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Trim69 Gene Detail
Summary
  • Symbol
    Trim69
  • Name
    tripartite motif-containing 69
  • Synonyms
    4921519C19Rik, Rnf36, Trif
  • Feature Type
    protein coding gene
  • IDs
    MGI:1918178
    NCBI Gene: 70928
  • Alliance
  • Transcription Start Sites
    4 TSS
Location &
Maps
more
  • Sequence Map
    Chr2:121991189-122009503 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 2, 60.55 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    547 from dbSNP Build 142
  • Strain Annotations
    19
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1918178
protein coding gene Chr2:121991181-122009508 (+)
129S1/SvImJ ENSMUSG00200045180
protein coding gene Chr2:118922512-118942657 (+)
A/J ENSMUSG00195024877
protein coding gene Chr2:118961616-118981109 (+)
AKR/J ENSMUSG00220039673
protein coding gene Chr2:118884923-118905022 (+)
BALB/cJ ENSMUSG00180040244
protein coding gene Chr2:118762363-118781854 (+)
C3H/HeJ ENSMUSG00175024333
protein coding gene Chr2:119236268-119255759 (+)
C57BL/6NJ ENSMUSG00215020837
protein coding gene Chr2:118910018-118928352 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0024207
protein coding gene Chr2:115004375-115025542 (+)
CAST/EiJ ENSTCUG00005015997
protein coding gene Chr2:118178009-118196417 (+)
CBA/J ENSMUSG00210007139
protein coding gene Chr2:119077121-119096612 (+)
DBA/2J ENSMUSG00185041850
protein coding gene Chr2:118759503-118778994 (+)
FVB/NJ ENSMUSG00205031549
protein coding gene Chr2:117985277-118005378 (+)
JF1/MsJ ENSUMUG00000007864
protein coding gene Chr2:118658269-118676595 (+)
LP/J ENSMUSG00230019686
protein coding gene Chr2:120581944-120603677 (+)
NOD/ShiLtJ ENSMUSG00190029823
protein coding gene Chr2:119009427-119029525 (+)
NZO/HlLtJ ENSMUSG00225003036
protein coding gene Chr2:128483748-128503239 (+)
PWK/PhJ ENSLUMG00010039611
protein coding gene Chr2:118595039-118613621 (+)
SPRET/EiJ ENSMSPG00010036105
protein coding gene Chr2:120989139-121013445 (+)
WSB/EiJ ENSIUOG00005024454
protein coding gene Chr2:118732727-118752830 (+)



Homology
more
  • Human Ortholog
    TRIM69, tripartite motif containing 69
  • Vertebrate Orthologs
    4
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    TRIM69, tripartite motif containing 69
  • Synonyms
    HSD-34, HSD34, RNF36, Trif
  • Links
    NCBI Gene ID: 140691
    UniProt: Q86WT6

  • Chr Location
    15q21.1; chr15:44728988-44767829 (+)  GRCh38

Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    2 phenotypes from 2 alleles in 2 genetic backgrounds
    11 phenotype references
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
integument
immune system
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
neoplasm
vision/eye

Click cells to view annotations.
Mice homozygous for a knock-out allele are viable and exhibit normal body development, fertility and behavior. Male mice show normal spermatogenesis with no detectable alterations in sperm morphology, count or motility.
Gene Ontology
(GO)
Classifications
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  • All GO Annotations
  • GO References
Molecular Function

carbohydrate derivative binding
cytoskeletal protein binding
DNA binding
enzyme regulator
hydrolase
ligase
lipid binding
oxidoreductase
RNA binding
signaling receptor activity
signaling receptor binding
transcription
transferase
transporter
Biological Process

carbohydrate derivative metabolism
cell differentiation
cell population proliferation
cellular component organization
DNA-templated transcription
establishment of localization
homeostatic process
immune system process
lipid metabolic process
programmed cell death
protein metabolic process
response to stimulus
signaling
system development
Cellular Component

cell projection
cytoplasmic vesicle
cytoskeleton
cytosol
endoplasmic reticulum
endosome
extracellular region
Golgi apparatus
mitochondrion
membraneless organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
protein-containing complex
synapse
vacuole
Click cells to view annotations.
Expression
less
Expression Overview

early conceptus
embryo ectoderm
embryo endoderm
embryo mesoderm
embryo mesenchyme
extraembryonic component
alimentary system
auditory system
branchial arches
cardiovascular system
connective tissue
endocrine system
exocrine system
hemolymphoid system
integumental system
limbs
liver and biliary system
musculoskeletal system
nervous system
olfactory system
reproductive system
respiratory system
urinary system
visual system
Click cells to view annotations.


  • Assay Results
  • Tissues
  • cDNA Data
  • Literature Summary
Sequences &
Gene Models
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Representative SequencesLengthStrain/SpeciesFlank
genomic 70928 NCBI Gene Model | MGI Sequence Detail 18315 C57BL/6J ±  kb
transcript NR_166637 RefSeq | MGI Sequence Detail 1753 C57BL/6  
polypeptide Q80X56 UniProt | EBI | MGI Sequence Detail 500 Not Applicable  
For the selected sequence
Protein
Information
less
Molecular
Reagents
less
  • All nucleic 10
    cDNA 10

    Microarray probesets 3
References
more
  • Summaries
    All 39
    Developmental Gene Expression 2
    Gene Ontology 7
    Phenotypes 11
  • Earliest
    J:109968 Roderick TH, et al., Nineteen paracentric chromosomal inversions in mice. Genetics. 1974 Jan;76(1):109-17
  • Latest
    J:345621 Adams DJ, et al., Genetic determinants of micronucleus formation in vivo. Nature. 2024 Mar;627(8002):130-136

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Funding Information
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last database update
09/08/2026
MGI 6.24
The Jackson Laboratory