TUBA1A Gene

HGNC Family	Tubulins (TUB)
Name	tubulin, alpha 1a
Description	Microtubules of the eukaryotic cytoskeleton perform essential and diverse functions and are composed of a heterodimer of alpha and beta tubulins. The genes encoding these microtubule constituents belong to the tubulin superfamily, which is composed of six distinct families. Genes from the alpha, beta and gamma tubulin families are found in all eukaryotes. The alpha and beta tubulins represent the major components of microtubules, while gamma tubulin plays a critical role in the nucleation of microtubule assembly. There are multiple alpha and beta tubulin genes, which are highly conserved among species. This gene encodes alpha tubulin and is highly similar to the mouse and rat Tuba1 genes. Northern blot studies have shown that the gene expression is predominantly found in morphologically differentiated neurologic cells. This gene is one of three alpha-tubulin genes in a cluster on chromosome 12q. Mutations in this gene cause lissencephaly type 3 (LIS3) - a neurological condition characterized by microcephaly, intellectual disability, and early-onset epilepsy caused by defective neuronal migration. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2017]
Summary	{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nTUBA1A encodes a neuron‐specific α‐tubulin that is a fundamental structural subunit of microtubules. It is essential for the formation of tubulin heterodimers and the assembly of a dynamic microtubule network that underlies neuronal migration and proper lamination of the cerebral cortex. Studies in both mouse models and human patients have demonstrated that mutations in TUBA1A disrupt GTP binding, heterodimer formation, and interactions with microtubule‐associated proteins, leading to abnormal cortical architecture and impaired neuronal displacement."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "4"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nMutations in TUBA1A are now recognized as one of the major causes of “tubulinopathies,” a group of neurodevelopmental disorders that include lissencephaly, pachygyria, polymicrogyria, and other complex malformations such as agenesis or dysgenesis of the corpus callosum, cerebellar hypoplasia, and hippocampal anomalies. Notably, de novo missense mutations in this gene have also been implicated in conditions ranging from severe fetal brain malformations to cerebral palsy, highlighting its critical expression during central nervous system development."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "5", "end_ref": "11"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nInsights into the molecular mechanisms reveal that many TUBA1A mutations result in reduced efficiency of chaperone‐assisted folding, compromised heterodimer stability, and defective integration into the microtubule lattice. In some cases, mutant TUBA1A protein incorporates into microtubules and exerts a dominant-negative “poisoning” effect on microtubule dynamics—altering microtubule polymerization properties, stability, and interactions with motor proteins—which in turn perturbs nucleus–centrosome coupling and neuronal migration."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "12", "end_ref": "16"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nBeyond its established role in neural migration and cortical development, altered TUBA1A expression has also been linked to aberrant cell dynamics in other biological contexts such as tumor cell behavior. For instance, high levels of TUBA1A expression have been associated with pathways that might influence tumor–microenvironment interactions and chemotherapeutic resistance in gastric cancer, suggesting that TUBA1A function and regulation may have broader implications for cellular morphogenesis and pathology."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "17"}]}, {"type": "t", "text": ""}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "David A Keays, Guoling Tian, Karine Poirier, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell (2007)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.cell.2006.12.017"}], "href": "https://doi.org/10.1016/j.cell.2006.12.017"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17218254"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17218254"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Karine Poirier, David A Keays, Fiona Francis, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A)."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Hum Mutat (2007)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/humu.20572"}], "href": "https://doi.org/10.1002/humu.20572"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17584854"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17584854"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Ravinesh A Kumar, Daniela T Pilz, Timothy D Babatz, et al. "}, {"type": "b", "children": [{"type": "t", "text": "TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulins."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Hum Mol Genet (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/hmg/ddq182"}], "href": "https://doi.org/10.1093/hmg/ddq182"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20466733"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20466733"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Thomas D Cushion, William B Dobyns, Jonathan G L Mullins, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Overlapping cortical malformations and mutations in TUBB2B and TUBA1A."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Brain (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/brain/aws338"}], "href": "https://doi.org/10.1093/brain/aws338"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23361065"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23361065"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Catherine Fallet-Bianco, Laurence Loeuillet, Karine Poirier, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Neuropathological phenotype of a distinct form of lissencephaly associated with mutations in TUBA1A."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Brain (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/brain/awn155"}], "href": "https://doi.org/10.1093/brain/awn155"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18669490"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18669490"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "N Bahi-Buisson, K Poirier, N Boddaert, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Refinement of cortical dysgeneses spectrum associated with TUBA1A mutations."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Med Genet (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1136/jmg.2008.058073"}], "href": "https://doi.org/10.1136/jmg.2008.058073"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18728072"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18728072"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "D J Morris-Rosendahl, J Najm, A M A Lachmeijer, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Refining the phenotype of alpha-1a Tubulin (TUBA1A) mutation in patients with classical lissencephaly."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Clin Genet (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1111/j.1399-0004.2008.01093.x"}], "href": "https://doi.org/10.1111/j.1399-0004.2008.01093.x"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18954413"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18954413"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "A C Jansen, A Oostra, B Desprechins, et al. "}, {"type": "b", "children": [{"type": "t", "text": "TUBA1A mutations: from isolated lissencephaly to familial polymicrogyria."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Neurology (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1212/WNL.0b013e31821043f5"}], "href": "https://doi.org/10.1212/WNL.0b013e31821043f5"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21403111"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21403111"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Karine Poirier, Yoann Saillour, Franck Fourniol, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Expanding the spectrum of TUBA1A-related cortical dysgenesis to Polymicrogyria."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Eur J Hum Genet (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/ejhg.2012.195"}], "href": "https://doi.org/10.1038/ejhg.2012.195"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22948023"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22948023"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Catherine Fallet-Bianco, Annie Laquerrière, Karine Poirier, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephaly."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Acta Neuropathol Commun (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1186/2051-5960-2-69"}], "href": "https://doi.org/10.1186/2051-5960-2-69"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25059107"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25059107"}]}, {"type": "r", "ref": 11, "children": [{"type": "t", "text": "Sheng Chih Jin, Sara A Lewis, Somayeh Bakhtiari, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Mutations disrupting neuritogenesis genes confer risk for cerebral palsy."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Genet (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s41588-020-0695-1"}], "href": "https://doi.org/10.1038/s41588-020-0695-1"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32989326"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32989326"}]}, {"type": "r", "ref": 12, "children": [{"type": "t", "text": "Guoling Tian, Xiang-Peng Kong, Xavier H Jaglin, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A pachygyria-causing alpha-tubulin mutation results in inefficient cycling with CCT and a deficient interaction with TBCB."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Biol Cell (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1091/mbc.e07-09-0861"}], "href": "https://doi.org/10.1091/mbc.e07-09-0861"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18199681"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18199681"}]}, {"type": "r", "ref": 13, "children": [{"type": "t", "text": "Guoling Tian, Xavier H Jaglin, David A Keays, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Disease-associated mutations in TUBA1A result in a spectrum of defects in the tubulin folding and heterodimer assembly pathway."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Hum Mol Genet (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/hmg/ddq276"}], "href": "https://doi.org/10.1093/hmg/ddq276"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20603323"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20603323"}]}, {"type": "r", "ref": 14, "children": [{"type": "t", "text": "Yohei Bamba, Tomoko Shofuda, Mitsuhiro Kato, et al. "}, {"type": "b", "children": [{"type": "t", "text": "In vitro characterization of neurite extension using induced pluripotent stem cells derived from lissencephaly patients with TUBA1A missense mutations."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Brain (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1186/s13041-016-0246-y"}], "href": "https://doi.org/10.1186/s13041-016-0246-y"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27431206"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27431206"}]}, {"type": "r", "ref": 15, "children": [{"type": "t", "text": "Richard Belvindrah, Kathiresan Natarajan, Preety Shabajee, et al. 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"}, {"type": "b", "children": [{"type": "t", "text": "Tubulin mutations in brain development disorders: Why haploinsufficiency does not explain TUBA1A tubulinopathies."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cytoskeleton (Hoboken) (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/cm.21567"}], "href": "https://doi.org/10.1002/cm.21567"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31574570"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31574570"}]}, {"type": "r", "ref": 17, "children": [{"type": "t", "text": "Dazhi Wang, Zheng Jiao, Yinghui Ji, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Elevated TUBA1A Might Indicate the Clinical Outcomes of Patients with Gastric Cancer, Being Associated with the Infiltration of Macrophages in the Tumor Immune Microenvironment."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Gastrointestin Liver Dis (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.15403/jgld-2834"}], "href": "https://doi.org/10.15403/jgld-2834"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33331338"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33331338"}]}]}]}
Synonyms	B-ALPHA-1, LIS3, TUBA3
Proteins	TBA1A_HUMAN
NCBI Gene ID	7846
API
Download Associations
Predicted Functions
Co-expressed Genes
Expression in Tissues and Cell Lines

