| Name | endosome-lysosome associated apoptosis and autophagy regulator 1 |
| Description | Expression of this gene is induced by estrogen and the encoded protein has been characterized as a transmembrane protein. The encoded protein has been found in to correlate with survival in certain carcinomas (PMID: 21102415) and may be important for cellular response to stress (PMID: 21072319). Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2012] |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\n Although several of the provided abstracts discuss different genes and pathways, a subset of them focuses on the estrogen‐induced gene 121 (EIG121; also known in some studies by its systematic name KIAA1324), which appears to be the gene of interest here. EIG121 is expressed in a hormone‐responsive, tissue‐ and developmental stage–specific manner. In normal and hyperestrogenic tissues – for example, in the endometrium during the proliferative phase or in grade 1 estrogen‐related endometrial adenocarcinomas – EIG121 is markedly up‐regulated."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": " Its transcription can be driven by alternative promoters, leading to the production of isoforms that may differ in size and temporal expression."}]}, {"type": "t", "text": "\n \n "}, {"type": "p", "children": [{"type": "t", "text": "\n Functionally, EIG121 encodes a transmembrane protein that localizes predominantly to the plasma membrane as well as late endosome–lysosome compartments. Overexpression studies have demonstrated that increased levels of EIG121 promote the formation of autophagic vacuoles and lysosomal degradation of long-lived proteins, thereby activating autophagy. This enhancement of autophagy appears to provide a cytoprotective role for cells under stressful conditions such as starvation or exposure to cytotoxic agents. Conversely, knockdown of EIG121 impairs autophagic flux and makes cells more susceptible to apoptosis when challenged by these stressors."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n \n "}, {"type": "p", "children": [{"type": "t", "text": "\n Furthermore, because of its regulation by estrogen and its differential expression between hormone‐dependent tumor types, EIG121 has been proposed as a potential biomarker. In cancers such as endometrial and ovarian carcinomas, its expression level has been correlated with disease phenotype and prognosis. In some contexts, high EIG121 expression is associated with a protective autophagy mechanism that supports cell survival, whereas in others it may identify tumors that are more responsive to hormonal manipulation. Thus, EIG121 (ELAPOR1, as referenced here) appears to represent a multifunctional protein acting at the crossroads of estrogen signaling, autophagy regulation, and cell survival, with potential utility both as a prognostic marker and as a therapeutic target in hormone‐driven cancers.\n "}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Lei Deng, Russell R Broaddus, Adrienne McCampbell, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Identification of a novel estrogen-regulated gene, EIG121, induced by hormone replacement therapy and differentially expressed in type I and type II endometrial cancer."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Clin Cancer Res (2005)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1158/1078-0432.CCR-05-1189"}], "href": "https://doi.org/10.1158/1078-0432.CCR-05-1189"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "16322283"}], "href": "https://pubmed.ncbi.nlm.nih.gov/16322283"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Tetsuro Araki, Morioh Kusakabe, Eisuke Nishida "}, {"type": "b", "children": [{"type": "t", "text": "Expression of estrogen induced gene 121-like (EIG121L) during early Xenopus development."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Gene Expr Patterns (2007)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.modgep.2007.03.004"}], "href": "https://doi.org/10.1016/j.modgep.2007.03.004"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17475571"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17475571"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "L Deng, J Feng, R R Broaddus "}, {"type": "b", "children": [{"type": "t", "text": "The novel estrogen-induced gene EIG121 regulates autophagy and promotes cell survival under stress."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Death Dis (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/cddis.2010.9"}], "href": "https://doi.org/10.1038/cddis.2010.9"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21072319"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21072319"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Xiaomin Ran, Ping Zhou, Keqiang Zhang "}, {"type": "b", "children": [{"type": "t", "text": "Autophagy plays an important role in stemness mediation and the novel dual function of EIG121 in both autophagy and stemness regulation of endometrial carcinoma JEC cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Int J Oncol (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3892/ijo.2017.4047"}], "href": "https://doi.org/10.3892/ijo.2017.4047"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28656197"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28656197"}]}]}]}
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| NCBI Gene ID | 57535 |
| API | |
| Download Associations | |
| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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ELAPOR1 has 2,593 functional associations with biological entities spanning 6 categories (chemical, functional term, phrase or reference, disease, phenotype or trait, cell line, cell type or tissue, gene, protein or microRNA, sequence feature) extracted from 32 datasets.
