| Name | major facilitator superfamily domain containing 14A |
| Description | Predicted to enable transmembrane transporter activity. Predicted to be involved in transmembrane transport. Predicted to act upstream of or within acrosome assembly; sperm mitochondrion organization; and spermatid nucleus differentiation. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nThe collection of abstracts provided details a wide array of cellular regulatory mechanisms—including nuclear transport, centrosome integrity, autophagy, gene imprinting, and cell migration—that are orchestrated by proteins such as nucleoporins (Nup62, Nup107), chaperone‐associated factors, and autophagic receptors like p62. However, none of these studies make any mention of MFSD14A nor do they shed light on its function. Consequently, no insights into the functional role of MFSD14A can be gleaned from this literature."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "10"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nSeveral of the abstracts emphasize the critical role of nuclear pore-associated proteins and chaperone complexes in regulating the intracellular trafficking and localization of key regulatory molecules. For example, research described in abstract 1 (PMID 19581287) focuses on the chaperone‐mediated nuclear import of the glucocorticoid receptor via interactions with the nuclear pore complex, while abstracts 2 (PMID 24107630) and 10 (PMID 32554220) explore how nucleoporins such as Nup62 affect centrosome integrity and cellular differentiation. Abstract 5 (PMID 30022050) further underscores the importance of specific nucleoporins in gene imprinting and chromatin regulation.\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nOther studies in this collection shift attention to cellular stress responses and quality control pathways. Abstracts 6 (PMID 37802024) and 9 (PMID 37620146) examine the regulation of selective autophagy through the dynamics of p62 and its interaction with ubiquitinated cargo, whereas abstract 7 (PMID 34571994) investigates the role of GDF-15 in modulating autophagic processes in atherosclerosis. Additionally, abstract 4 (PMID 22683860) links nuclear pore interactions with cellular migration, and abstract 8 (PMID 36908815) addresses hippocampal impairment post-traumatic brain injury. Despite these extensive insights into cellular homeostasis and signaling, MFSD14A remains unaddressed in all these reports.\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Pablo C Echeverría, Gisela Mazaira, Alejandra Erlejman, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Nuclear import of the glucocorticoid receptor-hsp90 complex through the nuclear pore complex is mediated by its interaction with Nup62 and importin beta."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell Biol (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1128/MCB.00649-09"}], "href": "https://doi.org/10.1128/MCB.00649-09"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19581287"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19581287"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Chieko Hashizume, Akane Moyori, Akiko Kobayashi, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Nucleoporin Nup62 maintains centrosome homeostasis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Cycle (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.4161/cc.26671"}], "href": "https://doi.org/10.4161/cc.26671"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24107630"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24107630"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Yayoi Kinoshita, Richard G Hunter, Jason D Gray, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Role for NUP62 depletion and PYK2 redistribution in dendritic retraction resulting from chronic stress."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Proc Natl Acad Sci U S A (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1073/pnas.1418896111"}], "href": "https://doi.org/10.1073/pnas.1418896111"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25349423"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25349423"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Olivier Béaslas, Terhi Vihervaara, Jiwei Li, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Silencing of OSBP-related protein 8 (ORP8) modifies the macrophage transcriptome, nucleoporin p62 distribution, and migration capacity."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Exp Cell Res (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.yexcr.2012.05.026"}], "href": "https://doi.org/10.1016/j.yexcr.2012.05.026"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22683860"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22683860"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Saqib S Sachani, Lauren S Landschoot, Liyue Zhang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Nucleoporin 107, 62 and 153 mediate Kcnq1ot1 imprinted domain regulation in extraembryonic endoderm stem cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Commun (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s41467-018-05208-2"}], "href": "https://doi.org/10.1038/s41467-018-05208-2"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30022050"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30022050"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Xue Huang, Jia Yao, Lu Liu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "S-acylation of p62 promotes p62 droplet recruitment into autophagosomes in mammalian autophagy."