ZMP
otud5a
Ensembl ID:
ZFIN ID:
Description:
OTU domain-containing protein 5-A [Source:UniProtKB/Swiss-Prot;Acc:Q08BW0]
Human Orthologue:
OTUD5
Human Description:
OTU domain containing 5 [Source:HGNC Symbol;Acc:25402]
Mouse Orthologue:
Otud5
Mouse Description:
OTU domain containing 5 Gene [Source:MGI Symbol;Acc:MGI:1859615]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34303 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41124 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa34304 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45310 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21204 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34303
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 |
---|---|---|---|---|---|
ENSDART00000081999 | None | None | 464 | 2 | 10 |
ENSDART00000139150 | None | None | 283 | None | 7 |
ENSDART00000144986 | Nonsense | 76 | 560 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 8 (position 9406164)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 8822746 |
GRCz11 | 8 | 8861331 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCGCCGGCGTCCAGAGAGGACAGGCGAACTGAATCCAGCTCCCGGCCG[C/T]AGCAGGCCTCTCCTCCGCCGGTGGGTGCCGGGTCCTCGGGTGGCCCCGGG
Long Flanking Sequence:
TTCAGAAGCCGAAAGGCGGAACAAGCAGCGAGACGGAAATGACGTGATGGCGTCGTCAGCTGTATGTTGATGTTGTGTGGCAACAGCAGGACCGAGGGACGGAAGACGGTTTGTTTTTGTTCTGTTATCCGCCGTTTTTACCCTCAAAATCACCTCGAGTTGAATCAAATTCGCTCCGGGGTGAAAGGGGCGAACATTACAACACACAAGACGCTCAAGTTTAAATGTTAAACCGCGTTCGGAGGCGTTAAAACGGACACCCTTCCTGAACGGTCATGACGATCCTGCCGAAGAAGAAGCCGAACTCGTCGGTCGGTGTGTCCGATCACCCTGACGACCCCGACCGACGGACCGGCTCCGACCCGCACCAGCATCAGCACCAACACTCCCACGGGGTCCGGCCGGGTGCGAGGCCCCGCGCTTCCCCGCCACCCTGGTCCTATCAAGCCGCTCCGCCGGCGTCCAGAGAGGACAGGCGAACTGAATCCAGCTCCCGGCCG[C/T]AGCAGGCCTCTCCTCCGCCGGTGGGTGCCGGGTCCTCGGGTGGCCCCGGGGACGCGACAGGGATGGCGTGCGTGTCAGGCAATCGGGCTGAGCTGTCAGGTGGGGTGGGCTGTGGAGGTGGCATGGGAGGTTGCTGTTCGGGGCCTGGGCTCAGTAAGAGAAGACGACAAGCGACTTGCTCCGGTGGGGTGGCCGGTGGAGGCACCGGACCCGGGGCTGCGGGGGGTGGAGGCGGCGGTGGTGGAGGAGGTGGAGTAGGGGGTCCCAGTCCCGAGCAGGAGGAAGGAGCCGGGTATAACAGTGAGGATGAGTATGAGAATGCTTCCAGACTACAGTCAGAGGACCCAGCGACTGTTGAACAGGTATGTGGATGGATGATGTCACCTAATGCTGAGAGTCATAAACAACTGTTTAATGTGTGACACGTGGTCTGACAATGTTCAGACAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41124
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 |
---|---|---|---|---|---|
ENSDART00000081999 | Essential Splice Site | 100 | 464 | None | 10 |
ENSDART00000139150 | None | None | 283 | None | 7 |
ENSDART00000144986 | Essential Splice Site | 196 | 560 | None | 9 |
Genomic Location (Zv9):
Chromosome 8 (position 9406528)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 8823110 |
GRCz11 | 8 | 8861695 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGAATGCTTCCAGACTACAGTCAGAGGACCCAGCGACTGTTGAACAGG[T/A]ATGTGGATGGATGATGTCACCTAATGCTGAGAGTCATAAACAACTGTTTA
Long Flanking Sequence:
GCACCAGCATCAGCACCAACACTCCCACGGGGTCCGGCCGGGTGCGAGGCCCCGCGCTTCCCCGCCACCCTGGTCCTATCAAGCCGCTCCGCCGGCGTCCAGAGAGGACAGGCGAACTGAATCCAGCTCCCGGCCGCAGCAGGCCTCTCCTCCGCCGGTGGGTGCCGGGTCCTCGGGTGGCCCCGGGGACGCGACAGGGATGGCGTGCGTGTCAGGCAATCGGGCTGAGCTGTCAGGTGGGGTGGGCTGTGGAGGTGGCATGGGAGGTTGCTGTTCGGGGCCTGGGCTCAGTAAGAGAAGACGACAAGCGACTTGCTCCGGTGGGGTGGCCGGTGGAGGCACCGGACCCGGGGCTGCGGGGGGTGGAGGCGGCGGTGGTGGAGGAGGTGGAGTAGGGGGTCCCAGTCCCGAGCAGGAGGAAGGAGCCGGGTATAACAGTGAGGATGAGTATGAGAATGCTTCCAGACTACAGTCAGAGGACCCAGCGACTGTTGAACAGG[T/A]ATGTGGATGGATGATGTCACCTAATGCTGAGAGTCATAAACAACTGTTTAATGTGTGACACGTGGTCTGACAATGTTCAGACAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAAGACAGACACCAGTTGAATGGATAGATATACAGACAAGATAAGATAAACTGAATGATTTGACAGATTGATGTTGACAGCTACTGTTAGTCTTTATAAATGCAAGGAATACACCAGGTTTACTATTGTATTTATATTATTATTAATTATTGCGTTTACATTGCCTATTACTGTGAGAATCAAACAAATAAACAAAACAAATATGTGACACCTGATGACAAGATTAGTCTGTTGCTGCAAGGCGGGTATATTATTATTAATACATTTTACAACTCAAAATGATTTTTTATACCAAAAATCATTAAACTTGCAAGTAAAGATTGTGTTTAATATATTATATTATATTATATACTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34304
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081999 | Nonsense | 163 | 464 | 5 | 10 |
ENSDART00000139150 | Nonsense | 23 | 283 | 3 | 7 |
ENSDART00000144986 | Nonsense | 259 | 560 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 8 (position 9449845)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 8866427 |
GRCz11 | 8 | 8905012 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTGCGATATTTGCTTGCAGATGAAAAATGCAGATTACTTCTCAAACTA[T/A]GTGACAGAGGACTTCACTACATACATCAACAGAAAGAGGAAGAACAACTG
Long Flanking Sequence:
CACACAGAAATGCCAACTGACCAGCAACCTTCTTGCTGTGAGGCGACAGTGCTACCCATTGCACCACCGTGCCACCTGCAAATAATAAACACCTAAAAATATTAAAGTTTCATGTGATTTTCTCAACTAGCAGTGTTTTGAAATTAATGAAAGCATAAAAATCATAACCGTGAAACTGTGATTATTTCTCAGACTGTAATCGTATAACCAAAATCTATAATCGTTCCATCCCTATTGTGCAGCAGACACTACAATAAATGCTATATTAGTCATATGTTTACTCATAACCCTGGTATTGTTCTTTTTACAGCTGATCAAGTTTACGGAGACCAGGATATGCACGAAGTCGTTCGCAAGCACTGCATGGATTACTTGGTACGTACTTTTTTTTTTTTTTTTTGGCATGAATCATCGATGTGTAGAGAACCGGTTTAATTAAATTCAGGCTTTCTCTGCGATATTTGCTTGCAGATGAAAAATGCAGATTACTTCTCAAACTA[T/A]GTGACAGAGGACTTCACTACATACATCAACAGAAAGAGGAAGAACAACTGTCATGGCAACCACATTGAGATGCAGGCAATGGCAGAGATGTACAATCGGCCAGTTGAAGTTTATCAGTCCGGCACAGGTTAGTTTAATTTGCATGATGCTGCCTGTGAAACTGAACTATGGACATTTAATTATGTATTCCTCCATGCGGTTGCCTTGATGAATACTAGATTTTTCTCCTATATCATATTTATATGCATGCAGTGTCCTAATAGATACTGTTGAGTCCCATAAGTTGACCTGTATCTCTAAATAATTCTGCTTTTATTTGATGGCTTCTTTCAGAACCAATCAACACGTTCCATGGCATCCATCAAAATAATGACGAGCCAATCAGAGTTAGTTACCATCGAAATATTCACTATAACTCTGTAGTGAATCCCAACAAAGCCACTATTGGAGTTGGGCTCGGACTTCCTGCCTTCAAACCCGGGGTGAGTACATGCAAGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45310
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 |
---|---|---|---|---|---|
ENSDART00000081999 | Nonsense | 244 | 464 | 6 | 10 |
ENSDART00000139150 | Nonsense | 104 | 283 | 4 | 7 |
ENSDART00000144986 | Nonsense | 340 | 560 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 8 (position 9450292)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 8866874 |
GRCz11 | 8 | 8905459 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCGAAATATTCACTATAACTCTGTAGTGAATCCCAACAAAGCCACTATT[G/T]GAGTTGGGCTCGGACTTCCTGCCTTCAAACCCGGGGTGAGTACATGCAAG
Long Flanking Sequence:
TTTCTCTGCGATATTTGCTTGCAGATGAAAAATGCAGATTACTTCTCAAACTATGTGACAGAGGACTTCACTACATACATCAACAGAAAGAGGAAGAACAACTGTCATGGCAACCACATTGAGATGCAGGCAATGGCAGAGATGTACAATCGGCCAGTTGAAGTTTATCAGTCCGGCACAGGTTAGTTTAATTTGCATGATGCTGCCTGTGAAACTGAACTATGGACATTTAATTATGTATTCCTCCATGCGGTTGCCTTGATGAATACTAGATTTTTCTCCTATATCATATTTATATGCATGCAGTGTCCTAATAGATACTGTTGAGTCCCATAAGTTGACCTGTATCTCTAAATAATTCTGCTTTTATTTGATGGCTTCTTTCAGAACCAATCAACACGTTCCATGGCATCCATCAAAATAATGACGAGCCAATCAGAGTTAGTTACCATCGAAATATTCACTATAACTCTGTAGTGAATCCCAACAAAGCCACTATT[G/T]GAGTTGGGCTCGGACTTCCTGCCTTCAAACCCGGGGTGAGTACATGCAAGTGAATGAGCATTTGTGTCCTGTTTTCATAATCTACTTTTGAGTTTTTGAGTGAGGCAGGATATGCAATGAGAGCTAATTCTATTTAAATAGAATTGATTTGATTATTAAAAGTCTTTACATTTGATCAAATGGGTTACTGTGGAATTTTATAAAGTCCATTCGCCACAAAAAATAACTTTGCGCCACTTTATTAGGTACACCTGTCCAACTCCTCGTTAACGCAAATTTCTAACCAGCCAATAATATGCCAGCAACTCAATGCATGTAGACATGGTCAAAACGATCTGCTGCAGCTCAAACTGAGCATCAGAATGGGGTATGAGTATTTCAGAAACTGCTGATCTGCTGGGAGTTTCATGCACCACCATCTATAGAGTTTTCAGAGAATGGTCCGAAAAAGAGAAAATATCCAGTGAGCGGCAGTTCTGTGGGCGCAAATGCCTTGTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21204
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 |
---|---|---|---|---|---|
ENSDART00000081999 | Nonsense | 342 | 464 | 8 | 10 |
ENSDART00000139150 | Nonsense | 202 | 283 | 6 | 7 |
ENSDART00000144986 | Nonsense | 438 | 560 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 8 (position 9463843)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 8880425 |
GRCz11 | 8 | 8919010 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGCTCTGCCACGGCTGCGGCCTCCAGTGGTTTGGAAGAATGGAATGCT[C/T]GATCTCCACGGCAACGAAGCTCCGCCCCTTCTCCGGAGATTCCTGATCCC
Long Flanking Sequence:
TCTTTGCTATTACTGGTTATATACCTCAACATATCCTTTGAGGGTGCAGCTTCTGAAATAAGACACATCTATTGACCTCCATAGTGGAAAAAAAATTACAATGGAAGTCAATGGGTACCATCACCCGGCATTTTTCAAAACGGTCTTCCTTTGTGTTCAACACAAGAAAGAAACTCAAATAGGTGTTGAACAAGTAATAAGGGAGTAAATAATGACAGTGTTTAAATTTGGTGATTAAACTATTCCTTTAATACTTTTGATTGTTTTTGATAAAAAAAATGCAGCCTTCCTGAGCAAAAGTCATCCCAAACGTAGAAGCGCTAGTGTATCTTGCGTAAGCATTTAGTAAATGCCCTGATGTAAGAATGTTAACTGTTCTCAAGTGACAAAGTGGCTCATTTGTGAATGAATGTGTTTACTGTTGCCAGCCTCGTAAGGCCAGTGCTACGTGCAGCTCTGCCACGGCTGCGGCCTCCAGTGGTTTGGAAGAATGGAATGCT[C/T]GATCTCCACGGCAACGAAGCTCCGCCCCTTCTCCGGAGATTCCTGATCCCGCACACTCGGACACAGCGGCCAAACCCCCGTCCCCCGCCGGAGCCCTCGCTCTGTCCAAACCTCCGTCGCCCTGCGCACCAGGTCTGTTATCAGGAGACGCTGTCATTAGCTTTATCAGGCCAACTGGGTGATGCATTTCCTCCAGCAGGACAATATATAGAGTAAATGCCATATGCTGTTTGCTGATAATTAAAATTAATTACAATGGAAAATGGTGTCAGGATCATGACTGGGTCGTATTTCTGCCCAAAATCTTAAGGAATATATACAGTTGAAGGCAAAATTATTATTATTATTATATGTTTGTAAAAATTACATTTTTTTAAAAATATTTCCCTTATTTTCACAGTATTTTAAATAAAAGTTTTTTCTTCTGGATAAAGTTTTATTTATATTATTTTATTTTTTTGTATAATTTTTTTTTTCCAATGACTTGCCTTTTTGATCAA
Associated Phenotype:
Not determined