ZMP
ubin
Ensembl ID:
ZFIN ID:
Description:
ubiquilin-4 [Source:RefSeq peptide;Acc:NP_998521]
Human Orthologue:
UBQLN4
Human Description:
ubiquilin 4 [Source:HGNC Symbol;Acc:1237]
Mouse Orthologue:
Ubqln4
Mouse Description:
ubiquilin 4 Gene [Source:MGI Symbol;Acc:MGI:2150152]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa9131 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa15580 | Nonsense | Available for shipment | Available now |
| sa22943 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9131
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000058327 | Nonsense | 43 | 497 | 1 | 9 |
| ENSDART00000074919 | Nonsense | 43 | 599 | 1 | 11 |
| ENSDART00000142698 | Nonsense | 43 | 497 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 16 (position 49732746)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 46699600 |
| GRCz11 | 16 | 46666316 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTAAGGTTACCGTCAAAACACCGAAGGATAAAGAAGAAATAGCCAWCGCC[G/T]AGGACGCATCTGTCGCACAAGYGAGTTTATTCGCGGTTTCTTGTAGTTTG
Long Flanking Sequence:
CTAAATTTGCTTTGAGTCACTGCCTTGTGGCTGGCTGATTAGAAATTTGCGTTAACAAGCAGTTGGACAGGTGTACCTAATAAAGTGGCCGGTGAGTGTAAGTATTTACACTATTTTCCTTTTTGAAATATAGATTTTTTTATTTACATATATTGTTTACTATATTATTCTTTATTCTCTTGTTTAATCCTTGTTGTTTCATTCATGCATGCGAAATACTTTTCTAGTATACTAAAACTGCACGCTTGTTCTTGTACGGTGAATTCGCGGACACGCCACACCACTAGAGGCCGCTGTGGAACAACCGGCGTTTGCAGCACTTTTCTCCGCTGCTTGTTGGTGCGATGATGTAATGAAGTAAAAGAAGAGTAAAGATGGCGGAGAATAGCGGCACGGATCCTGCCGTGGAGACGAACACTGAAGAAAATGCCGCCGCTAGCGCGACTATCATTAAGGTTACCGTCAAAACACCGAAGGATAAAGAAGAAATAGCCATCGCC[G/T]AGGACGCATCTGTCGCACAAGTGAGTTTATTCGCGGTTTCTTGTAGTTTGTTTCACCCGGGCGTTCATTACACCAGCGGCTAACAGCTTTAGCCGACGAGCTAGCAGTTGACGACGCACAGTCCCAGCCGAAACCAGTCGCCTTGGACATCGAAAACAAATTCATGCTCATGTTATTAGTTAGATGTGGTTATTTTGATCGTGTTATGTGTAGTTTTGTGTTTTTTAAAACCAGTGTAATGTGTGATACTCTAACTCGGCGTTGTCGTTAAACAAACGGCCTGCTCTGGTATAGAAGGTTCTAGTCTGTCATCTTTGGTCGCGCTCTTTCTGTTTTGATTTCTATTGTTGACTTTAGGATCATTCGAGGGATTTAAATAACATGTTAACTGATCTTTTAATCAAAAGGTTGTGTTTATAGTGTTTATGTGCGTTCATTTGACCAACAGCGGTTATATGTTGAGGTCTAAGTTACAATATCAGGTTGAATAAAAGGAACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15580
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000058327 | None | None | 497 | None | 9 |
| ENSDART00000074919 | Nonsense | 415 | 599 | 7 | 11 |
| ENSDART00000142698 | Nonsense | 415 | 497 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 16 (position 49725867)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 46706479 |
| GRCz11 | 16 | 46673195 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTATATGCGCACCATGATGCAATCCCTSGCCCAGAATCCTGATGTTGYCT[C/A]ACAGGTAGCCGGACAATAATTTAAAAGCTCCCTGGTGTTTTCAGATTTCT
Long Flanking Sequence:
