ZMP
trim33
Ensembl ID:
ZFIN ID:
Description:
E3 ubiquitin-protein ligase TRIM33 [Source:UniProtKB/Swiss-Prot;Acc:Q6E2N3]
Human Orthologue:
TRIM33
Human Description:
tripartite motif-containing 33 [Source:HGNC Symbol;Acc:16290]
Mouse Orthologue:
Trim33
Mouse Description:
tripartite motif-containing 33 Gene [Source:MGI Symbol;Acc:MGI:2137357]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa1735 | Essential Splice Site | Available for shipment | Available now |
| sa15516 | Nonsense | Available for shipment | Available now |
| sa16614 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1735
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000020116 | Essential Splice Site | 194 | 1176 | 1 | 20 |
| ENSDART00000111005 | Essential Splice Site | 76 | 1058 | 2 | 21 |
| ENSDART00000139603 | None | None | 104 | None | 2 |
Genomic Location (Zv9):
Chromosome 8 (position 11702684)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 10966440 |
| GRCz11 | 8 | 11004145 |
KASP Assay ID:
554-1680.1 (used for ordering genotyping assays)
KASP Sequence:
AAGMTCACCATGCCGGTGCAAGGCCCCCACGGACAGGACACTCGAATCGG[T/A]AAGTTCGGAAAGGGGAAGTGTGATTGGTAAATTCTGTCCCGAAGGATCCA
Long Flanking Sequence:
GACGGTGGCGCAAAAGAGCCTGAGGCGGTTGTTTCAATCGACACGGAGCCGAAAGAAGCAGCAGACGAGGCCAAATCTCAAGAGACCGTTCCCCAGGCGCCGACGACATCCAGCGATAGCAGCAGCAGTGGCGGCGGCGGCGAAGCTACAGACGGGACCCCGAATGCTGAAAGCGCGGATCCTCCTCCTCCACCACCACCACCTCCGCCGCCGCCACCGTCCACCCCAGCGGACAGCACCGCAGCTGCCGCATCACCCGCTGTGGTTACCGAGATGTCGCCTCCTCCACCAGCATCCACATCTTCATCATCTTCCACCCCTGCCGCCCCGATAAACCTGCTGGATACGTGCGCTGTGTGTAAACAGAGTCTCCAGAACCGCGACTGTGAACCCAAACTCCTGCCCTGCTTGCACTCCTTTTGCCTCAAGTGCATCCCACAGCCCGATCGTAAGATCACCATGCCGGTGCAAGGCCCCCACGGACAGGACACTCGAATCGG[T/A]AAGTTCGGAAAGGGGAAGTGTGATTGGTAAATTCTGTCCCGAAGGATCCAGAAGCTACGCATTGCTCAACTGTTTACACTTCATGGCATGTGCAGTCAGTCACATACATGTGAGATCATCAGATCACCTGGTGTTTGGTGTTTAACCCATGCAGTTTTGGTTCTACTTTCTGACTGTAAGTTAGCTTAAAGTAAACGGGTGTCTGTCAGGACGTATTTTAGCTGATAAGTACAGCCATGTGCAGGTAGATAAACACTAGGTCGTTAAACCGTACATTCTCTCTGCACATGGATGCACAGATCCAGGGGGTCATACCTTATCTTCACCCAACAGACCCCAATTATAAGCCTAAATAATTCCTCATCCTAACATTTTTAAGGCTTGTATTTTTACAGTGGGAATAAAGAATGTGTGTGAAGTTGTTAGCTTGAACTGTCTGTGGCATATTTATTTATTCATTTTAGTATCGTCTAATTAAATGCAGCTTATTTTGTGCAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15516
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 |
|---|---|---|---|---|---|
| ENSDART00000020116 | Nonsense | 758 | 1176 | 12 | 20 |
| ENSDART00000111005 | Nonsense | 640 | 1058 | 13 | 21 |
| ENSDART00000139603 | None | None | 104 | None | 2 |
Genomic Location (Zv9):
Chromosome 8 (position 11734451)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 10934673 |
| GRCz11 | 8 | 10972378 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGCTTGAAGATGCYGGCTCTAGCACACTGGATAATATCCTAAGTCGGTA[T/A]ATTTCTGCTAATGCATATCCTACTGTCGGACCCACAAACCCATCRCCAGG
