Busch Lab

ZMP

USP10

Ensembl ID:
ENSDARG00000076116
Description:
ubiquitin specific peptidase 10 [Source:HGNC Symbol;Acc:12608]
Human Orthologue:
USP10
Human Description:
ubiquitin specific peptidase 10 [Source:HGNC Symbol;Acc:12608]
Mouse Orthologue:
Usp10
Mouse Description:
ubiquitin specific peptidase 10 Gene [Source:MGI Symbol;Acc:MGI:894652]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa34233 Nonsense Available for shipment Available now
sa21137 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa34233
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111762 Nonsense 494 870 8 18
Genomic Location (Zv9):
Chromosome 7 (position 70363533)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 68938278
GRCz11 7 69161049
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCATCTGATGAAGTCTATCCCCCTTTTCAGCGAGACTCAGAGACCCTG[C/A]ACATCCACCCCCATGATGGATAACTTGTAAGTTTCAAGTGTTTTTTTTTT
Long Flanking Sequence:
TGCATCAATCACAGGATGCGAAGTTGGCATAATGAACATAACATCTTTCTAATTGGTGTAGACTGCTCTTCAGGTTTATTTTGCTTGTTGTTATGGAGGTATATGGCCCACTAAATGCTAAACTTTGACTTACGTGACCTCTGATCATTAATGAATTGAAGACTGTCTGGTTGTCCATGCAGTTGTTAATCTTACCAATGATGTATATTTTTTTCTTTCCACCCATCTATCAGAGTTAATAGAGAATGTGAAGTTGATACACAAACCTGTGTCTTTGCAACCAAGAGGACTGATAAACAAGGGAAACTGGTGCTATATCAATGCTGTATCCTTTCGTCTTTGCTCAAGTTGACTCCATTCTGTATTGGTCAAGTCTGCCTCGTCTTTTGTTTATCCTCCCTTGACTCTGAGCTTTAGACCCTGCAGGCTCTGATTGCGTGTCCCCCTATGTATCATCTGATGAAGTCTATCCCCCTTTTCAGCGAGACTCAGAGACCCTG[C/A]ACATCCACCCCCATGATGGATAACTTGTAAGTTTCAAGTGTTTTTTTTTTCTGCCCTTAATATTGCCATGATACAATGTGTTTATATGAACAGGATGTGGAATAAGTCACAACATGACTTTTTACGGTCACACTTTACAATAAGGTTCATTATTTAACATGAACTAGTTACAAACTATACTTGTACAGCATTAATCATAGTTCAACATTTACTGATGTATTATTAACCTCCAAACCCATGCTTGTTAACATTAGTTATGCTCCATGAGTTAAAGGTGCAGTAGGTGATCTGCCAAAATGCTAACCGCTTAGCATATTATCTTTGGACGGCGGGGAAGGACTGTGATTCAAAGCCACGCCTCCTGAAATCGAGAAAACGTGCACCATTTCACAACAGCAGACAACCCACTAGTTCATGTCATTGTCCAGTTTAGATGGTGTTTGGCCAGTGGCGTGCGGGAATTACATTTATTACTAAGCCAAACTTGCATGCTATTTCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21137
Status:
Mutation detected in F1 DNA
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
ENSDART00000111762 Nonsense 841 870 17 18
Genomic Location (Zv9):
Chromosome 7 (position 70376388)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 68925423
GRCz11 7 69148194
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGCACACAATCTCACACACTCAACCACGTGTCTCAACAGGAACACTGCC[C/T]GACTTCACAATTGTCCTTCTTCCCTCGACCCTGCTATTCCAGAGAGCCAG
Long Flanking Sequence:
AATCTGGACAAAAGCATATCGATTTATGGACTTCAATGATCACACAAGTTACGTAATGCTGGAGTTTGTGACTGCTTGGCTACTGTAAAAGATCAAACTCCACAGGATTTAGCTGCTTGGCGTTGTTCAGCAATATATTTCCAGAAATAGGTTGACGGCTAAATCTGTTTAACATAATTGATTTGCATGCTGAATCCTGTGTGTTTTCCCGCAGTCGTCTATCACCATGGGAACAGTGCCACGGGTGGCCACTACACTACAGATGTCTTCCACATCGGTCTGAACGGCTGGCTGCGCATTGATGACCAGGCGGTGAAGATCATCAATCAGCATCAGGTGGTGAAGCAGACTGCAGAGCGCACTGCCTACCTGCTGTACTACCGCCGCGTGGACCTGATGTAGAAACCATACGCATACAACACAAACACACATACACGTTTACATGCAGACACGCACACAATCTCACACACTCAACCACGTGTCTCAACAGGAACACTGCC[C/T]GACTTCACAATTGTCCTTCTTCCCTCGACCCTGCTATTCCAGAGAGCCAGCTTTTCCAATTTTTCTTTTCCGTTTTGGGAAGACGTATCTAAAGACTTTTTCTGTAACGGTGTTTTCCCCCTCTGCACACGGTCTGGAGAAGCCGAGGGGAGAATTGTTAGCACTGCAGAACGCTCCAATTTGGAGAGACAGACCTGAATCACTGCAAATGTCCACAGCCTTTTTTGTTTGACTGGCCAGAGTGTGGATCCCTGCTGAAAGGACTCAAACCAGGCTGATGGACTGCTGGAGAAAATCATTGTTTCTTTGATTTTTGTTTAATCTACTTTTTAAAAATGGCATAGGAAAAAAAAATATGAAGTGTTTTGCCTTTTAGCAAGAGGAGTTGTCGGCCTAATTTGCAGCAGTTAAGTGGAGCCTGTTCAATTCTTGACTGAAGCATCAGTGGCCAACACCAGCAAGCTACCAAAATAATTTGTGAAAATCTCAATGTTTGGAGT
Associated Phenotype:
Not determined