Busch Lab

ZMP

nr0b1

Ensembl ID:
ENSDARG00000056541
ZFIN ID:
ZDB-GENE-070130-1
Description:
nuclear receptor subfamily 0 group B member 1 [Source:RefSeq peptide;Acc:NP_001076416]
Human Orthologue:
NR0B1
Human Description:
nuclear receptor subfamily 0, group B, member 1 [Source:HGNC Symbol;Acc:7960]
Mouse Orthologue:
Nr0b1
Mouse Description:
nuclear receptor subfamily 0, group B, member 1 Gene [Source:MGI Symbol;Acc:MGI:1352460]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa30950 Nonsense Mutation detected in F1 DNA Not yet available
sa41861 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa30950
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079060 Nonsense 263 264 2 2
ENSDART00000128468 Nonsense 291 292 2 2
ENSDART00000079060 Nonsense 263 264 2 2
ENSDART00000128468 Nonsense 291 292 2 2
Genomic Location (Zv9):
Chromosome 11 (position 30560307)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 29436293
GRCz11 11 29683467
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGTCATTGGCGCGGTCAACATGGAGGAACTTCTTCTGGAGATGTTTTAT[G/T]GAAAATAAACTTTGAAAAAAACTGGGAGAGAATTATCAGACTTGGAAAGA
Long Flanking Sequence:
CTGTCTTAAATAAATACCCCCAAGAGTCATACTTAATTAAAAACAAAAAATCTTTTTTTTTGCATTGGCGTAATAAAACAAATTCATAGTAATGTATTAATCAAACAAGAATCATGACTCGTTGATCATAAATTGTTCCCAAGAAATTGAGAGTGCTAATCAAATATACAGGTAGTACATTTTATTGGTTTAATGAGGGTAATTTCATGTCATTCATATCTTCCTGGCATACAATATAACAAGTTTCACTTAATCTCTTGTTCTCAGATGTTGCTGGGCTGCAGTGTCAACATTACATCCAGGCCCTGCAGAGCGAGGCGAACCAGGCACTTAATGAATATGTCAAAATGATTCACCGCGGGGACAGTGCGAGATTCGCCAAACTCTTCCTCGCTCTCTCCATGCTGAGATCCATCAACGCCAATGTAGTGGCTGGGCTCTTCTTCAAACCCGTCATTGGCGCGGTCAACATGGAGGAACTTCTTCTGGAGATGTTTTAT[G/T]GAAAATAAACTTTGAAAAAAACTGGGAGAGAATTATCAGACTTGGAAAGAGCGACAGTCACTGTTGGAGGGACAGATTTTGAAAATGACTGATTCCTTTTTACACATGCTATTTTTGTACAATATATAAGAGCTCTCCTTTTTGCCTTCTGAGTTGAACTCATCACTGAATCCAAAGTTGATGACAATATTTTTCCCATTTGGGGAAAGAGCTTTATAACTTTGTTCTGATTGTTTTTTGTTTACTTGCTTATTATCTGTAATGTCTTGTTGCATTTTGAAGAATGTTTATTTGATTCTGGGAGACACTTTATAATAACTTTCTTAAGGAAATCATTTACAAACATTCATTTAAATATGTGCTCCGTTTAAGAAATACATTGAAATGTAATTATATTTGATGTAAATATATTACATTTAATAATAGCCTAATATATGATCTTATGTTTCCTGATATTATTTGTTATCTCATGAACTGTTTTGCATTATTAAATGTAATGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41861
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079060 Nonsense 263 264 2 2
ENSDART00000128468 Nonsense 291 292 2 2
ENSDART00000079060 Nonsense 263 264 2 2
ENSDART00000128468 Nonsense 291 292 2 2
Genomic Location (Zv9):
Chromosome 11 (position 30560307)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 29436293
GRCz11 11 29683467
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGTCATTGGCGCGGTCAACATGGAGGAACTTCTTCTGGAGATGTTTTAT[G/T]GAAAATAAACTTTGAAAAAAACTGGGAGAGAATTATCAGACTTGGAAAGA
Long Flanking Sequence:
CTGTCTTAAATAAATACCCCCAAGAGTCATACTTAATTAAAAACAAAAAATCTTTTTTTTTGCATTGGCGTAATAAAACAAATTCATAGTAATGTATTAATCAAACAAGAATCATGACTCGTTGATCATAAATTGTTCCCAAGAAATTGAGAGTGCTAATCAAATATACAGGTAGTACATTTTATTGGTTTAATGAGGGTAATTTCATGTCATTCATATCTTCCTGGCATACAATATAACAAGTTTCACTTAATCTCTTGTTCTCAGATGTTGCTGGGCTGCAGTGTCAACATTACATCCAGGCCCTGCAGAGCGAGGCGAACCAGGCACTTAATGAATATGTCAAAATGATTCACCGCGGGGACAGTGCGAGATTCGCCAAACTCTTCCTCGCTCTCTCCATGCTGAGATCCATCAACGCCAATGTAGTGGCTGGGCTCTTCTTCAAACCCGTCATTGGCGCGGTCAACATGGAGGAACTTCTTCTGGAGATGTTTTAT[G/T]GAAAATAAACTTTGAAAAAAACTGGGAGAGAATTATCAGACTTGGAAAGAGCGACAGTCACTGTTGGAGGGACAGATTTTGAAAATGACTGATTCCTTTTTACACATGCTATTTTTGTACAATATATAAGAGCTCTCCTTTTTGCCTTCTGAGTTGAACTCATCACTGAATCCAAAGTTGATGACAATATTTTTCCCATTTGGGGAAAGAGCTTTATAACTTTGTTCTGATTGTTTTTTGTTTACTTGCTTATTATCTGTAATGTCTTGTTGCATTTTGAAGAATGTTTATTTGATTCTGGGAGACACTTTATAATAACTTTCTTAAGGAAATCATTTACAAACATTCATTTAAATATGTGCTCCGTTTAAGAAATACATTGAAATGTAATTATATTTGATGTAAATATATTACATTTAATAATAGCCTAATATATGATCTTATGTTTCCTGATATTATTTGTTATCTCATGAACTGTTTTGCATTATTAAATGTAATGA
Associated Phenotype:
Not determined