ANKRD26 Gene

HGNC Family	Ankyrin repeat domain containing (ANKRD)
Name	ankyrin repeat domain 26
Description	This gene encodes a protein containing N-terminal ankyrin repeats which function in protein-protein interactions. Mutations in this gene are associated with autosomal dominant thrombocytopenia-2. Pseudogenes of this gene are found on chromosome 7, 10, 13 and 16. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]
Summary	{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\n ANKRD26 is emerging as a multifunctional gene with critical roles in both hematopoietic and metabolic regulation as well as in oncogenesis. In the hematopoietic compartment, germline mutations—most notably single‐nucleotide substitutions in the 5′ untranslated region—lead to autosomal‐dominant thrombocytopenia characterized by dysmegakaryopoiesis, mild bleeding, and an increased risk of myeloid malignancies including acute myeloid leukemia. These mutations disrupt normal transcriptional silencing during late megakaryocyte differentiation by impairing the binding of transcription factors such as RUNX1 and FLI1, resulting in persistent ANKRD26 expression, aberrant MPL signaling, and defective proplatelet formation (1,2,3,4,11,13,14,15). Alterations in cell surface receptor profiles, including reduced CXCR4 expression in platelets, further underscore its role in proper platelet biogenesis (17)."}]}, {"type": "t", "text": "\n \n "}, {"type": "p", "children": [{"type": "t", "text": "\n In addition to its hematologic functions, studies in mouse and zebrafish models have demonstrated that ANKRD26 is a key regulator of energy homeostasis. Partial inactivation of Ankrd26 leads to hyperphagia, obesity, insulin resistance, and enhanced adipogenesis—phenotypes that are linked to abnormal MAPK/ERK signaling and perturbed adipose tissue insulin responsiveness. Epigenetic modifications, such as promoter hypermethylation leading to decreased expression, have been correlated with a pro‐inflammatory profile and increased cardiometabolic risk in obese subjects (5,6,7,8,9,12)."}]}, {"type": "t", "text": "\n \n "}, {"type": "p", "children": [{"type": "t", "text": "\n Moreover, structural alterations of ANKRD26, including N‐terminal truncating mutations and fusion events (for example, the formation of a WAC–ANKRD26 or ANKRD26–RET fusion protein), highlight its potential oncogenic role in diverse tissue types (10,16). Collectively, these findings reveal that ANKRD26 functions as a pivotal regulator of megakaryopoiesis and platelet production, while also modulating appetite, adipocyte differentiation, and tumorigenic processes. As such, ANKRD26 continues to represent an important diagnostic marker and molecular target in both hematologic and metabolic disorders.\n "}]}, {"type": "t", "text": "\n \n "}, {"type": "p", "children": [{"type": "t", "text": "\n <!-- Hyperlinked citations -->."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "17"}]}, {"type": "t", "text": ""}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Patrizia Noris, Silverio Perrotta, Marco Seri, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Blood (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1182/blood-2011-02-336537"}], "href": "https://doi.org/10.1182/blood-2011-02-336537"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21467542"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21467542"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Tommaso Pippucci, Anna Savoia, Silverio Perrotta, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Mutations in the 5' UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Am J Hum Genet (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.ajhg.2010.12.006"}], "href": "https://doi.org/10.1016/j.ajhg.2010.12.006"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21211618"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21211618"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Dominique Bluteau, Alessandra Balduini, Nathalie Balayn, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Thrombocytopenia-associated mutations in the ANKRD26 regulatory region induce MAPK hyperactivation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Clin Invest (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1172/JCI71861"}], "href": "https://doi.org/10.1172/JCI71861"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24430186"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24430186"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Vittorio Necchi, Alessandra Balduini, Patrizia Noris, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Ubiquitin/proteasome-rich particulate cytoplasmic structures (PaCSs) in the platelets and megakaryocytes of ANKRD26-related thrombo-cytopenia."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Thromb Haemost (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1160/TH12-07-0497"}], "href": "https://doi.org/10.1160/TH12-07-0497"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23223974"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23223974"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Tapan K Bera, Xiu-Fen Liu, Masanori Yamada, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A model for obesity and gigantism due to disruption of the Ankrd26 gene."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Proc Natl Acad Sci U S A (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1073/pnas.0710978105"}], "href": "https://doi.org/10.1073/pnas.0710978105"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18162531"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18162531"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Zhaoliang Fei, Tapan K Bera, Xiufen Liu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Ankrd26 gene disruption enhances adipogenesis of mouse embryonic fibroblasts."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M111.248435"}], "href": "https://doi.org/10.1074/jbc.M111.248435"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21669876"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21669876"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Gregory A Raciti, Rosa Spinelli, Antonella Desiderio, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Specific CpG hyper-methylation leads to Ankrd26 gene down-regulation in white adipose tissue of a mouse model of diet-induced obesity."