ZMP
si:ch73-140j6.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
USP53
Human Description:
ubiquitin specific peptidase 53 [Source:HGNC Symbol;Acc:29255]
Mouse Orthologue:
Usp53
Mouse Description:
ubiquitin specific peptidase 53 Gene [Source:MGI Symbol;Acc:MGI:2139607]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa19503 | Nonsense | Available for shipment | Available now |
| sa39617 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa32683 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa39616 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa14536 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19503
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109714 | Nonsense | 29 | 1029 | 1 | 16 |
| ENSDART00000145012 | Nonsense | 29 | 391 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 24768606)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 25220377 |
| GRCz11 | 1 | 25911206 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACATGTCTGGCACAGGTGCAAGGAGTGGGACGGGGCTGAGCAAGTCCTA[T/A]CAGCCGGGCAGCATGATCTCTCTCGCTTTGACCAAAGGACTTCTAAATGA
Long Flanking Sequence:
GATTTGTTCTTCTATCTGCGTCCATCCTCATATTGCCTGTGTGCCTGGATGCAGAGGAATCCACACATGCAGTGGAGACAGAGCCAGATCATTGTTATAGTAACTGCTGGACTGATAAAGCAATGTGCTTCAACTTGTGGCTGAATGCCACATGCTTGCGTTAAATGTAAAGCAACTGAATAATTTCTTATATCCCAATGGTGTGCTGTCAAATTCTGCACATCGAAAAAAAATCTGTTGCAATATATTTTGCTCTTTTGTCGGGGGGCATTATACAGTTGGCTTTCAGCTACAGGGACTGCCAGGACTAATGTTGCCTAAAACAGATCCATCAGCCTCAAGTTGCTCAAGATCCATCAGCCTCAAGAGTAATTGACTGGTTATTTGCTGGAGAGAGGGCCAGGCTCCAACCTCATGGCATGGGTCAAACTGTTTAAAAAGCCTGGAGGCAACATGTCTGGCACAGGTGCAAGGAGTGGGACGGGGCTGAGCAAGTCCTA[T/A]CAGCCGGGCAGCATGATCTCTCTCGCTTTGACCAAAGGACTTCTAAATGAGCCAGGCCAGAACAGCTGCTTTCTCAACAGTGCGGTGCAGGTGAGTGAAGCTATATTGAAAACCTACTGTATGCTGGTGTACAATTGAACAAACACTGAAACTGAATATAAAATATTCTTTAAATGGGGTGGAATGTGTGACCCTGGACTTGAAAACCATTTATTGGGGTAATTGTCTATAGATACGCCACATGAAGACAGAATCAAAAATCTGTTGAGATAGGACATTATTTGGCTAAGATATAAGATAAAATCTGTAATCTGAGGGTTAAAAAATAGAGAAATTTGCATTAAAAAGACATTGAAATTGTGGCATTCACTCGAGTAAATTATGATGTTGATTTTTATGCGTTCACTAGAGGAAATAATATGATTAACGCTAGCTCCACAGCTAACTATCAGGCACCTGTAGAGTTAATGCGTTCCAGTAAAATATAGCTATACAAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39617
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109714 | Nonsense | 476 | 1029 | 12 | 16 |
| ENSDART00000145012 | None | None | 391 | None | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 24721139)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 25172910 |
| GRCz11 | 1 | 25863739 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCTGAATTGCTTACTAATGAAAATTATTTTGATTTCAGATATGACATA[T/A]CCACGCTTATCCTCTCCACCTGAGAATGGCCCAAGGTTTCATTGTGAGCA
Long Flanking Sequence:
