ZMP
si:ch211-175l6.6
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q1MT08]
Human Orthologue:
TRIM35
Human Description:
tripartite motif-containing 35 [Source:HGNC Symbol;Acc:16285]
Mouse Orthologue:
Trim35
Mouse Description:
tripartite motif-containing 35 Gene [Source:MGI Symbol;Acc:MGI:1914104]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa39995 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa33093 | Nonsense | Available for shipment | Available now |
| sa15080 | Nonsense | Available for shipment | Available now |
| sa17828 | Essential Splice Site | Available for shipment | Available now |
| sa25241 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa25994 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa13253 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39995
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 |
|---|---|---|---|---|---|
| ENSDART00000028695 | Nonsense | 34 | 292 | 1 | 5 |
| ENSDART00000133133 | Nonsense | 32 | 448 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 3 (position 8151021)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 8054581 |
| GRCz11 | 3 | 7940421 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGAAATCTTCAAGAATCCTGTAGTTTTATCATGCAGTCACAGTGTGTG[T/A]AAAGAGTGTCTTCAACAGTACTGGAGAACCAAGACAACTCAGGAGTGTCC
Long Flanking Sequence:
ATATATATATATATATATATATATATATATATATATATTTCAACATGAATAAACAAGTTTTGTTGTTGTTGTTTTGTTGGTGTTCTAGTAATCCTAAAGGTCTTTTTAATAGCTGTGTTTCTTCTGTGACTTATTATTTTACCTGAAAATCCTTGTGCAATCTTTGACCTTTTTTACCACACCCAAATGAGATCAAAAGTCCAGTATTTTACAGTTCTGTCCAGGAAAAGACTGGCTTGTTATTTCTGCTTTCTGTCACACTGACTCTCTTTATTTCTGTACTGGATTTAAAAAAGAATCAGAAATCAGCAAATAATGAAGGCAAAGATCTTAGTGATTGACTTTTGAAGCCGCCATTCAGAAAGTGAAAGTCAGGTTCAGATTTCTGGAGCTCAAACTGTGGAAATGGCTTCACTAAATGTATCCGAAGATCTTTCTTGTCCTGTGTGCTGTGAAATCTTCAAGAATCCTGTAGTTTTATCATGCAGTCACAGTGTGTG[T/A]AAAGAGTGTCTTCAACAGTACTGGAGAACCAAGACAACTCAGGAGTGTCCTGTTTGCCGGAGAAGATCTTCAAAAGGTGAACCTCCAGTTAATCTTGCATTAAAAAACCTGTGTGAGTTGTTCCTGAAGGAGAGAAATGAGAGATGTTCATCAGCATCTGAGGAGATCTGCAGTTTACACAGTGAGAAACTCAAACTCTTCTGTCTGGAGGACAAACAGCCTGTGTGTGTGATGTGTGTTACTTTACAACAACACGACAATCACAAATTCAGACCCATCAGTGAAGTGGCTTCTTCATACAAGGTAAGACAAGAGTTTCTTTATTCATATACTAACATCTGTTTACAACATTACTCCACAATCAATATTATATATTGTTTACGTTCATAGACATGTATATATACATGTAATTTCATTGTTGCCAATTCTACAATTTCTTCTTTCCTTACTGTGCACATGACAATAAACAAATTGAACTGAATTGAATATGTAAAGAACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33093
