ZMP
c13orf22l
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC445403 [Source:RefSeq peptide;Acc:NP_001003880]
Human Orthologue:
USPL1
Human Description:
ubiquitin specific peptidase like 1 [Source:HGNC Symbol;Acc:20294]
Mouse Orthologue:
Uspl1
Mouse Description:
ubiquitin specific peptidase like 1 Gene [Source:MGI Symbol;Acc:MGI:2442342]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34950 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa34951 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34950
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 |
|---|---|---|---|---|---|
| ENSDART00000043802 | Nonsense | 287 | 1014 | 4 | 9 |
The following transcripts of ENSDARG00000034825 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 37687512)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 36499673 |
| GRCz11 | 10 | 36443431 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATTGCTCACACTGAGGAGAAACCTGTGTCTCTTGTTCACACTGAGGAT[C/T]AACATTTGTCTATTGATCAAACAGAGGAACAACCCATCTCAATTGATCCC
Long Flanking Sequence:
ATGCTGAAGTCAATGATGCCACCCTTCCAGACGACACTGTCAAAACTCAAACGTTTACAGATCAACAGTCAGCACCTGCAGAGACTATTTCTCTTGATAAAACTGAAGAACAACCTGTTTCTATAGAAGACATTAAGGAACAACCTATCTCTCATGATGCCACTGAGGGGCAACCTATATCTATTGATCAAACTGAGGAGCAACCCGTTTCTATTCTTCACACTGAGGAGCAACCTATAGTTCTTGATCTCATAGAAGTAAAACCTATGTCTGTTGATCATTCTGAGGAACAACCTATCTGTATTGATAACACCAAGGAACGACCTGTTTCTATTGTTCACACTGAGGAGCAATCCATAGTTCTTGACCTCTTTGAAGTTAAACCTATGTCTATTGCTCACACTGAGGAGAAACCTACATCTTTTGATCACATTGAGGAGAAGCCTATGTCTATTGCTCACACTGAGGAGAAACCTGTGTCTCTTGTTCACACTGAGGAT[C/T]AACATTTGTCTATTGATCAAACAGAGGAACAACCCATCTCAATTGATCCCACAGAGGAGCAACAACCCGAGGAATTACCTGCTGTCTCTGATGAGGATGTAGACTTGTGTGAAAGGAAGGAGGATTGTGTATCCAGTACTCAAGATGAGATGGAGGAGGAGGTCTTGGAGAGTTCTTCAGAGCTGGTCCCGGTTCATTCTGAACTCTTCTGGAAAAACGAGGAGAACATGTGCTGGTTGGATGCGATGTTGGTGATGCTGGTGCACTGCAGGACCATCAGAGGGACTCCATGTCGGGGCATAAAGCTGAGCGATAAGTTGGCAACAGTGCCTTGCAATGATTCTGTCGTCTGGAAACTTTGCTGGAGATATGATAAAACGTGTGCCTATCTCCAAGCCAGGAAGAAACAGAGCGAAGGTAAGAAAAAGACATATATTGGCATTTGTACAGTGTTTGATTTTTGACCCCCTGATTTTGAACCATTAAAGGATGTGGAATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34951
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 |
|---|---|---|---|---|---|
| ENSDART00000043802 | Nonsense | 360 | 1014 | 4 | 9 |
The following transcripts of ENSDARG00000034825 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 37687731)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 36499892 |
| GRCz11 | 10 | 36443650 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGTTCTTCAGAGCTGGTCCCGGTTCATTCTGAACTCTTCTGGAAAAAC[G/T]AGGAGAACATGTGCTGGTTGGATGCGATGTTGGTGATGCTGGTGCACTGC
Long Flanking Sequence:
ACACTGAGGAGCAACCTATAGTTCTTGATCTCATAGAAGTAAAACCTATGTCTGTTGATCATTCTGAGGAACAACCTATCTGTATTGATAACACCAAGGAACGACCTGTTTCTATTGTTCACACTGAGGAGCAATCCATAGTTCTTGACCTCTTTGAAGTTAAACCTATGTCTATTGCTCACACTGAGGAGAAACCTACATCTTTTGATCACATTGAGGAGAAGCCTATGTCTATTGCTCACACTGAGGAGAAACCTGTGTCTCTTGTTCACACTGAGGATCAACATTTGTCTATTGATCAAACAGAGGAACAACCCATCTCAATTGATCCCACAGAGGAGCAACAACCCGAGGAATTACCTGCTGTCTCTGATGAGGATGTAGACTTGTGTGAAAGGAAGGAGGATTGTGTATCCAGTACTCAAGATGAGATGGAGGAGGAGGTCTTGGAGAGTTCTTCAGAGCTGGTCCCGGTTCATTCTGAACTCTTCTGGAAAAAC[G/T]AGGAGAACATGTGCTGGTTGGATGCGATGTTGGTGATGCTGGTGCACTGCAGGACCATCAGAGGGACTCCATGTCGGGGCATAAAGCTGAGCGATAAGTTGGCAACAGTGCCTTGCAATGATTCTGTCGTCTGGAAACTTTGCTGGAGATATGATAAAACGTGTGCCTATCTCCAAGCCAGGAAGAAACAGAGCGAAGGTAAGAAAAAGACATATATTGGCATTTGTACAGTGTTTGATTTTTGACCCCCTGATTTTGAACCATTAAAGGATGTGGAATGTCTTATTTTATATACACAAAGTTATTTAGTAAAAAAGGCAAACTATGGCTTATCACAGAATATATGAGTGTTATGATGCACAAAAGTTAAGCGTTTATTTACTGCAGTCTAATCACCTTATTATTGTTTGGTTCTTCCTTATATAAGCCAGAGCTGCACAAATAATCGAAAAAAGATCGCGATCTCGATTCGACCCCCTAGACCAGGTGTGACCAACCCT
Associated Phenotype:
Not determined