ftr25

Ensembl ID:
ENSDARG00000093651
ZFIN ID:
ZDB-GENE-070912-323
Description:
Novel protein with Zinc finger, C3HC4 type (RING finger) and B-box zinc finger domains [Source:UniPr
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
sa5168 Essential Splice Site Mutation detected in F1 DNA During 2014

Mutation Details

Allele Name:
sa5168
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:
G > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098047 Essential Splice Site 307 553 3 8
ENSDART00000143023 Essential Splice Site 307 360 3 4
Genomic Location:
Chromosome 2 (position 48042771)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
CTGAGCTGGAGCAGCTTTCACACACTGATGATCACATACATTTCCTACAG[G/A]TAGCAGTGAAATGGAAAACATGAACTTTAGGATCATCCTATTATCACAGA
Associated Phenotype:
Not determined

GWAS

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

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

Register

If you would like to be informed when the status of this gene changes (for example, a new allele is generated or an allele is made available for distribution) then please enter your details below:

* quick link - http://q.sanger.ac.uk/q94qmkho