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e.g. ENSDARG00000093395 or slc2a11b or ENSG00000135862 or LAMC1 or sa457
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ftr07
- Ensembl ID:
- ENSDARG00000078446
- ZFIN ID:
- ZDB-GENE-070912-229
- Description:
- Novel protein [Source:UniProtKB/TrEMBL;Acc:B0S719]
- 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 |
---|---|---|---|
sa17121 | Nonsense | Available for shipment | Available now |
Mutation Details
- Allele Name:
- sa17121
- 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:
- C > T
- Consequence:
- Nonsense
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022008 | Nonsense | 339 | 541 | 4 | 6 |
ENSDART00000141210 | None | 278 | None | 3 |
- Genomic Location (Zv9):
- Chromosome 2 (position 42413732)
- Other Location(s):
-
Assembly Chromosome Position GRCz10 2 42463196 GRCz11 2 42312614 - KASP Assay ID:
- None (used for ordering genotyping assays from LGC Genomics)
- KASP Sequence:
- CWTCTGTCTCTGAGTTAAAYGAGAAACTCCAGCAGWCTTTGAATGTTGAA[C/T]RAGAAAACATATTTCGGATTGGTAAAGTWTACTATTGACACTATTAATTT
- 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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