ZMP
si:ch211-198a12.4
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B8A692]
Human Orthologue:
TRIM65
Human Description:
tripartite motif-containing 65 [Source:HGNC Symbol;Acc:27316]
Mouse Orthologue:
Trim65
Mouse Description:
tripartite motif-containing 65 Gene [Source:MGI Symbol;Acc:MGI:2442815]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa42173 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa38931 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa1784 | Nonsense | Available for shipment | Available now |
| sa31919 | Essential Splice Site | Available for shipment | Available now |
| sa22269 | Essential Splice Site | Available for shipment | Available now |
| sa42174 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42173
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000108779 | Nonsense | 85 | 506 | 1 | 6 |
| ENSDART00000136024 | Nonsense | 68 | 419 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 18582179)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 18402214 |
| GRCz11 | 13 | 18533206 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCTGACTTGCTTAACCTCCTTTTGTGAAGCGCATCTCCAGGCTCATTA[T/G]GAGTATCCAGCTCTCATGAAGCACAAACTGGTGGCGGCGACAGGGCAACT
Long Flanking Sequence:
GTCACATTATTCTGTCACAGCATATTTTCAACACCAAAGAGGTGTTTAACCACTTGTAAAACCACAGTTGTTTCCACTTTATGGTTAACCATCAACAAGGCCTTTGTATAAAGAAGTCTCATTGTTTACGTTACATTTTTTTCCTTTTCTCTTCTGACATAAGCTGTCACACCCATTCAGAAGATGTCATCCTCTAACCTGGTTAACTGGTTTATCACACATGGTTCACATTCCTCTATAAAATGAATGAGTCAGTACAGTTTCATTGAAACTCTGTTTAACATTCAGCTTTCTAACATGTCTCGGAGCAGTACAGCAAGCCAAAGCCGATATGGCACTCAGGAGAAACCCCGCCGATCTGGAAGATACAGCAGCTCCAGCAGCCGCAGCAGCTCTAGAGACGTGCTGTGTGATTTTTGTATGATTAAGAAAAACAAGGCAGTAAAATCGTGTCTGACTTGCTTAACCTCCTTTTGTGAAGCGCATCTCCAGGCTCATTA[T/G]GAGTATCCAGCTCTCATGAAGCACAAACTGGTGGCGGCGACAGGGCAACTGCGTGAAAAGATCTGCGGCGAACATGACAAACTTCTGGAGGTTTTCTGTCGTTCTGACCAAATGTGTGTTTGTGTTTTGTGTATTATGGAGGAACATAAAAAACATGACATTGTTTCAGCAGCAGCTGAAAGGACGGAAAAGCAGGTGAGATGCTCAGTAGACAACCACTCATGCTCAATGCAACTAAATGATGACATGATACAAGTCAATATGCAGTGCAACGATTAACTGTGAGAAGATTAACGTTAAAACACTAACTTTTTCAACAGAAACAGCTTGGGGCTAAACTAATGACTTCACAGCAGAAAATTGAGGAAAGGATGAAGAAATGGCAAGATCTCAGGCAGGCAGTGGCATCTCTAAAGGTAAGCCTTTCAGAAATTATGGGCTCTATTTTAACAATCTAAGTGCAAAGTCTAAAGTGTAGGGTGCAAAAGCATTAAAGGCGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38931
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000108779 | Nonsense | 112 | 506 | 1 | 6 |
| ENSDART00000136024 | Nonsense | 95 | 419 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 18582258)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 18402293 |
