ZMP
nr2f1a
Ensembl ID:
ZFIN IDs:
Description:
Nuclear receptor subfamily 2 group F member 1-A [Source:UniProtKB/Swiss-Prot;Acc:Q06725]
Human Orthologue:
NR2F1
Human Description:
nuclear receptor subfamily 2, group F, member 1 [Source:HGNC Symbol;Acc:7975]
Mouse Orthologue:
Nr2f1
Mouse Description:
nuclear receptor subfamily 2, group F, member 1 Gene [Source:MGI Symbol;Acc:MGI:1352451]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa20527 | Nonsense | Available for shipment | Available now |
| sa11358 | Nonsense | Available for shipment | Available now |
| sa40551 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa45227 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa14691 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20527
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000051263 | Nonsense | 72 | 411 | 1 | 3 |
| ENSDART00000133384 | Nonsense | 72 | 410 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 5 (position 51528488)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 49094186 |
| GRCz11 | 5 | 49745697 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCAGGGACGGCTGGCGACAAGGGCAGCCAGAATTCTGGACAGAGTCAA[C/T]AGCATATAGAATGTGTTGTTTGCGGGGACAAATCAAGCGGCAAGCACTAT
Long Flanking Sequence:
TTTATATTACGTCTGGGATCGCTTTCTTCATTCACGATTGGGTTCCCGAATGGCTGACTGCAATTTACCTTGGAACTGGCCTCCCGACAACTGCATATCCTGATCGGGTGCCTTTCTATCGACTCCGGTATTTTGAATGTATTGACCATTTTCTGCTTCTACTTTTTTCCCTATGAGATTGAGTGCTCCGATTTGAATTCGCGCTGCCGTTCGTCCAAGACTTCCCTTTTCCCTGCTCCGATATCCGAGCGACCAGTTCGCTTGAAAGCACTTTTCGGGCCCGAGATATGGCAATGGTAGTTAGCGTCTGGCGAGATCCGCAGGAAGACGTGGCTGGAGGACCTCCGAGCGGCCCCAATCCAGCAGCTCAGCCGGCGAGGGAGCAACAGCAGGCGGCGTCAGCGGCACCACACACTCCGCAGACCCCCAGTCAGCCAGGACCTCCGTCCACACCAGGGACGGCTGGCGACAAGGGCAGCCAGAATTCTGGACAGAGTCAA[C/T]AGCATATAGAATGTGTTGTTTGCGGGGACAAATCAAGCGGCAAGCACTATGGTCAATTCACCTGCGAAGGATGCAAAAGTTTCTTCAAGAGGAGTGTCCGAAGGAACTTAACATATACATGTCGTGCCAACAGGAACTGTCCTATTGACCAACACCATCGTAATCAGTGCCAATATTGTCGGCTGAAGAAGTGTTTAAAAGTGGGCATGCGGCGGGAAGGTGAATATATTTTTCTGAATACATCACACTTGCTACACAAACAGGTTTATTGTTTAAAGCAAGGTTATGCAGACCTCGCAATATTAATATGCAAACGCAAAATACTATCGTATTGAATTATTGCTAAAGAGTGTCAGAGGGCGCGTTTGTAAATACACGCGTATATATGCAAGATCAGCATGGATCTATTATAGTTTTTTTTACATAGATTGGCAAATATCGTATGCACCAATTTCAACTCGCAAATAACAATATATATTATAAAGTCACCCAGTAAACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11358
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000051263 | Nonsense | 93 | 411 | 1 | 3 |
| ENSDART00000133384 | Nonsense | 93 | 410 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 5 (position 51528553)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 49094251 |
| GRCz11 | 5 | 49745762 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTGTTTGCGGGGACAAAKCAAGCGGCAAGCACTATGGTCAATTCACCTG[C/A]GAAGGAWGCAAAAGTTTCTTCAAGAGGAGTGTCCGAAGGAACTTAACATA
Long Flanking Sequence:
