ZMP
NP_001082871.1
Ensembl ID:
Description:
ubiquitin carboxyl-terminal hydrolase 43 [Source:RefSeq peptide;Acc:NP_001082871]
Human Orthologue:
USP43
Human Description:
ubiquitin specific peptidase 43 [Source:HGNC Symbol;Acc:20072]
Mouse Orthologue:
Usp43
Mouse Description:
ubiquitin specific peptidase 43 Gene [Source:MGI Symbol;Acc:MGI:2444541]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45247 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33838 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40665 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9269 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa45247
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085669 | Nonsense | 13 | 1154 | 1 | 15 |
ENSDART00000112731 | None | None | 1011 | None | 15 |
Genomic Location (Zv9):
Chromosome 6 (position 18260791)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 23193491 |
GRCz11 | 6 | 19664812 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGACGGACTAAACATGGATTCGCTGAGGGAAACCAGGAAACAAACAATC[A/T]AAGCTAAATCGGCGAAGCGCAAGAACAAAACGCACAAGTCCCAAAAGCTG
Long Flanking Sequence:
CAAAGTAAACCAGGCTAATAAGATTCATTGTGGGAGGGTAACGCCGTGCATCTACCATTCATACGCATACTCCAACCACAAGCCAGAGCAAGAGAGAGCGGGCGAAATACAGCCAGTAATGGGCATCCACACACGAGCACGCAGGTAGGTGTGGTGTAAAAGAACGAGAGTTGTGTCTGAAGCATGGAGTTCAGCCCAGTGTATTTCCAGGTGCGTACGAGAGCGTCATGGATAAATCGAAAGTAGCGCAGCAGAGAACAGCGATAAGGAATGTCGGGGACGCGATAATTACGAGCCTCGGTGCAAAAACCGGTGCCTTTAGAGTGTTTTTTTCATCGTCGTGATGGTTTAGCGATGAAGGATTTTGAGACGCACAGGTGGGAGCGACGTGTCTTTACACCGCCGTGCACTTGTTTCTCTTACTGACGTCCACCGCTCGGTTTGGGCGAAACGACGGACTAAACATGGATTCGCTGAGGGAAACCAGGAAACAAACAATC[A/T]AAGCTAAATCGGCGAAGCGCAAGAACAAAACGCACAAGTCCCAAAAGCTGTTCCGAAGGAAATCGTTAAAATCGCTGGGAAATTTTATGAGCAGGATTGTCAAAACTTTGGGCACTTTGGCACACTTGGGGGACGCGGATCAGCCGGACGCAGCAGCGGAGGATGATGATGGTGGATTTGGAGACACGGCGAGTGTCCACAACTCTGGGAACTACAGAGAGAGCTCGGCGAGGAAAAGCTCTTCTTACGGGTCTGTGAAAGAAAGACTGTCCTGGTGTTACGGAGAGAAAACACCGGGAGTTCAGGGTCTGAAGAATCACGGAAACACCTGTTTTATGAACGCTGTGGTGCAGTGTCTGAGTAACACAGAACTTCTGGCTGAATATCTGGGTCTGGAGCAGTATAAATATGAATTAAATGAGCGGAGGATCAACGGGATGATGAAGAGTGAGGAGGTCAGAGGGGAAGTCACGGACAAGCTGGCATCGTTAGTAAGGGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33838
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 |
---|---|---|---|---|---|