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 |
|---|---|---|---|---|---|
| ENSDART00000028695 | Nonsense | 74 | 292 | 1 | 5 |
| ENSDART00000133133 | Nonsense | 72 | 448 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 3 (position 8151140)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 8054462 |
| GRCz11 | 3 | 7940302 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAAAAGGTGAACCTCCAGTTAATCTTGCATTAAAAAACCTGTGTGAGT[T/A]GTTCCTGAAGGAGAGAAATGAGAGATGTTCATCAGCATCTGAGGAGATCT
Long Flanking Sequence:
TCTTCTGTGACTTATTATTTTACCTGAAAATCCTTGTGCAATCTTTGACCTTTTTTACCACACCCAAATGAGATCAAAAGTCCAGTATTTTACAGTTCTGTCCAGGAAAAGACTGGCTTGTTATTTCTGCTTTCTGTCACACTGACTCTCTTTATTTCTGTACTGGATTTAAAAAAGAATCAGAAATCAGCAAATAATGAAGGCAAAGATCTTAGTGATTGACTTTTGAAGCCGCCATTCAGAAAGTGAAAGTCAGGTTCAGATTTCTGGAGCTCAAACTGTGGAAATGGCTTCACTAAATGTATCCGAAGATCTTTCTTGTCCTGTGTGCTGTGAAATCTTCAAGAATCCTGTAGTTTTATCATGCAGTCACAGTGTGTGTAAAGAGTGTCTTCAACAGTACTGGAGAACCAAGACAACTCAGGAGTGTCCTGTTTGCCGGAGAAGATCTTCAAAAGGTGAACCTCCAGTTAATCTTGCATTAAAAAACCTGTGTGAGT[T/A]GTTCCTGAAGGAGAGAAATGAGAGATGTTCATCAGCATCTGAGGAGATCTGCAGTTTACACAGTGAGAAACTCAAACTCTTCTGTCTGGAGGACAAACAGCCTGTGTGTGTGATGTGTGTTACTTTACAACAACACGACAATCACAAATTCAGACCCATCAGTGAAGTGGCTTCTTCATACAAGGTAAGACAAGAGTTTCTTTATTCATATACTAACATCTGTTTACAACATTACTCCACAATCAATATTATATATTGTTTACGTTCATAGACATGTATATATACATGTAATTTCATTGTTGCCAATTCTACAATTTCTTCTTTCCTTACTGTGCACATGACAATAAACAAATTGAACTGAATTGAATATGTAAAGAACAGTAATTGGTCAGAAGCACAGATAACAGCACATTCATGCTCTCAATATTTTTCTCAGCTATTTTATTCATCCTAAAATGACAAACATCTATTTATTGTTATGCTCGTGCTAATTTTAAGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15080
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 |
|---|---|---|---|---|---|
| ENSDART00000028695 | Nonsense | 93 | 292 | 1 | 5 |
| ENSDART00000133133 | Nonsense | 91 | 448 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 3 (position 8151197)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 8054405 |
| GRCz11 | 3 | 7940245 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAGGAGAGAAATGAGAGATGTTCATCAGCATCTGAGGAGATCTGCAGTT[T/A]ACACAGTGAGAARCTCAAACTCTTCTGTCTGGAGGACAAACAGCCTGTGT
Long Flanking Sequence:
