Gene Gene information from NCBI Gene database.
Entrez ID 84134
Gene name Translocase of outer mitochondrial membrane 40 like
Gene symbol TOMM40L
Synonyms (NCBI Gene)
TOMM40B
Chromosome 1
Chromosome location 1q23.3
miRNA miRNA information provided by mirtarbase database.
215
miRTarBase ID miRNA Experiments Reference
MIRT533583 hsa-miR-27a-3p PAR-CLIP 22012620
MIRT533582 hsa-miR-27b-3p PAR-CLIP 22012620
MIRT533581 hsa-miR-6895-5p PAR-CLIP 22012620
MIRT533580 hsa-miR-7160-3p PAR-CLIP 22012620
MIRT533579 hsa-miR-4512 PAR-CLIP 22012620
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
17
GO ID Ontology Definition Evidence Reference
GO:0003674 Function Molecular_function ND
GO:0005739 Component Mitochondrion HTP 34800366
GO:0005739 Component Mitochondrion IEA
GO:0005741 Component Mitochondrial outer membrane IEA
GO:0005742 Component Mitochondrial outer membrane translocase complex IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q969M1
Protein name Mitochondrial import receptor subunit TOM40B (Protein TOMM40-like)
Protein function Potential channel-forming protein implicated in import of protein precursors into mitochondria.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01459 Porin_3 26 302 Eukaryotic porin Family
Sequence
Sequence length 308
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  Mitophagy - animal
Amyotrophic lateral sclerosis
Pathways of neurodegeneration - multiple diseases
 
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
IGA GLOMERULONEPHRITIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
TOMM40L-related disorder Likely benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations