ZMP
TRIM69 (3 of 3)
Ensembl ID:
Description:
tripartite motif-containing 69 [Source:HGNC Symbol;Acc:17857]
Human Orthologue:
TRIM69
Human Description:
tripartite motif-containing 69 [Source:HGNC Symbol;Acc:17857]
Mouse Orthologue:
Trim69
Mouse Description:
tripartite motif-containing 69 Gene [Source:MGI Symbol;Acc:MGI:1918178]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22821 | Nonsense | Available for shipment | Available now |
sa10274 | Nonsense | Available for shipment | Available now |
sa36104 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa36103 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22820 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22821
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 |
---|---|---|---|---|---|
ENSDART00000083822 | Nonsense | 11 | 308 | 1 | 6 |
ENSDART00000123717 | Nonsense | 11 | 463 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 16 (position 23984385)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 21995123 |
GRCz11 | 16 | 21799375 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTACAGCAGGTGAATCATGGCTTCAGCTCTGTCTCTTTACCTCATGTG[T/A]CCGGTGTGTCTGAGTGACTTCAAAGTTCCAGTAAGTTTGCCCTGTGAACA
Long Flanking Sequence:
TATGGATCCATCCTGCCTTGTATCAACAGTCAGGCTGCTGGTGGTGGTGCAATGGTGTGGGGGATATTTTCTTGCCACACTTAGGGCCCATTAGTTTAAATTGAACATCATGTCAATGCCACAGCCTACCTAAGTATCGTTGTTGACCATGTCGAAGGTTTAAGGCAGTAAAGTGGGTCCAAGCCAGTACTAGTAAGCTGTACCTAATAAAGTGAGTGTATATCAGCAATGCAATTACTTCAATTTTCATGACAGTTAGTCGTACCATCTTGTAAGTTGTTGTCAGTAAGTTGTTGTCTTGTAAGTTTTTATTTTCAGTCTAGAAGTATGTGAAGCATCTTGTTCCCTGATGTGAAAGGGTGTGATCTGACACAAAAAGGCCTAAATAAACACTACACCGCCATTGTTTCATCAGCAAAGTGTATACTTAATAGTCTGACATACTAGTCTGACTACAGCAGGTGAATCATGGCTTCAGCTCTGTCTCTTTACCTCATGTG[T/A]CCGGTGTGTCTGAGTGACTTCAAAGTTCCAGTAAGTTTGCCCTGTGAACATGTTCTCTGTCGGCAGTGTGCTTCCAGGTATTTAGAATCCAGCAAAGGACCTCATAAATGCCCAGAATGCAGACAAAACTTCACCAGGACGGATCTTAAAGGTATTCGAGTTCTGAGAAATGTTGTGGACGCCATACAAGAACAGCGTAAGAAAAAGCAATTGATTCAACCGAACGCAGAGGAAATGCTGTGTTCTGAGCACAAGGAGCCGCTTAAACTTTTCTGTGTCAATGACCAGAGATTAGTTTGCCTCATCTGCAAAGAGGGAATGAAACACAGCGGACACAGTTTCAAACCTGTAAAGGAAGCTAAGGAGATGAGTGAGGTTGAAACAACATATTTGAATTTAACAGCTAATTTCATATGAATTACTGTGACATGAATATGTGTGGAATAACAGATATTTTTGTTGTTGTTATTATAATTTAGAAAATGGTGAACAAAGCATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10274
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 |
---|---|---|---|---|---|
ENSDART00000083822 | Nonsense | 43 | 308 | 1 | 6 |
ENSDART00000123717 | Nonsense | 43 | 463 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 16 (position 23984291)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 21995029 |
GRCz11 | 16 | 21799281 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GYGAACATGTTCTCTGTCGGCAGTGTGCTTCCAGGTATTTAGAATCCAGC[A/T]AAGGACCTCATAAATGCCCAGAATGCAGACAAAACTTYACCRGGACGGAT
Long Flanking Sequence:
TTTAAATTGAACATCATGTCAATGCCACAGCCTACCTAAGTATCGTTGTTGACCATGTCGAAGGTTTAAGGCAGTAAAGTGGGTCCAAGCCAGTACTAGTAAGCTGTACCTAATAAAGTGAGTGTATATCAGCAATGCAATTACTTCAATTTTCATGACAGTTAGTCGTACCATCTTGTAAGTTGTTGTCAGTAAGTTGTTGTCTTGTAAGTTTTTATTTTCAGTCTAGAAGTATGTGAAGCATCTTGTTCCCTGATGTGAAAGGGTGTGATCTGACACAAAAAGGCCTAAATAAACACTACACCGCCATTGTTTCATCAGCAAAGTGTATACTTAATAGTCTGACATACTAGTCTGACTACAGCAGGTGAATCATGGCTTCAGCTCTGTCTCTTTACCTCATGTGTCCGGTGTGTCTGAGTGACTTCAAAGTTCCAGTAAGTTTGCCCTGTGAACATGTTCTCTGTCGGCAGTGTGCTTCCAGGTATTTAGAATCCAGC[A/T]AAGGACCTCATAAATGCCCAGAATGCAGACAAAACTTCACCAGGACGGATCTTAAAGGTATTCGAGTTCTGAGAAATGTTGTGGACGCCATACAAGAACAGCGTAAGAAAAAGCAATTGATTCAACCGAACGCAGAGGAAATGCTGTGTTCTGAGCACAAGGAGCCGCTTAAACTTTTCTGTGTCAATGACCAGAGATTAGTTTGCCTCATCTGCAAAGAGGGAATGAAACACAGCGGACACAGTTTCAAACCTGTAAAGGAAGCTAAGGAGATGAGTGAGGTTGAAACAACATATTTGAATTTAACAGCTAATTTCATATGAATTACTGTGACATGAATATGTGTGGAATAACAGATATTTTTGTTGTTGTTATTATAATTTAGAAAATGGTGAACAAAGCATTGAGTTTTATTTTAGATGACAACAAGCAAATGGGTGACATGATCCTGAATCAGACGCTTGAAATCACAAAATCCAAGGTGGGTTAAAAGACATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36104
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083822 | Essential Splice Site | 246 | 308 | 3 | 6 |
ENSDART00000123717 | Essential Splice Site | 246 | 463 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 16 (position 23981953)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 21992691 |
GRCz11 | 16 | 21796943 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATATTGGAGTCAGGACTAAAGATAAACCAGCCAGAGAGGTTTTTAGAGG[T/A]AACGTTGTTCTGTAGCACATTCCAGAAACATGTTTAGACTCAGCATGGTG
Long Flanking Sequence:
GCTTTTTTACAATAGAAGTCAGTTGCTAGAGTGCCGTAAGTGGTTGCTAGGGTGTGGCTAGTAACTTGAAAGGTCATCTGTGATTGGCAGATTGGTAGTCTAAATGAAATGAGCAGAAAGAATAATAAGTTAATGTAGTATAACAGTATTGTCTTTCTCAAGCCATCATAATGAAAGCTTGTTGTATATTGTGACTGAAAAAATGTATTATCGTTATTTTGGCTGCTTCACTTTTTTGTTCTCAAAGTCAAATGTGAATCTACAGGAAAGGGCCAAACATCTTGAGACCCTTATGCATGCTCAGTTTAAGAAAATGCATGACTTCTTGTTGAAAAAGGAGGAGGATGCAATGAGACAGATCCAGAAAGCAGCAAACAGTGCTGAGGAATCAATGAAGCATAATGGGTCGTTGTTGTCAAAGTTGCAAATAAAAGGAAACAGCCAGGTGTCCATATTGGAGTCAGGACTAAAGATAAACCAGCCAGAGAGGTTTTTAGAGG[T/A]AACGTTGTTCTGTAGCACATTCCAGAAACATGTTTAGACTCAGCATGGTGGATTTCATAACACCTCAAATCTGTTTCTATTATTTTCAGTGGTGGAGTAAAGACGGGTTTCCTTTGGTTAATGAAATCAGCGAGAGCAAAAACATCAAGTTTGCCATTCCAACCAAGTAAGATAGAAAATGCTTTTTAGCTGATATTTTGGACACTTTTACACAGCCATTTCTTAATATTACTGCATTACAACACAACAAAACTCCATACATGCTTAAAAATATTTTTTATCGACAGATTTGAACCGTTTTAAATGAAATTATAGTCTATCAAATACATAAGCTAATCATGTAATACCATTACTAATACATATTAGGTGTCTGCATAATATTATTATTTTTTAATACATTTTAAGGGTTTGTTGGTTGTTCCTTGGTGAGCTCTTTCAAGCAAATGAAAAAAAGACGCTTTTCCACTTTGCACAGCTTGGCTGACTTCAGTTCTTGCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36103
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083822 | Nonsense | 269 | 308 | 5 | 6 |
ENSDART00000123717 | None | None | 463 | None | 6 |
Genomic Location (Zv9):
Chromosome 16 (position 23979883)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 21990621 |
