Gene Gene information from NCBI Gene database.
Entrez ID 6902
Gene name Tubulin folding cofactor A
Gene symbol TBCA
Synonyms (NCBI Gene)
-
Chromosome 5
Chromosome location 5q14.1
Summary The product of this gene is one of four proteins (cofactors A, D, E, and C) involved in the pathway leading to correctly folded beta-tubulin from folding intermediates. Cofactors A and D are believed to play a role in capturing and stabilizing beta-tubuli
miRNA miRNA information provided by mirtarbase database.
82
miRTarBase ID miRNA Experiments Reference
MIRT001495 hsa-miR-155-5p pSILAC 18668040
MIRT001495 hsa-miR-155-5p Reporter assay;Other 20584899
MIRT001495 hsa-miR-155-5p Proteomics 18668040
MIRT664211 hsa-miR-3156-5p HITS-CLIP 23824327
MIRT664210 hsa-miR-4733-5p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
18
GO ID Ontology Definition Evidence Reference
GO:0003723 Function RNA binding HDA 22681889
GO:0005515 Function Protein binding IPI 21044950, 32353859, 33060197
GO:0005730 Component Nucleolus IDA
GO:0005737 Component Cytoplasm IEA
GO:0005737 Component Cytoplasm TAS 16130169
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
610058 11579 ENSG00000171530
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O75347
Protein name Tubulin-specific chaperone A (TCP1-chaperonin cofactor A) (Tubulin-folding cofactor A) (CFA)
Protein function Tubulin-folding protein; involved in the early step of the tubulin folding pathway.
PDB 1H7C
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02970 TBCA 9 95 Tubulin binding cofactor A Domain
Sequence
Sequence length 108
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
5
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
CARDIOMYOPATHY, HYPERTROPHIC CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HYPERTROPHIC CARDIOMYOPATHY Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MULTIPLE MYELOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PELVIC ORGAN PROLAPSE 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
Alzheimer Disease Alzheimer disease Pubtator 39392298 Associate
★☆☆☆☆
Found in Text Mining only
Ankylosing spondylitis Ankylosing Spondylitis BEFREE 31128893
★☆☆☆☆
Found in Text Mining only
Arthritis Arthritis BEFREE 24405551, 31834562
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Hepatocellular carcinoma Pubtator 34557456 Associate
★☆☆☆☆
Found in Text Mining only
Dementia Dementia BEFREE 19939808
★☆☆☆☆
Found in Text Mining only
Depressive disorder Mental Depression BEFREE 31106586
★☆☆☆☆
Found in Text Mining only
Dermatitis, Atopic Dermatitis BEFREE 23671420
★☆☆☆☆
Found in Text Mining only
Disturbance in mood Mood Disorder BEFREE 28049104
★☆☆☆☆
Found in Text Mining only
Eczema Eczema BEFREE 23671420
★☆☆☆☆
Found in Text Mining only
Hypertrophic Cardiomyopathy Hypertrophic cardiomyopathy CTD_human_DG 9527842
★★☆☆☆
Found in Text Mining + Unknown/Other Associations