TACCTTGGAACTGGCCTCCCGACAACTGCATATCCTGATCGGGTGCCTTTCTATCGACTCCGGTATTTTGAATGTATTGACCATTTTCTGCTTCTACTTTTTTCCCTATGAGATTGAGTGCTCCGATTTGAATTCGCGCTGCCGTTCGTCCAAGACTTCCCTTTTCCCTGCTCCGATATCCGAGCGACCAGTTCGCTTGAAAGCACTTTTCGGGCCCGAGATATGGCAATGGTAGTTAGCGTCTGGCGAGATCCGCAGGAAGACGTGGCTGGAGGACCTCCGAGCGGCCCCAATCCAGCAGCTCAGCCGGCGAGGGAGCAACAGCAGGCGGCGTCAGCGGCACCACACACTCCGCAGACCCCCAGTCAGCCAGGACCTCCGTCCACACCAGGGACGGCTGGCGACAAGGGCAGCCAGAATTCTGGACAGAGTCAACAGCATATAGAATGTGTTGTTTGCGGGGACAAATCAAGCGGCAAGCACTATGGTCAATTCACCTG[C/A]GAAGGATGCAAAAGTTTCTTCAAGAGGAGTGTCCGAAGGAACTTAACATATACATGTCGTGCCAACAGGAACTGTCCTATTGACCAACACCATCGTAATCAGTGCCAATATTGTCGGCTGAAGAAGTGTTTAAAAGTGGGCATGCGGCGGGAAGGTGAATATATTTTTCTGAATACATCACACTTGCTACACAAACAGGTTTATTGTTTAAAGCAAGGTTATGCAGACCTCGCAATATTAATATGCAAACGCAAAATACTATCGTATTGAATTATTGCTAAAGAGTGTCAGAGGGCGCGTTTGTAAATACACGCGTATATATGCAAGATCAGCATGGATCTATTATAGTTTTTTTTACATAGATTGGCAAATATCGTATGCACCAATTTCAACTCGCAAATAACAATATATATTATAAAGTCACCCAGTAAACACTGTGTGTGTCAAAAAGAAAGATAAAGATTAAGTGTGTAGCTAAGCCTACGTGCTTTTACGTGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40551
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000051263 | Nonsense | 332 | 411 | 3 | 3 |
| ENSDART00000133384 | Nonsense | 331 | 410 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 5 (position 51533111)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 49098809 |
| GRCz11 | 5 | 49750320 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTTTTGTCTACTCAGACGCTTGCGGCCTGTCAGATGCTGCACACATC[G/T]AGAGTCTGCAGGAGAAGTCTCAGTGCGCCCTGGAGGAGTACGTGAGGAGC
Long Flanking Sequence:
TCCAGCGGCCTTGCCTCCTCATTCAAACTCACAGCAGAGGCAACTGCTGGTACAGGGAGAAATAACTCGGTAGCATCTGGAGAGCAATTAGGTCATAATTTGGTTATTACCATGCCCAATTCTCTGTCAGATATGCGGCTGGATATTTCCATATTTGACACAAGACATGAAGGCCTTCTCCATCCTCTTCAGTCGAGCTTACTGTGCACCCTCGTCTCAGCGTACTCTTTGTTTTGTCTGATTTGTGAGCGTGCATGTGGTATGTCCCCTACGACGCAGGGAATACGTCCTGTTACTCTTGAGGGATTGCTCAGTCGTATTGTTTATTTATATTACAGGCAGCCTCATACGCTGCGTGATGCATGATGTTGGGCTCGTGTTTGTTCATCTCACTTTGTCAACAACACGTAATGCTGATGCTGAATGATAACCTGGGCCTCTTTTCTGTGCTGTGTTTTGTCTACTCAGACGCTTGCGGCCTGTCAGATGCTGCACACATC[G/T]AGAGTCTGCAGGAGAAGTCTCAGTGCGCCCTGGAGGAGTACGTGAGGAGCCAGTACCCGAACCAGCCCAGTCGCTTTGGCAAGCTTTTACTGCGACTGCCTTCTCTCCGCACTGTCTCTTCGTCAGTAATTGAACAGCTGTTCTTCGTTCGCTTGGTAGGTAAAACTCCCATTGAAACCCTCATCAGGGATATGTTATTATCCGGGAGCAGCTTCAACTGGCCCTACATGTCCATTCAATGATCCGAATGAGCGAGTGAAACAAAAAGACTAAAGGACCAAAATTCTGCAAGCCCTTTCAAGAAGACTATATATATAGGACCTAATTTCTGACCACTTAGGAAGACACTTTTTTGTCTTCTGGGACCGAATGGAATATGAAATGTACAAAGATTAAAGAACTGGACGTACCCCCTGTAAATCCATCGTCGTCATCAAGAACACTCTCCATTTTGTAAAATACTAGTCTTTATTTTATTTTCTTTTTTCTCTCATTTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45227
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000051263 | Nonsense | 340 | 411 | 3 | 3 |
| ENSDART00000133384 | Nonsense | 339 | 410 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 5 (position 51533137)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 49098835 |
