| SLC38A10 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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| Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Aliases | SLC38A10, PP1744, solute carrier family 38 member 10 | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | OMIM: 616525; MGI: 1919305; HomoloGene: 41556; GeneCards: SLC38A10; OMA: SLC38A10 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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| Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Putative sodium-coupled neutral amino acid transporter 10, also known as solute carrier family 38 member 10, [5] is a protein that in humans is encoded by the SLC38A10 gene. [6]
Cellular localization
Cellular localization study of SLC38A10 protein was investigated on different cell lines and primary cortex neuronal cells using Immunocytochemistry and GFP SLC38A10 vector. SLC38A10 localized on Golgi apparatus and ER organelles. [7]
Recent study on SLC38A10 knockout model provided some insight on possible association with p53 protein and cell survival. [8]
Cancer
A SLC38A family member has been observed progressively downregulated in Human papillomavirus-positive neoplastic keratinocytes derived from uterine cervical preneoplastic lesions at different levels of malignancy. [9] For this reason, SLC38A is likely to be associated with tumorigenesis and may be a potential prognostic marker for uterine cervical preneoplastic lesions progression. [9]
References
- ^ a b c GRCh38: Ensembl release 89: ENSG00000157637 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000061306 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "SLC38A10 - Function". www.nextprot.org. Retrieved 2021-11-29.
- ^ "Entrez Gene: solute carrier family 38, member 10". Retrieved 2011-08-30.
- ^ Tripathi R, Hosseini K, Arapi V, Fredriksson R, Bagchi S (December 2019). "SLC38A10 (SNAT10) is Located in ER and Golgi Compartments and Has a Role in Regulating Nascent Protein Synthesis". International Journal of Molecular Sciences. 20 (24): 6265. doi: 10.3390/ijms20246265. PMC 6940841. PMID 31842320.
- ^ Tripathi R, Aggarwal T, Fredriksson R (2021). "SLC38A10 Transporter Plays a Role in Cell Survival Under Oxidative Stress and Glutamate Toxicity". Frontiers in Molecular Biosciences. 8: 671865. doi: 10.3389/fmolb.2021.671865. ISSN 2296-889X. PMC 8133219. PMID 34026845.
- ^ a b Rotondo JC, Bosi S, Bassi C, Ferracin M, Lanza G, Gafà R, et al. (April 2015). "Gene expression changes in progression of cervical neoplasia revealed by microarray analysis of cervical neoplastic keratinocytes". Journal of Cellular Physiology. 230 (4): 806–12. doi: 10.1002/jcp.24808. hdl: 11392/2066612. PMID 25205602. S2CID 24986454.
Further reading
- Yashin AI, Wu D, Arbeev KG, Ukraintseva SV (September 2010). "Joint influence of small-effect genetic variants on human longevity". Aging. 2 (9): 612–20. doi: 10.18632/aging.100191. PMC 2984609. PMID 20834067.
 | This article on a gene on human chromosome 17 is a stub. You can help Wikipedia by expanding it. |
| SLC38A10 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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| Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Aliases | SLC38A10, PP1744, solute carrier family 38 member 10 | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | OMIM: 616525; MGI: 1919305; HomoloGene: 41556; GeneCards: SLC38A10; OMA: SLC38A10 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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| Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
| |||||||||||||||||||||||||||||||||||||||||||||||||||
Putative sodium-coupled neutral amino acid transporter 10, also known as solute carrier family 38 member 10, [5] is a protein that in humans is encoded by the SLC38A10 gene. [6]
Cellular localization
Cellular localization study of SLC38A10 protein was investigated on different cell lines and primary cortex neuronal cells using Immunocytochemistry and GFP SLC38A10 vector. SLC38A10 localized on Golgi apparatus and ER organelles. [7]
Recent study on SLC38A10 knockout model provided some insight on possible association with p53 protein and cell survival. [8]
Cancer
A SLC38A family member has been observed progressively downregulated in Human papillomavirus-positive neoplastic keratinocytes derived from uterine cervical preneoplastic lesions at different levels of malignancy. [9] For this reason, SLC38A is likely to be associated with tumorigenesis and may be a potential prognostic marker for uterine cervical preneoplastic lesions progression. [9]
References
- ^ a b c GRCh38: Ensembl release 89: ENSG00000157637 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000061306 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "SLC38A10 - Function". www.nextprot.org. Retrieved 2021-11-29.
- ^ "Entrez Gene: solute carrier family 38, member 10". Retrieved 2011-08-30.
- ^ Tripathi R, Hosseini K, Arapi V, Fredriksson R, Bagchi S (December 2019). "SLC38A10 (SNAT10) is Located in ER and Golgi Compartments and Has a Role in Regulating Nascent Protein Synthesis". International Journal of Molecular Sciences. 20 (24): 6265. doi: 10.3390/ijms20246265. PMC 6940841. PMID 31842320.
- ^ Tripathi R, Aggarwal T, Fredriksson R (2021). "SLC38A10 Transporter Plays a Role in Cell Survival Under Oxidative Stress and Glutamate Toxicity". Frontiers in Molecular Biosciences. 8: 671865. doi: 10.3389/fmolb.2021.671865. ISSN 2296-889X. PMC 8133219. PMID 34026845.
- ^ a b Rotondo JC, Bosi S, Bassi C, Ferracin M, Lanza G, Gafà R, et al. (April 2015). "Gene expression changes in progression of cervical neoplasia revealed by microarray analysis of cervical neoplastic keratinocytes". Journal of Cellular Physiology. 230 (4): 806–12. doi: 10.1002/jcp.24808. hdl: 11392/2066612. PMID 25205602. S2CID 24986454.
Further reading
- Yashin AI, Wu D, Arbeev KG, Ukraintseva SV (September 2010). "Joint influence of small-effect genetic variants on human longevity". Aging. 2 (9): 612–20. doi: 10.18632/aging.100191. PMC 2984609. PMID 20834067.
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| This article on a gene on human chromosome 17 is a stub. You can help Wikipedia by expanding it. |