ZMP
nr2f6b
Ensembl ID:
ZFIN ID:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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