ZMP
zgc:194780
Ensembl ID:
ZFIN ID:
Description:
nuclear receptor binding protein [Source:RefSeq peptide;Acc:NP_001124089]
Human Orthologue:
NRBP2
Human Description:
nuclear receptor binding protein 2 [Source:HGNC Symbol;Acc:19339]
Mouse Orthologue:
Nrbp2
Mouse Description:
nuclear receptor binding protein 2 Gene [Source:MGI Symbol;Acc:MGI:2385017]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa37926 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa25217 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37926
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000128943 | Essential Splice Site | 81 | 504 | 2 | 18 |
Genomic Location (Zv9):
Chromosome 24 (position 34476472)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 33328292 |
| GRCz11 | 24 | 33242712 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGGAACGAGGTTTTCTTCCAGGACAAGAAGGTCTTTAAGACAGTGGAG[G/A]TGAGTTCTTAAATAATAGTTTTAAGTTTACTAAAAGCTACTTTAAAAAAA
Long Flanking Sequence:
CAAGATCACGAAATACAGCTCTCAGTCTACATAAATCATACTTTCAAATTTCAACTTAAACCAAAGCAAGGCATGCTTAACAAATGCTGGTCAACAAATATATGTTGTTATTGGTTGGTGCTGATTTCATCATTTCATATTTAATCAAATATAAACAAATATATGCATGTAAACAACATAAAAAATGATAAAATTGAAATATTTTCCTTATAAAATATTTATCTAAATTTTAAATCTAATCAATTATGTATAAAATATAATGTTGATGGTGGATGTTAATTATCTGAATCTTCTTTGTGCATTTTTTAAAGATTTGTCCTTAAATATCCTCTGTTTTGACAGTGGATGTAAAAGTGGTTGTGTGTCTCCCTCTGCAGGTCAGTCAGGGGAATGTGCCCGGAGTGGAGAGCGCGTCTCTGGCCATGGACACTGAAGAGGGTGTTGAGGTGGTCTGGAACGAGGTTTTCTTCCAGGACAAGAAGGTCTTTAAGACAGTGGAG[G/A]TGAGTTCTTAAATAATAGTTTTAAGTTTACTAAAAGCTACTTTAAAAAAAACTCTTAAAACGGAAAATTGTTAGAAAAATTAAAGTTTCTGAAAAGGTTTCACCAAGGTTACGTGGAATTGATTATACTTTACTTGATGTTGAAAACATGCCAAAAAAAAAACACCTTAAAGAAGCGAATTGATTTGTTGTCAATTTATTACCTTGGCATCATTCAATTGGTAACATTGGTGTTAAAAAACACAAAAATATATATTACAGGACAGTCGATTTTTGACGTTTTTTTTGTGCATTTGTGTAGGACAAAATGAAGGAGATGTTTGAGAACCTGACACAGGTGGATCATCCCAACATTGTCAAATTCCACAAATACTGGCTGGACATTAGAGACAACCATGCTAGGGTAACACATACACACAAACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACGTTTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25217
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 |
|---|---|---|---|---|---|
| ENSDART00000128943 | Nonsense | 348 | 504 | 12 | 18 |
Genomic Location (Zv9):
Chromosome 24 (position 34468046)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 33319866 |
| GRCz11 | 24 | 33234286 |
KASP Assay ID:
554-7755.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGAAAACCAAATCCTTCGACCCAAATGGAGTCATGGCAGAGATTATTTA[C/A]GGAGATCGTTCTCGCGTTCAGCTCAAGTAAGTCTCAACTTAAGCTACATT
Long Flanking Sequence:
TTGTCTTTTCCTGTCCCTTATTCTGACTTATAAGGAGTCTCTGAAATATGCTACACAGAAGATGGTTTTTTATGTTATTGGCAAAAAAACACTGACTTGAAAATGGATCTGACATATATATATATATATATATATATATATACACACACATGAGTATACATAACCATATATATAAATTATTGTTTTTTTCTTGGCATTTTGAAAAAAATTTCAGTTCTACTTTTTCTATTTCAGTTAGTATTATATTCAGAATTATAAAAAAAACTATAAATATGAACAAAATATTTATTTACAGTTATTTTGTTGTAAAGGATTAAATGAGGATTCTAATATATTAAAAGTATAATTGATTATAATGGTTAAAAAATACATTTTTATTGTTATTTTGTTTATTTTTATATTAAATTTTTATTGGTGTTTAAAGACATGCTACCTGAAAACTGCGTGGAGGAGAAAACCAAATCCTTCGACCCAAATGGAGTCATGGCAGAGATTATTTA[C/A]GGAGATCGTTCTCGCGTTCAGCTCAAGTAAGTCTCAACTTAAGCTACATTCAATTCTATTTTATATTTTATTTTTATTACTATTATTATTATTATTTGTTTTATTATTATTATTATTATTATTAATATTAAAGGAATGAATGTTATTATTTGTCTTAACAAATTAAATTGATCAAAAGTAACTTGAAATTTCATTCATTGATTAATTTTCTTTTTGGCTCAGTCCCTTTATTAATCTGGGGACGCCACAGCAGAATGAACCACTAACTTATCCAGCATATGTTTTTATGCAGTGGATGCACTCCCAGCCGCAACCCATCACTCGGAAACATCCATACACACTCATAACTTGAAAATGTTACACAAATTTCTGTTTCAAATTTATGCCGTTCTTTTGTACTAGTTGCTGTTCTGTTCATTAGAGAACACTTATAGTTTCACAGTTTTAAAGTTAAACTTAAACAATAAATGAGCATATCAGAATAACATCTAAAGGATCAT
Associated Phenotype:
Not determined