Functional Associations

TUBA1A has 14,312 functional associations with biological entities spanning 8 categories (molecular profile, organism, functional term, phrase or reference, chemical, disease, phenotype or trait, structural feature, cell line, cell type or tissue, gene, protein or microRNA) extracted from 139 datasets.

Click the + buttons to view associations for TUBA1A from the datasets below.

If available, associations are ranked by standardized value

Harmonizome 3.0

TUBA1A Gene

Functional Associations

Please acknowledge the Harmonizome in your publications by citing the following reference(s):

	Dataset	Summary
	Achilles Cell Line Gene Essentiality Profiles	cell lines with fitness changed by TUBA1A gene knockdown relative to other cell lines from the Achilles Cell Line Gene Essentiality Profiles dataset.
	Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles	tissues with high or low expression of TUBA1A gene relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
	Allen Brain Atlas Aging Dementia and Traumatic Brain Injury Tissue Sample Gene Expression Profiles	tissue samples with high or low expression of TUBA1A gene relative to other tissue samples from the Allen Brain Atlas Aging Dementia and Traumatic Brain Injury Tissue Sample Gene Expression Profiles dataset.
	Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray	tissue samples with high or low expression of TUBA1A gene relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
	Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq	tissue samples with high or low expression of TUBA1A gene relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
	Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles	tissues with high or low expression of TUBA1A gene relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
	Biocarta Pathways	pathways involving TUBA1A protein from the Biocarta Pathways dataset.
	BioGPS Cell Line Gene Expression Profiles	cell lines with high or low expression of TUBA1A gene relative to other cell lines from the BioGPS Cell Line Gene Expression Profiles dataset.
	BioGPS Human Cell Type and Tissue Gene Expression Profiles	cell types and tissues with high or low expression of TUBA1A gene relative to other cell types and tissues from the BioGPS Human Cell Type and Tissue Gene Expression Profiles dataset.
	BioGPS Mouse Cell Type and Tissue Gene Expression Profiles	cell types and tissues with high or low expression of TUBA1A gene relative to other cell types and tissues from the BioGPS Mouse Cell Type and Tissue Gene Expression Profiles dataset.
	Carcinogenome Chemical Perturbation Carcinogenicity Signatures	small molecule perturbations changing expression of TUBA1A gene from the Carcinogenome Chemical Perturbation Carcinogenicity Signatures dataset.
	CCLE Cell Line Gene CNV Profiles	cell lines with high or low copy number of TUBA1A gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset.
	CCLE Cell Line Gene Expression Profiles	cell lines with high or low expression of TUBA1A gene relative to other cell lines from the CCLE Cell Line Gene Expression Profiles dataset.
	CellMarker Gene-Cell Type Associations	cell types associated with TUBA1A gene from the CellMarker Gene-Cell Type Associations dataset.
	ChEA Transcription Factor Binding Site Profiles	transcription factor binding site profiles with transcription factor binding evidence at the promoter of TUBA1A gene from the CHEA Transcription Factor Binding Site Profiles dataset.
	ChEA Transcription Factor Targets	transcription factors binding the promoter of TUBA1A gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets dataset.
	ChEA Transcription Factor Targets 2022	transcription factors binding the promoter of TUBA1A gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
	ClinVar Gene-Phenotype Associations	phenotypes associated with TUBA1A gene from the curated ClinVar Gene-Phenotype Associations dataset.
	ClinVar Gene-Phenotype Associations 2025	phenotypes associated with TUBA1A gene from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
	CMAP Signatures of Differentially Expressed Genes for Small Molecules	small molecule perturbations changing expression of TUBA1A gene from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores	cellular components containing TUBA1A protein from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores 2025	cellular components containing TUBA1A protein from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
	COMPARTMENTS Text-mining Protein Localization Evidence Scores	cellular components co-occuring with TUBA1A protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
	COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025	cellular components co-occuring with TUBA1A protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
	CORUM Protein Complexes	protein complexs containing TUBA1A protein from the CORUM Protein Complexes dataset.
	COSMIC Cell Line Gene CNV Profiles	cell lines with high or low copy number of TUBA1A gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset.
	COSMIC Cell Line Gene Mutation Profiles	cell lines with TUBA1A gene mutations from the COSMIC Cell Line Gene Mutation Profiles dataset.
	CTD Gene-Chemical Interactions	chemicals interacting with TUBA1A gene/protein from the curated CTD Gene-Chemical Interactions dataset.
	CTD Gene-Disease Associations	diseases associated with TUBA1A gene/protein from the curated CTD Gene-Disease Associations dataset.
	DeepCoverMOA Drug Mechanisms of Action	small molecule perturbations with high or low expression of TUBA1A protein relative to other small molecule perturbations from the DeepCoverMOA Drug Mechanisms of Action dataset.
	DepMap CRISPR Gene Dependency	cell lines with fitness changed by TUBA1A gene knockdown relative to other cell lines from the DepMap CRISPR Gene Dependency dataset.
	DISEASES Curated Gene-Disease Association Evidence Scores	diseases involving TUBA1A gene from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
	DISEASES Curated Gene-Disease Association Evidence Scores 2025	diseases involving TUBA1A gene from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
	DISEASES Experimental Gene-Disease Association Evidence Scores 2025	diseases associated with TUBA1A gene in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
	DISEASES Text-mining Gene-Disease Association Evidence Scores	diseases co-occuring with TUBA1A gene in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
	DISEASES Text-mining Gene-Disease Association Evidence Scores 2025	diseases co-occuring with TUBA1A gene in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
	DisGeNET Gene-Disease Associations	diseases associated with TUBA1A gene in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
	DisGeNET Gene-Phenotype Associations	phenotypes associated with TUBA1A gene in GWAS and other genetic association datasets from the DisGeNET Gene-Phenoptype Associations dataset.
	DrugBank Drug Targets	interacting drugs for TUBA1A protein from the curated DrugBank Drug Targets dataset.
	ENCODE Histone Modification Site Profiles	histone modification site profiles with high histone modification abundance at TUBA1A gene from the ENCODE Histone Modification Site Profiles dataset.