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.molcel.2023.09.004"}], "href": "https://doi.org/10.1016/j.molcel.2023.09.004"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "37802024"}], "href": "https://pubmed.ncbi.nlm.nih.gov/37802024"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Aline Heduschke, Kathrin Ackermann, Beate Wilhelm, et al. "}, {"type": "b", "children": [{"type": "t", "text": "GDF-15 Deficiency Reduces Autophagic Activity in Human Macrophages In Vitro and Decreases p62-Accumulation in Atherosclerotic Lesions in Mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cells (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3390/cells10092346"}], "href": "https://doi.org/10.3390/cells10092346"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34571994"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34571994"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Jianwei Zhao, Weihua Wang, Ke Yan, et al. "}, {"type": "b", "children": [{"type": "t", "text": "RNA-seq reveals Nup62 as a potential regulator for cell division after traumatic brain injury in mice hippocampus."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PeerJ (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.7717/peerj.14913"}], "href": "https://doi.org/10.7717/peerj.14913"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "36908815"}], "href": "https://pubmed.ncbi.nlm.nih.gov/36908815"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Riccardo Trapannone, Julia Romanov, Sascha Martens "}, {"type": "b", "children": [{"type": "t", "text": "p62 and NBR1 functions are dispensable for aggrephagy in mouse ESCs and ESC-derived neurons."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Life Sci Alliance (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.26508/lsa.202301936"}], "href": "https://doi.org/10.26508/lsa.202301936"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "37620146"}], "href": "https://pubmed.ncbi.nlm.nih.gov/37620146"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Patrick J Bishop, Yayoi Kinoshita, N Natalie Lopes, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Changes in Nup62 content affect contact-induced differentiation of cultured myoblasts."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Differentiation (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.diff.2020.05.001"}], "href": "https://doi.org/10.1016/j.diff.2020.05.001"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32554220"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32554220"}]}]}]}
|
| NCBI Gene ID | 64645 |
| API | |
| Download Associations | |
| Predicted Functions |
![]() |
| Co-expressed Genes |
![]() |
| Expression in Tissues and Cell Lines |
![]() |
MFSD14A has 655 functional associations with biological entities spanning 6 categories (functional term, phrase or reference, disease, phenotype or trait, chemical, cell line, cell type or tissue, gene, protein or microRNA, sequence feature) extracted from 16 datasets.
Click the + buttons to view associations for MFSD14A from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| CellMarker Gene-Cell Type Associations | cell types associated with MFSD14A gene from the CellMarker Gene-Cell Type Associations dataset. | |
| COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 | cellular components co-occuring with MFSD14A protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. | |
| DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 | diseases co-occuring with MFSD14A gene in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. | |
| GTEx eQTL 2025 | SNPs regulating expression of MFSD14A gene from the GTEx eQTL 2025 dataset. | |
| GTEx Tissue Gene Expression Profiles 2023 | tissues with high or low expression of MFSD14A gene relative to other tissues from the GTEx Tissue Gene Expression Profiles 2023 dataset. | |
| MoTrPAC Rat Endurance Exercise Training | tissue samples with high or low expression of MFSD14A gene relative to other tissue samples from the MoTrPAC Rat Endurance Exercise Training dataset. | |
| NIBR DRUG-seq U2OS MoA Box Gene Expression Profiles | drug perturbations changing expression of MFSD14A gene from the NIBR DRUG-seq U2OS MoA Box dataset. | |
| Replogle et al., Cell, 2022 K562 Essential Perturb-seq Gene Perturbation Signatures | gene perturbations changing expression of MFSD14A 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 MFSD14A 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 MFSD14A gene from the Replogle et al., Cell, 2022 RPE1 Essential Perturb-seq Gene Perturbation Signatures dataset. | |
| RummaGEO Drug Perturbation Signatures | drug perturbations changing expression of MFSD14A gene from the RummaGEO Drug Perturbation Signatures dataset. | |
| RummaGEO Gene Perturbation Signatures | gene perturbations changing expression of MFSD14A gene from the RummaGEO Gene Perturbation Signatures dataset. | |
| Tahoe Therapeutics Tahoe 100M Perturbation Atlas | drug perturbations changing expression of MFSD14A gene from the Tahoe Therapeutics Tahoe 100M Perturbation Atlas dataset. | |
| TISSUES Curated Tissue Protein Expression Evidence Scores 2025 | tissues with high expression of MFSD14A 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 MFSD14A 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 MFSD14A protein in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. | |