ENSDART00000085669 | Nonsense | 579 | 1154 | 11 | 15 |
ENSDART00000112731 | Nonsense | 439 | 1011 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 6 (position 18489111)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 23039439 |
GRCz11 | 6 | 19510760 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATTGAGGATGCAGAGAGTGTGAGAATCCAGCAGCAGAATCATGTACAA[C/T]AGCACAGCTGCACACTGGATGACTGTTTTCAGCTCTACACCAAAGAGGAG
Long Flanking Sequence:
CTTAATAACTAATTTACTATTAGCTAACCACACCCTTTAATTTACTACAGGAAAAAATAAATAAGGAATGTCACTGCATTTTCTATAACATTCAGCAGGGAGGTTGTCTTGCAATGCTCGCTCCTTCTCTGAATTCACTACACTGATTATTTTCTGCCCCCTGGTGGCTAAATTCCAAACCCACATTTGAATTGATTTTTCCTCTTCCAGAGCCCTCAAGTTATGTGGTCCAGGTGGTCCTTTGCATGTGAAGCTCATAATTGAATGGGACAACAAAATTAAAGAATGGTGAGATACATGCAGCAGCATAAATCTTCTTATTTTTTAGACATTCGTTTAATTTAAGATCACAGTAAGAGCCAAATGCCTTAGTATTAGTAAGAGTGCAACATAATTTGTAATTTACTATTCATATCTGTTTTAGCCTCTTTGGCAATATTCAAGAGGAGGTGATTGAGGATGCAGAGAGTGTGAGAATCCAGCAGCAGAATCATGTACAA[C/T]AGCACAGCTGCACACTGGATGACTGTTTTCAGCTCTACACCAAAGAGGAGCAGGTATTCTTTCATCCAGTTACTTTCCCTGTTTATTTATCTATCCTCACAAAGGCTGCATTTCTTTGATCAAAAATATACACTGCTCAAAAAAATTTAAGAAAACTCCTGGGATTATGATCTGATCAGTTGAAGTAACACTCCACTATTTGTGAAAATAGGCTCATTTTACAAGTCGCAAGTTCTATCATTTTTTAATCCATTCAGCCAATATCCAGGTCTGGTGGGAGAGCTTTTAGCTTAGCTAAGCAGAGTTAATTGAATCAGATTAGACCATTAGCATCCAGCTCAAACATTTTTGGTCATTTTTCAATTTAAAACTTGACACTTCTGTTGTTACATTGTGTACCTAGTTGAAAAGTTGCTATTTTCTAGGCCGATATGGCTGTTCTCTCATTCTGGTGTAATAATCAAGGAATGCAGTTGCCACAATGATCTTGGGGAAAGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40665
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085669 | Nonsense | 916 | 1154 | 15 | 15 |
ENSDART00000112731 | Nonsense | 773 | 1011 | 15 | 15 |
Genomic Location (Zv9):
Chromosome 6 (position 18517760)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 23010790 |
GRCz11 | 6 | 19482111 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAAAACAGCCAAATCTTCCAGCCACAGTGGCCTCAGACCTCCAGAATA[T/G]CTGAAAATACCACAGGGTCAAGAAAGAAGTAGCTCAGAGAAAGCAATGGG
Long Flanking Sequence:
