Gene Gene information from NCBI Gene database.
Entrez ID 90580
Gene name Translocase of inner mitochondrial membrane 29
Gene symbol TIMM29
Synonyms (NCBI Gene)
C19orf52TIM29
Chromosome 19
Chromosome location 19p13.2
miRNA miRNA information provided by mirtarbase database.
136
miRTarBase ID miRNA Experiments Reference
MIRT724330 hsa-miR-590-3p HITS-CLIP 19536157
MIRT724329 hsa-miR-483-5p HITS-CLIP 19536157
MIRT724328 hsa-miR-4735-5p HITS-CLIP 19536157
MIRT724327 hsa-miR-4775 HITS-CLIP 19536157
MIRT531649 hsa-miR-4781-3p HITS-CLIP 21572407
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
16
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 27554484, 27718247, 28514442, 33961781
GO:0005739 Component Mitochondrion HTP 34800366
GO:0005739 Component Mitochondrion IEA
GO:0005743 Component Mitochondrial inner membrane IDA 27554484, 27718247, 32901109
GO:0005743 Component Mitochondrial inner membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
617380 25152 ENSG00000142444
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9BSF4
Protein name Mitochondrial import inner membrane translocase subunit Tim29 (TIM29)
Protein function Component of the TIM22 complex, a complex that mediates the import and insertion of multi-pass transmembrane proteins into the mitochondrial inner membrane. The TIM22 complex forms a twin-pore translocase that uses the membrane potential as the
PDB 7CGP
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10171 Tim29 22 186 Translocase of the Inner Mitochondrial membrane 29 Family
Sequence
Sequence length 260
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
MYOCARDIAL INFARCTION GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations