Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6902
Gene name Gene Name - the full gene name approved by the HGNC.
Tubulin folding cofactor A
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TBCA
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
5
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
5q14.1
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 information of associated ontologies with gene provided by GO database.
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 TAS 16130169
GO:0005829 Component Cytosol IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
610058 11579 ENSG00000171530
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Hypertrophic cardiomyopathy Hypertrophic Cardiomyopathy, Hypertrophic obstructive cardiomyopathy rs63750743, rs104894655, rs121908987, rs587776643, rs28938173, rs121908989, rs121908991, rs267606977, rs267606978, rs193922384, rs121909374, rs886041030, rs886041031, rs121909375, rs121909377
View all (752 more)
9527842
Unknown
Disease term Disease name Evidence References Source
Multiple myeloma Multiple myeloma MM cells lacking PSMC6 also developed resistance against Carfilzomib (CAR) GWAS, CBGDA
Associations from Text Mining
Disease Name Relationship Type References
Alzheimer Disease Associate 39392298
Carcinoma Hepatocellular Associate 34557456