AGCTTCAGAGGATTAGAATCATCTGCTATCACACTTTGAATTGTTTTTATCATTTGTTGTTCCTTGTAAACCAATAGTCTTGGAGCAAGTCTTGAGTTTTGAAGGCGATTTTTGTCTCTAACTGAAAGTGAGGAGAACCAGCATTAAAGAAAAAGCTGAATATTCTCTTAATATAGGTAGTATTAATAACTAATCAGTATTAAAAACTACTCCGCATATATTTTTTTGTCTACAAAAAGAGTTCAGTTTCCTGAGAATTTGCAAGCAAATAATGTTAATGCACAGATTTGAGTGATTTTGTTCAATATAATATGACTTTTTATAATTTCAACTGGCTTAATTTCATGTTTATTTTTTGTGCTTAGGTATGTTTAACAGTCCTGGCATGCAAAGCCTAATGCAACAGATCTCGGAGAACCCTCAGCTTATGCAGAACATGATTTCTGCTCCTTATATGCGCACCATGATGCAATCCCTGGCCCAGAATCCTGATGTTGCCT[C/A]ACAGGTAGCCGGACAATAATTTAAAAGCTCCCTGGTGTTTTCAGATTTCTTTACTATTAAGTTCTAAAATGTGTTTTTTTCTTTCTAGGTATTGATGAACAACCCTCTCTTTGCGGGAAATCCACAACTGCAAGAGCAGATGAGACAGCAGCTACCTGTATTTCTACAGCAGGTGTGTCCAGCTGGAATCTTTGTGACTTCATTTAGATTATGTAATTTCACCTGGTAACTTTTGTTCTATTTCACTGGCAGATGCAGAACCCAGAAGCCCTTTCTGTCATGACAAATCCTCGAGCCATGAGAGCCCTAATGCAGATCCAGGAGGGACTGCAAACCCTTCAAACTGAAGCCCCTGGACTTATGCCCGGGTGCAGTTTCTCATTTTCTCTCATAGAAAAGTGGATTTGCAGAAGTATGCGGAAGGACTTTTAATTTGTCAGCAACTAGGGTTAAGCGCTTCCGGTGAATTGTATCCCATTACAAAATCTGCACGTTTAGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22943
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000058327 | Essential Splice Site | 447 | 497 | None | 9 |
| ENSDART00000074919 | Essential Splice Site | 549 | 599 | None | 11 |
| ENSDART00000142698 | Essential Splice Site | 447 | 497 | None | 9 |
Genomic Location (Zv9):
Chromosome 16 (position 49723379)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 46708967 |
| GRCz11 | 16 | 46675683 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGCTCATGCAGCAGATGCTACAGATGTTTGCTGGAGGGAGCGCATCGG[T/C]ACTCATGTTTTAATCTTTTTGCTAATAGCAGTTGTCAACAGTATTAATAG
Long Flanking Sequence:
AAGCACATGGTTTTATGAGGTGTGCATAATTTAGGTTAAAGCTAAACTGTGCAGAGCTGTGGCCCTCCAGAATCTGAGTGTGACACCCGTGTACTAAATGAATCAATATTTTAAGTATGTATATAGATAGTCAAATGTTTTGAGATGCTTTAGGCATAATACTTTTATCTAGACATTAAATCTAGATCACATTGCCCTAATTTTAATAAAGAAATTAAAAGTAAACAATATCCTCTTTAAGAGTTATTTCCCTCCTTTGTCGGGCTGAATCTCCAATTAAATCTTTCTGTATCTTTCTAGTCTGGGGCCTGGAGGAATGCCTGGTGGGATTCCCGTTGGTATGCCTGGTGCCCCACTGCCCACAGGAGTGACTGTGACACCTGAGAATCCTCCGCCTTCCAGCCAGGGCTCCACCCCAACCCCGACTGCTGGAGCCAGTCCTGCCCAGCAGCAGCTCATGCAGCAGATGCTACAGATGTTTGCTGGAGGGAGCGCATCGG[T/C]ACTCATGTTTTAATCTTTTTGCTAATAGCAGTTGTCAACAGTATTAATAGTATTTTTATAAAGCTGTCCTTTTTATCTTCAGTTTTATTTTTTAATGGTTATGTTTGAGGTGCAGGTCATTTTAGTATTTAATGGAGCCTATTCTTCTAGTTGTGACATGAATCTGAAGTCGCACAAATACTTGAGTCATTTTAATTGTGATTGCTTGCTGTAGCTCATACGGCATGTGCATAGAATGTGTTTTAATCAAATTGATTCACATTTGAATTGGTTTGAATTCTACATTTCTGGCTACCTGCTAGTTTTGGTTTGCTCTAAATAAATGTTAGGCTTGTCAAGTTATTTCTAGTGAATAGAATAACTCTGCAACTGTCTTGTTAAATTATGTGATAAATCGTATATATTGTAGGGTTGATACTATACTGGAATTTGGTACCAATCGATACTGAAATCTTAAAAACGTCCATTTCTCGCTAACATTTGAGCGCTGTTGAGCATGT
Associated Phenotype:
Not determined