ZMP
usp45
Ensembl ID:
ZFIN ID:
Human Orthologue:
USP45
Human Description:
ubiquitin specific peptidase 45 [Source:HGNC Symbol;Acc:20080]
Mouse Orthologue:
Usp45
Mouse Description:
ubiquitin specific petidase 45 Gene [Source:MGI Symbol;Acc:MGI:101850]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13100 | Nonsense | Available for shipment | Available now |
sa12916 | Essential Splice Site | Available for shipment | Available now |
sa42767 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa36194 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36193 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa28695 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13100
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 |
---|---|---|---|---|---|
ENSDART00000112360 | Nonsense | 148 | 830 | 5 | 23 |
ENSDART00000137232 | None | None | 803 | None | 18 |
Genomic Location (Zv9):
Chromosome 16 (position 35036219)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 32767719 |
GRCz11 | 16 | 32721749 |
KASP Assay ID:
2260-9951.1 (used for ordering genotyping assays)
KASP Sequence:
TGCAAAAGCAGTCAGCAAAAGCCACCTCAGGTAATTAATCCACAGAAAAA[C/T]AAGGAGAACAATGTTAAANNNNNNNNAATTTTAGGAACATGAYAYATTTT
Long Flanking Sequence:
TAAGCAATGACACACACTTTTCAAAAATGTACATGCAACATATACTCCTTTGTATTGGACATAAAAGCCATAATAGAGGGCAGCAGTTGAGTTCTAGACTTAAATAATCCATTCTCCACAGGGAAATTGATTTTTAACATTACCTGACAAGTCCTTACAGATAGACCTGTTGTGAGGTCCGAAGATGTTAATCGATTTAATATGCTTTCGCTGACCTATTGATCTCTTTGCAATAATCCACTTTATTTTGAATTCATGCAGAAAAATGACTTTAAGCATTATTCTGTAAAGAAAATACCTCTAGGTTAGAGAGTCAGAGACAAATTGCACTACGAATTGTGTTTTACCGTTAGATGATGCTTTTGTTCTTGTTTAACAGGTGCTTTGAATGTAAGGAAGAGCTGTCCACTCACTGCAATAAGAAAGCATTGGCTCAGACTCTGGACTTTCTGCAAAAGCAGTCAGCAAAAGCCACCTCAGGTAATTAATCCACAGAAAAA[C/T]AAGGAGAACAATGTTAAACTTTGTTCAATTTTAGGAACATGACACATTTTTCTGCTGTTAGTAGTGAAGGTTGTTGAACTTTTGTGAATGTACGTTATTATAGCGGCTTGCTTTTTTATTTAATGGATTAAAAACAGAACATTTTCTCTTTTTCCTGTGCTATGGTGCGTTCAAAGATGAGCTGTTTCTTTCAGATGGCTCTTTTAAAAAGCTCTTCATTGTTTCTCTGTGCAAACAGCAATGCCATGTTAGCACATCTGTCGTCACTGACCTTTGTCCTCAGATCACTAGGTTTTAGCTTTCCAGATACAATTAGGAGAGGACTTATGTCATTGCAGTCTTTAGTTAACCTAAATGCATTGTGATATTGCAAAGACTTCAATTTATTTCTTGTATTTACATGAATTGATTTTAAAAAAAGAACAATAAAAAAAATGTTCCTTCATACTTGAAATGGTTGACCTTGAGTAAATGACATCCAGGGTTATTTTGACTTGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12916
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112360 | Essential Splice Site | 319 | 830 | 12 | 23 |
ENSDART00000137232 | Essential Splice Site | 313 | 803 | 9 | 18 |
Genomic Location (Zv9):
