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e.g. ENSDARG00000093395 or slc2a11b or ENSG00000135862 or LAMC1 or sa457
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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:
-
Order Allele From ZIRC
Order Allele From EZRC - 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 (Zv9):
- Chromosome 3 (position 50171464)
- Other Location(s):
-
Assembly Chromosome Position GRCz10 3 44865884 GRCz11 3 49011295 - 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/.)
Register
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