CIBAR1 Gene

Name CBY1 interacting BAR domain containing 1
Description Enables phospholipid binding activity. Involved in several processes, including inner mitochondrial membrane organization; limb morphogenesis; and membrane tubulation. Located in several cellular components, including centriole; ciliary base; and mitochondrial crista. [provided by Alliance of Genome Resources, Mar 2025]
Summary
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\n FAM92A1 (also known as BARMR1) is a multifunctional BAR domain–containing protein with diverse roles in cellular organization, energy regulation, development, and cancer. In the context of ciliogenesis, FAM92A1 interacts with the coiled‐coil protein Chibby1 to recruit small vesicles that mediate ciliary vesicle formation and basal body docking—processes essential for both primary and multiciliated cell function."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n Additionally, FAM92A1 localizes to the matrix side of the mitochondrial inner membrane where it induces membrane curvature and maintains mitochondrial ultrastructure, a function crucial for optimal bioenergetics."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n Alternative splicing generates isoforms such as FAM92A1‐289, which have been implicated in tumorigenesis. Overexpression of these isoforms promotes cell proliferation, migration, and resistance to treatment by engaging signaling cascades (for example, the ERK pathway) and modulating the expression of oncogenic mediators—findings documented in renal, cervical, and glioblastoma models."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "5", "end_ref": "8"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n Moreover, genetic variants in FAM92A1 have been linked to congenital limb malformations such as postaxial polydactyly, underscoring its contribution to developmental patterning."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "9"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n Studies in developmental models further support an essential role for FAM92A1 homologs during embryogenesis, where perturbation of its expression leads to defects in ectoderm and mesoderm differentiation and subsequent developmental abnormalities."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "10"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n Collectively, these findings illustrate that FAM92A1 is a critical organizer of membrane architecture—functioning in both the formation of cilia and mitochondria—and a modulator of proliferative and developmental processes. Its multifaceted activities position FAM92A1 as an important candidate for therapeutic targeting in ciliopathies, mitochondrial dysfunction, and cancer.\n "}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Feng-Qian Li, Xingwang Chen, Cody Fisher, et al. "}, {"type": "b", "children": [{"type": "t", "text": "BAR Domain-Containing FAM92 Proteins Interact with Chibby1 To Facilitate Ciliogenesis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell Biol (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1128/MCB.00160-16"}], "href": "https://doi.org/10.1128/MCB.00160-16"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27528616"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27528616"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Xu Zhi Ruan, Xin Rong Guo, Xuan Bin Wang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "BARMR1/FAM92A1, a novel gene encoding BAR domain protein with multi-functions."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Gene (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.gene.2020.145074"}], "href": "https://doi.org/10.1016/j.gene.2020.145074"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32891772"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32891772"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Liang Wang, Ziyi Yan, Helena Vihinen, et al. "}, {"type": "b", "children": [{"type": "t", "text": "FAM92A1 is a BAR domain protein required for mitochondrial ultrastructure and function."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Biol (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1083/jcb.201806191"}], "href": "https://doi.org/10.1083/jcb.201806191"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30404948"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30404948"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Zuoneng Wang, Carsten Mim "}, {"type": "b", "children": [{"type": "t", "text": "Optimizing purification of the peripheral membrane protein FAM92A1 fused to a modified spidroin tag."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Protein Expr Purif (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.pep.2021.105992"}], "href": "https://doi.org/10.1016/j.pep.2021.105992"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34648955"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34648955"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Shufang Liang, Fengming Gong, Xinyu Zhao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Prokaryotic expression, purification of a new tumor-relative protein FAM92A1-289 and its characterization in renal cell carcinoma."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cancer Lett (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.canlet.2008.10.043"}], "href": "https://doi.org/10.1016/j.canlet.2008.10.043"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19059705"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19059705"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Hui Gui, Xing-Rong Guo, Juan Fang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The Tumor-promoting Effects of FAM92A1-289 in Cervical Carcinoma Cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Anticancer Res (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.21873/anticanres.11090"}], "href": "https://doi.org/10.21873/anticanres.11090"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27798880"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27798880"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Xing Rong Guo, Mu Yu Wu, Long Jun Dai, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Nuclear FAM289-Galectin-1 interaction controls FAM289-mediated tumor promotion in malignant glioma."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Exp Clin Cancer Res (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1186/s13046-019-1393-7"}], "href": "https://doi.org/10.1186/s13046-019-1393-7"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31492191"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31492191"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Xu Zhi Ruan, Fei Yan, Xin Yu Zhao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Identification and characterization of two novel variants of the DUF1208 protein FAM92A1."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cells (2007)"}]}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17646714"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17646714"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Isabelle Schrauwen, Arnaud Pj Giese, Abdul Aziz, et al. "}, {"type": "b", "children": [{"type": "t", "text": "FAM92A Underlies Nonsyndromic Postaxial Polydactyly in Humans and an Abnormal Limb and Digit Skeletal Phenotype in Mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Bone Miner Res (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/jbmr.3594"}], "href": "https://doi.org/10.1002/jbmr.3594"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30395363"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30395363"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Xu Zhi Ruan, Han Suo Yang, Shao Hua Yao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Isolation and characterization of a novel Xenopus gene (xVAP019) encoding a DUF1208 domain containing protein."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Reprod Dev (2007)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/mrd.20739"}], "href": "https://doi.org/10.1002/mrd.20739"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17440976"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17440976"}]}]}]}
NCBI Gene ID 137392
API
Download Associations
Predicted Functions View CIBAR1's ARCHS4 Predicted Functions.
Co-expressed Genes View CIBAR1's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View CIBAR1's ARCHS4 Predicted Functions.

