ZMP
usp5
Ensembl ID:
ZFIN ID:
Description:
ubiquitin carboxyl-terminal hydrolase 5 [Source:RefSeq peptide;Acc:NP_999920]
Human Orthologue:
USP5
Human Description:
ubiquitin specific peptidase 5 (isopeptidase T) [Source:HGNC Symbol;Acc:12628]
Mouse Orthologue:
Usp5
Mouse Description:
ubiquitin specific peptidase 5 (isopeptidase T) Gene [Source:MGI Symbol;Acc:MGI:1347343]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9178 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14716 | Nonsense | Available for shipment | Available now |
sa17405 | Nonsense | Available for shipment | Available now |
sa22772 | Essential Splice Site | Available for shipment | Available now |
sa36058 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36057 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9178
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 |
---|---|---|---|---|---|
ENSDART00000029121 | Nonsense | 117 | 853 | 4 | 20 |
Genomic Location (Zv9):
Chromosome 16 (position 13732302)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 12091393 |
GRCz11 | 16 | 11982295 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
YTNGCAGGTATTGAGGGAGGGTTYGATGTTGAGCAGGAGCAGTATGAAGAA[G/T]AGGTCAAGGTGGTTCTTTTCCCAGAYCGACAGGAAGTGACACTGGATGAT
Long Flanking Sequence:
ATTTTTTAGGAAAGTTATACCACGGTTGTCTGTGTAAAATATGTAAATGTAAATTTGCCGCATTCTATGAACTAAACATGTATTGCATTTGCAAGTACTTTTCAAAAGTGTGCAGTGTTTCCATACAAATATACAAAGTGATATTGCCGTCAACAACATTAATCTATGGACAGAACTTTTGAGTAATACGAAGGAAACTTCATTTTATCATTTCTCTCTCTGTTCTTCTGGCAAACATATACTAACCTTATCTGTCTTTCAGAAGGAGGATGATCCCAATTCAGGATCAGGTGATCCTCCTAAAAAGAAGCCCACAAGACTGGCCATTGGTAGGCACCTGTGTTCTTTTGCCTTTGAAGTCTTTGCTTCATATTTTTGTACATGCTAATTTTAACTGAGAGTCTGTTTAATTTACGAAACAAAAAAGGCTGTAAGGTTTGTATGTGTTTCCTGCAGGTATTGAGGGAGGGTTCGATGTTGAGCAGGAGCAGTATGAAGAA[G/T]AGGTCAAGGTGGTTCTTTTCCCAGACCGACAGGAAGTGACACTGGATGATCTCTCCTCCATGCCAGATGTTGTTCGGGAGCGGGTGGGTATCTTTTACTATACTGAATTACTTAACGAACATTAGGATAGTGTGTTGATAATTTGCTTATTAAAATTATATAGGTCTGTAGATATATAGATAGAGAGAGAGAGAGTTTTTTTTTTGTTTGTTTTACATACTTGTAGTTTGATAAAGTGCTGGGTGATTAATTTAAAGCAATCCTTCATGTGCATTTGGTCAGTAAAGCCAGTTCTAGTAAATCACCTGCATGTGCTTTCATATGGAGCAGCATTTACTACAAAGAGCTGATGTTCACTGACAATTCATTCTGATTCTGTAGTCATATGATTATTAGTCACCTCGAATCCAATTACGTTTAAGATCCAAAAGTGCTCAAAGTTGTATTTTCGTGTGAGGATTATCCGACTGGACGAAACATGTAAATGTAATGAACAGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14716
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 |
---|---|---|---|---|---|
ENSDART00000029121 | Nonsense | 197 | 853 | 6 | 20 |
