ZMP
usp42
Ensembl ID:
ZFIN ID:
Description:
Ubiquitin carboxyl-terminal hydrolase [Source:UniProtKB/TrEMBL;Acc:Q802X0]
Human Orthologue:
USP42
Human Description:
ubiquitin specific peptidase 42 [Source:HGNC Symbol;Acc:20068]
Mouse Orthologue:
Usp42
Mouse Description:
ubiquitin specific peptidase 42 Gene [Source:MGI Symbol;Acc:MGI:1924050]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42004 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35250 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10774 | Essential Splice Site | Available for shipment | Available now |
sa35249 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42004
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003375 | Essential Splice Site | 244 | 1047 | 6 | 16 |
ENSDART00000134597 | None | None | 74 | None | 4 |
Genomic Location (Zv9):
Chromosome 12 (position 18653542)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 17464119 |
GRCz11 | 12 | 17585993 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAACCACTTTTGTACATCAGATTTTTGGAGGATATCTGAGATCCAGAGG[T/C]AGGTCACTCATTTCGTTTGACTCGGATTTAATGTATTTGTATTTGAATGT
Long Flanking Sequence:
CACACAAACTGGTACAATTCCAAATATGGCTTTTTCATGGCTCTTGGAGACAGCCCCAAGATAAGGGTTGAGAGTTAAGCAAATAAATATTGAGGTTAAACCATGATGTTAATATAAAAACAAGAACAGTGATAAGGAATGGCATGGGATGACAGCTATTTTTAAAACATGGTCCACTGATATTTTGTTCTTCTCCTCAGGGATTGGAAAGCATTTTAGATTTGGAAGTCAAGAAGATGCCCACGAGTTCTTGAGGTACACTGTGGATGCTATGCAAAAGTCCTGCCTTCCTGGAAACAAGTGAGTTCACATAATGCTGTTTTGTTTGCCAGTTTACAAGCAGTGTAAGGCATGAAACTTAACATTTCCACATTTGTCGATGCAATGACTTCGTTATTACCTCCATTTTAACACTACTTTTATCTTGTCAGACTGGACAGGCAAACTCAGGCAACCACTTTTGTACATCAGATTTTTGGAGGATATCTGAGATCCAGAGG[T/C]AGGTCACTCATTTCGTTTGACTCGGATTTAATGTATTTGTATTTGAATGTAATAATTAGTTTGCTCTAGATTTCTTGTATTTGTTGGCATCAGTTGTTAATGAACATTTCTTTTTCACAGTCAAATGTCTGAATTGCAAAGCAGTCTCTGATACTTTCGATCCATATTTGGATATTTCATTGGAGATAAAGGTGAAAGATTTTTTCTCTCTTAACATCAATTCTTGCAGTTTATGCACAAGTTTTAAAGATTGAAATGGTGACTTTGTGTGCTTCTTCGCAGACGGCTCAGACACTCTCTAAGGCGTTTGAGCAATTTGTAAAACCTGAGCAACTTGATGGGGACAATGCCTATAAATGCTCCAAGTAAGTCTTCTGTTCATATGAATACCACATCATTGTATTATTCAAGAATTTAATTTGTGCAATGGTATTGCATTTATACTTTCACTTTCATTCAAGCTGACAGTAATCTTTTTTTTGTCTTGTCAGATGTAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35250
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 |
---|---|---|---|---|---|