Chromosome 16 (position 35012136)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 32743636 |
GRCz11 | 16 | 32697666 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAATTGCTGCATTACCYCCTGGACTCTATGAGAGTGGAGGAGACAAAGG[T/G]GAGTGTGTGAGATCGTGTNNTTTTTTNCCTTCTCTTCTATTAATAAAGATTWA
Long Flanking Sequence:
TAAATTCCAATCTTGGATTTGTAATTCAGCTGAATGAGAGAATTGGTTAAAGGTCTGAATGTGTTTATGCGTCTGTTTGTGTGTGTGACCAACTGACCTCGGCTGGTTGAATGATGAAATGAAAGTGAATGAAAGTTGTCAGGGAAATAATAATAGCAGCCTCAGAGTTCCAGAAACCTGCAGCGAGCAGCGCGAGTCTCCTCGTGCAGTGTCAGAGGAAAGGCCTTGAGAGAAGATTATGGTCATTCTTCTCTCGTCTTTACTCCTCTATATGCTGCCGATTGGTTTTTGTGTGTGGCTAATTGGTGTTTGCGTGGCTTCGGCTGCTTTTGTCCCCGTAGATGTATTTACACTTGTGCCAATGCATTTGTAAGATGGAGAAGCTCATTGTGTGTGTGTGTGTGTTTGCAGGGCTCCTCGTTTTAAGGGTTACCAGCAGCAGGACAGTCAGGAATTGCTGCATTACCTCCTGGACTCTATGAGAGTGGAGGAGACAAAGG[T/G]GAGTGTGTGAGATCGTGTTTTTTTCCTTCTCTTCTATTAATAAAGATTAACTTAAGACCCGTTTGCTTGTAACTAAGGTTGGAGTAAGATATATACCAAAGTAGTGTATCTGCATAAAATTCAGAATTACATATTTAACATTTTATTAATTAATAACAAATGCAAATTAGTTCAAGTTAACTTTTTTATGAAGGTGCAGTAGATCAAAATGCTCTTTGTTCAATAATAACAGTTTATTGTAAATAAATAATAAGTTTATTTATTTGAACAAATGTACTTTTTATTATAATAATAATAATATTATTATTATTAATAATAATAATAATAATATTAATAATAATTCTCCATCGATATCAAAGCAGACGACTCGCTTCATTCTAGATGTCTTTCAGGATTGTAATTGTAGGCCTAACTACTCTGTATAACATACCGATATTGTGTAGTCCTACAATGTGACGAAGCCACAGACATATGCAAGAGGCAGTGCACACTTTTTTCGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42767
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112360 | Essential Splice Site | 346 | 830 | 13 | 23 |
ENSDART00000137232 | Essential Splice Site | 340 | 803 | 10 | 18 |
Genomic Location (Zv9):
Chromosome 16 (position 35001391)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 32732891 |
GRCz11 | 16 | 32686921 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACCCCACAGAGAAGACTGCAGACGAGGAGACCAAACGACAAGTGAAGG[G/A]TGATTCAGCTCTGCTTCCGTCACATCACTCAAAACAATAGTGCCATCTAG
Long Flanking Sequence:
AAATATTGTGGATTCTGTAATTCAGAAAATACTGCAAACTGATGTAATAAAATGTAGATAATCAATGTATGCATGAACATCTCTGTCTGTAAAAGCTTTCAGAATATTGATATGAATAAAGTGCTGCTGAAGTCAAGATATATGGTGCAGTCCAATAAAAGAAATCCCTTAAAAAATGTATAATTGAAATGTTCTTTTACAAATAGATAAAGTGTCATTAAAATAAACTTATAATGTGTTTTTATGATAATTCTAATAGATAGAAAAACTTGAAAACAGTTTTGGTCTGCAGTGTTTCACTTTAAAGACGGAAGTCTTTTACTGTGCTCCTTTTATTTTGAATGTGATGATAAATGGAGCTTTTTGTGACCACTTTATTATCTAACCAAGTGGCATGCCATTGTGTTTTCACTGACAGCGCATTAAAGCGGGGATCCTTAAAGCCTTTAACAACCCCACAGAGAAGACTGCAGACGAGGAGACCAAACGACAAGTGAAGG[G/A]TGATTCAGCTCTGCTTCCGTCACATCACTCAAAACAATAGTGCCATCTAGTGACCGCTTGCTTTCTTTACCTTCTAGAAATAGTTATGCGTTAAATCAGAATTTGAAAAATGATCTGTTAATTGCGTTCTGCTTACTAGTATCTGTTTTATGGTGTTTATATTAATTAGATATTTTTATGCTTTACAGCTTATGGAAAAGAAGGAGTGAAATTAAATTTTGTTGATCGAATCTTTGTCGGAGAGCTGACCAGCACCATAATGTGTGAAGAGTGTGAGCATGTACGTTTTTTAAATTCCTGATCATTTGTGTTATCTATGATCAGTCTTTTTAGCTCAAAAGTTTCATTGCATAGCTAAAAAAGAAAGTCTACATTACACTTCTTTTTGGCTTTGATGCTTCAAAACCATGGGTCTGAAACTGGATTCCTGGAGGGCCGCAGCTCTGCACAGTTTTGCTTCAATCCTAATCAAACACATCTAAACCAACTAATCAAGGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36194
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112360 | Nonsense | 532 | 830 | 19 | 23 |
ENSDART00000137232 | Nonsense | 504 | 803 | 14 | 18 |
Genomic Location (Zv9):
Chromosome 16 (position 34997625)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 32729125 |
GRCz11 | 16 | 32683155 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCAGGACAGCAGTAACGATGCAGACAGCGAGGCCTCTGAAAGTGAATG[G/A]TCTCCCCGAATCCCATCAGTGTCCAGTCACAGCAGCACATCAGATAAAAC
Long Flanking Sequence:
ATCACGCTGCTTTGTTTACTTCAGTAACCAAGGCAACACCATTATTTCTGCAGTTCAATAGGCACCAACCTGCTGAATTAGCTAGATTTAATAGATTTTCATTCAGTATATGAATTATGTTTTAGTTTTGGATTAGTTTCTTACATTAATATTTAGTAAATATATTGTACAATTAAAATCTCGGCAGTGTTTCCGGTTGAAACCTAAAGTGGTTATGAGTTCTTAAAGTATATTAAAAGGTTGTTGAATTTTTTTTTTTTTTTATTGACTATACGACTCTGTTTTCAGAAGCTACAGAGCCGCCATTCGTCCACGTCTCATGATGACCGAGGCCCAGACACTGTTTCTAGCCGTCAAGAGGAGGATCTCTGTGTGGCTGGCCGTGGCCTATCCAGTTACAGGACTGATACAATGGGCAGCCAGTCAGACTGCAGTGAAAAAGAGTCAAACCTGCAGGACAGCAGTAACGATGCAGACAGCGAGGCCTCTGAAAGTGAATG[G/A]TCTCCCCGAATCCCATCAGTGTCCAGTCACAGCAGCACATCAGATAAAACCTCAATCACCACAACTCTATCCACAACAACACACAATCCAAGTTTAAAATCGAACCCAAGCTCCACTCCATTACCCTCCATTAGGCCCCAGCAGGGCGGCGCTGTGGAGCAGCTTGTCAGCGCTGTGTCCAAACTGGGCCTGGTTCACACATCCACTGATACTCTACCCATCAGCCACAGCCAAGAGGAGCTGAGTGAGACCCGGGACAGAGACCGTCAACACCATCAAGGGGCCTTTCAAGTCCTCTGTCACAGCTACACCCCCAGCTCAAAAGAGTGCTCTGTCCAGTCCTGCCTTCATCAGTTTACCTCTATTGAGCTGCTTATGGGAAACAACAAGCTGCTCTGTGAAAACTGCACTGACAGGAGGCAGAGGCAGATGAAGAGGAGCGGTATGTATTACCGACACATTTTCAAAACTTTACTATATATGTGGCTTAGGGCTGTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36193
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112360 | Essential Splice Site | 742 | 830 | None | 23 |
ENSDART00000137232 | Essential Splice Site | 714 | 803 | None | 18 |
Genomic Location (Zv9):
Chromosome 16 (position 34994102)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 32725602 |
GRCz11 | 16 | 32679632 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGAGTTTACAGTGTTCTTCCCAATATAGATTTGTTGTTTATGTTTGGC[A/T]GAACCTCGGGTCAGGAGAGCGTGTGCTTTACAGTTTGTATGGCATTGTGG
Long Flanking Sequence:
