ZMP
nr2f2
Ensembl ID:
Description:
COUP transcription factor 2 [Source:RefSeq peptide;Acc:NP_571258]
Human Orthologue:
NR2F2
Human Description:
nuclear receptor subfamily 2, group F, member 2 [Source:HGNC Symbol;Acc:7976]
Mouse Orthologue:
Nr2f2
Mouse Description:
nuclear receptor subfamily 2, group F, member 2 Gene [Source:MGI Symbol;Acc:MGI:1352452]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa18083 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18083
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 |
|---|---|---|---|---|---|
| ENSDART00000059976 | Nonsense | 83 | 428 | 1 | 3 |
| ENSDART00000130163 | Nonsense | 83 | 422 | 1 | 3 |
| ENSDART00000133361 | None | None | 49 | None | 6 |
| ENSDART00000134910 | Nonsense | 44 | 140 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 18 (position 23658496)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 23888269 |
| GRCz11 | 18 | 23874801 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAACCCCGACGAACCAGACGACGCAGAGCCARTCGGAAAAGCAGCAGCCA[C/T]AGCATMTAGAGTGCGTGGTTTGCGGGGACAAATCCAGCGGTAAACACTAT
Long Flanking Sequence:
GCTGCTATTCGGCTTGCTTCAATTTTAACCACATGCCAGGTAACGCTATTTCAGTCAAGAAATAGACTACTGTTTCTCGTCGGTGCGCAACTTTGAACGGACATTCAGACTCTAACCGACCGTGCCGATCCTGAATTATTTATTTTACCCTCCTAAGTGATAGAGGCACCGTGCTGCGATATTATTTTTTTAAACAAAGCATTCCGAAACCAAAAACGGGGAACAAAAAGTTTTTTTAACGTTGACTGATAGATATGGCAATGGTAGTGTGGAGAGGCTCCCAGGACGATGTGGCCGAGACCCATGGCACCCTCTCATCGCAAACCCAAGGAGGACTATCCCTTCCGACCCCTCAACCAGGCCAGCTGGGTCTGACGGCCTCTCAGGTTGCCCCTCCGACCCCTCAGACACCCGTTCAAGGACCCCCGAACAACAATAACAACACACAGTCAACCCCGACGAACCAGACGACGCAGAGCCAGTCGGAAAAGCAGCAGCCA[C/T]AGCATATAGAGTGCGTGGTTTGCGGGGACAAATCCAGCGGTAAACACTATGGCCAGTTCACTTGCGAGGGGTGCAAAAGCTTTTTCAAACGGAGCGTACGAAGGAACCTCACTTACACATGCCGTGCCAACAGGAATTGTCCCATTGACCAGCACCATCGCAATCAGTGTCAGTACTGCCGCCTCAAAAAATGCCTCAAAGTTGGCATGAGACGGGAAGGTATTCGGATTTTTGTTGTTTTACTGCTGTCTTTGTCTTTGTCTTCTGTATTTAGCCTGACTTAATCGCGCATGCTTCTTCCTGTATTTTATCCCCGACTCCTCTCTCTCAATCTGCCCGTCCACAGCATGCGAAGGAACCGCCTATAGCGCTCGAGACTGAGCGTTATCACGGCGCCCTTAATGCTCGAATAAAGAACACCCTCTCCTTAGCGACTATTTCGCATTGCACATGTTCGCAGCTTTAAACTAACCATTGCTTTTATTAGGCGACGAAAACAT
Associated Phenotype:
Not determined