AGAGTCACCAGTTTTTAAAAATGAACCCTCAATTGAGGAAAGAGGTCAGTTTAACCACAAAGTTTTTTTTTCTTGTGATTGTAACCAGAATTCAACGACCTTTTAAATAGATTTCATAATAATTATTTCTTCATTTGTTGTTGTGGACAAGTGTCTTCCACCATGTTCTGAATATTTGCGTTTATGCCAGTGTCTTTAGGTGGGTTTGAAAGCAGACCTTTTGTGCGAGGAATCCAAGGTCGTAGTGTAAGCATGAGAAGTCCCACCAAGAGTAAAGTGCTCCCACTGCGATGGTCTTTTGGAAATAAAGACCGCCACAAACCTGTGCCGGCTTCTGAGCAGTCTCCTGCAGAACTGGTGGAGTATTTAGAGTCTGGGAGGAGACCAAGATGTACCAAAGACCCTATTGTTTCCCTAATGACTCGACCTTCAGACAAAGACAACGATGCAAAAAAAACAGCCAAATCTTCCAGCCACAGTGGCCTCAGACCTCCAGAATA[T/G]CTGAAAATACCACAGGGTCAAGAAAGAAGTAGCTCAGAGAAAGCAATGGGCCAACAACCTGCCAGCAGCAGTAGATCAAGAGAAGAAGGGACCTTGACCAGACGGAGCAGCAGAAAATCTAAACCGGACCAATCACACTCCAGGAAGAGCTCTGGAGCAGGGATCCAGTCCAGTTGTAGTACTCCAAGTGGCTGGGAAACAGCACAGAAGCATGAGTCGAGTGACAAGCGTGACCAATCAGAGGATAAACATAAAAAAGGGCAGGAGACTAAACGTCATGATGTCTTCGCTTTTCTCAAAGGTGGCTTTATCAAGAAGGATTCCCTTCGGAAGTCTCGGGATAATGATTCTGTCAAAAAGGCTGATTCAGGGGTGAAGAGCCCATCTGGAGTTTCCCTCTCCAACGGGACACATAATAAAAATCCAGAAGGTAAAGTCAGTACTATGAACCATGGTAGCAGGCACGGAAGTGAACTGGCAAATGGCAAGGTGAGTCGTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9269
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 |
---|---|---|---|---|---|
ENSDART00000085669 | Nonsense | 935 | 1154 | 15 | 15 |
ENSDART00000112731 | Nonsense | 792 | 1011 | 15 | 15 |
Genomic Location (Zv9):
Chromosome 6 (position 18517815)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 23010735 |
GRCz11 | 6 | 19482056 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAATACCACAGGGTCAAGAAAGAAGTAGCTCAGAGAAAGCAATGGGCCAA[C/T]AACCTGCCAGCAGCAGTAGATCAAGAGAAGAAGGGACYTTGACCAGACGG
Long Flanking Sequence:
CACAAAGTTTTTTTTTCTTGTGATTGTAACCAGAATTCAACGACCTTTTAAATAGATTTCATAATAATTATTTCTTCATTTGTTGTTGTGGACAAGTGTCTTCCACCATGTTCTGAATATTTGCGTTTATGCCAGTGTCTTTAGGTGGGTTTGAAAGCAGACCTTTTGTGCGAGGAATCCAAGGTCGTAGTGTAAGCATGAGAAGTCCCACCAAGAGTAAAGTGCTCCCACTGCGATGGTCTTTTGGAAATAAAGACCGCCACAAACCTGTGCCGGCTTCTGAGCAGTCTCCTGCAGAACTGGTGGAGTATTTAGAGTCTGGGAGGAGACCAAGATGTACCAAAGACCCTATTGTTTCCCTAATGACTCGACCTTCAGACAAAGACAACGATGCAAAAAAAACAGCCAAATCTTCCAGCCACAGTGGCCTCAGACCTCCAGAATATCTGAAAATACCACAGGGTCAAGAAAGAAGTAGCTCAGAGAAAGCAATGGGCCAA[C/T]AACCTGCCAGCAGCAGTAGATCAAGAGAAGAAGGGACCTTGACCAGACGGAGCAGCAGAAAATCTAAACCGGACCAATCACACTCCAGGAAGAGCTCTGGAGCAGGGATCCAGTCCAGTTGTAGTACTCCAAGTGGCTGGGAAACAGCACAGAAGCATGAGTCGAGTGACAAGCGTGACCAATCAGAGGATAAACATAAAAAAGGGCAGGAGACTAAACGTCATGATGTCTTCGCTTTTCTCAAAGGTGGCTTTATCAAGAAGGATTCCCTTCGGAAGTCTCGGGATAATGATTCTGTCAAAAAGGCTGATTCAGGGGTGAAGAGCCCATCTGGAGTTTCCCTCTCCAACGGGACACATAATAAAAATCCAGAAGGTAAAGTCAGTACTATGAACCATGGTAGCAGGCACGGAAGTGAACTGGCAAATGGCAAGGTGAGTCGTGGTTCCTCAGACATCAAACGCTCACAAAGCTCATCCAATATTCAAAGCAAAACTGAT
Associated Phenotype:
Not determined