ENSDART00000003375 | Nonsense | 296 | 1047 | 9 | 16 |
ENSDART00000134597 | None | None | 74 | None | 4 |
Genomic Location (Zv9):
Chromosome 12 (position 18653047)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 17463624 |
GRCz11 | 12 | 17585498 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCACTTTCATTCAAGCTGACAGTAATCTTTTTTTTGTCTTGTCAGATG[T/A]AAGAAAATGGTTACTGCCTCAAAGAGATTCACCGTTCATCGCAGTTCTAA
Long Flanking Sequence:
AGAGGTAGGTCACTCATTTCGTTTGACTCGGATTTAATGTATTTGTATTTGAATGTAATAATTAGTTTGCTCTAGATTTCTTGTATTTGTTGGCATCAGTTGTTAATGAACATTTCTTTTTCACAGTCAAATGTCTGAATTGCAAAGCAGTCTCTGATACTTTCGATCCATATTTGGATATTTCATTGGAGATAAAGGTGAAAGATTTTTTCTCTCTTAACATCAATTCTTGCAGTTTATGCACAAGTTTTAAAGATTGAAATGGTGACTTTGTGTGCTTCTTCGCAGACGGCTCAGACACTCTCTAAGGCGTTTGAGCAATTTGTAAAACCTGAGCAACTTGATGGGGACAATGCCTATAAATGCTCCAAGTAAGTCTTCTGTTCATATGAATACCACATCATTGTATTATTCAAGAATTTAATTTGTGCAATGGTATTGCATTTATACTTTCACTTTCATTCAAGCTGACAGTAATCTTTTTTTTGTCTTGTCAGATG[T/A]AAGAAAATGGTTACTGCCTCAAAGAGATTCACCGTTCATCGCAGTTCTAATGTTCTCACAATCTCACTAAAGCGGTTTACCAACTTTAATGGAGGAAAAATAACAAAGGTGAAGCAGATAATTGTGTTACTGCTTGCTAAGTTCCTGTTGTGACCAGACCCATCACCTGTATTATTGTCTCCTTTATACATGACCTTTTACATATAGTTTTAAATGGATTTATTGTCTTTTAGAAACATTAAAATCTTATCAGTAAATACATTTGTTATTCCATTATCACTTCACAGGATGTGAGGTACGCAGAGCATCTAGATCTGCGTCCATTCATGTCTCAGTCTCATGGGGAGCCACAAATCTATGCTCTGTATGCTGTGTTGGTTCATTCTGGGTTCAGTTGCCACGCTGGACATTACTACTGCTACATTAAGGTATGTTGTCAAGAGCAGAACTGTATTCTTCTTTACTTTAATAGAATTTATAAATTAACATATTTATTTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10774
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003375 | Essential Splice Site | 464 | 1047 | 12 | 16 |
ENSDART00000134597 | None | None | 74 | None | 4 |
Genomic Location (Zv9):
Chromosome 12 (position 18652169)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 17462746 |
GRCz11 | 12 | 17584620 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACCACCACGTCCTTCATTGGCCCTCAACTGCCACCTCATATGCTGAAGG[T/A]AMTGCAAGACAATRAAACATCCTAGCAAAATCAGCACTGTGATGGATGTT
Long Flanking Sequence:
