ZMP
si:ch211-175l6.9
Ensembl ID:
ZFIN ID:
Description:
ubinuclein 2 [Source:RefSeq peptide;Acc:NP_001098410]
Human Orthologue:
UBN2
Human Description:
ubinuclein 2 [Source:HGNC Symbol;Acc:21931]
Mouse Orthologue:
Ubn2
Mouse Description:
ubinuclein 2 Gene [Source:MGI Symbol;Acc:MGI:2444236]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17456 | Splice Site, Nonsense | Available for shipment | Available now |
| sa45131 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17456
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:
Splice Site, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000074147 | Splice Site, Nonsense | 92 | 1065 | 1 | 15 |
| ENSDART00000136453 | Splice Site, Nonsense | 92 | 262 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 3 (position 8194702)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 8010900 |
| GRCz11 | 3 | 7896740 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCAGAAATCAGCRGAGTTTAACTACGGCGAGCTKATCACCKCCAGCCTG[C/T]AGGTGAGACCCTGRAACACCACTRTGSTGGGTTTAWAACCGGATTCATGG
Long Flanking Sequence:
CCACAGATGCTGCCGAGATTTCACACAAACAAAAACTACTTTCACACTCGACTAAATGAAACGGAAGCAACCTGAATGCAGAGAGGAAATAATTTATGACCTAAAACGGAGTTCGTTTCCTTTCGTGTCAGCGTTAAAGTATTGTTTGGGAGTGTGAGCGCTAATTTTAGCTCAAGCTAACAGTCAGGGGCGCGCGTGTCCGGGCTCGAGCAGAACCGGAGAGCCCAATGGCTGACCCGAGAAAAGTCCCGTTCGTCACCCTCGCCTCTTTCAGCACCACACCGGCGGCGCCCGAGACTAAAAAACGCCGACGGGAGGATGAGGAGAATGAGCCGACCCCCGGTGTCACCGGCGGGGGGCTGTTCGGTAATGTTACCGCGAAACCGGCTACGGATCCCGGCGAACCCAAACGCACCGTCCGACTAAACCTGAGCCTGTCAGAGCCGAATGAGCAGAAATCAGCAGAGTTTAACTACGGCGAGCTGATCACCTCCAGCCTG[C/T]AGGTGAGACCCTGGAACACCACTATGCTGGGTTTAAAACCGGATTCATGGGTTTAAACCCCCGATTGATTTGTCAGAAGCGAACTTTTAGTATATAAGATGTAACTTAAGACACTTTCAGTGAAAGTTTGTTTTCAACTCTGTCCTTTGTCGACAAATTAAGGTAACGTTGAGCAATTCCAGCGTCATGGTTGTGACATTTGCAGTAAAAACTTAAACATAAATTCATAGAGAAAGCATATGTTGACTAATTATGTTGAAAACCTGTTTATATTTTTCAAAACAACTTAAAGGAGCAGAAAGGCATCCCTATGTACTAAAATGTTTATTTTAAATCAGGAAAATAAGCTTGGATTATAGAAGTGACCAAAAAAACTGCAAGTTTAAGGTATGCAACAAACTTTGTACAAATTCTGTGAACTGCACAACCCAAAAGAAATGGTGATCATTAAAAAGATAAGTTTGCTCTCTATAGAACAAACTTGACTGATTTTAATTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45131
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000074147 | Nonsense | 118 | 1065 | 2 | 15 |
| ENSDART00000136453 | Nonsense | 118 | 261 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 3 (position 8204617)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 8000985 |
| GRCz11 | 3 | 7886825 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCAGCTCTGGACCCCAGCGATCCGTTTGCAGACGAAGACAAAGAGCGG[C/T]AGGAAGTCGAGGCTCTGGCCAGGAAGTTTGAGAGCAAATATGTATGTATC
Long Flanking Sequence:
AAGTAAGAAACTTAATTGTTTTATGTTCAATCCACTTAAATATTTAAAAAACAGTTTGAATAACTTAATTAATTTGTGTTGGGACAGCATGAAGGGAAGCGTTTTTTACAGTGTACAGTCTAACAGTATTCATTTACAGGCAATGAATAGTGTTGTAAAATTACACTGCATAATCTACAACTAAAAATGATAGTTTTTATAGGAAATTAGTCTTCATTAAAGTTTAAAACGGCACAATTTCTTATGCCCAAGTGCATTAACCCTTTATTAATTCTGAAATAGGCTATAGTGCAGCCCTAATAATAAAATATTGACGTTCTATTGCACACTGATGAGTAGCAGAAACCTATAATGCATAACTCATACCTTTTTGCATGTAAACAATTGGATTAGTTTTGTCTGACCTGTTTTATTTGCTCCTGAAGGTGAGGAAAGCTCCTCAGGGTCTCACTCCAGCTCTGGACCCCAGCGATCCGTTTGCAGACGAAGACAAAGAGCGG[C/T]AGGAAGTCGAGGCTCTGGCCAGGAAGTTTGAGAGCAAATATGTATGTATCGTACATCAGCACCTGTCATTGAGTGTTGCATGTTTTTAAGCTGATTGTGCCTAAAGGTCCCATGAAGTGCCTTGAAAATGCATTTTGTTTTATGTAATCGCAGTTTAAACATGGAGAGGGCGGAGCTTATAGTAGCTCCTCCCCTTTAACACAGCCAATAGAGTTTTGATTTTATCAGAGCTCTGCCATTGAGAGTAGTTGAGCTCAAGCATCAAATGAAAAGCTAAGGAGGCTGGGAGTGTCAGATATTAGAGGGCATTTGATTGGTCAAGACTGAAGTATGAGGTGACGTAAAAAAAAAAGTTGATTCATTTTGGCGGAAGGGAGCTCTACACAGGGTTTCTGCAGGGTCTTAAAATGTCTTAAATCTTAAATTCAAAATTTTAGGCCTTAAAAAGTCCTACATTTGCTGAAATATTGTGTTGTAAGTCTTAAATATCTTTTTAAACA
Associated Phenotype:
Not determined