ZMP
usp22
Ensembl ID:
ZFIN ID:
Description:
Ubiquitin carboxyl-terminal hydrolase 22 [Source:UniProtKB/Swiss-Prot;Acc:A6H8I0]
Human Orthologues:
USP22, USP51
Human Descriptions:
ubiquitin specific peptidase 22 [Source:HGNC Symbol;Acc:12621]
ubiquitin specific peptidase 51 [Source:HGNC Symbol;Acc:23086]
ubiquitin specific peptidase 51 [Source:HGNC Symbol;Acc:23086]
Mouse Orthologues:
Usp22, Usp27x, Usp51
Mouse Descriptions:
ubiquitin specific peptidase 22 Gene [Source:MGI Symbol;Acc:MGI:2144157]
ubiquitin specific peptidase 27, X chromosome Gene [Source:MGI Symbol;Acc:MGI:1859645]
ubiquitin specific protease 51 Gene [Source:MGI Symbol;Acc:MGI:3588217]
ubiquitin specific peptidase 27, X chromosome Gene [Source:MGI Symbol;Acc:MGI:1859645]
ubiquitin specific protease 51 Gene [Source:MGI Symbol;Acc:MGI:3588217]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14142 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14142
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 |
---|---|---|---|---|---|
ENSDART00000059143 | Essential Splice Site | 403 | 466 | 10 | 13 |
Genomic Location (Zv9):
Chromosome 12 (position 1699058)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 1492951 |
GRCz11 | 12 | 1521269 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGAACGGACAGTACCAGCAGCCAGTAGACTCATTAAACAATGATAACAA[G/A]TAAGTCCACGTCCATATTTATATAAAAAATATATATTCATATTATATTTA
Long Flanking Sequence:
CATCTGCTGTTAATTACTAGCCTATAGCGCCATCTACTGTTAAAATCTAGCCTAGAGCGCGATCTGCTGTTTAAAACTAGCCTAGAGCGCCATCTTCTGTTAAAAACTAGCCTACAGCACAGCCTGCTGTTAAATAGTAGCCTAGAGAGCACAGTCTGCTGTTAAATACCAGCCTAGAGTACCGTCTGCTGTTAAATACCAGCCTAGAGCGCCATTAGCTGTAAAATACCAGCCTAGAGCACCGTCTGCTGTTAAATACCAGCTTAGAGGGCCATCTGCTGTTTAAAAACTAGCCTAGAACGCCATCTGCTGTTAAAAACTAACCTAGAGCGCCATCTGCAGTTAAAACTATGCTAGAGCGTGTCTTCATTATCATCAGTGTGTGATAGAAATAAAAGTATCGAGTTTAACGTTGATGTCTTGGGTTTTTCCTGCAGTAAAGAGAGCCGAATGAACGGACAGTACCAGCAGCCAGTAGACTCATTAAACAATGATAACAA[G/A]TAAGTCCACGTCCATATTTATATAAAAAATATATATTCATATTATATTTATATTTTTTATAATTATTTGATATATTTTTATTCATTTAATGTTTATTTTATTATTATATTAATTAATAAACTTTATTTTTATATTATATTCTATTTATTTTTATATTTATTTATTTATTTATTTAATATAATTTTAGTTTAATTAATTTTGCCAATGGAGCAGGTCACTTATTTTGCAGAAAACAAACATGAATGAGAATGAATCAAGATAGACTCGAGCTCCAAATGATAAGAGTAAAGCCGACTAATATTGTTTGTTTACTGTTTGCTGTAGAAGCTGAAACTGAAGATTACAGTAAGCAACAGTACATTTGCAGCACCTGCTTGAGGTGTTTGACCAATCACAGCACAGTGGCAGTGACATTAGCCAATCAGAGCTCTCTGGGCTTTTGAGAAGGCGGGGCTTGTAGAAACTGTAACTCAAGTGTGTGGTTATGTGTATGTGTTCAG
Associated Phenotype:
Not determined