LOC566988

Ensembl ID:: ENSDARG00000070943
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 is 1 allele of this gene:

Allele name	Consequence	Status	Availability Estimate
sa11244	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:: sa11244
Current Status:: Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:: A > C
Consequence:: Essential Splice Site

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000074445	Essential Splice Site	352	544	5	6

Genomic Location:: Chromosome 3 (position 50171464)
KASP Assay ID:: None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:: TGTAACATCATWTTAGAAACATGCATGACACTTACACCAATACAYCAATT[A/C]TGTKTTTTGATTTTCCCAGTGACAAAAAMTAGTCCCAAGACCAGGAACGA
Associated Phenotype:: Not determined

GWAS

This gene's human homologue has been identified in the following GWAS studies:

White matter hyperintensity burden: Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium. (View Study)

(GWAS data comes from http://www.genome.gov/gwastudies/.)

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