ZMP
nr1d2a
Ensembl ID:
ZFIN ID:
Description:
nuclear receptor subfamily 1, group D, member 2a [Source:RefSeq peptide;Acc:NP_001124064]
Human Orthologue:
NR1D2
Human Description:
nuclear receptor subfamily 1, group D, member 2 [Source:HGNC Symbol;Acc:7963]
Mouse Orthologue:
Nr1d2
Mouse Description:
nuclear receptor subfamily 1, group D, member 2 Gene [Source:MGI Symbol;Acc:MGI:2449205]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa18069 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18069
Status:
Available for shipment
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For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000099040 | Essential Splice Site | 78 | 504 | 3 | 8 |
| ENSDART00000128167 | Essential Splice Site | 78 | 505 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 16 (position 53626734)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 49896395 |
| GRCz11 | 16 | 50100715 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACACAGTGAGCACATCTGACAGGATTTACCGACTCTGACGTGTGTTTTCT[A/G]GAGCTGAATGGGATGGTGYTGCTGTGTAAAGTGTGTGGAGACGTCGCCTC
Long Flanking Sequence:
CTGTCGTCATGGCAAAGAGAAAATAAATCTTTTATTAGAAATGAGTTACTTAAACTATTATGTTTAGAAATTAAACAGACATTGGGAAAAATATACAGGAGGGCTAATAATTCTCACACTAGCTGTATTTTTTATGTATTAACTACTGTGCATACCTAGTTATAGTCTTTAAATGAAGGATTTTCTGCTGTGTTTTCGTTTGTCCAGGAGGTGTGATAGCTTATGTCTGCTCCTCAAGCTCGGCCTCCAGCCCTGAGTCCTGCATGAGTGACAGCTCTGCCAGCCAATCGCCATCCTCCTCTCCTCCTCTGCCCACTAAAGCGAGCCGTGCCACAGATCTGTCCATCAGCGCAGGAATGCTGAAACACACACGTGGACACACATCTGATAAAAGCCTCGCTAACAAGAGCTCCATCACCAGTGAGTACACACACACACACACACATACAAACACAGTGAGCACATCTGACAGGATTTACCGACTCTGACGTGTGTTTTCT[A/G]GAGCTGAATGGGATGGTGTTGCTGTGTAAAGTGTGTGGAGACGTCGCCTCTGGCTTCCACTATGGTGTTCATGCCTGTGAAGGCTGCAAGGTGAGGAGGCGCATAATTTTTTGGGGTCTTTTCCAAAAGCGCTTATCTATGGGTATTTTAAGGCATCTTTGCTAAGCTAACATAGATATGTACTAATGAATCAATTTAGTTGCTTGCAGTCCAAAAAATTCGCAGTTTTAGCATGTATCTGTAAGTGCACTGTATGTATTAGTTTATTAATTTTAGATTTGTTCCTATGACTATTTACAATAGTCGACAGTTTTAGGATTTGTACCCCATTTTATTTTTAATTTGAGTCATTTTGAGCAGTTTGAGTTGAGTAGTCATTATTTCTTATATAATATTAGATCATAGCTTATATATACACTCACTGGCCACTTTATTAAGTACACCGTACTATTAACGGGTTAGATCCCCTTTTGACTTCAGAACTGCCTTAATCCTTCATG
Associated Phenotype:
Not determined