Click the + buttons to view associations for ELAPOR1 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 ELAPOR1 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 ELAPOR1 gene from the Carcinogenome Chemical Perturbation Carcinogenicity Signatures dataset. | |
| CCLE Cell Line Proteomics | Cell lines associated with ELAPOR1 protein from the CCLE Cell Line Proteomics dataset. | |
| CellMarker Gene-Cell Type Associations | cell types associated with ELAPOR1 gene from the CellMarker Gene-Cell Type Associations dataset. | |
| CM4AI KOLF21J CRISPRi Gene Perturbation Atlas | gene perturbations changing expression of ELAPOR1 gene from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas dataset. | |
| COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 | cellular components co-occuring with ELAPOR1 protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. | |
| DepMap CRISPR Gene Dependency | cell lines with fitness changed by ELAPOR1 gene knockdown relative to other cell lines from the DepMap CRISPR Gene Dependency dataset. | |
| DisGeNET Gene-Disease Associations | diseases associated with ELAPOR1 gene in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. | |
| GlyGen Glycosylated Proteins | ligands (chemical) binding ELAPOR1 protein from the GlyGen Glycosylated Proteins dataset. | |
| GO Biological Process Annotations 2023 | biological processes involving ELAPOR1 gene from the curated GO Biological Process Annotations 2023 dataset. | |
| GO Biological Process Annotations 2025 | biological processes involving ELAPOR1 gene from the curated GO Biological Process Annotations2025 dataset. | |
| GO Cellular Component Annotations 2023 | cellular components containing ELAPOR1 protein from the curated GO Cellular Component Annotations 2023 dataset. | |
| GO Cellular Component Annotations 2025 | cellular components containing ELAPOR1 protein from the curated GO Cellular Component Annotations 2025 dataset. | |
| GO Molecular Function Annotations 2023 | molecular functions performed by ELAPOR1 gene from the curated GO Molecular Function Annotations 2023 dataset. | |
| GTEx eQTL 2025 | SNPs regulating expression of ELAPOR1 gene from the GTEx eQTL 2025 dataset. | |
| GTEx Tissue Gene Expression Profiles 2023 | tissues with high or low expression of ELAPOR1 gene relative to other tissues from the GTEx Tissue Gene Expression Profiles 2023 dataset. | |
| GWAS Catalog SNP-Phenotype Associations 2025 | phenotypes associated with ELAPOR1 gene in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. | |
| HuBMAP Azimuth Cell Type Annotations | cell types associated with ELAPOR1 gene from the HuBMAP Azimuth Cell Type Annotations dataset. | |
| IMPC Knockout Mouse Phenotypes | phenotypes of mice caused by ELAPOR1 gene knockout from the IMPC Knockout Mouse Phenotypes dataset. | |
| JASPAR Predicted Human Transcription Factor Targets 2025 | transcription factors regulating expression of ELAPOR1 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 ELAPOR1 gene predicted using known transcription factor binding site motifs from the JASPAR Predicted Mouse Transcription Factor Targets 2025 dataset. | |
| LINCS L1000 CMAP Chemical Perturbation Consensus Signatures | small molecule perturbations changing expression of ELAPOR1 gene from the LINCS L1000 CMAP Chemical Perturbations Consensus Signatures dataset. | |
| LINCS L1000 CMAP CRISPR Knockout Consensus Signatures | gene perturbations changing expression of ELAPOR1 gene from the LINCS L1000 CMAP CRISPR Knockout Consensus Signatures dataset. | |
| MGI Mouse Phenotype Associations 2023 | phenotypes of transgenic mice caused by ELAPOR1 gene mutations from the MGI Mouse Phenotype Associations 2023 dataset. | |
| Rummagene Transcription Factor Associations 2026 | transcription factors regulating expression of ELAPOR1 gene from the Rummagene Transcription Factor Associations 2026 dataset. | |
| RummaGEO Drug Perturbation Signatures | drug perturbations changing expression of ELAPOR1 gene from the RummaGEO Drug Perturbation Signatures dataset. | |
| RummaGEO Gene Perturbation Signatures | gene perturbations changing expression of ELAPOR1 gene from the RummaGEO Gene Perturbation Signatures dataset. | |
| Sci-Plex Drug Perturbation Signatures | drug perturbations changing expression of ELAPOR1 gene from the Sci-Plex Drug Perturbation Signatures dataset. | |
| Tahoe Therapeutics Tahoe 100M Perturbation Atlas | drug perturbations changing expression of ELAPOR1 gene from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset. | |
| TISSUES Curated Tissue Protein Expression Evidence Scores 2025 | tissues with high expression of ELAPOR1 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 ELAPOR1 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 ELAPOR1 protein in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. | |