Gene Gene information from NCBI Gene database.
Entrez ID 80305
Gene name TraB domain containing
Gene symbol TRABD
Synonyms (NCBI Gene)
LP6054PP2447
Chromosome 22
Chromosome location 22q13.33
miRNA miRNA information provided by mirtarbase database.
100
miRTarBase ID miRNA Experiments Reference
MIRT005240 hsa-let-7b-5p pSILAC 18668040
MIRT005240 hsa-let-7b-5p Proteomics;Other 18668040
MIRT005240 hsa-let-7b-5p CLASH 23622248
MIRT050774 hsa-miR-17-3p CLASH 23622248
MIRT1450648 hsa-miR-1197 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
4
GO ID Ontology Definition Evidence Reference
GO:0005739 Component Mitochondrion HTP 34800366
GO:0005741 Component Mitochondrial outer membrane IDA 38843396
GO:0008053 Process Mitochondrial fusion IMP 38843396
GO:0160204 Function Mitochondrion-mitochondrion outer membrane tether activity IMP 38843396
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
621246 28805 ENSG00000170638
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9H4I3
Protein name TraB domain-containing protein (Protein TTG2)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01963 TraB 64 311 TraB family Family
Sequence
Sequence length 376
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
TYPE 2 DIABETES MELLITUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Acute lymphocytic leukemia Lymphocytic Leukemia BEFREE 8142620
★☆☆☆☆
Found in Text Mining only
Celiac Disease Celiac disease BEFREE 30023063
★☆☆☆☆
Found in Text Mining only
insulinoma Insulinoma BEFREE 29654212
★☆☆☆☆
Found in Text Mining only
leukemia Leukemia BEFREE 1923511
★☆☆☆☆
Found in Text Mining only
Neoplasms Neoplasms BEFREE 25173755
★☆☆☆☆
Found in Text Mining only
Stomach Neoplasms Stomach neoplasms Pubtator 25173755 Associate
★☆☆☆☆
Found in Text Mining only
Tendinopathy Tendinopathy BEFREE 21710445
★☆☆☆☆
Found in Text Mining only