ftr23

Ensembl ID:
ENSDARG00000067985
ZFIN ID:
ZDB-GENE-070912-322
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
sa33022 Nonsense Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
sa33022
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 2017.
Mutation:
C > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000029400 Nonsense 542 552 6 6
ENSDART00000098049   None 489 None 6
ENSDART00000098051   None 158 None 3
ENSDART00000122206   None 358 None 5

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 48047557)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 48079221
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GACAACATTCACTCAACCGCTCTACCCTGGGTTTGGGATTAATTTTGGAT[C/A]AACAATAAAACTTCTATTGTTGAAGTCCTTATGAACTATAAGATAATTTA
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/.)

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