ZMP

nr4a2b

Ensembl ID:

ENSDARG00000044532

ZFIN IDs:

ZDB-GENE-040718-103, ZDB-GENE-990415-184

Description:

nuclear receptor subfamily 4, group A, member 2b [Source:RefSeq peptide;Acc:NP_001002406]

Human Orthologue:

NR4A2

Human Description:

nuclear receptor subfamily 4, group A, member 2 [Source:HGNC Symbol;Acc:7981]

Mouse Orthologue:

Nr4a2

Mouse Description:

nuclear receptor subfamily 4, group A, member 2 Gene [Source:MGI Symbol;Acc:MGI:1352456]

Alleles

There are 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa40651	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa40651

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 > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000065385	Essential Splice Site	449	586	7	8

Genomic Location (Zv9):

Chromosome 6 (position 12377100)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	12230322
GRCz11	6	12465180

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GATCTACATTTTTAAAAGACATAATATAATAACTTTTCAATTTTCTCACC[A/T]GATCTAACCTGCCAGAGGACAAACTCATCTTTTGCAACGGAATGGTTTTA

Long Flanking Sequence:

CACCCGTCAATCTCCTGAACGCACTAGTGAGAGCGCACATAGACTCCAACCCCTCCATGGCCCGTCTGGACTACTCTAAAGTGAGCTTCAAACTTCCAACATTCTGTAAAATAAATTTAAGTTTTAAGTCAAATTGACAATTTAATTATTGTTTTAGAATATGACCAAAATACATTTACTCTATTATATTCCATTAACAGTTTTGTATTACATCTTAGTTTCAGACGAGTCCGGAGTATCACAGTGGAGGAGATGAATCTCTGCACATTCAGCAGTTCTACGATCTACTCACTGCCTCAATGAGCATCATTCGCGGATGGGCCGAAAAAATCCCCGGCTTTACCGAGCTGCCCAAATGCGACCAGGAGCTCCTTTTCGAGTCTGCCTTCCTTGAACTCTTCGTGTTGCGGCTGGCGTACAGGTAGGCTAAGTATCATTGGAATTTAGATGGATCTACATTTTTAAAAGACATAATATAATAACTTTTCAATTTTCTCACC[A/T]GATCTAACCTGCCAGAGGACAAACTCATCTTTTGCAACGGAATGGTTTTACACAAGTTGCAGTGCGTGCGAGGCTTTGGGGAGTGGATCGACTCTATTGTCGAGTTTTCTTCTAATCTTCAGAGCATGAGCTTAGACGTGTCTGCCTTCTCCTGCATAGCCGCTCTCACCATAGTAACAGGTAAGACATGTCTGACCTTTTCCAAGTGATGCACAGAATATACAGCATGTTTCAGAGCTCTGACGGGTTTTTTCTTATCTCCATAGAGAGACACGGACTAAAGGAGCCCAAGAAAGCAGAGGAACTTCAAAACAAGCTCATAAACTGTCTGAAGGATCAGGTGTCCTGCAGTGGTGAATTGTCTAAACTGTTGGAGAAGCTGCCGGAGGTGCGCGCGCTGTGCACGCAGGGTCTGCAGCGCATCTTTTACTTGAAACTGGAGGATTTGGTGCCCACGCCTGCGATCATTGATAAACTCTTTCATGACACTTTACCATTCT

Associated Phenotype:

Not determined