WDR35 Gene

HGNC Family	Intraflagellar transport proteins (IFT), WD repeat domain containing (WDR)
Name	WD repeat domain 35
Description	This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. Two patients with Sensenbrenner syndrome / cranioectodermal dysplasia (CED) were identified with mutations in this gene, consistent with a possible ciliary function.[provided by RefSeq, Sep 2010]
Summary	{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nWDR35, also known as IFT121, is a critical component of the intraflagellar transport (IFT) machinery that governs cilia assembly and function. It is indispensable for retrograde IFT, ensuring proper trafficking of selected cargoes—including key signaling molecules such as EVC, EVC2, and Smoothened—into and out of the ciliary compartment. Structural studies suggest that WDR35 bears homology to proteins involved in vesicular trafficking (for example, COPI coatamers), underscoring its role in coordinating the fusion of Rab8 vesicles and regulating centriolar satellite organization. Mutations disrupting its normal splicing or protein structure perturb these processes, thereby implicating WDR35 in the pathogenesis of ciliopathies."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "5"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nDefective WDR35 function is increasingly recognized as the genetic basis of a spectrum of skeletal and multisystem ciliopathies, including Sensenbrenner syndrome (cranioectodermal dysplasia), Ellis–van Creveld syndrome, and short‐rib polydactyly. In these disorders, compound heterozygous or homozygous mutations in WDR35 lead to impaired ciliary protein targeting and aberrant Hedgehog signaling, causing characteristic craniofacial, skeletal, ectodermal, and visceral manifestations. Clinical reports further highlight considerable intrafamilial and interfamilial variability, emphasizing that while the same WDR35 alleles can underlie these disorders, additional genetic or environmental modifiers may influence disease severity."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "6", "end_ref": "12"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nBeyond its well‐established role in ciliary transport, emerging evidence points to additional functions for WDR35 in cell signaling. It interacts with small GTPases such as RagA, RagB, and RagC to negatively influence mTORC1 activity and is found to associate with chaperone complexes (e.g., the CCT complex) that regulate the distribution of acetylated α‑tubulin within or near the primary cilium. Intriguingly, the TTC32–WDR35 gene cluster has also been linked to coronary artery disease, suggesting that WDR35 might have broader implications in cellular homeostasis beyond ciliogenesis."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "13", "end_ref": "15"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Christian Gilissen, Heleen H Arts, Alexander Hoischen, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Am J Hum Genet (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.ajhg.2010.08.004"}], "href": "https://doi.org/10.1016/j.ajhg.2010.08.004"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20817137"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20817137"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Pleasantine Mill, Paul J Lockhart, Elizabeth Fitzpatrick, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis."}]}, {"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.2011.03.015"}], "href": "https://doi.org/10.1016/j.ajhg.2011.03.015"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21473986"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21473986"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Carlos A Bacino, Shweta U Dhar, Nicola Brunetti-Pierri, et al. "}, {"type": "b", "children": [{"type": "t", "text": "WDR35 mutation in siblings with Sensenbrenner syndrome: a ciliopathy with variable phenotype."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Am J Med Genet A (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/ajmg.a.35608"}], "href": "https://doi.org/10.1002/ajmg.a.35608"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22987818"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22987818"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "José A Caparrós-Martín, Alessandro De Luca, François Cartault, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Specific variants in WDR35 cause a distinctive form of Ellis-van Creveld syndrome by disrupting the recruitment of the EvC complex and SMO into the cilium."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Hum Mol Genet (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/hmg/ddv152"}], "href": "https://doi.org/10.1093/hmg/ddv152"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25908617"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25908617"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Wenxiang Fu, Lei Wang, Sehyun Kim, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Role for the IFT-A Complex in Selective Transport to the Primary Cilium."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Rep (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.celrep.2016.10.018"}], "href": "https://doi.org/10.1016/j.celrep.2016.10.018"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27806291"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27806291"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Joanna Walczak-Sztulpa, Anna Wawrocka, Agata Sobierajewicz, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Intrafamilial phenotypic variability in a Polish family with Sensenbrenner syndrome and biallelic WDR35 mutations."