Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
401505
Gene name Gene Name - the full gene name approved by the HGNC.
Translocase of outer mitochondrial membrane 5
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TOMM5
Synonyms (NCBI Gene) Gene synonyms aliases
C9orf105, Tom5, bA613M10.3
Chromosome Chromosome number
9
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
9p13.2
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT049947 hsa-miR-30a-5p CLASH 23622248
MIRT041447 hsa-miR-193b-3p CLASH 23622248
MIRT504062 hsa-miR-548m PAR-CLIP 23446348
MIRT504061 hsa-miR-548ag PAR-CLIP 23446348
MIRT504060 hsa-miR-548ai PAR-CLIP 23446348
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005739 Component Mitochondrion HTP 34800366
GO:0005739 Component Mitochondrion IDA
GO:0005739 Component Mitochondrion IEA
GO:0005741 Component Mitochondrial outer membrane IEA
GO:0005741 Component Mitochondrial outer membrane NAS 18331822
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
616169 31369 ENSG00000175768
Protein
UniProt ID Q8N4H5
Protein name Mitochondrial import receptor subunit TOM5 homolog
PDB 7CK6 , 7CP9 , 7VBY , 7VC4 , 7VD2 , 7VDD , 8XVA , 9EIH , 9EII , 9EIJ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10642 Tom5 1 50 Mitochondrial import receptor subunit or translocase Family
Sequence
Sequence length 51
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Pink/Parkin Mediated Mitophagy
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Sarcoidosis Sarcoidosis N/A N/A GWAS
Schizophrenia Schizophrenia N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Carcinoma Hepatocellular Associate 37114494
Huntington Disease Associate 38447791
Intervertebral Disc Degeneration Associate 38041088
Mitochondrial Diseases Stimulate 21467644
Obesity Associate 24455749