Busch Lab

ZMP

nr2f6b

Ensembl ID:
ENSDARG00000003165
ZFIN ID:
ZDB-GENE-040426-2351
Description:
nuclear receptor subfamily 2, group F, member 6b [Source:RefSeq peptide;Acc:NP_998404]
Human Orthologue:
NR2F6
Human Description:
nuclear receptor subfamily 2, group F, member 6 [Source:HGNC Symbol;Acc:7977]
Mouse Orthologue:
Nr2f6
Mouse Description:
nuclear receptor subfamily 2, group F, member 6 Gene [Source:MGI Symbol;Acc:MGI:1352453]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa21843 Nonsense Available for shipment Available now
sa35012 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa21843
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
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000027666 Nonsense 47 404 2 5
ENSDART00000123931 Nonsense 47 404 2 5
ENSDART00000139816 None None 315 None 3
Genomic Location (Zv9):
Chromosome 11 (position 6151909)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 6120092
GRCz11 11 6117347
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGCTCGCCCCAGGCAGGGAACAGCGATGTGGAAGGTGGCGAGGAGGAC[A/T]AGGCCTGCGTGGTGGACTGTGTTGTGTGTGGAGACAAATCCAGCGGGAAG
Long Flanking Sequence:
CGTTTATCTGTAATTTATTGTTTCCTGTGAAAAGGGCGAGGTAAGCTGTCCAACTCTCAGCTGCTCATTGATTCAAAGCAATCTTGGGATCTTCAGAGACTTTTTTGTGGTTAGAGGACAAGAAGAAAAGCACCGGGATGAGTGTTCCCCTGACAGGATTTTGATATGACATTTGGCGGCAAAAACATGTCAGCCTGGTAAGCTTCGGAGGTCTTCAGAGTGCTGTTAAACGTGTTTTTTTCCCCCTCAGACTCTGACTTCTTCGGCTTACTGTCTGCAGCTTAAAGGGATTCGCTCCAGGGCGGCTCTGAATTCTCGACGCAGGAAGGTTTCTCGAGCAGCTCCTGCTGGTGTACACAGAGATGGCCATGGTGAGCGGGGGATGGGCCAACCCCAATGGCAGTGCTAATGGACTCGGTGAGAAAGGTTACCTGCGGGGGGAGGAGGAGGGAAGCTCGCCCCAGGCAGGGAACAGCGATGTGGAAGGTGGCGAGGAGGAC[A/T]AGGCCTGCGTGGTGGACTGTGTTGTGTGTGGAGACAAATCCAGCGGGAAGCACTATGGTGTTTTCACCTGTGAAGGGTGCAAGAGTTTCTTCAAAAGGAGCATCAGACGGAACCTCAACTACACCTGCAGGTGAGACACCCACACACACACGTGTATTATTATTTCTATGGTTGAGCACACTAGTTTACGTTTTTTCTGCATACTTAAAAAAATTGTGACTGCTCAGACACAACAGCCAATCACACGCTGTTTCCAGATGCAGCTCAGTAAAGGAATTTGGCTGAACTTTCGGTGAACTCTGTTAACCTCTTACTGACATTTCAATTAGAGTGTGTGTAAGTGAACATAAACGCACTGATGAATCAGAGTCTGTAATAGAGGAGATTAATAATAGTAATTATGTTTTTGTATTAATCATGTTTTGAAAGCTGTTACGACTTAGATTTTTATACCCAAGACGACTATTTTTTTTAAATTGCCCTAAGCAGTTATAATTCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35012
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
ENSDART00000027666 Nonsense 95 404 3 5
ENSDART00000123931 Nonsense 95 404 3 5
ENSDART00000139816 Nonsense 6 315 1 3
Genomic Location (Zv9):
Chromosome 11 (position 6158577)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 6126760
GRCz11 11 6124015
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATCATCTCAAAGCTATCTATCCTACATTTACAGATCAAACAGAGAATG[T/A]CAGATTGATCAGCATCACCGTAACCAGTGTCAGTACTGCCGTCTGAAGAA
Long Flanking Sequence:
GTAGGTGTACATATTTAATTTGTATTTTTTTGTGTGACCACCATTACAAAGGACTGGATATCTATAAAGAATTGTGCACAGAATATATATTCAGATATTGCAGGAAAGGACATTGTGATGTTTTAAAGATTAGTGTTGGAGAATTAGCTACGCTTTAATGTTCTCATTCTTATGAAAAACATTTGAAGTTCTAAAGCAGCTGTGCCCTTGAAAAAGACGTGATAGTGTCATTAGAAACTGAATTGGAAATAAGGTTATTTTAATATAGTCAGTCGTGAACTGATGGGCCGGTCTAAGGCTTAAAATTCTAGGGCTGAAAAGGCGTTGCACTCCGGCCCAGGGTTTACAACTATTCATTTGATACTATTTATTTATACAATTTTTATTTATTTATTCATTTTAATCCTATTGAAAAGTGTTAAACCTTAAATAGTGTTCCTCTCATGTATTATATCATCTCAAAGCTATCTATCCTACATTTACAGATCAAACAGAGAATG[T/A]CAGATTGATCAGCATCACCGTAACCAGTGTCAGTACTGCCGTCTGAAGAAGTGCTTCCGGGTCGGTATGAGGAAAGAAGGTCAGCAAACCCCTAGTAAACCATTTATGTATATTATAATATTTATATCTATTTTTTATAACTCTGATAGTGTAATTTTACTTGCATTATTCAAAACGAGATTTGTTTGGATCATTATACTGAGTTTTCCCGCCCTCTTTTTTTTCCAGCTGTTCAGCGTGGCCGAATTCCTCCATCCCACGCAGGCATCAGCCCAGCCTCCATGGTAGGAGCAGGTGGTGATGTTGGAGGAGGTCCGGGCATGGGTGCTGATTTTTTTAATGGTCAGCCAGTGTCTGAACTCATCTCTCAACTACTGAGAGCAGAGCCGTACCCCAACAGCCGTTATGGAGCCCAGTGTGGCCAGCAGCTCCAAGGCGCCAACAGCTCCATGATGGGCATTGACAATATATGTGAGCTTGCAGCCCGGCTGCTGTTCAGC
Associated Phenotype:
Not determined