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C57BL/6JCya-Retnlgem1flox/Cya
Common Name:
Retnlg-flox
Product ID:
S-CKO-08657
Background:
C57BL/6JCya
Product Type
Age
Genotype
Sex
Quantity
Price:
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Basic Information
Strain Name
Retnlg-flox
Strain ID
CKOCMP-245195-Retnlg-B6J-VA
Gene Name
Retnlg
Product ID
S-CKO-08657
Gene Alias
Fizz3; Relmg; Xcp1
Background
C57BL/6JCya
NCBI ID
245195
Modification
Conditional knockout
Chromosome
16
Phenotype
MGI:2667763
Document
Click here to download >>
Application
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Rare Disease Data Center >>
Note
Note: When using this mouse strain in a publication, please cite “C57BL/6JCya-Retnlgem1flox/Cya mice (Catalog S-CKO-08657) were purchased from Cyagen.”
Strain Description
Ensembl Number
ENSMUST00000065666
NCBI RefSeq
NM_181596
Target Region
Exon 3~4
Size of Effective Region
~2.4 kb
Detailed Document
Click here to download >>
Overview of Gene Research
Retnlg, encoding resistin-like molecule (RELM)-γ, is associated with immune-related functions [2]. It may play roles in pathways related to immune cell regulation and inflammation, and is of biological importance in understanding immune-mediated processes [1,2,3,4,5,6,7,8,9]. Genetic models such as KO/CKO mouse models can be valuable for further exploring its functions.

In skin wound healing, the expression of Retnlg was associated with migrating neutrophils in a study on the impact of human umbilical cord mesenchymal stem cell-derived exosomes [1]. In the context of mesenchymal stem/stromal cell-induced myeloid-derived suppressor cells (MDSCs), these MSC-induced MDSCs highly expressed Retnlg, though RELM-γ encoded by Retnlg had no direct effects on T cell proliferation, Treg expansion, or splenocyte activation [2].

In acute inflammatory lung injury, differential expression of Retnlg was seen in mice with acute lung injury caused by pulmonary and extrapulmonary factors [3]. In bladder cancer, a subpopulation of RETNLG+LCN2+ senescence-like neutrophils preferentially accumulated in the male tumor microenvironment, exerting an immunosuppressive effect [4].

In gastric pre-neoplastic and neoplastic development, Retnlg was among the genes highly enriched in gastric CD11b+Ly6G+ granulocytic MDSCs following Helicobacter felis infection [5]. In atopic dermatitis in mice, topical emollient treatment downregulated genes in the lung involved in leucocyte chemotaxis, including Retnlg [6].

In Clonorchis sinensis -infected mouse livers, Retnlg was up-regulated at both the gene and protein levels, associated with liver fibrosis and inflammation [7]. In preeclampsia, pro-inflammatory macrophages at the maternal-fetal interface inhibited the production of Ly6g+S100a8+S100a9+Retnlg+Wfdc21+ gMDSCs, leading to PE-like symptoms in mice [8]. In ulcerative colitis, Retnlg was identified as a biomarker for assessing BPA-induced colitis [9].

In conclusion, Retnlg is mainly involved in immune-related biological functions, including immune cell regulation, inflammation, and chemotaxis. Studies using mouse models have revealed its roles in various disease areas such as skin wound healing, bladder cancer, gastric diseases, atopic dermatitis, liver fibrosis, and preeclampsia, providing insights into disease mechanisms and potential biomarker discovery.

References:
1. Liu, Yuanyuan, Zhang, Mingwang, Liao, Yong, Zhang, Xingyue, Yang, Rongya. 2023. Human umbilical cord mesenchymal stem cell-derived exosomes promote murine skin wound healing by neutrophil and macrophage modulations revealed by single-cell RNA sequencing. In Frontiers in immunology, 14, 1142088. doi:10.3389/fimmu.2023.1142088. https://pubmed.ncbi.nlm.nih.gov/36999022/
2. Lee, Hyun Ju, Choi, Yoo Rim, Ko, Jung Hwa, Ryu, Jin Suk, Oh, Joo Youn. 2024. Defining mesenchymal stem/stromal cell-induced myeloid-derived suppressor cells using single-cell transcriptomics. In Molecular therapy : the journal of the American Society of Gene Therapy, 32, 1970-1983. doi:10.1016/j.ymthe.2024.04.026. https://pubmed.ncbi.nlm.nih.gov/38627968/
3. Kang, Zhi-Ying, Huang, Qian-Yu, Zhen, Ning-Xin, Zhang, Zhao-Cai, Tian, Bao-Ping. 2024. Heterogeneity of immune cells and their communications unveiled by transcriptome profiling in acute inflammatory lung injury. In Frontiers in immunology, 15, 1382449. doi:10.3389/fimmu.2024.1382449. https://pubmed.ncbi.nlm.nih.gov/38745657/
4. Zhu, Qingchen, Zhang, Guiheng, Cao, Ming, Qin, Jun, Xiao, Yichuan. 2025. Microbiota-shaped neutrophil senescence regulates sexual dimorphism in bladder cancer. In Nature immunology, 26, 722-736. doi:10.1038/s41590-025-02126-6. https://pubmed.ncbi.nlm.nih.gov/40217111/
5. Kao, Krystal D, Grasberger, Helmut, El-Zaatari, Mohamad. 2023. The Cxcr2+ subset of the S100a8+ gastric granylocytic myeloid-derived suppressor cell population (G-MDSC) regulates gastric pathology. In Frontiers in immunology, 14, 1147695. doi:10.3389/fimmu.2023.1147695. https://pubmed.ncbi.nlm.nih.gov/37744359/
6. Zhang, Jiayi, Xu, Xintian, Wang, Xiaopan, Chen, Lihong, Zheng, Jie. 2023. Topical emollient prevents the development of atopic dermatitis and atopic march in mice. In Experimental dermatology, 32, 1007-1015. doi:10.1111/exd.14806. https://pubmed.ncbi.nlm.nih.gov/37029953/
7. Zhan, Tingzheng, Wu, Yuhong, Deng, Xueling, Liu, Dengyu, Tang, Zeli. 2023. Multi-omics approaches reveal the molecular mechanisms underlying the interaction between Clonorchis sinensis and mouse liver. In Frontiers in cellular and infection microbiology, 13, 1286977. doi:10.3389/fcimb.2023.1286977. https://pubmed.ncbi.nlm.nih.gov/38076459/
8. Fei, Haiyi, Lu, Xiaowen, Shi, Zhan, Zhang, Songying, Jiang, Lingling. 2025. Deciphering the preeclampsia-specific immune microenvironment and the role of pro-inflammatory macrophages at the maternal-fetal interface. In eLife, 13, . doi:10.7554/eLife.100002. https://pubmed.ncbi.nlm.nih.gov/40152904/
9. Huang, Chen, Wang, Yuqin, Lin, Xiao, Lai, Keng Po, Li, Rong. 2022. Uncovering the functions of plasma proteins in ulcerative colitis and identifying biomarkers for BPA-induced severe ulcerative colitis: A plasma proteome analysis. In Ecotoxicology and environmental safety, 242, 113897. doi:10.1016/j.ecoenv.2022.113897. https://pubmed.ncbi.nlm.nih.gov/35999755/
Quality Control Standard
Sperm Test

Pre-cryopreservation: Measurement of sperm concentration, determination of sperm viability.

Post-cryopreservation: A vial of cryopreserved sperms is selected for in-vitro fertilization from each batch.

Environmental Standards:SPF
Available Region:Global
Source:Cyagen
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