TCTCTTCAGCTTAAAAGGATGCTGTTTGCTCGCTCCAGGTGTGCTTATATGCTGGGATAATTGGCAATGAAGCACACCTGTGCAAGCTTACGCTGCCAATTCATTGCATTCATTGGCCCATTCAATACTTTTTCAGACAAGCGGCTTCTGATCCGAATCCTCCCATTCGTGGATTTCAATCAATCCACTCTATGGCACTTCCGTTCCCCTCCTCGGGGAACGAAGGGTTACTTCTGTAACCTCGAACGTTTGTGCCTCATTTTGTGAGCCAACTGACAGTTGTTCACTTCCCTTTTTTCTCTGCTTTGCTGGCCATGCCCAATCGCAGCACTCCACACCCATCATAAAGCTTTTTTTTTTTTTAAATCTAAGGTACACTTGAACTAAAAGAAAGGGATTTCATGACCCTTTAAAACACACACAGCAACCCATTGATTATCTCAAACTTATAATCTGAATTGCTTACTAATGAAAATTATTTTGATTTCAGATATGACATA[T/A]CCACGCTTATCCTCTCCACCTGAGAATGGCCCAAGGTTTCATTGTGAGCAGAGGCCGCGAACTTTGCCCTCACGGGTCTCTCGAACTGAGCACTCTTCTGTTCATCCTCGTGTATCACCCCAGGAGTCTCGCTCAAACCAGGGGATGGCATCTGGAGTCAGTCGTCACGCTGATTCATCATCGCTTTCCCATCGTGGCTCCACAAATCCCACTGAGCGTGGCAAGTCCAAGCCCTCATGGAGACCAGTACGGGAGGTCCTCAATGTAGACAGTGTGCTGAGCGAACTAGAGCGACGACAGCAGCAGCAACAGCAGCAACAGCGTGGAAGCCCTCGATGTGTGCGTCGATTCGCCCATGAGAGGGGGCTGATGAAGGACAAGCAGAAGGGTCTGATGACTATTTATGAAGATGACTCACGGCTGGAGACTGAAAGTCAAAGCTCCCAGGAGTCTCAACGACAGATGATGGTGACCAGGTCTAAAGGTGGAGCAAATGTAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32683
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 |
|---|---|---|---|---|---|
| ENSDART00000109714 | Nonsense | 583 | 1029 | 12 | 16 |
| ENSDART00000145012 | None | None | 391 | None | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 24720820)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 25172591 |
| GRCz11 | 1 | 25863420 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGTGTGCTGAGCGAACTAGAGCGACGACAGCAGCAGCAACAGCAGCAA[C/T]AGCGTGGAAGCCCTCGATGTGTGCGTCGATTCGCCCATGAGAGGGGGCTG
Long Flanking Sequence:
CAATCGCAGCACTCCACACCCATCATAAAGCTTTTTTTTTTTTTAAATCTAAGGTACACTTGAACTAAAAGAAAGGGATTTCATGACCCTTTAAAACACACACAGCAACCCATTGATTATCTCAAACTTATAATCTGAATTGCTTACTAATGAAAATTATTTTGATTTCAGATATGACATATCCACGCTTATCCTCTCCACCTGAGAATGGCCCAAGGTTTCATTGTGAGCAGAGGCCGCGAACTTTGCCCTCACGGGTCTCTCGAACTGAGCACTCTTCTGTTCATCCTCGTGTATCACCCCAGGAGTCTCGCTCAAACCAGGGGATGGCATCTGGAGTCAGTCGTCACGCTGATTCATCATCGCTTTCCCATCGTGGCTCCACAAATCCCACTGAGCGTGGCAAGTCCAAGCCCTCATGGAGACCAGTACGGGAGGTCCTCAATGTAGACAGTGTGCTGAGCGAACTAGAGCGACGACAGCAGCAGCAACAGCAGCAA[C/T]AGCGTGGAAGCCCTCGATGTGTGCGTCGATTCGCCCATGAGAGGGGGCTGATGAAGGACAAGCAGAAGGGTCTGATGACTATTTATGAAGATGACTCACGGCTGGAGACTGAAAGTCAAAGCTCCCAGGAGTCTCAACGACAGATGATGGTGACCAGGTCTAAAGGTGGAGCAAATGTAGCACAGCGAAGTGATAACTGGGTAATACAGAGGACAGAGTCAGGATATGAGAGCAGTGATAGGCTGAGCAGCGGCTCTACCAATCCTGACTCACCTGGAGTTGAGAACTTTACCGGCAAAGAGCTGAGACTCAGTCAAGATGCACAGCACCTCAGGTAGGAGAAATGAAGTAATGATGTGTATGTTATTTATTCTTTGAGTTACTTGCTCTTGATTTAGTGATGTATTCCCTCAGGGATCAAGGCCATAATAATCAAGATGACTCAAAAATGGAGGCGGCGCGTTCTCCACTGTACCACGGTAAGTATTAACGTTACACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39616
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109714 | Nonsense | 794 | 1029 | 15 | 16 |
| ENSDART00000145012 | None | None | 391 | None | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 24712908)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 25164679 |