CCACACCCAAATGAGATCAAAAGTCCAGTATTTTACAGTTCTGTCCAGGAAAAGACTGGCTTGTTATTTCTGCTTTCTGTCACACTGACTCTCTTTATTTCTGTACTGGATTTAAAAAAGAATCAGAAATCAGCAAATAATGAAGGCAAAGATCTTAGTGATTGACTTTTGAAGCCGCCATTCAGAAAGTGAAAGTCAGGTTCAGATTTCTGGAGCTCAAACTGTGGAAATGGCTTCACTAAATGTATCCGAAGATCTTTCTTGTCCTGTGTGCTGTGAAATCTTCAAGAATCCTGTAGTTTTATCATGCAGTCACAGTGTGTGTAAAGAGTGTCTTCAACAGTACTGGAGAACCAAGACAACTCAGGAGTGTCCTGTTTGCCGGAGAAGATCTTCAAAAGGTGAACCTCCAGTTAATCTTGCATTAAAAAACCTGTGTGAGTTGTTCCTGAAGGAGAGAAATGAGAGATGTTCATCAGCATCTGAGGAGATCTGCAGTT[T/A]ACACAGTGAGAAACTCAAACTCTTCTGTCTGGAGGACAAACAGCCTGTGTGTGTGATGTGTGTTACTTTACAACAACACGACAATCACAAATTCAGACCCATCAGTGAAGTGGCTTCTTCATACAAGGTAAGACAAGAGTTTCTTTATTCATATACTAACATCTGTTTACAACATTACTCCACAATCAATATTATATATTGTTTACGTTCATAGACATGTATATATACATGTAATTTCATTGTTGCCAATTCTACAATTTCTTCTTTCCTTACTGTGCACATGACAATAAACAAATTGAACTGAATTGAATATGTAAAGAACAGTAATTGGTCAGAAGCACAGATAACAGCACATTCATGCTCTCAATATTTTTCTCAGCTATTTTATTCATCCTAAAATGACAAACATCTATTTATTGTTATGCTCGTGCTAATTTTAAGTCATCAAACAAAATGCAATGCCAACATTCATTCATTTTCTTTTTGACTGAGTCCCCTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17828
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000028695 | Essential Splice Site | 167 | 292 | 2 | 5 |
| ENSDART00000133133 | Essential Splice Site | 165 | 448 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 3 (position 8152476)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 8053126 |
| GRCz11 | 3 | 7938966 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAATGAAGAAAKGAAAGCAGAGTTTGAGAAAACAKTTCAACACATCAAGG[T/C]GAGGAAAMATTTCAATTCAAACATTTTCATTGCAGCCGCAGGAGACACTA
Long Flanking Sequence:
GTGAGGCGATCGAGCTATCCCCTGCGCCACCATGACGCCATCCCATGATCCAAACAATGATAACTGTGATCATGTATTTCACTGCTGTGGTGGGTTTTGACTGACTGCATTAGTTTGGCAACATAAAAAAAATAAAAAATAAATAAAGCTGCTTTATATTGCCTGAAGCTCTATCAGTTTGACTGCACTGACACTATTGTCAGTAATCAGACTTGTTGCATCTTTCCTCTTTTACAACATAATGAATGCAGTTTCATAGACCAGAAACTGTCCTTGTTTTACTTTACAGTAGATATTCATTTCTGAATCAGTTTAGTAGGAAATTCTGCTGAATACAGCACCAAATGACTTCTCATCGCAGTCATTTGGCATTTTATTTGTTTTTAAATTGTTTAATTTTCAGGAGGAGCTCAATACAGCACTGAAGTCTTTACAAGTGAAACTGAAACGCAATGAAGAAAGGAAAGCAGAGTTTGAGAAAACAGTTCAACACATCAAGG[T/C]GAGGAAACATTTCAATTCAAACATTTTCATTGCAGCCGCAGGAGACACTATTAAATAAATGACTTGTTATTTTTAAAATAATGTATTCCTTTTGCTAATAATAAACATCATTAGGCTTCTGGGTCTGTTGACTGTCTGAGTTTATTTTGGATATTTATGTTGTTATGTTGATGTGTCGTGACTTTTGATTATTAAATGTCTCTGTGGTTTGCTTTCAGTCTCAAGCCGATCACACAGAGCGTCAGGTTAAGCATGAGTTTGAGAAGCTTCATCAGTTTCTCCGAGATGAAGAAGAAGCTACAATCACTGCACTGAGGGAGGAAGAGGAGCAGAAGAAGCAGATGATGAAGGAGAAGCTGGAGGAGATGAACACACACATCTCAGCTCTTTCACACACGATCAAAGACACGGAGGAGATGCTGAAAGCCAAGGACGTCTGCTTTCTAAAGGTCTGATTTCAGATCAGTGATTGATTGATTGATGATGGATTGAGCTCTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25241
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000028695 | Essential Splice Site | 245 | 292 | 4 | 5 |
| ENSDART00000133133 | Essential Splice Site | 243 | 448 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 3 (position 8153001)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 8052601 |
| GRCz11 | 3 | 7938441 |
KASP Assay ID:
554-7321.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATTGATGATGGATTGAGCTCTTGATGATCAGTTGTGTGTTTGTTCTGC[A/T]GGAGTTTCCAGTCTCGATGGAAAGGTGAGTGATCTGCTGGTGTCTCTGCT
Long Flanking Sequence:
TTTCATTGCAGCCGCAGGAGACACTATTAAATAAATGACTTGTTATTTTTAAAATAATGTATTCCTTTTGCTAATAATAAACATCATTAGGCTTCTGGGTCTGTTGACTGTCTGAGTTTATTTTGGATATTTATGTTGTTATGTTGATGTGTCGTGACTTTTGATTATTAAATGTCTCTGTGGTTTGCTTTCAGTCTCAAGCCGATCACACAGAGCGTCAGGTTAAGCATGAGTTTGAGAAGCTTCATCAGTTTCTCCGAGATGAAGAAGAAGCTACAATCACTGCACTGAGGGAGGAAGAGGAGCAGAAGAAGCAGATGATGAAGGAGAAGCTGGAGGAGATGAACACACACATCTCAGCTCTTTCACACACGATCAAAGACACGGAGGAGATGCTGAAAGCCAAGGACGTCTGCTTTCTAAAGGTCTGATTTCAGATCAGTGATTGATTGATTGATGATGGATTGAGCTCTTGATGATCAGTTGTGTGTTTGTTCTGC[A/T]GGAGTTTCCAGTCTCGATGGAAAGGTGAGTGATCTGCTGGTGTCTCTGCTCTCTCTGCTTCTGAATCCTGCAGTTCTGACTCCTGAATGTTCCTCCAGAGTCCAGATCTCACAGCCGGATCCACAGACGCCTTCTGGAGCTTTGATTCATGTGGCTGGCTACTTGGGGAACCTGACATACAGAGTCTGGAAGAAGATGCAGGACATCGTCCACTACAGTGAGTCTCTACAATATCTGTATGCTAAATTATGAAAGGGTATGTAGTAAGGTGTCTGCAGCTGGAGGTCTGTGTCGGGCTAGGGCTGGCAGGGCAAGGAACCTGAAACCACTCTGGAGCCAACACTGGCAGGCATTCTAAGGCTGAGGAGGCCCTCCTCTAGCTCCTCTTCTAAGTGGGGAACAACAGGAAGCTAGGACCAAGATGGTTTGCGGGTGGAAAGAACGTCCAGATTTTCTCTGGAGGCCCTTTTTGGGCTGTTTGACAAACCAGAGGTCCAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25994
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000028695 | Essential Splice Site | 252 | 292 | 4 | 5 |
| ENSDART00000133133 | Essential Splice Site | 250 | 448 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 3 (position 8153026)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 8052576 |
| GRCz11 | 3 | 7938416 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGATCAGTTGTGTGTTTGTTCTGCAGGAGTTTCCAGTCTCGATGGAAAG[G/T]TGAGTGATCTGCTGGTGTCTCTGCTCTCTCTGCTTCTGAATCCTGCAGTT
Long Flanking Sequence:
ATTAAATAAATGACTTGTTATTTTTAAAATAATGTATTCCTTTTGCTAATAATAAACATCATTAGGCTTCTGGGTCTGTTGACTGTCTGAGTTTATTTTGGATATTTATGTTGTTATGTTGATGTGTCGTGACTTTTGATTATTAAATGTCTCTGTGGTTTGCTTTCAGTCTCAAGCCGATCACACAGAGCGTCAGGTTAAGCATGAGTTTGAGAAGCTTCATCAGTTTCTCCGAGATGAAGAAGAAGCTACAATCACTGCACTGAGGGAGGAAGAGGAGCAGAAGAAGCAGATGATGAAGGAGAAGCTGGAGGAGATGAACACACACATCTCAGCTCTTTCACACACGATCAAAGACACGGAGGAGATGCTGAAAGCCAAGGACGTCTGCTTTCTAAAGGTCTGATTTCAGATCAGTGATTGATTGATTGATGATGGATTGAGCTCTTGATGATCAGTTGTGTGTTTGTTCTGCAGGAGTTTCCAGTCTCGATGGAAAG[G/T]TGAGTGATCTGCTGGTGTCTCTGCTCTCTCTGCTTCTGAATCCTGCAGTTCTGACTCCTGAATGTTCCTCCAGAGTCCAGATCTCACAGCCGGATCCACAGACGCCTTCTGGAGCTTTGATTCATGTGGCTGGCTACTTGGGGAACCTGACATACAGAGTCTGGAAGAAGATGCAGGACATCGTCCACTACAGTGAGTCTCTACAATATCTGTATGCTAAATTATGAAAGGGTATGTAGTAAGGTGTCTGCAGCTGGAGGTCTGTGTCGGGCTAGGGCTGGCAGGGCAAGGAACCTGAAACCACTCTGGAGCCAACACTGGCAGGCATTCTAAGGCTGAGGAGGCCCTCCTCTAGCTCCTCTTCTAAGTGGGGAACAACAGGAAGCTAGGACCAAGATGGTTTGCGGGTGGAAAGAACGTCCAGATTTTCTCTGGAGGCCCTTTTTGGGCTGTTTGACAAACCAGAGGTCCAAAAACTGTTGATATAAAAAGCCCCCCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13253
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000028695 | None | None | 292 | None | 5 |
| ENSDART00000133133 | Nonsense | 352 | 448 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 3 (position 8170942)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 8034660 |
| GRCz11 | 3 | 7920500 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGGWTCAGAGGGTTTCATCTCAGGGAAACACTGCTGGGATGTGGAGGTC[A/T]AAGAAAGTTTATACTGGAAYTTTGGAGTAWCTACAGCATCAAACCAGAGG
Long Flanking Sequence:
TCAAATATTCACTCCAGGTTGACAGATGAGATGTTTCAAGCTTACCAGGGAAAAGATTAATGTACTTCTCATCATTTGCTCTAAAGTTATGACCAAGTTCTTATTGGTGCCAACAAATGTTGGGAGAAAGTTGTCAAAAGCGGGTCGATTTGTTGCGAAAAGATGCTGAATAATGATGTAATGTCATTACGTGATGGTGCTAACACGTGCAGCAAAGCTGTGCTATCGTATAGAATACAGTAATTGTATAATAATAATATTAATAATAAGAATAAATAATATAATCAAATGTATTATGTGATTTTGTCTCTTCAGCTCCTGTAATTCTGGATCCAAACACTGCTCATCCAGGTCTAATCCTGTCTGATGATCTGACCACTTTGAGAAATAGAAGGAACACACAGCCATCTCCTGATAATCCGGAGAGGTTTGACCAAATGTACTGTGTTCTGGGTTCAGAGGGTTTCATCTCAGGGAAACACTGCTGGGATGTGGAGGTC[A/T]AAGAAAGTTTATACTGGAATTTTGGAGTAACTACAGCATCAAACCAGAGGAAGGGGTTCTTTAGCACTGGTGTCTGGAGTGTGCGGTGTGAACTATCTTTTGGTTCTGGCTTCATTGTTAAACAGAGTCTTGAGCGTGTGAGAGTTGATCTGGACTGTGACAGAGGAACAGTGTCTTTCTCTGATCCTCTTAAAAACACACATCTACACACATTCACAACCACCTTCACTGAGTCGGTCTTTCCTTACTTCTATTTTAATGATATAGTCAATTGTTTGAAGATTTTACCATGTTAAACTGCTTGCATCAACAGAAAATCATCAAAGTTTTTTAAAATCCATTGCTGAGGATTATAGGTCTTCAATTTTGCACTTTTTACTAGACGTAAAAAAAAAAGTCTTTTGCTTCTTTAGAATGGGTCCGTGAAGTTTTAGGTCAAAATACTCATCAGATTCTTTATTTTACCCCCCTGAATATGCCCATTTTGAGCTCAAAGCAAG
Associated Phenotype:
Not determined