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 |
sa2432 | Nonsense | F2 line generated | Not yet available |
sa27135 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa27136 | Nonsense | Mutation detected in F1 DNA | Not yet available |
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:
sa2432
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000020116 | Nonsense | 325 | 1176 | 4 | 20 |
ENSDART00000111005 | Nonsense | 207 | 1058 | 5 | 21 |
ENSDART00000139603 | None | None | 104 | None | 2 |
Genomic Location (Zv9):
Chromosome 8 (position 11717960)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 10951164 |
GRCz11 | 8 | 10988869 |
KASP Assay ID:
554-2924.1 (used for ordering genotyping assays)
KASP Sequence:
AGAYCTGYGACACTCTGACCTGCAGAGACTGCCAGCTACTTGAACACAAA[G/T]AACACAGGTCAGCCGGACAGCACTGTTTACACTTTACACACAACAANNNC
Long Flanking Sequence:
ACTAATTAATTTGCATATTAATCTGCTTTTATTTGCAAGGCAGTTACGATATGATCGTTTTCGTTATGACTTTGCTTTGCTCTAGTGGCGCGGTTGACGTTTGGATCTTTCTGCAACTGTGTACGGAGTGTCTGTTTTTCGCATTAAGCAGGCAGTACCGTAGTACAGTTGCTATGGCAACAGGCAGAGTTTTAGAGAGAGTCGCTTGCTCGGCCTGTACTGTTTTCATTAAAGCTAACCCACTTAGTTTTCCTCATTTCGATAGAGTTTGGCAAGGGGCATATGAGAACATATGGGAGTCGTAGACTGTGAGAATAAAGTACAGCAGGGAGAAGTAATCGAAACAACGTGCATTTGATTGGTTGTGTGTTGTAGAGTCTGTTGGGACATCAGGCCAGAGACCAGTTTTCTGTCCGGTACACAAACAAGAGGCCCTCAAGCTCTTCTGTGAGACCTGCGACACTCTGACCTGCAGAGACTGCCAGCTACTTGAACACAAA[G/T]AACACAGGTCAGCCGGACAGCACTGTTTACACTTTACACACAACAACATCATCATCATCATCATAATAATAATCATCTTCATCTGCACTGTAGTTAATCACCTGGCATTGCATGAAGGGATTTTTAAGCAAGAATATTAAATTGACTTTAGGTACCTCGAATTAAACATCACATTAAAGGAATAGATGACCAGAAATTTCTTTTGTCCTTTGATTTCAGTGATGTGGAAAAGGCAGAATCCAGTCATTAAAAAGTGATTTACTTTACAACGCAGAAAATGTCACATTCATTCATTCATTTTCTTTTCGGCTTAGACCCCTTATTAATCTGAGGTCACCACAGCAGAATGAACCACCAACTTATCCCGCATATGTTTTACGCTGTGGATGCCCTTCCAGCTGCAACCCATCACTGGGAAAAGAAAATGTCACATAATTTGGCAAATTCTAGCTGAATAAATCAAAAGTAGGACTGCACACATACAAATTATGATATGTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27135
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 |
---|---|---|---|---|---|
ENSDART00000020116 | Nonsense | 572 | 1176 | 9 | 20 |
ENSDART00000111005 | Nonsense | 454 | 1058 | 10 | 21 |
ENSDART00000139603 | None | None | 104 | None | 2 |
Genomic Location (Zv9):
Chromosome 8 (position 11728810)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 10940314 |
GRCz11 | 8 | 10978019 |
KASP Assay ID:
554-6565.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAACAACAACAACACCAACACCAACAACAGCAGCAGCAACAACAACAA[C/T]AACAACAACAACAGCAGCAGCAACAACAACAACAGCAACACCAGCAACAA
Long Flanking Sequence:
TTTTCAGACTTGGTGTGAACAGGCATTTACATGCTTTATAATTAATTTTTGTTCTGGCAATCTTTTATTTAATATTTTATGTTCTTTTTAAGTGTTTGTGTTTGTAATTTGTTTTCTGAAATATACTACAGCATTTTTAAAACCTTTTATTCTAATAAACAATGTCCATTATTTCATAATACATTTGATTTCTTTTAATTTATGCATTTTCTCCTTTTTGTTCTGGCAATATTTTTGATCTTCTCTTTTTTTTTAATCATTCAGGCAATCTAGTCATTGAAAAAGTTGCTCCTACTGCTCCTCCGTCCAACATGATGGTCAATCAGCAGATCTCTCCCGGTCACAACCACCCAGGTAAGCACTCAGGACAGATCAACCTGGCCCAGCTGAGGCTGCAGCACATGCAGCAGGCAGCGATTGCTCAGAAACATCAGCAGCAACACCAACACCACCAACAACAACAACACCAACACCAACAACAGCAGCAGCAACAACAACAA[C/T]AACAACAACAACAGCAGCAGCAACAACAACAACAGCAACACCAGCAACAAATTCAGCAGCAGATGCGCATCGCCTCTCAGATGTCCCAGCATCCCAGACAAGGAGCTCCACAAATGATTCAGCAACCTGTAAGTTAGGAATTAGCTCTTTCCTACTTTACATGTTTGATTTATTCTGGACCAGGATAATTGTGTGTGCTTGTGAAGCTGGTTGCACAATCAAGTCTTAAAAGATAAGCTTAATATTTATCAAAATGCATTTTAGTTAGAATAATTAGCAGGGCTGTGTGATTGAAGACAAATATGAAATGTGATGGCCAGATGATCATAATAATTACTTATTACCTGTGATAAAATAAGTGAAGCGCTATGAATACTTTGCAAGTAGCAAGATTTCATCTGACAGTGAAGTCGCAATTGTGATTGAGTTTTATTATGTGATCATTTTTGCTTTGCTAGTTATTACACATTGTTTAATATGTACTGAGTATTTATGTTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27136
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 |
---|---|---|---|---|---|
ENSDART00000020116 | Nonsense | 576 | 1176 | 9 | 20 |
ENSDART00000111005 | Nonsense | 458 | 1058 | 10 | 21 |
ENSDART00000139603 | None | None | 104 | None | 2 |
Genomic Location (Zv9):
Chromosome 8 (position 11728822)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 10940302 |
GRCz11 | 8 | 10978007 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACACCAACACCAACAACAGCAGCAGCAACAACAACAACAACAACAACAA[C/T]AGCAGCAGCAACAACAACAACAGCAACACCAGCAACAAATTCAGCAGCAG
Long Flanking Sequence:
GTGTGAACAGGCATTTACATGCTTTATAATTAATTTTTGTTCTGGCAATCTTTTATTTAATATTTTATGTTCTTTTTAAGTGTTTGTGTTTGTAATTTGTTTTCTGAAATATACTACAGCATTTTTAAAACCTTTTATTCTAATAAACAATGTCCATTATTTCATAATACATTTGATTTCTTTTAATTTATGCATTTTCTCCTTTTTGTTCTGGCAATATTTTTGATCTTCTCTTTTTTTTTAATCATTCAGGCAATCTAGTCATTGAAAAAGTTGCTCCTACTGCTCCTCCGTCCAACATGATGGTCAATCAGCAGATCTCTCCCGGTCACAACCACCCAGGTAAGCACTCAGGACAGATCAACCTGGCCCAGCTGAGGCTGCAGCACATGCAGCAGGCAGCGATTGCTCAGAAACATCAGCAGCAACACCAACACCACCAACAACAACAACACCAACACCAACAACAGCAGCAGCAACAACAACAACAACAACAACAA[C/T]AGCAGCAGCAACAACAACAACAGCAACACCAGCAACAAATTCAGCAGCAGATGCGCATCGCCTCTCAGATGTCCCAGCATCCCAGACAAGGAGCTCCACAAATGATTCAGCAACCTGTAAGTTAGGAATTAGCTCTTTCCTACTTTACATGTTTGATTTATTCTGGACCAGGATAATTGTGTGTGCTTGTGAAGCTGGTTGCACAATCAAGTCTTAAAAGATAAGCTTAATATTTATCAAAATGCATTTTAGTTAGAATAATTAGCAGGGCTGTGTGATTGAAGACAAATATGAAATGTGATGGCCAGATGATCATAATAATTACTTATTACCTGTGATAAAATAAGTGAAGCGCTATGAATACTTTGCAAGTAGCAAGATTTCATCTGACAGTGAAGTCGCAATTGTGATTGAGTTTTATTATGTGATCATTTTTGCTTTGCTAGTTATTACACATTGTTTAATATGTACTGAGTATTTATGTTTTGACCAAAGTCATA
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