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Sci Rep (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/srep43526"}], "href": "https://doi.org/10.1038/srep43526"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28266632"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28266632"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "G A Raciti, T K Bera, O Gavrilova, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Partial inactivation of Ankrd26 causes diabetes with enhanced insulin responsiveness of adipose tissue in mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Diabetologia (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s00125-011-2263-9"}], "href": "https://doi.org/10.1007/s00125-011-2263-9"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21842266"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21842266"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Antonella Desiderio, Michele Longo, Luca Parrillo, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Epigenetic silencing of the ANKRD26 gene correlates to the pro-inflammatory profile and increased cardio-metabolic risk factors in human obesity."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Clin Epigenetics (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1186/s13148-019-0768-0"}], "href": "https://doi.org/10.1186/s13148-019-0768-0"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31801613"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31801613"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Lara Wahlster, Jeffrey M Verboon, Leif S Ludwig, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Familial thrombocytopenia due to a complex structural variant resulting in a WAC-ANKRD26 fusion transcript."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Exp Med (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1084/jem.20210444"}], "href": "https://doi.org/10.1084/jem.20210444"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33857290"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33857290"}]}, {"type": "r", "ref": 11, "children": [{"type": "t", "text": "Caterina Marconi, Ilaria Canobbio, Valeria Bozzi, et al. "}, {"type": "b", "children": [{"type": "t", "text": "5'UTR point substitutions and N-terminal truncating mutations of ANKRD26 in acute myeloid leukemia."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Hematol Oncol (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1186/s13045-016-0382-y"}], "href": "https://doi.org/10.1186/s13045-016-0382-y"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28100250"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28100250"}]}, {"type": "r", "ref": 12, "children": [{"type": "t", "text": "Peter Acs, Peter O Bauer, Balazs Mayer, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A novel form of ciliopathy underlies hyperphagia and obesity in Ankrd26 knockout mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Brain Struct Funct (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s00429-014-0741-9"}], "href": "https://doi.org/10.1007/s00429-014-0741-9"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24633808"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24633808"}]}, {"type": "r", "ref": 13, "children": [{"type": "t", "text": "C Zaninetti, V Santini, M Tiniakou, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Inherited thrombocytopenia caused by ANKRD26 mutations misdiagnosed and treated as myelodysplastic syndrome: report on two cases."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Thromb Haemost (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1111/jth.13855"}], "href": "https://doi.org/10.1111/jth.13855"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28976612"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28976612"}]}, {"type": "r", "ref": 14, "children": [{"type": "t", "text": "Meri Ouchi-Uchiyama, Yoji Sasahara, Atsuo Kikuchi, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Analyses of Genetic and Clinical Parameters for Screening Patients With Inherited Thrombocytopenia with Small or Normal-Sized Platelets."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Pediatr Blood Cancer (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/pbc.25668"}], "href": "https://doi.org/10.1002/pbc.25668"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26175287"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26175287"}]}, {"type": "r", "ref": 15, "children": [{"type": "t", "text": "Juliana Perez Botero, Dong Chen, Rong He, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Clinical and laboratory characteristics in congenital ANKRD26 mutation-associated thrombocytopenia: A detailed phenotypic study of a family."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Platelets (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3109/09537104.2016.1171305"}], "href": "https://doi.org/10.3109/09537104.2016.1171305"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27123948"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27123948"}]}, {"type": "r", "ref": 16, "children": [{"type": "t", "text": "Julia Isabelle Staubitz, Thomas Johannes Musholt, Arno Schad, et al. "}, {"type": "b", "children": [{"type": "t", "text": "ANKRD26-RET - A novel gene fusion involving RET in papillary thyroid carcinoma."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cancer Genet (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.cancergen.2019.07.002"}], "href": "https://doi.org/10.1016/j.cancergen.2019.07.002"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31425920"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31425920"}]}, {"type": "r", "ref": 17, "children": [{"type": "t", "text": "Juan P Salim, Ana C Glembotsky, Paola R Lev, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Differential expression of SDF-1 receptor CXCR4 in molecularly defined forms of inherited thrombocytopenias."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Platelets (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1080/09537104.2016.1254763"}], "href": "https://doi.org/10.1080/09537104.2016.1254763"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28032520"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28032520"}]}]}]}
Synonyms	BA145E8.1, THC2
Proteins	ANR26_HUMAN
NCBI Gene ID	22852
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Predicted Functions
Co-expressed Genes
Expression in Tissues and Cell Lines

Functional Associations

ANKRD26 has 5,143 functional associations with biological entities spanning 9 categories (molecular profile, organism, chemical, disease, phenotype or trait, functional term, phrase or reference, structural feature, cell line, cell type or tissue, gene, protein or microRNA, sequence feature) extracted from 108 datasets.