Long Flanking Sequence:
TAAGTTAGCAGTTATATACCTGGCCCGGTTAGTCATAGATTGCAAGTTCAGATCTGTGAAAGTGTGATCATGAGGGTACATATCTAATAAATGGGTGGAAATGCAATAAAGATTCTAAATGTAATAACTTGTGGGTCTAAATCTAATAAAGCAATTAAATGTAATAACTTTTAAAGCCCAAATGCAATAAACCCCTAAACATAATTACGTTTAAGGCACCTAAGGCAACAGAACAAAGACAATCCCTGTACTTGGATCTGTTAATAATGGTCTTCATATAGCAGATGCTTCCTTTACCAAAGCTAAATTAAACAAAGCTCAAACTGACTTTATTTATGAAAAGATACATTCAGGTTGGAGGAGAAAACAAAATATGACTAAATAAAAAAGAAATAAAATGAAGAGACTTTTTATTTATTTATTAATTAATTTATTTATTTATTTTATCTCCAGCTTGAAGATGCCGGCTCTAGCACACTGGATAATATCCTAAGTCGGTA[T/A]ATTTCTGCTAATGCATATCCTACTGTCGGACCCACAAACCCATCGCCAGGACCTTCCACACATTCTCCGGGATCGTCAGGTACTTCAGAACAAAATGTGGAAATTTCTGCAGCAAATCATTGACATGAATTGTTTTGCATTTGAATGTCTGTATAGGTTAGCTTGCATTTACATAATGTCATGAAATATTCATGCAGATGCGTGTTTTTGTATGTATGATATGCTTATATATACCATACTACCCTGCCCTCTTGTACTATATGGCTAAAACTCCCATTCAACCAACCATATGCACCAAAACCCAAGGGCTAAGGCTGTGTCAGCTCTGCTGGCGCCATTAATTCCTGCTCAGCGCTCCAGGTTCCTTATGGCATAATCTGCTGTCCAACCATATGCACAAACCCTGAGGCTAAGACTGCATTCTGCTGCCCTCGTGAATTTGTGCTCCGTCCCAAATGGTGTGCTACCAAACTGCCTCCAAAGCTCGCTAGCACATTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16614
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 |
|---|---|---|---|---|---|
| ENSDART00000020116 | Nonsense | 1090 | 1176 | 19 | 20 |
| ENSDART00000111005 | Nonsense | 972 | 1058 | 20 | 21 |
| ENSDART00000139603 | None | None | 104 | None | 2 |
Genomic Location (Zv9):
Chromosome 8 (position 11749397)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 10919727 |
| GRCz11 | 8 | 10957432 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTTTTTTTCCTTTTGTTTCTGTGCTGTCGTTGCCCTTTTTAGATGTCT[C/T]GAATAATCCAGGTTTATGATGAGGAGAAACAGAGTAATGTCCAGGTAAGANANN
Long Flanking Sequence:
ATGGGCAGCACAAATGTCTTGATACCTCAGGCTGTTGATGTTGCCATCCACTCTGCAGATCTCTCGCACGCCCCCATACTGAATGTAACCCCAACCATGATTTTTCCATCACCAGACTTGACTGATTTGTGTGAGAATCTTGGGTCCATGCAGGTTCCAGTAGGTCTTTGCAGTATTTGTGGTGATTGAGATGCAGTTCAACAGATAATTAATCAGAAAATTTATCTTCTGCCACTTTTCCAAATGATCAACTAGAATTTATTTGTTGCTCTTACAACTGGGATCGACGACAAGACTTTTGTCAGGTAGTGTCGTGTCTTAAAAACCGGAAGGCATTTAATTATGCGCAAAGCCCCAAATTGTGCTCCTTGGACATTTTTACGTACAGATGAGGATGCGACCTCACTGTATAGATGGTATAAAATCTTTCTTCCCCCTTTTCTTTTTGTATTTTTTTTTTCCTTTTGTTTCTGTGCTGTCGTTGCCCTTTTTAGATGTCT[C/T]GAATAATCCAGGTTTATGATGAGGAGAAACAGAGTAATGTCCAGGTAAGATGTTTCGTGCACCACACCGATGGGTTCAGCAGTGCTGGCACTCGAAAGCATCCAAAGCAGGAGTTTTTAACCCTGTCTGTGATTCTCTCCTCCTCTTCCTTCTCCTCTTCATCCGTTCTTCATCCATTCTGGGCCTGCATTTCACCTCCTGGCATTTCCACACTCTTTACCCTCTCCCTCCCTCTTCTAGGCCGATTCGGAAGTGGCAGAAGCTGGAAAAGCCGTGAGTCTGTACTTTGAGGAGCGATTGCTGGAGATTTTTCCAGAGCAGACGTTCCCGGTGGTGATGGAGAAGGAAACTCAAATCGAGGCCGAAAAGGAGGATTCGGACGACTCCGATGATGACATCATACAACCCAAACGCAAACGCTTAAAAGTGGACACAGAGATGCTGCTGCACATCAAGTGAGGAAGAAGATCATGAGGAAACGTCTGAAAGAAATAAACCGT
Associated Phenotype:
Not determined