| GRCz11 | 13 | 18533285 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTGGCGGCGACAGGGCAACTGCGTGAAAAGATCTGCGGCGAACATGAC[A/T]AACTTCTGGAGGTTTTCTGTCGTTCTGACCAAATGTGTGTTTGTGTTTTG
Long Flanking Sequence:
TATGGTTAACCATCAACAAGGCCTTTGTATAAAGAAGTCTCATTGTTTACGTTACATTTTTTTCCTTTTCTCTTCTGACATAAGCTGTCACACCCATTCAGAAGATGTCATCCTCTAACCTGGTTAACTGGTTTATCACACATGGTTCACATTCCTCTATAAAATGAATGAGTCAGTACAGTTTCATTGAAACTCTGTTTAACATTCAGCTTTCTAACATGTCTCGGAGCAGTACAGCAAGCCAAAGCCGATATGGCACTCAGGAGAAACCCCGCCGATCTGGAAGATACAGCAGCTCCAGCAGCCGCAGCAGCTCTAGAGACGTGCTGTGTGATTTTTGTATGATTAAGAAAAACAAGGCAGTAAAATCGTGTCTGACTTGCTTAACCTCCTTTTGTGAAGCGCATCTCCAGGCTCATTATGAGTATCCAGCTCTCATGAAGCACAAACTGGTGGCGGCGACAGGGCAACTGCGTGAAAAGATCTGCGGCGAACATGAC[A/T]AACTTCTGGAGGTTTTCTGTCGTTCTGACCAAATGTGTGTTTGTGTTTTGTGTATTATGGAGGAACATAAAAAACATGACATTGTTTCAGCAGCAGCTGAAAGGACGGAAAAGCAGGTGAGATGCTCAGTAGACAACCACTCATGCTCAATGCAACTAAATGATGACATGATACAAGTCAATATGCAGTGCAACGATTAACTGTGAGAAGATTAACGTTAAAACACTAACTTTTTCAACAGAAACAGCTTGGGGCTAAACTAATGACTTCACAGCAGAAAATTGAGGAAAGGATGAAGAAATGGCAAGATCTCAGGCAGGCAGTGGCATCTCTAAAGGTAAGCCTTTCAGAAATTATGGGCTCTATTTTAACAATCTAAGTGCAAAGTCTAAAGTGTAGGGTGCAAAAGCATTAAAGGCGTGTCAGAATCCACTTTTTCTATTTTGAGGACAAAAAAAATAAGCTCTGCGCCGCATGATCTAACAGGGCTAAGCTAATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1784
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 |
|---|---|---|---|---|---|
| ENSDART00000108779 | Nonsense | 239 | 506 | 3 | 6 |
| ENSDART00000136024 | Nonsense | 222 | 419 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 18586413)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 18406448 |
| GRCz11 | 13 | 18537440 |
KASP Assay ID:
554-1777.1 (used for ordering genotyping assays)
KASP Sequence:
GACCAATGCAGAGAGACATTTGGCCAGACTAGAGGAAGAGATTACCCTGT[T/A]AAGGAAGAAACACACTGACTTGGAGCAGCTCTCACAGTCTGATGATCACA
Long Flanking Sequence:
ACCTGTTTGGAAGTTTCTAGTATACCTAAAAAGAACTTGATTAGCTGGTTGTGGTATGTCTAATTGTGGTTAAAACTAAACTCTTCAGGACACTGGTCCTTCAGGAACAAATTTGCACACCCCTGCGTTAAGGGTCCTTTCAGAAGTTTTCTTGGACATTGAATTTTTATTTAACTTTTTCCACTATAAAAAAAGGTTTTATGGAACATTAAATTTCCATATATAAGATTCATATATAAATTTCCAATTTATAAGAGTGCCAAATGTAATTGGTAAATGAAATCTAAGGATATAACTGTCACGTTGATGTTTTGTTTTTCTATCATGATAGCATTCATCACAGAGTGTGCTGGATGAGAATGAACGTATTTTTGCTGAGCTGCTGCGAGCGTTGGAGAGGAGGCATGGAGAAGTGAAGGAGATGATTCGAGCTCAAGAAGTCCTTCTGCTGACCAATGCAGAGAGACATTTGGCCAGACTAGAGGAAGAGATTACCCTGT[T/A]AAGGAAGAAACACACTGACTTGGAGCAGCTCTCACAGTCTGATGATCACATTCATTTCTTACAGGTACTGAGCAAAAACCAGTGTTTGTATGTAGTTCTCTAAAGTATTATAAAATAAAACAGCTACTTTATTTCCCCTAGAGCTGGCAGTCTCTTTCTGCTCCTTCTGGATATGAAGATTTGTCTAAGGTGACATTAGCGCCTCACCACACATTTGACAATGCAAAGAAAGCCATCTCTGACTTAAAGGTGCAAATGGAAGACATAAGCAAGGAAGAACTGAACAAAATCTCTTCAGCAGGTTGTTAAAACTCATAAATATACCGTATGTTGCAAACTTACCACAGAAGTGTTTTTTACTTTGTCTTTGTTTGTAGTGTAGACTTATGTGGGAATACAGTAATTTAAAGCTGTTTAGCATACACGTGTAACTTTTTTACACTTGTCTTGTGAAATATTATTGCAGTTTAAACAATTTCAAAGAATATTAAACATTAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31919
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000108779 | Essential Splice Site | 333 | 506 | 5 | 6 |
| ENSDART00000136024 | Essential Splice Site | 316 | 419 | 5 | 6 |
| ENSDART00000108779 | Essential Splice Site | 333 | 506 | 5 | 6 |
| ENSDART00000136024 | Essential Splice Site | 316 | 419 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 18588501)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 18408536 |
| GRCz11 | 13 | 18539528 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAAATTCTCCAGACTGTGGACCCAGCAAAACGAGAGGAGTTCTTTGAAT[G/T]TAAGTTCAGAAATAGTGAGATTCTCATTTTATATAAACACATTGTTGATG
Long Flanking Sequence:
TAAAAACTCTGTAATAAAAATTCAAGGATATTGGAAAATATATTAAGTGATCTAATACAATTAATTAGGCTTGTATTTTGGGGTAGCACTGTAATACTTAAATAGACTGAATGGCAAGTAACTAAACCACTCCAACTCACAACAAAAAGCAGAAACATAATCCAGAATCATATGACAAAACAAATGGGTTTAAATACACAGAGAACAAAATCCGGATTAAGACACATAGCTGAAAAATTTACAATACACAATCAAAGGAGCAAAAGAACATGGGAAATTGTCCTCTAGTGTCTTTTATAGGCACTACAGCTTAAGGTTCTGAGGAACTGTAGCAATATTATATCTTGTTGCCTTAATGCTTAAAACCCCTTTCATCTTTTATCAATAATGTAATTTATCCAATTATAAATCCTTTACACATGTCAAAATTCTATCTGCAGTGAATGAGGTTAAAATTCTCCAGACTGTGGACCCAGCAAAACGAGAGGAGTTCTTTGAAT[G/T]TAAGTTCAGAAATAGTGAGATTCTCATTTTATATAAACACATTGTTGATGCTGATTAATCTAAACACTCCTTTTCCATCTAGATTCCTGTCAGCTATCAATAGATCCTTTAACAGCCCATCCAAACCTGGTCCTGTCAGACAGAAACACTGTGGTGCAGATGAGCAATGAGCCCAGACCGTACCCAGATCATCCTGACCGCTTCGACTATTGGCAACAGGCACTGTGTAAGCCGGGTCTGGCAGGAGGACGATATTACTGGGAGCTGGACTGGAGAGGCACTGAAGTGGACATTGCTGTCACCTACAAAGGGATCCAGAGGAAAGGAAATGACAAACCTGGCAGCTTCGGAAGGAATGACAAGTCTTGGAGTTTGTACTGCTCTGAATCCGAATACTCGTTTATGCACAACAGCAAAAGCACGGCTGTATCTGTGCCCAGGTCCTCAAGGATTGGGGTTTATGTTGACTATGAGTCTGGGACACTGGCATTTTATAGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22269
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000108779 | Essential Splice Site | 333 | 506 | 5 | 6 |
| ENSDART00000136024 | Essential Splice Site | 316 | 419 | 5 | 6 |
| ENSDART00000108779 | Essential Splice Site | 333 | 506 | 5 | 6 |
| ENSDART00000136024 | Essential Splice Site | 316 | 419 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 18588501)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 18408536 |
| GRCz11 | 13 | 18539528 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAAATTCTCCAGACTGTGGACCCAGCAAAACGAGAGGAGTTCTTTGAAT[G/T]TAAGTTCAGAAATAGTGAGATTCTCATTTTATATAAACACATTGTTGATG
Long Flanking Sequence:
TAAAAACTCTGTAATAAAAATTCAAGGATATTGGAAAATATATTAAGTGATCTAATACAATTAATTAGGCTTGTATTTTGGGGTAGCACTGTAATACTTAAATAGACTGAATGGCAAGTAACTAAACCACTCCAACTCACAACAAAAAGCAGAAACATAATCCAGAATCATATGACAAAACAAATGGGTTTAAATACACAGAGAACAAAATCCGGATTAAGACACATAGCTGAAAAATTTACAATACACAATCAAAGGAGCAAAAGAACATGGGAAATTGTCCTCTAGTGTCTTTTATAGGCACTACAGCTTAAGGTTCTGAGGAACTGTAGCAATATTATATCTTGTTGCCTTAATGCTTAAAACCCCTTTCATCTTTTATCAATAATGTAATTTATCCAATTATAAATCCTTTACACATGTCAAAATTCTATCTGCAGTGAATGAGGTTAAAATTCTCCAGACTGTGGACCCAGCAAAACGAGAGGAGTTCTTTGAAT[G/T]TAAGTTCAGAAATAGTGAGATTCTCATTTTATATAAACACATTGTTGATGCTGATTAATCTAAACACTCCTTTTCCATCTAGATTCCTGTCAGCTATCAATAGATCCTTTAACAGCCCATCCAAACCTGGTCCTGTCAGACAGAAACACTGTGGTGCAGATGAGCAATGAGCCCAGACCGTACCCAGATCATCCTGACCGCTTCGACTATTGGCAACAGGCACTGTGTAAGCCGGGTCTGGCAGGAGGACGATATTACTGGGAGCTGGACTGGAGAGGCACTGAAGTGGACATTGCTGTCACCTACAAAGGGATCCAGAGGAAAGGAAATGACAAACCTGGCAGCTTCGGAAGGAATGACAAGTCTTGGAGTTTGTACTGCTCTGAATCCGAATACTCGTTTATGCACAACAGCAAAAGCACGGCTGTATCTGTGCCCAGGTCCTCAAGGATTGGGGTTTATGTTGACTATGAGTCTGGGACACTGGCATTTTATAGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42174
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 |
|---|---|---|---|---|---|
| ENSDART00000108779 | Nonsense | 390 | 506 | 6 | 6 |
| ENSDART00000136024 | Nonsense | 373 | 419 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 18588751)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 18408786 |
| GRCz11 | 13 | 18539778 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTCGACTATTGGCAACAGGCACTGTGTAAGCCGGGTCTGGCAGGAGGA[C/T]GATATTACTGGGAGCTGGACTGGAGAGGCACTGAAGTGGACATTGCTGTC
Long Flanking Sequence:
ATCAAAGGAGCAAAAGAACATGGGAAATTGTCCTCTAGTGTCTTTTATAGGCACTACAGCTTAAGGTTCTGAGGAACTGTAGCAATATTATATCTTGTTGCCTTAATGCTTAAAACCCCTTTCATCTTTTATCAATAATGTAATTTATCCAATTATAAATCCTTTACACATGTCAAAATTCTATCTGCAGTGAATGAGGTTAAAATTCTCCAGACTGTGGACCCAGCAAAACGAGAGGAGTTCTTTGAATGTAAGTTCAGAAATAGTGAGATTCTCATTTTATATAAACACATTGTTGATGCTGATTAATCTAAACACTCCTTTTCCATCTAGATTCCTGTCAGCTATCAATAGATCCTTTAACAGCCCATCCAAACCTGGTCCTGTCAGACAGAAACACTGTGGTGCAGATGAGCAATGAGCCCAGACCGTACCCAGATCATCCTGACCGCTTCGACTATTGGCAACAGGCACTGTGTAAGCCGGGTCTGGCAGGAGGA[C/T]GATATTACTGGGAGCTGGACTGGAGAGGCACTGAAGTGGACATTGCTGTCACCTACAAAGGGATCCAGAGGAAAGGAAATGACAAACCTGGCAGCTTCGGAAGGAATGACAAGTCTTGGAGTTTGTACTGCTCTGAATCCGAATACTCGTTTATGCACAACAGCAAAAGCACGGCTGTATCTGTGCCCAGGTCCTCAAGGATTGGGGTTTATGTTGACTATGAGTCTGGGACACTGGCATTTTATAGTGTTTCTGACAAAATGACACTGCTGTACAAGGTGCAAACTAAATTTACTGAGCCTCTTTACCCTGGCATTGGAGTTTGGGGATACGGGACAACAGTGCGACTGTAATAAATCTACGCTGTAAAAACTATATAATCAGTAAATCATGACAACATATTCTTTTTATTGTAATTTCACTCACTCACTATCCTTCGGTGAGAAGCCCACACTAGTGGACATTAATTCCATGTGGGCCTTTTGAGGGCTTTTTGTGAG
Associated Phenotype:
Not determined