TRIM69 (3 of 3)

Ensembl ID:
ENSDARG00000059905
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 3 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa22821 Nonsense Mutation detected in F1 DNA During 2014
sa10274 Nonsense Available for shipment Available now
sa22820 Essential Splice Site Mutation detected in F1 DNA During 2014

Mutation Details

Allele Name:
sa22821
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2014.
Mutation:
T > A
Consequence:
Nonsense
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:
Chromosome 16 (position 23984385)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GACTACAGCAGGTGAATCATGGCTTCAGCTCTGTCTCTTTACCTCATGTG[T/A]CCGGTGTGTCTGAGTGACTTCAAAGTTCCAGTAAGTTTGCCCTGTGAACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10274
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Nonsense
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:
Chromosome 16 (position 23984291)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
GYGAACATGTTCTCTGTCGGCAGTGTGCTTCCAGGTATTTAGAATCCAGC[A/T]AAGGACCTCATAAATGCCCAGAATGCAGACAAAACTTYACCRGGACGGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22820
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2014.
Mutation:
T > C
Consequence:
Essential Splice Site
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:
Chromosome 16 (position 23979713)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GACCTTCCGCTCATGGTTTGGCGAGACATGCTGGGTCCTGTTAAACGAGG[T/C]GAGTTGAGCTTTCATGAACATCTCTAATAAAGAAACACATTTTTATACTG
Associated Phenotype:
Not determined

Register

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* quick link - http://q.sanger.ac.uk/9inv3duv