ZMP
zgc:171747
Ensembl ID:
ZFIN ID:
Description:
ubinuclein 1 [Source:RefSeq peptide;Acc:NP_001098588]
Human Orthologue:
UBN1
Human Description:
ubinuclein 1 [Source:HGNC Symbol;Acc:12506]
Mouse Orthologue:
Ubn1
Mouse Description:
ubinuclein 1 Gene [Source:MGI Symbol;Acc:MGI:1891307]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa19430 | Essential Splice Site | Available for shipment | Available now |
| sa8896 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa19430
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000092071 | Essential Splice Site | 147 | 827 | 3 | 16 |
| ENSDART00000114876 | Essential Splice Site | 17 | 315 | 3 | 8 |
| ENSDART00000132812 | Essential Splice Site | 17 | 148 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 8352422)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 8592227 |
| GRCz11 | 1 | 9276338 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGCTTTGGTTACGATGAGTCCGATTCATTCATTGATAACTCTGAGGCT[G/A]TGAGTTCTGGCCAGTCTTTGTATATCCAGATGATATTATAGAATATCAAA
Long Flanking Sequence:
CTTCTTTCACTTAAATGGATTAAAGTCACAGTATTCATCTGGAATAGTTTTTGAATTTAAATGGTTTGTAGCAATCGGTTTCCTCAATTGGTTTGAGTTACCTTAACTTTTTGGGTTTTACAGTGTAAATAAAATGCTGGTTGTTATGAAGTTTTATTGTTCTTGTTGTATTTACTATTATTCTTTAACCCTTTATCAGGTGAGGAACCTGATTACAATATAATTTGTTTCATTATTTTTTTTCATAAGTTTTTTCATAAGTCATAAAAGTCTTGTAATTACCAGGTTTTACCAGAGTATTTCAGTGAGTGCCCTTTAAAGGGTTAACTGTGAAGCAGGTGATATTTTAGTTTTATCCCTCTCCAATACATGCAGTAAATATCTCCAGTGTTCTTGCTTAGGGTGGAGCCGGCAAAAGGAAAAAAGACAGATTACAGGACCTGGTGGATATGGGCTTTGGTTACGATGAGTCCGATTCATTCATTGATAACTCTGAGGCT[G/A]TGAGTTCTGGCCAGTCTTTGTATATCCAGATGATATTATAGAATATCAAATACCCTTATAGAAAAGGTTTTACTCAAGTCAACATTTTTCCTCTATGCCACCGCGTCCACAGTATGACGAGCTCGTCCCAGCTTGTCTGACCACCAGATATGGAGGCTTTTACATCAACTCTGGGACTCTGCAGTTCCGGCCAGCTTCTGATGAAGGAGAGAACGAGAATGATTTTGAGGACAGTGGCCTTAAACCCAAGGTGTGTAAACACATTTAAGAATTCTTCAACCTGTCTAATAACCTCTACACTAGAAAAAAAATGATTAACTTTTTTTAGTGAACATTTTATAAGAGCTGAATTTACACAAACAAACTAAATTTAGTAATATTTAACTTAATTTGTTAGTTCAAAGGTGCTGTGTACATTTTTCACTCTTCTAAAGCATAAAAATGGCTTTATATGTTTGCAGATATTAAGGAAACTTGCTAAGTAAGCATTCTTGTTTATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8896
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 |
|---|---|---|---|---|---|
| ENSDART00000092071 | Essential Splice Site | 480 | 827 | 10 | 16 |
| ENSDART00000114876 | None | None | 315 | None | 8 |
| ENSDART00000132812 | None | None | 148 | None | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 8341986)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 8581791 |
| GRCz11 | 1 | 9265902 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTCACTCTGMTTGTRTTGTTATATTTGWGTGTTCTTCTGTGTGCTTTAA[G/A]ACTCGAGGCTGAGAAAGAGCGAGYGATTGATGGATCTGATGAGGAAGAAG
Long Flanking Sequence:
TTGTAAAAGTGCTATAGAAATAAAGATGAATTGAAATTGAAAAATTGAATCAAAAATCGCTGTTTACATTGGTAGACTCTTAATCAGAACAGTGTCTTAATCGTATTAACATCAGGTTATTGGTGTCCATGTTAACGTACTCCATGTTTTTTAAAAACGTGTTACGATGAATGGAGTTTCAATAAATGTCTTTTGTAAATCATGGTAAAAAGTAGACAATTATTACTCGGAAATAAAAACATTTTAACCTTGATTCATATACTATATATAAATTAAATGCTGTATGTCATCAGGATGAGCAGATGCAGGAGCTGCTGAAGAAGCTGGAGAATGCTGTCGCCAGATCCATGCCAGAGCAGATCACCCGCTTCCAGAATCACTGCCAGGCTCACTCTGAAGCCAGAGCTGCCAAGTAATCGGACATCACTGCGCTTTTATTGATGTTTTAATTTTCACTCTGCTTGTGTTGTTATATTTGTGTGTTCTTCTGTGTGCTTTAA[G/A]ACTCGAGGCTGAGAAAGAGCGAGCGATTGATGGATCTGATGAGGAAGAAGAAGAGAGGAGTGGAAAACGGGTATTTGGGCCTCGCAAGCGATTCAGATGGAATGAAGAGATCAGGTCGGGACTCTTGTGTGTACATGATTATTCATAGATGCTAGTAAATGACACAAAAACGGAGCGTTCGTTCTCATCAAATATTCTATTAATCTAATGAGAACCAGGTTTTGTAATAAAATCAAGCATCGTTTTATTATGTGACCTTTGATCATGGGTATACACAAATGTCGCTGTGTGTTTTGACAGGGAGCTGCTCTGTGAGATTGTCAATGTGAAAATGATGATTTATGATTCAGAGTCGCCCTCCTGCTCTAGTTTAGAGGAGTATCTGAAAGCGTTCCTGGAGGCGGATGTTAAATCACTTTGGCCCAAAGGGTGGATGCAGTCCAGGTATACAAAGCAAACATTGATACTTTAAAATTATGAAAATTGTCAAATCGATACAA
Associated Phenotype:
Not determined