ZMP
usp2a
Ensembl ID:
ZFIN ID:
Description:
ubiquitin carboxyl-terminal hydrolase 2 [Source:RefSeq peptide;Acc:NP_001008574]
Human Orthologue:
USP2
Human Description:
ubiquitin specific peptidase 2 [Source:HGNC Symbol;Acc:12618]
Mouse Orthologue:
Usp2
Mouse Description:
ubiquitin specific peptidase 2 Gene [Source:MGI Symbol;Acc:MGI:1858178]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa8592 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14898 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa8592
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 |
---|---|---|---|---|---|
ENSDART00000018185 | None | None | 391 | None | 12 |
ENSDART00000123148 | Nonsense | 110 | 600 | 1 | 15 |
ENSDART00000134053 | None | None | 394 | None | 12 |
Genomic Location (Zv9):
Chromosome 15 (position 19887018)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 20989644 |
GRCz11 | 15 | 20925376 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGCACTCCAGTAAAGGGCTATGGCTCAGGCCTGAATGGGGGCTCCGGATA[C/A]AGCAGCTACAGCTACACTCCGGCCCCCAGCAGCTACCTCTCCTCCTCGCC
Long Flanking Sequence:
AGACATTAATTGTTCAAAGGATGTTTTTGTCAGTAACAACAAAAGGATGCGTCATTGATATCTGCTCCTGCTACATTTAATATTACTACTTTTTAAAATGACAACTGCTCTTCTTTCTTCCACAGAGTCCATGCAGCCTGAAATTGCCTTACGTACGGCTGAGCACCCAGCATGTCTCGTGTCTCCTCTACGGCGAAGCGCTACGCCGGTTCGTCTTATACCAGTCACTACAGCTCCTATGGCTCCTCCTTGACTCCATCGCTTGGCTCATACGAGCGGGACAAGCTGCCCTATAAGAGCTCCTCCTCGGGCTTCTCCTCCTCATCCTCTAGCTACCTAAGCTCAAGTGCCAGCCGCTCCCGCAACTACAGCTCGTCATCCGAGCCGGACCGGGGTCGCCCTATCCCTCGCACTGATTTGCTGGGTGGCCGGCGCAGCGAGAGCCTGAGCCGCACTCCAGTAAAGGGCTATGGCTCAGGCCTGAATGGGGGCTCCGGATA[C/A]AGCAGCTACAGCTACACTCCGGCCCCCAGCAGCTACCTCTCCTCCTCGCCTGTGTCCTCCAGCATTTCCCTCAGTCGCAGGAAGTCTGTGAGTCAGAGCGATTTGACGCACGATCTGTCGGCTCTGGGACTGAGCGAAACCTCTAGTGGCAGTGGCCTAAAGCAGTCCTACCTAAGCCGAGGCAGTGACGTATCTGACTCCTACAGCAGCTCTCGCTCCAGCCTAGGCCTCTCACGGAGCTCCACACAGGAGGGGTTAGGCAGCAGTGGCCTGAAGAGCAGCAGCCGATTCTCCTCCAGCTATCGCTCCACCTCACCCGTCAGAGAGTCTTTGGTAAGTCATGTTTTTTATATTTTGATATCCTTTTTTTAATATACGGTTGAATTCTGAATTATTAGCCTTTCTGAATTATAAGCCCCCTGCATATTTTCCCCAATTTCTGTTTAACAGAGAGAAGTTTTTTTTTCATCACATTTCTGAACACATTAGTTTTAATAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14898
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 |
---|---|---|---|---|---|
ENSDART00000018185 | Essential Splice Site | 182 | 391 | 5 | 12 |
ENSDART00000123148 | Essential Splice Site | 392 | 600 | 8 | 15 |
ENSDART00000134053 | Essential Splice Site | 185 | 394 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 15 (position 19869570)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 20972196 |
GRCz11 | 15 | 20907928 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGGTCACRGTCCGGCCACGRGGAAACACAGAAGATTTTGACCACTTGCC[G/A]TAAGTGTRCTATACTTATTTTCCTCCATATANNNNNNNNTATGCAAGATTTTATGATT
Long Flanking Sequence:
AAAACACAGATTCAGAGATACGCCCCCAGATTTGTGGGCTACAAGTAAGTCTAATCCTACGTCCATCTTATTCTGCTCGAAGTCCAAGCATCGTAATGTCACAGTACTAGGCCTTGCATATATAAGTGCCCTCTCATAATTATGTAAAATAATGTTGTTGTTTTTTGACAAACTATACAAACTGTTGTTTTACTTTTTCCCTCATTATTGGATTTAATATTGTACAATATAATGTTAAAATGAATAAATCAAGTAGTATAATTATTGCATTAATTTATGTTAATGGCCAAAACATAAATTATAAGTAAATGAAAATCTTATAATGTCTCGTATGTCAATAGCTAGCTGTAGTTGTGTTATGCTTTAAGCTGTTTATGTTATCTCTCCAGTCAACAGGATGCTCAGGAGTTTCTACGGTTCCTGCTTGACGGCTTGCACAATGAAGTAAACAGGGTCACGGTCCGGCCACGGGGAAACACAGAAGATTTTGACCACTTGCC[G/A]TAAGTGTACTATACTTATTTTCCTCCATATATATGCAAGATTTTATGATTTATGTATCTTGTTAATTCTTTTTAGTGATGAAGAAAAAGGGAAAAAGATGTGGTCTAAGTATTTAGAGAGAGAAGACAGCAAAATTGTAGGTAAGTAAACATTACACCAGTGTTTGTAGTATTATTGATATACTATTAAATTAGCACTGCATTACAGCTGAAAGTGTTTTCGGTGTGTTTCTTCATTAAGTGTAACATCGCTATGTGTCTGTCTGTCCTCAGATCTGTTTGTAGGCCAGCTAAAGAGCTCTCTGACCTGCAGCGAATGCGGTTATTGTTCCACTGTGTTCGATCCCTTCTGGGATCTTTCCTTACCTATCGCCAAGGTCAGTTTAGCTAGTTTGTACATTACAGTGTTCATTTTGGCATTTGCAGAAATGAGTGGGTGTTAATGGTGTTCTTCTGCCTAGAAGGGCTATGGAGAGGTGAGCCTAATGGACTGCATGCGGC
Associated Phenotype:
Not determined