| GRCz11 | 1 | 25855508 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGAAAGCCCATTACTGCGCCGCCTGGGCAAGATCAGCAGTTCAGAGTG[T/A]AACAGTTCTGATGAACTCACTAACCCTCTGTCAGAGCAGGAGGACAGTGC
Long Flanking Sequence:
TAACTTGCCTCATTACCCTAACCTGCCAAGTTAACCTAATTAACCTAATTAAGCCTTTAAATGTCACTTTAAGCTGTATAGAAGTGCCTTGAAAAATGTCAAAAATTATTTACTGCCATCATGGCAAAAAGAAAATAAATCACTTTTTTGAAATGAGTTAAGAAAACTATTATGTTTAGAAATGTTTTAAAAACATTTCGCTCCGTTAAGTAGAAATTGGGTAAAAAATAAACAGAGGGTATAATAATTCAGAGGGGCTAATAATTCTGACTTCAACTTTATATATCTAAAAGTAAAATAAATTACTAAATGAGATTGCTCATGTTTCACAGAAGGAAGCTTCGATATTCATCCTGTGGTACCAGGAAAGCAGGCAACACAGAGAAAGACCCGTCAGGTGTGGATCTTCCACCAGAGCAGCAGGAACTTTCCATGCAATGGCACCACAGCCCAGAAAGCCCATTACTGCGCCGCCTGGGCAAGATCAGCAGTTCAGAGTG[T/A]AACAGTTCTGATGAACTCACTAACCCTCTGTCAGAGCAGGAGGACAGTGCTTATCGTTCCAGCACCAGTGAAGTCGCTCCACATGAGTCACCGGGTCCCAATCGCTCTAGTTACCCATGGGAAGAATCAGCCATCCAATCAGGACCCTCGATTGCAAGCCACTCCAAACACGCTCAGCGACCGATCGAGATAAAGACTCCACCTTTCCGCCCCAGAATCTTACAGGAACCATCTCAAACAGCTTCAAGAGCATCTGGCCGTGGTGCTCCATCATCTTCACACAGTGGCGCAGTACACAGGCGAATGGAGATCAATGGCACGTGCCCCAGCTCGTCAGACGTGAGCTCAAAATCGGGATCAGACCAGGAAAGAGGGGAGCAGGTGTCCAGCGAGCCCGAGGGTTGGGATAAGCCATCTTCTTCTGTGTCTCCAGGATCTGGAGTGGCGCTGACCACTTATTTCTCTGTGGATAATTGCATGACAGACACCTACAGACTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14536
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109714 | Nonsense | 812 | 1029 | 15 | 16 |
| ENSDART00000145012 | None | None | 391 | None | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 24712854)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 25164625 |
| GRCz11 | 1 | 25855454 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTTCTGATGAACTCACTAACCCTCTGTCAGAGCAGGAGGACAGTGCTTA[T/A]CGTTCCAGCACCAGTGAAGTCGCTCCACAKGAGTCACCGGGTCCCAATCG
Long Flanking Sequence:
CTTTAAATGTCACTTTAAGCTGTATAGAAGTGCCTTGAAAAATGTCAAAAATTATTTACTGCCATCATGGCAAAAAGAAAATAAATCACTTTTTTGAAATGAGTTAAGAAAACTATTATGTTTAGAAATGTTTTAAAAACATTTCGCTCCGTTAAGTAGAAATTGGGTAAAAAATAAACAGAGGGTATAATAATTCAGAGGGGCTAATAATTCTGACTTCAACTTTATATATCTAAAAGTAAAATAAATTACTAAATGAGATTGCTCATGTTTCACAGAAGGAAGCTTCGATATTCATCCTGTGGTACCAGGAAAGCAGGCAACACAGAGAAAGACCCGTCAGGTGTGGATCTTCCACCAGAGCAGCAGGAACTTTCCATGCAATGGCACCACAGCCCAGAAAGCCCATTACTGCGCCGCCTGGGCAAGATCAGCAGTTCAGAGTGTAACAGTTCTGATGAACTCACTAACCCTCTGTCAGAGCAGGAGGACAGTGCTTA[T/A]CGTTCCAGCACCAGTGAAGTCGCTCCACATGAGTCACCGGGTCCCAATCGCTCTAGTTACCCATGGGAAGAATCAGCCATCCAATCAGGACCCTCGATTGCAAGCCACTCCAAACACGCTCAGCGACCGATCGAGATAAAGACTCCACCTTTCCGCCCCAGAATCTTACAGGAACCATCTCAAACAGCTTCAAGAGCATCTGGCCGTGGTGCTCCATCATCTTCACACAGTGGCGCAGTACACAGGCGAATGGAGATCAATGGCACGTGCCCCAGCTCGTCAGACGTGAGCTCAAAATCGGGATCAGACCAGGAAAGAGGGGAGCAGGTGTCCAGCGAGCCCGAGGGTTGGGATAAGCCATCTTCTTCTGTGTCTCCAGGATCTGGAGTGGCGCTGACCACTTATTTCTCTGTGGATAATTGCATGACAGACACCTACAGACTGAAGTATCACCACCAGAGGCCATTGGTCCTCTCCATGCCTGAGCCTAGAGGAGCTGG
Associated Phenotype:
Not determined