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Am J Med Genet A (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/ajmg.a.38163"}], "href": "https://doi.org/10.1002/ajmg.a.38163"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28332779"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28332779"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Dinu Antony, Narayanan Nampoory, Chiara Bacchelli, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Exome sequencing for the differential diagnosis of ciliary chondrodysplasias: Example of a WDR35 mutation case and review of the literature."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Eur J Med Genet (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.ejmg.2017.08.019"}], "href": "https://doi.org/10.1016/j.ejmg.2017.08.019"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28870638"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28870638"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Joanna Walczak-Sztulpa, Anna Wawrocka, Anna Swiader-Lesniak, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Clinical and molecular genetic characterization of a male patient with Sensenbrenner syndrome (cranioectodermal dysplasia) and biallelic WDR35 mutations."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Birth Defects Res (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/bdr2.1151"}], "href": "https://doi.org/10.1002/bdr2.1151"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "29134781"}], "href": "https://pubmed.ncbi.nlm.nih.gov/29134781"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Joanna Walczak-Sztulpa, Anna Wawrocka, Beata Leszczynska, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Prenatal genetic diagnosis of cranioectodermal dysplasia in a Polish family with compound heterozygous variants in WDR35."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Am J Med Genet A (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/ajmg.a.61785"}], "href": "https://doi.org/10.1002/ajmg.a.61785"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32804427"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32804427"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Joanna Walczak-Sztulpa, Anna Wawrocka, Małgorzata Stańczyk, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Interfamilial clinical variability in four Polish families with cranioectodermal dysplasia and identical compound heterozygous variants in WDR35."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Am J Med Genet A (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/ajmg.a.62067"}], "href": "https://doi.org/10.1002/ajmg.a.62067"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33421337"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33421337"}]}, {"type": "r", "ref": 11, "children": [{"type": "t", "text": "Zhongren Hu, Shurong Hong, Yu Zhang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Down-regulated WDR35 contributes to fetal anomaly via regulation of osteogenic differentiation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Gene (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.gene.2019.02.034"}], "href": "https://doi.org/10.1016/j.gene.2019.02.034"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30790652"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30790652"}]}, {"type": "r", "ref": 12, "children": [{"type": "t", "text": "Carlos Córdova-Fletes, Luis E Becerra-Solano, Martha M Rangel-Sosa, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Uncommon runs of homozygosity disclose homozygous missense mutations in two ciliopathy-related genes (SPAG17 and WDR35) in a patient with multiple brain and skeletal anomalies."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Eur J Med Genet (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.ejmg.2017.11.011"}], "href": "https://doi.org/10.1016/j.ejmg.2017.11.011"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "29174089"}], "href": "https://pubmed.ncbi.nlm.nih.gov/29174089"}]}, {"type": "r", "ref": 13, "children": [{"type": "t", "text": "Takeshi Sekiguchi, Nobuaki Furuno, Takashi Ishii, et al. "}, {"type": "b", "children": [{"type": "t", "text": "RagA, an mTORC1 activator, interacts with a hedgehog signaling protein, WDR35/IFT121."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Genes Cells (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1111/gtc.12663"}], "href": "https://doi.org/10.1111/gtc.12663"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30570184"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30570184"}]}, {"type": "r", "ref": 14, "children": [{"type": "t", "text": "Takeshi Sekiguchi, Takashi Ishii, Hideki Kobayashi, et al. "}, {"type": "b", "children": [{"type": "t", "text": "WDR35 is involved in subcellular localization of acetylated tubulin in 293T cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochem Biophys Res Commun (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.bbrc.2021.01.092"}], "href": "https://doi.org/10.1016/j.bbrc.2021.01.092"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33610917"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33610917"}]}, {"type": "r", "ref": 15, "children": [{"type": "t", "text": "Ying Xu, Yang Zhuo, Mengliang Ye, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Association study of genetic variants at TTC32-WDR35 gene cluster with coronary artery disease in Chinese Han population."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Clin Lab Anal (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/jcla.23594"}], "href": "https://doi.org/10.1002/jcla.23594"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33009702"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33009702"}]}]}]}
Synonyms	IFT121, SRTD7, CED2, IFTA1
Proteins	WDR35_HUMAN
NCBI Gene ID	57539
API
Download Associations
Predicted Functions
Co-expressed Genes
Expression in Tissues and Cell Lines