TGTACACCAGTGCCCGTAAACAGATGCTCATATCTGCACTTCCTCCAGTCGTCACTCTTCACCTCAAACGCTTTCACCAGGTCTTTAATAATCTGCACTCATCTTAAGTACTTTAGCTGTCATTTCAGTTTATTTGCAAGCTAAACTCATCTGTTAAAAGTGAATGTAAGGCTTAATGTGATTGAATGCTCATTCGTCTACTTGGACGAAAAAGAAGATCTCTGGTGGGCATTTTAAAAAATCTATAGCAATTTTTTTTTCCACCAAGTGTGTAAAATGCTTCGTTCTTTGCCAATGCTCTTATTGAGTTGTTTGCATCTTTTCAGGCTGGGATGAATCTGAGGAAAGTTAATAGACATGTGGACTTTCCTCTTTTGCTGGACCTGGCACCTTTTTGCTCCGCCACTTGTAAGGTACTGATCAGAGTTCTAGCATTCAAGACCTGTGATTTGTGAGTTTACAGTGTTCTTCCCAATATAGATTTGTTGTTTATGTTTGGC[A/T]GAACCTCGGGTCAGGAGAGCGTGTGCTTTACAGTTTGTATGGCATTGTGGAGCACAGTGGATCGATGCGAGGTGGGCATTATGCAGCCTATGTAAAGGTCCGAACACCTCAACGTAAACCTGAGCAGCGCCGGAACCAGTCAGGTACAAAGCTGCATGGGCAGCATTTCATGCATCAATACATTTTCTTTGCAGCTGGCTCTGAATGGCTTGAATAAAACCTGTGAATAAACAAAGATTGTTTTCATTATGGCATTGGACCTGCATTCACTGCAACCTTGAATAAGTAGCTTGTTCAGTAAAGGCCAAGTGGGTTTTGTTTTTTGTTGATCTATCGATGTGTTCTTCTTCACTCACTACTCAAGGAGAGCGTCTACGTTACAGCATTGTTTGGAAGTAAGAGTAAATGGGCTGTGAGAAGCGATTGAACACACTTTGGTAGTTAACTACTGTTGTGCGCAAATTGAAAATGAATTGTTGCAAGGTTATAATTAAGTTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28695
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112360 | Essential Splice Site | 779 | 830 | None | 23 |
ENSDART00000137232 | None | 751 | 803 | 17 | 18 |
Genomic Location (Zv9):
Chromosome 16 (position 34993987)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 32725487 |
GRCz11 | 16 | 32679517 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCGAGGTGGGCATTATGCAGCCTATGTAAAGGTCCGAACACCTCAACG[T/A]AAACCTGAGCAGCGCCGGAACCAGTCAGGTACAAAGCTGCATGGGCAGCA
Long Flanking Sequence:
GCTGTCATTTCAGTTTATTTGCAAGCTAAACTCATCTGTTAAAAGTGAATGTAAGGCTTAATGTGATTGAATGCTCATTCGTCTACTTGGACGAAAAAGAAGATCTCTGGTGGGCATTTTAAAAAATCTATAGCAATTTTTTTTTCCACCAAGTGTGTAAAATGCTTCGTTCTTTGCCAATGCTCTTATTGAGTTGTTTGCATCTTTTCAGGCTGGGATGAATCTGAGGAAAGTTAATAGACATGTGGACTTTCCTCTTTTGCTGGACCTGGCACCTTTTTGCTCCGCCACTTGTAAGGTACTGATCAGAGTTCTAGCATTCAAGACCTGTGATTTGTGAGTTTACAGTGTTCTTCCCAATATAGATTTGTTGTTTATGTTTGGCAGAACCTCGGGTCAGGAGAGCGTGTGCTTTACAGTTTGTATGGCATTGTGGAGCACAGTGGATCGATGCGAGGTGGGCATTATGCAGCCTATGTAAAGGTCCGAACACCTCAACG[T/A]AAACCTGAGCAGCGCCGGAACCAGTCAGGTACAAAGCTGCATGGGCAGCATTTCATGCATCAATACATTTTCTTTGCAGCTGGCTCTGAATGGCTTGAATAAAACCTGTGAATAAACAAAGATTGTTTTCATTATGGCATTGGACCTGCATTCACTGCAACCTTGAATAAGTAGCTTGTTCAGTAAAGGCCAAGTGGGTTTTGTTTTTTGTTGATCTATCGATGTGTTCTTCTTCACTCACTACTCAAGGAGAGCGTCTACGTTACAGCATTGTTTGGAAGTAAGAGTAAATGGGCTGTGAGAAGCGATTGAACACACTTTGGTAGTTAACTACTGTTGTGCGCAAATTGAAAATGAATTGTTGCAAGGTTATAATTAAGTTTGAGGTCTGCGTAAAAGACTTCTTTAACAGGAGGAGGAGCTGAAAATCCACATTTCGCCTGTGTTTTGGTGTTAAGTGTTTTCTTTTTTATGACTGTTTAAAATGGCGAAATTCAATA
Associated Phenotype:
Not determined