GRCz11 | 16 | 21794873 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAATGTTAATTTTCATGAGAATGTTGCAAGTTCATAGTGCAGTCCTAGCT[C/A]AATTTCATGTGTGCAATGTTGCTGTAAACATTTTAACGGTTGTTTTCTAT
Long Flanking Sequence:
AACAGCCTTCACTAAGATCAATGGCCCAGTTCAGTGTTGCCATCTAGGAAAAAAATAATTAGTGCAAATAAGAATTCTAAATTTACATGCAAACATATTCAAAATACGTATGGTAATAAAGTATAGGGGAACAGATACATTAAATGCTTACTTTTCTTGTGACAAAATGTATGTCATGAGCGCTGTATGCAAACACGTGTATAAAACTGAAGCATGCTTTGGGTTTATTGCACATGCATTGTGCATGTTGAACTTTGCACTATTTAATATGTCCACAAGGTGTCAACACTGAGCTGGCCTGCTGTTATACTGTCAACTAAGGTACAGGAGCCAGAACAGTTTACTAAAAGTGTCTGAAAACTTTATTAAAATGTTCTTTTTATTGTTGAAAAAAAAGAGAGAGAGAAAAGACTCATGTTCCAGACACTGAGCAAATATCTTTTTGTGCTCTAATGTTAATTTTCATGAGAATGTTGCAAGTTCATAGTGCAGTCCTAGCT[C/A]AATTTCATGTGTGCAATGTTGCTGTAAACATTTTAACGGTTGTTTTCTATAGATTTAAGTCGAAACATGATGGCGTTCGAGTGATTTGTGACCATTTTACCCTTGGGCCTTATGAAACTGACCTTCCGCTCATGGTTTGGCGAGACATGCTGGGTCCTGTTAAACGAGGTGAGTTGAGCTTTCATGAACATCTCTAATAAAGAAACACATTTTTATACTGTGTTTCTGCCATTAATCTTATTATAACCACTATATTTTATCAGTGGTTATAATGTTTTACTCCAAGGCCCCCAAATACATTATTTAAAGATACCCTTAAATGTTTCTTTATATGCATCCTTATATGTTAAAAGCTTGTTTAATGTCAAAGCTGCTATATTTGTACTATGTTATGTTATTATGTATTAGCACATTAAAATAATTAAAATGATTAAATTCCTTAATTTTCGTAAGCGAATAGTTTCATGTTTTTTATTACCAAGGAAGTTAAATTACTTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22820
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 |
---|---|---|---|---|---|
ENSDART00000083822 | None | None | 308 | None | 6 |
ENSDART00000123717 | Essential Splice Site | 311 | 463 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 16 (position 23979713)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 21990451 |
GRCz11 | 16 | 21794703 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCTTCCGCTCATGGTTTGGCGAGACATGCTGGGTCCTGTTAAACGAGG[T/C]GAGTTGAGCTTTCATGAACATCTCTAATAAAGAAACACATTTTTATACTG
Long Flanking Sequence:
ATGTCATGAGCGCTGTATGCAAACACGTGTATAAAACTGAAGCATGCTTTGGGTTTATTGCACATGCATTGTGCATGTTGAACTTTGCACTATTTAATATGTCCACAAGGTGTCAACACTGAGCTGGCCTGCTGTTATACTGTCAACTAAGGTACAGGAGCCAGAACAGTTTACTAAAAGTGTCTGAAAACTTTATTAAAATGTTCTTTTTATTGTTGAAAAAAAAGAGAGAGAGAAAAGACTCATGTTCCAGACACTGAGCAAATATCTTTTTGTGCTCTAATGTTAATTTTCATGAGAATGTTGCAAGTTCATAGTGCAGTCCTAGCTCAATTTCATGTGTGCAATGTTGCTGTAAACATTTTAACGGTTGTTTTCTATAGATTTAAGTCGAAACATGATGGCGTTCGAGTGATTTGTGACCATTTTACCCTTGGGCCTTATGAAACTGACCTTCCGCTCATGGTTTGGCGAGACATGCTGGGTCCTGTTAAACGAGG[T/C]GAGTTGAGCTTTCATGAACATCTCTAATAAAGAAACACATTTTTATACTGTGTTTCTGCCATTAATCTTATTATAACCACTATATTTTATCAGTGGTTATAATGTTTTACTCCAAGGCCCCCAAATACATTATTTAAAGATACCCTTAAATGTTTCTTTATATGCATCCTTATATGTTAAAAGCTTGTTTAATGTCAAAGCTGCTATATTTGTACTATGTTATGTTATTATGTATTAGCACATTAAAATAATTAAAATGATTAAATTCCTTAATTTTCGTAAGCGAATAGTTTCATGTTTTTTATTACCAAGGAAGTTAAATTACTTTCTCAGTTGTTCTGTAAATAGATTAGTTTTAGTTTTAGTATATTTTGTGGTTTGGTTTGGTTTATTTATACTTATTTATTTAAAAATACTTTTTAAATTGCTTATCAAATAAAATATTTTAGAGCTTGGTGTTATTTAAAAAATATAAAGTACCTGTAATTAAATTGATTAGG
Associated Phenotype:
Not determined