGCTGAAAATGAACTGCTGAACAGCGCACACTGTGTGGACAAATAGTTTTATATTGGAGTTACTTAGTGTAATTGTGTTTGAGGATGTCCCACTGCCAATCGTTTTCATCGTTTCACAAAAGAACATTTTCTATGGTTCGTAACCACATATGATCTCTTATGTTAACTTCTTGAATGGAGCTTGACGTTTGGGGTTTAACTAAGCTTGGATTGGAAATGTACCACTTTTTCATGGTAACACTTTACGATGAGGTTCTGTTTGTAAAAATCAGCTAACATTGCTACACTGTAAAACTGAATAAGTTAAGGTAGCTCAAACCATGCAACAAACCATTTACATTCAAAAACTAATCCTAATGAGTACAGTGAACTTAATCCATTTGAGTAAACAAAGCAATTTGAGCACAGTGA[G/A]GCCCAATAAATGAAGAGAACTCAAACCTACTGAGTACTGTAATACCCAAGAAGTTAAGGCAACTCAAAATGTTTAAGGAAACCATTTAAGTTAAACTAATCTATACGAGCACTGTGAACTTCCTCCATTAACGTTGAAGTAATGAGGTATTTGAATTACTCATTACCTTTAACACAAGAGTTATAAACTCTTTTCAAATGAGTAGAATTAACTTTCAGTAAGTTTTGAGTTAACTACACTCATTTCATTTGATGAAGAGGACTGTTGGGTTCTACAGTGTAACAGTAGGTAGGGTATTGTGGCCAGATCAGGTCTGGGCCAGACAGAATTTGCTCATATGTCTTGCTATATCTGGGGGGAATAAGCTATTTATGCAGAATTTGAGATTATATTAACTAAAAACTTAAGGCATAAAATAAAAAATAGTACATTTTTAACAATAACCCTTTCCACAAACCCACTAATTCTTTGGAAAGCGGGCATGTGTGAACAGACCCTTA

Associated Phenotype:

Not determined