ZMP
otud7b
Ensembl ID:
ZFIN ID:
Description:
OTU domain-containing protein 7B [Source:RefSeq peptide;Acc:NP_001071212]
Human Orthologue:
OTUD7B
Human Description:
OTU domain containing 7B [Source:HGNC Symbol;Acc:16683]
Mouse Orthologue:
Otud7b
Mouse Description:
OTU domain containing 7B Gene [Source:MGI Symbol;Acc:MGI:2654703]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa42813 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa22940 | Essential Splice Site | Available for shipment | Available now |
| sa15023 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42813
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000041811 | Essential Splice Site | 86 | 917 | 3 | 12 |
| ENSDART00000124689 | Essential Splice Site | 86 | 545 | 3 | 12 |
| ENSDART00000128840 | Essential Splice Site | 86 | 920 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 16 (position 49030081)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 45999302 |
| GRCz11 | 16 | 45966018 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCACGGACAGGACGGCCCCTCTTACATCGACAAGATGAGGCTGTTCAAGG[T/C]AAGACTGTAAAATATTGTTTCGGCATTGATATTGCTGTGTGCACATCTGT
Long Flanking Sequence:
CAATGCATTTGTTTTGCACTAAATTAGTTATTGCTAATGTTGCATTGTTTTTGCAACGTGTTAGGCACTGCAAATGAATCGCAAGTTGTGGGATGTTGCAAAACATTTGCATCTTGTGTTTTATTAATAATGTCATAAGCGACTAGGCGACTCAACTTTTTTTTGGTAAAATAAGTCGACTTCCAAAAATCTAAAGTCATTCAACTCCTAGTATATGTAAATATGTAATTTGCTAAACTTGTGAAGTGCTAAAAAAAAGTTTGAAAATGCATCTAGAAAGTGCTTAAATTTGATCGTAATAACACTAAATACGGCTCTCCTTTCTCAGGAAAGAATTGGGACCTCTCAGCTGCACTGAGTGACTTTGAGCAGCTGAGACAAGTGCATGCTGGGAGCCTCTCATGCAGCTTTGTTGAGGAGAGTGAGTACCCCTCCATTGAGAAGGAGATGGCACGGACAGGACGGCCCCTCTTACATCGACAAGATGAGGCTGTTCAAGG[T/C]AAGACTGTAAAATATTGTTTCGGCATTGATATTGCTGTGTGCACATCTGTAATAGTCACGTCCAAGGATGTGCAATGTTGAGTTGGAATACTTGATCAGACACACAATTTAGAATACATGAGGTTTGTCAAGTCATTGCACTTTGAGTTTAGCCTTAATAGAGTAAAAGTTTTTCATTATATTTTTTCGCAATAACAATTTCAATTTTTGATTTTATACATTGAACACCATGTCATTTTATAGTCAGTTTTTTGTTGTTGATGATGTTTCTGTACCTGAACACTGTTATGCTGTGTTCACACCAAATGCAGTTAAAGCGTGTTGATTTACATGTTAAGTTAATGCAAAGACGCAAATAGACATCCTGCAGCTCAATTCGTTCAAATGATATAGCAGGAGTTAAACTTCTGCAGACATTCGCGCAGTGTTAACCAATCATGAGCTTGCTCTTGTAGACTATGAAGTAGTGCCTGTTGTTGGTGTCCCGAAGGGAAATCCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22940
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 |
|---|---|---|---|---|---|
| ENSDART00000041811 | Essential Splice Site | 237 | 917 | 6 | 12 |
| ENSDART00000124689 | Essential Splice Site | 238 | 545 | 6 | 12 |
| ENSDART00000128840 | Essential Splice Site | 238 | 920 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 16 (position 49035253)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 46004474 |
| GRCz11 | 16 | 45971190 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCTTTAAAGCGAAGGTGGAGATGGCAGCAAACCATGCAGAACAAAGAG[G/A]TTGGATCAGTTTATCTGTTAATTCATTATTTTGTACAAAACCCAAGGCAG