Genomic Location (Zv9):
Chromosome 16 (position 13729666)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 12088757 |
GRCz11 | 16 | 11979659 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGAGTAAGTAAYAGRAGGTGACTGTTYGCKCTTTCAGTGGCKGGAAGTG[T/A]GAGGTCTGTGAGCTGCAGGAGAACCTGTGGATGAATCTGAYGGACGGGAA
Long Flanking Sequence:
GTAACCTTTCATTTTAAAGTAATAGGTCATCCTACTGTATATAGTTTACACTATTAGCTAAGATGGATTTTTTTGTGTTCTTAAGAATATTTGAATAGAATATTTAGAGAATATTTAAGAAATATTAGTTTGAACCCAGATTAACACACATTTTTAGGAGCAAATTAAAAATTCCATCTTCCATTAGGCATATTTTACTGTTCTGTAATACCTCTCCTGCCTAAACCTTTACAAATTTTCAACTTAGTTCACACTATTTTGTAACATTTTTAAGAAAAAAAATGTTAAACATGATATTTAGTTTTATATAGCCATAGATCCTGACATAATGTTAAGTATTAAAAAAATAACAAAAATATACTCAATTTTGACTTCAAAATCAAGTTGTGAACCAAACCATCAAATATGTACACCTCTAACATGGACAGGTAAGCTTTGAGAACATGATCCCAGAGTAAGTAACAGAAGGTGACTGTTTGCTCTTTCAGTGGCTGGAAGTG[T/A]GAGGTCTGTGAGCTGCAGGAGAACCTGTGGATGAATCTGACGGACGGGAAAGTTTTGTGTGGCCGGAGATATTTTGATGGCTCTGGGGGGAATAACCATGCCCTCCTGTACTACCAGCAGACTGGATACCCACTAGCTGTTAAACTCGGCACAATAACACCTGACGGAGCAGGTCAGATTCTCACACCACATCTACAGGAATCAAATTCAGTTGTGTTTGTTTAATATTGAGTCAATAAAGTTATGTGTGCGTTACTGTTTATGGCCATTAAGGTTTTAATTTAGGTCTTTAAGTCTTTAGATTTAAGATATATTGCAAAATATTGTTCTTTTTAAATGAATTTTCCAAGGGGTAGTTTACCCAAATATGAAAATTGACATCTTTTAATCAACCTCCACTCTTTTCTAATGTATTTGAGTTTTTTCTGTTGAAAAAAAAAATACTGCTCAAAAAAATGAAGGGAATACTTAAACAACACAATGCAACTCCAAGTGTTTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17405
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029121 | Nonsense | 237 | 853 | 6 | 20 |
Genomic Location (Zv9):
Chromosome 16 (position 13729548)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 12088639 |
GRCz11 | 16 | 11979541 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GRTATTTTGATGGCTCTGGGGGGAATAACCATGCCCTCCTGTACTACCAG[C/T]AGACYGGATACCCAYTAGCTGTYAAACTCGGCACAATAACACCTGAYGGA
Long Flanking Sequence:
GAAATATTAGTTTGAACCCAGATTAACACACATTTTTAGGAGCAAATTAAAAATTCCATCTTCCATTAGGCATATTTTACTGTTCTGTAATACCTCTCCTGCCTAAACCTTTACAAATTTTCAACTTAGTTCACACTATTTTGTAACATTTTTAAGAAAAAAAATGTTAAACATGATATTTAGTTTTATATAGCCATAGATCCTGACATAATGTTAAGTATTAAAAAAATAACAAAAATATACTCAATTTTGACTTCAAAATCAAGTTGTGAACCAAACCATCAAATATGTACACCTCTAACATGGACAGGTAAGCTTTGAGAACATGATCCCAGAGTAAGTAACAGAAGGTGACTGTTTGCTCTTTCAGTGGCTGGAAGTGTGAGGTCTGTGAGCTGCAGGAGAACCTGTGGATGAATCTGACGGACGGGAAAGTTTTGTGTGGCCGGAGATATTTTGATGGCTCTGGGGGGAATAACCATGCCCTCCTGTACTACCAG[C/T]AGACTGGATACCCACTAGCTGTTAAACTCGGCACAATAACACCTGACGGAGCAGGTCAGATTCTCACACCACATCTACAGGAATCAAATTCAGTTGTGTTTGTTTAATATTGAGTCAATAAAGTTATGTGTGCGTTACTGTTTATGGCCATTAAGGTTTTAATTTAGGTCTTTAAGTCTTTAGATTTAAGATATATTGCAAAATATTGTTCTTTTTAAATGAATTTTCCAAGGGGTAGTTTACCCAAATATGAAAATTGACATCTTTTAATCAACCTCCACTCTTTTCTAATGTATTTGAGTTTTTTCTGTTGAAAAAAAAAATACTGCTCAAAAAAATGAAGGGAATACTTAAACAACACAATGCAACTCCAAGTGTTTGCTTTTTTTCAGCAGTCAATGTTTTGAAAAGATAACTTAAAGAATGCTGGGAAGTGGCAGCCATTGACTTCTGTAGTTTTCTTGTTCCTACAACGTTTTGTCTTCTAAAATATATTGTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22772
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 |
---|---|---|---|---|---|
ENSDART00000029121 | Essential Splice Site | 405 | 853 | 10 | 20 |
Genomic Location (Zv9):
Chromosome 16 (position 13724971)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 12084062 |
GRCz11 | 16 | 11974964 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAGCCCCAGACCCCGCAGATGAACCTAACACCTCTGCTGAACCCAGGG[T/C]ACACACACTTACAGTTCTCATGTATTGGGTTGTATTAAAAACAAATAGAT
Long Flanking Sequence:
TATTTTTGTCTCATCAATTGTCTGCTATCATATTTTTAGTATCTGGACAACACCACAAAAGTTATGCACTCGACCCAAGGTAACAAATAAGGGTTTGCTCTAGAGAAACTATATGTTACTATATGTAACAAATGCTGGGACTTTCTCATGTGATATAAATATAAATAATTATCAGGAAATCTTTATTTATGAGTGAACTATATTTTTTAAGAGGACTAAAGGGGCTTCAAAAATACCACACTTCCAGCAGAGGTCACTATACATAAATTCTTTATACAGTCTCAATGATAGAAAGAGGGAAAATACTCTGCTGTAATTTTGTCAATGAGCGTAAACTGCTTGCTTTTTTCCATAATATTAAATTTCTCAAATTAAAACTCTATTTCTTCATTTCCTTTTGAATTTCAGAGCAAAGCTGGGCTATGGCCTTTTGTCAGGAGAGTACTCTAAACCAGCCCCAGACCCCGCAGATGAACCTAACACCTCTGCTGAACCCAGGG[T/C]ACACACACTTACAGTTCTCATGTATTGGGTTGTATTAAAAACAAATAGATGAGTTAATATGCAAGTCTTTGATCATTTGATTACTGTAGAATGGGACAATTTACACACACAAGCGCACACACAAACACGCACACACATAAACTGAAATTAACTTGGCTCTTGCTCATTTGTTGAGGTTTGTTTTTCTTTGTGCAGGGTGACCAGGTTGGTATTGCACCTCGCATGTTCAAAGCTCTGGTTGGACGAGGCCACCCTGAGTTCTCCACCAATCGGCAACAGGATGCACAAGAGTTTCTTCTTCACTTCATAAATATGGTGGAGGTAATGATTATGACTTTCTCCTCCTATTTTTTTCTACCTTCAGGTGCATCTTCTCATTTTGTCTTGTCTTTGTTGTCCAGAGGAATTGTCGGTCAGGCATGAATCCTTCAGAAGCTTTCAGATTCTTGGTAGAGGAGAAGATTGTATGCCAACAATCACAAAAAGCCAAGTATACCCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36058
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 |
---|---|---|---|---|---|
ENSDART00000029121 | Nonsense | 432 | 853 | 11 | 20 |
Genomic Location (Zv9):
Chromosome 16 (position 13724697)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 12083788 |
GRCz11 | 16 | 11974690 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTCAAAGCTCTGGTTGGACGAGGCCACCCTGAGTTCTCCACCAATCGG[C/T]AACAGGATGCACAAGAGTTTCTTCTTCACTTCATAAATATGGTGGAGGTA
Long Flanking Sequence:
TACAGTCTCAATGATAGAAAGAGGGAAAATACTCTGCTGTAATTTTGTCAATGAGCGTAAACTGCTTGCTTTTTTCCATAATATTAAATTTCTCAAATTAAAACTCTATTTCTTCATTTCCTTTTGAATTTCAGAGCAAAGCTGGGCTATGGCCTTTTGTCAGGAGAGTACTCTAAACCAGCCCCAGACCCCGCAGATGAACCTAACACCTCTGCTGAACCCAGGGTACACACACTTACAGTTCTCATGTATTGGGTTGTATTAAAAACAAATAGATGAGTTAATATGCAAGTCTTTGATCATTTGATTACTGTAGAATGGGACAATTTACACACACAAGCGCACACACAAACACGCACACACATAAACTGAAATTAACTTGGCTCTTGCTCATTTGTTGAGGTTTGTTTTTCTTTGTGCAGGGTGACCAGGTTGGTATTGCACCTCGCATGTTCAAAGCTCTGGTTGGACGAGGCCACCCTGAGTTCTCCACCAATCGG[C/T]AACAGGATGCACAAGAGTTTCTTCTTCACTTCATAAATATGGTGGAGGTAATGATTATGACTTTCTCCTCCTATTTTTTTCTACCTTCAGGTGCATCTTCTCATTTTGTCTTGTCTTTGTTGTCCAGAGGAATTGTCGGTCAGGCATGAATCCTTCAGAAGCTTTCAGATTCTTGGTAGAGGAGAAGATTGTATGCCAACAATCACAAAAAGCCAAGTATACCCAGCGAGTTGACTATATCGTCCAGCTGCCCGTTCCCATGGACCAGGCAACTAATATGGGTTAGATAGTGACTAAAGTGTTGTTTATACTCTAAATCAGGGGTTCTCAACTGGTTTGGCCATGGGACCCACATTTTTACATGGTCATCAAGTCGCGACCCAAATTTTTAGGAACTATAATACAATTTTAGGAATTATAATTAATTTGTATTTATTCATTAACATAAACAAGTAGTAACAGATACGTCATAAGACATTCACCAAGACTTACAAATAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36057
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 |
---|---|---|---|---|---|
ENSDART00000029121 | Nonsense | 472 | 853 | 12 | 20 |
Genomic Location (Zv9):
Chromosome 16 (position 13724497)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 12083588 |
GRCz11 | 16 | 11974490 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCTTCAGAAGCTTTCAGATTCTTGGTAGAGGAGAAGATTGTATGCCAA[C/T]AATCACAAAAAGCCAAGTATACCCAGCGAGTTGACTATATCGTCCAGCTG
Long Flanking Sequence:
ACCTAACACCTCTGCTGAACCCAGGGTACACACACTTACAGTTCTCATGTATTGGGTTGTATTAAAAACAAATAGATGAGTTAATATGCAAGTCTTTGATCATTTGATTACTGTAGAATGGGACAATTTACACACACAAGCGCACACACAAACACGCACACACATAAACTGAAATTAACTTGGCTCTTGCTCATTTGTTGAGGTTTGTTTTTCTTTGTGCAGGGTGACCAGGTTGGTATTGCACCTCGCATGTTCAAAGCTCTGGTTGGACGAGGCCACCCTGAGTTCTCCACCAATCGGCAACAGGATGCACAAGAGTTTCTTCTTCACTTCATAAATATGGTGGAGGTAATGATTATGACTTTCTCCTCCTATTTTTTTCTACCTTCAGGTGCATCTTCTCATTTTGTCTTGTCTTTGTTGTCCAGAGGAATTGTCGGTCAGGCATGAATCCTTCAGAAGCTTTCAGATTCTTGGTAGAGGAGAAGATTGTATGCCAA[C/T]AATCACAAAAAGCCAAGTATACCCAGCGAGTTGACTATATCGTCCAGCTGCCCGTTCCCATGGACCAGGCAACTAATATGGGTTAGATAGTGACTAAAGTGTTGTTTATACTCTAAATCAGGGGTTCTCAACTGGTTTGGCCATGGGACCCACATTTTTACATGGTCATCAAGTCGCGACCCAAATTTTTAGGAACTATAATACAATTTTAGGAATTATAATTAATTTGTATTTATTCATTAACATAAACAAGTAGTAACAGATACGTCATAAGACATTCACCAAGACTTACAAATAAATACTATTTTATTGCTGTCATTAAACAAAATGGATCAAATTTTAGAAACATTACAAAGTAAAAACGACAAATACTGTTAATAATAAACTGTTAATAAAACATGTTTTCTGGTTTCTAAATGTTTTTTTTAATTTAAAAGGTTTCATGCTCTCTAGTGAGAGTACCTCACTACATATGACACCGAGGCTTTAAGTCTTTTTTG
Associated Phenotype:
Not determined