Click the + buttons to view associations for ANKRD26 from the datasets below.

If available, associations are ranked by standardized value

Harmonizome 3.0

ANKRD26 Gene

Functional Associations

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

	Dataset	Summary
	Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles	tissues with high or low expression of ANKRD26 gene relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
	Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles	tissues with high or low expression of ANKRD26 gene relative to other tissues from the Allen Brain Atlas Adult Mouse 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 ANKRD26 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 ANKRD26 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 ANKRD26 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 ANKRD26 gene relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
	BioGPS Cell Line Gene Expression Profiles	cell lines with high or low expression of ANKRD26 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 ANKRD26 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 ANKRD26 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 ANKRD26 gene from the Carcinogenome Chemical Perturbation Carcinogenicity Signatures dataset.
	CCLE Cell Line Gene CNV Profiles	cell lines with high or low copy number of ANKRD26 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 ANKRD26 gene relative to other cell lines from the CCLE Cell Line Gene Expression Profiles dataset.
	CCLE Cell Line Proteomics	Cell lines associated with ANKRD26 protein from the CCLE Cell Line Proteomics dataset.
	ChEA Transcription Factor Binding Site Profiles	transcription factor binding site profiles with transcription factor binding evidence at the promoter of ANKRD26 gene from the CHEA Transcription Factor Binding Site Profiles dataset.
	ChEA Transcription Factor Targets	transcription factors binding the promoter of ANKRD26 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 ANKRD26 gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
	ClinVar Gene-Phenotype Associations 2025	phenotypes associated with ANKRD26 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 ANKRD26 gene from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores	cellular components containing ANKRD26 protein from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores 2025	cellular components containing ANKRD26 protein from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
	COMPARTMENTS Experimental Protein Localization Evidence Scores	cellular components containing ANKRD26 protein in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores dataset.
	COMPARTMENTS Experimental Protein Localization Evidence Scores 2025	cellular components containing ANKRD26 protein in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores 2025 dataset.
	COMPARTMENTS Text-mining Protein Localization Evidence Scores	cellular components co-occuring with ANKRD26 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 ANKRD26 protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
	COSMIC Cell Line Gene CNV Profiles	cell lines with high or low copy number of ANKRD26 gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset.
	COSMIC Cell Line Gene Mutation Profiles	cell lines with ANKRD26 gene mutations from the COSMIC Cell Line Gene Mutation Profiles dataset.
	CTD Gene-Disease Associations	diseases associated with ANKRD26 gene/protein from the curated CTD Gene-Disease Associations dataset.
	DeepCoverMOA Drug Mechanisms of Action	small molecule perturbations with high or low expression of ANKRD26 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 ANKRD26 gene knockdown relative to other cell lines from the DepMap CRISPR Gene Dependency dataset.
	DISEASES Experimental Gene-Disease Association Evidence Scores 2025	diseases associated with ANKRD26 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 ANKRD26 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 ANKRD26 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 ANKRD26 gene in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
	DisGeNET Gene-Phenotype Associations	phenotypes associated with ANKRD26 gene in GWAS and other genetic association datasets from the DisGeNET Gene-Phenoptype Associations dataset.
	ENCODE Histone Modification Site Profiles	histone modification site profiles with high histone modification abundance at ANKRD26 gene from the ENCODE Histone Modification Site Profiles dataset.
	ENCODE Transcription Factor Binding Site Profiles	transcription factor binding site profiles with transcription factor binding evidence at the promoter of ANKRD26 gene from the ENCODE Transcription Factor Binding Site Profiles dataset.
	ENCODE Transcription Factor Targets	transcription factors binding the promoter of ANKRD26 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset.
	ESCAPE Omics Signatures of Genes and Proteins for Stem Cells	PubMedIDs of publications reporting gene signatures containing ANKRD26 from the ESCAPE Omics Signatures of Genes and Proteins for Stem Cells dataset.
	GDSC Cell Line Gene Expression Profiles	cell lines with high or low expression of ANKRD26 gene relative to other cell lines from the GDSC Cell Line Gene Expression Profiles dataset.
	GeneRIF Biological Term Annotations	biological terms co-occuring with ANKRD26 gene in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.