Functional Associations

WDR35 has 5,565 functional associations with biological entities spanning 9 categories (molecular profile, organism, disease, phenotype or trait, functional term, phrase or reference, chemical, 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 WDR35 from the datasets below.

If available, associations are ranked by standardized value

Harmonizome 3.0

WDR35 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 WDR35 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 WDR35 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 WDR35 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 WDR35 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 WDR35 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 WDR35 gene relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
	BioGPS Human Cell Type and Tissue Gene Expression Profiles	cell types and tissues with high or low expression of WDR35 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 WDR35 gene relative to other cell types and tissues from the BioGPS Mouse Cell Type and Tissue Gene Expression Profiles dataset.
	CCLE Cell Line Gene CNV Profiles	cell lines with high or low copy number of WDR35 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 WDR35 gene relative to other cell lines from the CCLE Cell Line Gene Expression Profiles dataset.
	CCLE Cell Line Proteomics	Cell lines associated with WDR35 protein from the CCLE Cell Line Proteomics dataset.
	CellMarker Gene-Cell Type Associations	cell types associated with WDR35 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 WDR35 gene from the CHEA Transcription Factor Binding Site Profiles dataset.
	ChEA Transcription Factor Targets	transcription factors binding the promoter of WDR35 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 WDR35 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 WDR35 gene from the curated ClinVar Gene-Phenotype Associations dataset.
	ClinVar Gene-Phenotype Associations 2025	phenotypes associated with WDR35 gene from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores	cellular components containing WDR35 protein from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores 2025	cellular components containing WDR35 protein from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
	COMPARTMENTS Experimental Protein Localization Evidence Scores	cellular components containing WDR35 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 WDR35 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 WDR35 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 WDR35 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 WDR35 gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset.
	COSMIC Cell Line Gene Mutation Profiles	cell lines with WDR35 gene mutations from the COSMIC Cell Line Gene Mutation Profiles dataset.
	CTD Gene-Disease Associations	diseases associated with WDR35 gene/protein from the curated CTD Gene-Disease Associations dataset.
	DeepCoverMOA Drug Mechanisms of Action	small molecule perturbations with high or low expression of WDR35 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 WDR35 gene knockdown relative to other cell lines from the DepMap CRISPR Gene Dependency dataset.
	DISEASES Curated Gene-Disease Association Evidence Scores	diseases involving WDR35 gene from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
	DISEASES Curated Gene-Disease Association Evidence Scores 2025	diseases involving WDR35 gene from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
	DISEASES Text-mining Gene-Disease Association Evidence Scores	diseases co-occuring with WDR35 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 WDR35 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 WDR35 gene in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
	DisGeNET Gene-Phenotype Associations	phenotypes associated with WDR35 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 WDR35 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 WDR35 gene from the ENCODE Transcription Factor Binding Site Profiles dataset.
	ENCODE Transcription Factor Targets	transcription factors binding the promoter of WDR35 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 WDR35 from the ESCAPE Omics Signatures of Genes and Proteins for Stem Cells dataset.
	GeneRIF Biological Term Annotations	biological terms co-occuring with WDR35 gene in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
	GeneSigDB Published Gene Signatures	PubMedIDs of publications reporting gene signatures containing WDR35 from the GeneSigDB Published Gene Signatures dataset.