| GRCz11 | 5 | 49750346 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCCTGTCAGATGCTGCACACATCGAGAGTCTGCAGGAGAAGTCTCAGTG[C/A]GCCCTGGAGGAGTACGTGAGGAGCCAGTACCCGAACCAGCCCAGTCGCTT
Long Flanking Sequence:
ACTCACAGCAGAGGCAACTGCTGGTACAGGGAGAAATAACTCGGTAGCATCTGGAGAGCAATTAGGTCATAATTTGGTTATTACCATGCCCAATTCTCTGTCAGATATGCGGCTGGATATTTCCATATTTGACACAAGACATGAAGGCCTTCTCCATCCTCTTCAGTCGAGCTTACTGTGCACCCTCGTCTCAGCGTACTCTTTGTTTTGTCTGATTTGTGAGCGTGCATGTGGTATGTCCCCTACGACGCAGGGAATACGTCCTGTTACTCTTGAGGGATTGCTCAGTCGTATTGTTTATTTATATTACAGGCAGCCTCATACGCTGCGTGATGCATGATGTTGGGCTCGTGTTTGTTCATCTCACTTTGTCAACAACACGTAATGCTGATGCTGAATGATAACCTGGGCCTCTTTTCTGTGCTGTGTTTTGTCTACTCAGACGCTTGCGGCCTGTCAGATGCTGCACACATCGAGAGTCTGCAGGAGAAGTCTCAGTG[C/A]GCCCTGGAGGAGTACGTGAGGAGCCAGTACCCGAACCAGCCCAGTCGCTTTGGCAAGCTTTTACTGCGACTGCCTTCTCTCCGCACTGTCTCTTCGTCAGTAATTGAACAGCTGTTCTTCGTTCGCTTGGTAGGTAAAACTCCCATTGAAACCCTCATCAGGGATATGTTATTATCCGGGAGCAGCTTCAACTGGCCCTACATGTCCATTCAATGATCCGAATGAGCGAGTGAAACAAAAAGACTAAAGGACCAAAATTCTGCAAGCCCTTTCAAGAAGACTATATATATAGGACCTAATTTCTGACCACTTAGGAAGACACTTTTTTGTCTTCTGGGACCGAATGGAATATGAAATGTACAAAGATTAAAGAACTGGACGTACCCCCTGTAAATCCATCGTCGTCATCAAGAACACTCTCCATTTTGTAAAATACTAGTCTTTATTTTATTTTCTTTTTTCTCTCATTTTTTTCTTTTTTCTTTTTATTTTTTTGTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14691
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000051263 | Nonsense | 361 | 411 | 3 | 3 |
| ENSDART00000133384 | Nonsense | 360 | 410 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 5 (position 51533199)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 49098897 |
| GRCz11 | 5 | 49750408 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTACRTGAGGAGCCAGTACCCGAACCAGCCCAGTCGCTTTGGCAAGCKTT[T/A]ACTGCGACTGCCTTCTCTCCGCACTGTCTCTTCGTCAGTAATTGAACAGC
Long Flanking Sequence:
TAGGTCATAATTTGGTTATTACCATGCCCAATTCTCTGTCAGATATGCGGCTGGATATTTCCATATTTGACACAAGACATGAAGGCCTTCTCCATCCTCTTCAGTCGAGCTTACTGTGCACCCTCGTCTCAGCGTACTCTTTGTTTTGTCTGATTTGTGAGCGTGCATGTGGTATGTCCCCTACGACGCAGGGAATACGTCCTGTTACTCTTGAGGGATTGCTCAGTCGTATTGTTTATTTATATTACAGGCAGCCTCATACGCTGCGTGATGCATGATGTTGGGCTCGTGTTTGTTCATCTCACTTTGTCAACAACACGTAATGCTGATGCTGAATGATAACCTGGGCCTCTTTTCTGTGCTGTGTTTTGTCTACTCAGACGCTTGCGGCCTGTCAGATGCTGCACACATCGAGAGTCTGCAGGAGAAGTCTCAGTGCGCCCTGGAGGAGTACGTGAGGAGCCAGTACCCGAACCAGCCCAGTCGCTTTGGCAAGCTTT[T/A]ACTGCGACTGCCTTCTCTCCGCACTGTCTCTTCGTCAGTAATTGAACAGCTGTTCTTCGTTCGCTTGGTAGGTAAAACTCCCATTGAAACCCTCATCAGGGATATGTTATTATCCGGGAGCAGCTTCAACTGGCCCTACATGTCCATTCAATGATCCGAATGAGCGAGTGAAACAAAAAGACTAAAGGACCAAAATTCTGCAAGCCCTTTCAAGAAGACTATATATATAGGACCTAATTTCTGACCACTTAGGAAGACACTTTTTTGTCTTCTGGGACCGAATGGAATATGAAATGTACAAAGATTAAAGAACTGGACGTACCCCCTGTAAATCCATCGTCGTCATCAAGAACACTCTCCATTTTGTAAAATACTAGTCTTTATTTTATTTTCTTTTTTCTCTCATTTTTTTCTTTTTTCTTTTTATTTTTTTGTAAAGAACAAAATACGTACAAATAAAACGAAGAACATCATATGCGCAGTAAATGAGCAAGACTTAG
Associated Phenotype:
Not determined