GTTCATTCTGGGTTCAGTTGCCACGCTGGACATTACTACTGCTACATTAAGGTATGTTGTCAAGAGCAGAACTGTATTCTTCTTTACTTTAATAGAATTTATAAATTAACATATTTATTTAATTGACCCTTTTATTTTAGGCTAGCAATGGGCAGTGGTATCAGATGAATGACTCGTCGGTATCTCTCAGCGATATAAGAACAGTTCTTAACCAACAAGCATACTTGCTCTTCTACATCAGGTAATATTCAAAATTCATTTGTCTCTTAAATGGGTAGTTAGTTGTATGAATGGAACTAAAAAAGATTCTGACAATTCATCAAAAAAATCTCCGTGTTAATTCAGGTCACCTGATGTAAAAAATGGAGGCGACTTTAGCCAGATGAACCATACTCCAGGTCAGTCTTCTCCAAGACCATCCATTCCACTCAAGATGAATGGGCCTCAGTATACCACCACGTCCTTCATTGGCCCTCAACTGCCACCTCATATGCTGAAGG[T/A]ACTGCAAGACAATGAAACATCCTAGCAAAATCAGCACTGTGATGGATGTTTTGAAAAATGTAGCTACAGGAAGAACTTTAAGTTATTTATTATATATCGGACTGAAAAATCATAAATGTAATTTTTTTTGTGTTACTGAATTATGAAGTTGTAATTACTATGTAATATGTTTTTATCTATATTAATCTTGCCATAAGTTCATAAGAAGGAACGTTCATAAGAATAAGTTCAGCCTTGATAAGCTTTTGTTTTTTCAATTTCTTCTGTTAAACTGGTCATTGTTTTTGCAGAACTCGTCATATGTTAATGGAAATGGTTCTTCAAAGGAATACCATGGTGGCTCTAAACCCAACAGAAATTTTGGTGGTGTGACCAAAATAGGCCCATCTCATACATCTTCCTCTGCATCTGCGTCCTCTTCTTCTTTGCCTGTTCGGTCCATGGGCATTCCAGATTCATCCAAAAGGCCGAAGCTGACGTTTCTCATTGGTCAAGGCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35249
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 |
---|---|---|---|---|---|
ENSDART00000003375 | Nonsense | 857 | 1047 | 15 | 16 |
ENSDART00000134597 | None | None | 74 | None | 4 |
Genomic Location (Zv9):
Chromosome 12 (position 18649251)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 17459828 |
GRCz11 | 12 | 17581702 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGTCAGGTGAGGACCGGAACAGAGGGTCAGATCGACCACATTTTTCTT[C/A]AACCCCGAAGGACAGGGAACGATACAGGCACTATAGGGATCATAGTGATA
Long Flanking Sequence:
ATCTTAATTTTTTGTGTCCTCAATCCGAGGCCATTTCTCATGTAATAAACTTCTTTTGGGTTTTCTTCATTCATTCAGAAGCTCCAATCCAGCAAGTTCTGATGACCATCCTTGTTCCTCACCTTCAAACAAAAGGTTGAACCTTCCTTCTGAGTCTTCATCTCAGTCTGTGGCACAGATACAATCTTCACCTAAAGAATCACTAGTCTTAAAGACTACAGATACTGACCTTCATACCGAGACCGCTTCTAAAGTTGAGTTGACTCAGAGGCATGCTACGCATACAGCAACTGGCACGTCAGACCTTCAGGTCAACAACAATGTTAGCCTTCATGTTAGTCATGGTCACACGAGTCCACACAAGTTAAAGGAGGTGTACAGGTGCAGTGAAGGAGAGAGCAAAGAGGCAAAACCATCACACTCAGACAAATTTGGCTCTGGAGATGGATGGAGGTCAGGTGAGGACCGGAACAGAGGGTCAGATCGACCACATTTTTCTT[C/A]AACCCCGAAGGACAGGGAACGATACAGGCACTATAGGGATCATAGTGATAGAAGCCGGAGTCGCTATGGGCACAGCTATCAAGATAGTCGTCGCTCCACCAGTAGAGAGCGCTATTATAGAGATCGAGATTTGGAGAGACACTGGGACAGATTCTCACACCACCGTCGAGAGCACCATTATTTCCAGAGAAGACACCGAGATGAACGCGACTGGAATAGAGATCGTAGGTTTGGGAGTGACTCTTATCGCCCTTCTGGATACCATAACAGGAATGGATATTCCAATCACAGTCATCGTGGGATGGAAGAGGCCCATGGAAGAGCGACTCATACAGTGAACGGTTCAAAAGGCAGGCCCTCGTCACCTCATTCCGTTAGTCCACTTCCTAGACATCACAAGCGGAAACGCAGTCCATCGGTTGATGCAAGGGAAAGTTCTGATGAGTGCAAAGCAAAGAAATCCAAAAAGAAAAAGAGAAACAAAGATAAACACAGGTAAG
Associated Phenotype:
Not determined