Functional Associations

CIBAR1 has 1,291 functional associations with biological entities spanning 5 categories (chemical, disease, phenotype or trait, functional term, phrase or reference, cell line, cell type or tissue, gene, protein or microRNA) extracted from 29 datasets.

Click the + buttons to view associations for CIBAR1 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
Allen Brain Atlas Aging Dementia and Traumatic Brain Injury Tissue Sample Gene Expression Profiles tissue samples with high or low expression of CIBAR1 gene relative to other tissue samples from the Allen Brain Atlas Aging Dementia and Traumatic Brain Injury Tissue Sample Gene Expression Profiles dataset.
Carcinogenome Chemical Perturbation Carcinogenicity Signatures small molecule perturbations changing expression of CIBAR1 gene from the Carcinogenome Chemical Perturbation Carcinogenicity Signatures dataset.
CellMarker Gene-Cell Type Associations cell types associated with CIBAR1 gene from the CellMarker Gene-Cell Type Associations dataset.
ClinVar Gene-Phenotype Associations 2025 phenotypes associated with CIBAR1 gene from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
CM4AI KOLF21J CRISPRi Gene Perturbation Atlas gene perturbations changing expression of CIBAR1 gene from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas dataset.
CM4AI U2OS Cell Map Protein Localization Assemblies assemblies containing CIBAR1 protein from integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
COMPARTMENTS Curated Protein Localization Evidence Scores 2025 cellular components containing CIBAR1 protein from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
COMPARTMENTS Experimental Protein Localization Evidence Scores 2025 cellular components containing CIBAR1 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 2025 cellular components co-occuring with CIBAR1 protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
GO Biological Process Annotations 2025 biological processes involving CIBAR1 gene from the curated GO Biological Process Annotations2025 dataset.
GO Cellular Component Annotations 2025 cellular components containing CIBAR1 protein from the curated GO Cellular Component Annotations 2025 dataset.
GTEx Tissue Gene Expression Profiles 2023 tissues with high or low expression of CIBAR1 gene relative to other tissues from the GTEx Tissue Gene Expression Profiles 2023 dataset.
GTEx Tissue-Specific Aging Signatures tissue samples with high or low expression of CIBAR1 gene relative to other tissue samples from the GTEx Tissue-Specific Aging Signatures dataset.
GWAS Catalog SNP-Phenotype Associations 2025 phenotypes associated with CIBAR1 gene in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
IMPC Knockout Mouse Phenotypes phenotypes of mice caused by CIBAR1 gene knockout from the IMPC Knockout Mouse Phenotypes dataset.
JASPAR Predicted Human Transcription Factor Targets 2025 transcription factors regulating expression of CIBAR1 gene predicted using known transcription factor binding site motifs from the JASPAR Predicted Human Transcription Factor Targets dataset.
JASPAR Predicted Mouse Transcription Factor Targets 2025 transcription factors regulating expression of CIBAR1 gene predicted using known transcription factor binding site motifs from the JASPAR Predicted Mouse Transcription Factor Targets 2025 dataset.
MoTrPAC Rat Endurance Exercise Training tissue samples with high or low expression of CIBAR1 gene relative to other tissue samples from the MoTrPAC Rat Endurance Exercise Training dataset.
Replogle et al., Cell, 2022 K562 Essential Perturb-seq Gene Perturbation Signatures gene perturbations changing expression of CIBAR1 gene from the Replogle et al., Cell, 2022 K562 Essential Perturb-seq Gene Perturbation Signatures dataset.
Replogle et al., Cell, 2022 K562 Genome-wide Perturb-seq Gene Perturbation Signatures gene perturbations changing expression of CIBAR1 gene from the Replogle et al., Cell, 2022 K562 Genome-wide Perturb-seq Gene Perturbation Signatures dataset.
Replogle et al., Cell, 2022 RPE1 Essential Perturb-seq Gene Perturbation Signatures gene perturbations changing expression of CIBAR1 gene from the Replogle et al., Cell, 2022 RPE1 Essential Perturb-seq Gene Perturbation Signatures dataset.
Rummagene Transcription Factor Associations 2026 transcription factors regulating expression of CIBAR1 gene from the Rummagene Transcription Factor Associations 2026 dataset.
RummaGEO Drug Perturbation Signatures drug perturbations changing expression of CIBAR1 gene from the RummaGEO Drug Perturbation Signatures dataset.
RummaGEO Gene Perturbation Signatures gene perturbations changing expression of CIBAR1 gene from the RummaGEO Gene Perturbation Signatures dataset.
Sci-Plex Drug Perturbation Signatures drug perturbations changing expression of CIBAR1 gene from the Sci-Plex Drug Perturbation Signatures dataset.
TISSUES Curated Tissue Protein Expression Evidence Scores 2025 tissues with high expression of CIBAR1 protein from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 tissues with high expression of CIBAR1 protein in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 tissues co-occuring with CIBAR1 protein in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
WikiPathways Pathways 2024 pathways involving CIBAR1 protein from the WikiPathways Pathways 2024 dataset.