Gene Gene information from NCBI Gene database.
Entrez ID 27175
Gene name Tubulin gamma 2
Gene symbol TUBG2
Synonyms (NCBI Gene)
-
Chromosome 17
Chromosome location 17q21.2
miRNA miRNA information provided by mirtarbase database.
42
miRTarBase ID miRNA Experiments Reference
MIRT1463548 hsa-miR-1273g CLIP-seq
MIRT1463549 hsa-miR-127-5p CLIP-seq
MIRT1463550 hsa-miR-3154 CLIP-seq
MIRT1463551 hsa-miR-320e CLIP-seq
MIRT1463552 hsa-miR-3622b-5p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
30
GO ID Ontology Definition Evidence Reference
GO:0000070 Process Mitotic sister chromatid segregation IBA
GO:0000166 Function Nucleotide binding IEA
GO:0000212 Process Meiotic spindle organization IBA
GO:0000242 Component Pericentriolar material IEA
GO:0000278 Process Mitotic cell cycle IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
605785 12419 ENSG00000037042
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NRH3
Protein name Tubulin gamma-2 chain (Gamma-2-tubulin)
Protein function Tubulin is the major constituent of microtubules, protein filaments consisting of alpha- and beta-tubulin heterodimers (PubMed:38305685). Gamma-tubulin is a key component of the gamma-tubulin ring complex (gTuRC) which mediates microtubule nucle
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00091 Tubulin 4 215 Tubulin/FtsZ family, GTPase domain Domain
PF03953 Tubulin_C 264 393 Tubulin C-terminal domain Domain
Sequence
Sequence length 451
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Motor proteins
Human papillomavirus infection
  Recruitment of mitotic centrosome proteins and complexes
Recruitment of NuMA to mitotic centrosomes
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PSORIASIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
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
Astrocytoma Astrocytoma Pubtator 18670637 Associate
★☆☆☆☆
Found in Text Mining only
Developmental Disabilities Developmental disability Pubtator 36672848 Associate
★☆☆☆☆
Found in Text Mining only
Microcephaly Microcephaly Pubtator 36672848 Associate
★☆☆☆☆
Found in Text Mining only
Perisylvian syndrome Perisylvian syndrome Pubtator 36672848 Associate
★☆☆☆☆
Found in Text Mining only
Polymicrogyria Polymicrogyria Pubtator 36672848 Associate
★☆☆☆☆
Found in Text Mining only