Long Flanking Sequence:
ACTCAACTAAATGACATCTTCAAAACATACTCTGACATTTTAATCTAAATTTAACTGAAACGTACTTTTGTAGCGCTACATATGCTGGCAGTGTGAATTACAACTCAATTACTTGTTTTGAAATTACTGGTGCTTTAAAAAGTCCTTGAATCTGGTGTTTATGAAATAGAGGGAATCCTGACTAATATGTTGTCACAAACAGATTCTCTGTCAGTCGAGTTCTGTTCATAATTTTCTAGTGTAGATGCTATCTATTTCCTAAACAACAGCAAAACGAATGCATGATCATCTAGAAACCACTACCAGATGTTATGTCAGATTTAATCTTAAGATTCAGGAATTATATTGAAAATATTGAACACTATAATGCAGGAATGTGGGGCTTCCATGATCGAGACCTGATGCTGCGGAAGTCTCTCTATGCACTGATGGATCATGGGCAGGAAAGGGAGGCTTTAAAGCGAAGGTGGAGATGGCAGCAAACCATGCAGAACAAAGAG[G/A]TTGGATCAGTTTATCTGTTAATTCATTATTTTGTACAAAACCCAAGGCAGTAGATAATAGTATTATTTGGTATTGTGCTTCCATAAAATATACGCTACTGCAGGATATTTGAAAAAAATTTTTAACAAGGACACATTAAGTAAATGTAAGGCGACAAAATAATGTTTAATACTACTACAAAAGGTTTATGTTTTAAATAAATTTTCTTTTTATTCATTGAAGAATCCTGAAAACACAAAAATACTGCATGAAAGTATTAAGTAAAGCAAATGATGTCAGCATTGTATCATATGTAAAAAGATCTGTTTCTTGAGCATCAAATTAGCAAAGTAAAATGATTAAAATATAACATTTTTAAAGGTATTAAAGAAGCACATAACATTTTAATGACCCCAATTATGAATATAAATGTCATTTTCAGCCTAATTAAATTTTTTATTTATTTATTTTTTTTTTTTTGCAGTCGGGACTGGTTTACACAGAGGAAGAGTGGCAGAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15023
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000041811 | Nonsense | 282 | 917 | 8 | 12 |
| ENSDART00000124689 | Nonsense | 283 | 545 | 8 | 12 |
| ENSDART00000128840 | Nonsense | 283 | 920 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 16 (position 49035956)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 46005177 |
| GRCz11 | 16 | 45971893 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAATGTGTGTTGCGTCCCGCAGTGCCGAATCGCAGGAGGAGCCRGTGTA[T/A]GAGAGCCTGGAGGAGTTTCATGTGTTCGTTCTTGCTCACGTGCTCCGCAG
Long Flanking Sequence:
TTTCTTTTTATTCATTGAAGAATCCTGAAAACACAAAAATACTGCATGAAAGTATTAAGTAAAGCAAATGATGTCAGCATTGTATCATATGTAAAAAGATCTGTTTCTTGAGCATCAAATTAGCAAAGTAAAATGATTAAAATATAACATTTTTAAAGGTATTAAAGAAGCACATAACATTTTAATGACCCCAATTATGAATATAAATGTCATTTTCAGCCTAATTAAATTTTTTATTTATTTATTTTTTTTTTTTTGCAGTCGGGACTGGTTTACACAGAGGAAGAGTGGCAGAAAGAGTGGAACGAGTTGTTAAAACTGGCATCTAGCGAACCAAGGATACACTACAGCACCAATGGCAGCAGCGGGTGTGTGTTTCTTTTTTATTTATTTTTTCCTCTTAATGTGAAGATGTAAACAGAGGATCTCTGGAGTGTCCTGCTCAAGCTGTGAATGTGTGTTGCGTCCCGCAGTGCCGAATCGCAGGAGGAGCCAGTGTA[T/A]GAGAGCCTGGAGGAGTTTCATGTGTTCGTTCTTGCTCACGTGCTCCGCAGGCCCATAGTCGTGGTTGCTGACACCATGCTACGGGACTCTGGAGGAGAAGGTAAATGATGGCTGAATATTTATATTTTGAGCTACTTCGTACATGACTTTTATATATTGTTTTCATCTTTTAACAATGAAAACAATATATACTTCCTAATGCATATTTCCTTACTGTTGTTAACAGGAAGGCCATGAGCTCTTAAAGTCTTACGGTGCTTTCACACCTGTGAATCGATTCATTTGTTCCAAAACGGGGATTAAAATTGTTACACTGCTCTTTGTTCTTGGTGCGGTTCGCTTTCACACAGCAAAGTTTCGAAACAGCCCAAAATAGCTAAAACAAGTCACGTGTGAATAAACTCTCCTCACATTGGTCAAAGTTTCACGGTTTATTTTGCTGACTCCCGCTCAGCTGTCAGGCGAGGTGGTGGTTTTTTGGTGTTTGACAGGGTGCGCGC
Associated Phenotype:
Not determined