SLC39A11

SLC39A11
Identifiers
Aliases	SLC39A11 , C17orf26, ZIP11, solute carrier family 39 member 11, ZIP-11
External IDs	OMIM: 616508; MGI: 1917056; HomoloGene: 12331; GeneCards: SLC39A11; OMA:SLC39A11 - orthologs
Gene location (Human)
Chr.	Chromosome 17 (human)
End	73,092,712 bp
Gene location (Mouse)
Chr.	Chromosome 11 (mouse)
End	113,540,905 bp
RNA expression pattern
	Top expressed in
	bone marrow cells; ; mucosa of ileum; ; pancreatic ductal cell; ; epithelium of colon; ; monocyte; ; nasal epithelium; ; rectum; ; skin of arm; ; liver; ; right lobe of liver;
	Top expressed in
	epithelium of stomach; ; pyloric antrum; ; parotid gland; ; mucous cell of stomach; ; submandibular gland; ; lacrimal gland; ; crypt of lieberkuhn of small intestine; ; duodenum; ; left colon; ; molar;
	More reference expression data
	n/a
Gene ontology
Molecular function	metal ion transmembrane transporter activity ; zinc ion transmembrane transporter activity ;
Cellular component	cytoplasm ; integral component of membrane ; plasma membrane ; Golgi apparatus ; nucleus ; membrane ; fungal-type vacuole membrane ;
Biological process	metal ion transport ; zinc ion transport ; ion transport ; transmembrane transport ; zinc ion transmembrane transport ;
	Sources:Amigo / QuickGO
Orthologs
	201266
	69806
	ENSG00000133195 ; ENSG00000282291
	ENSMUSG00000041654
	Q8N1S5
	Q8BWY7
	NM_001159770 ; NM_139177 ; NM_001352691 ; NM_001352692 ; NM_001352693 Contents See also ; References ; Further reading ;
NM_001166503 ; NM_027216 ; NM_001362937 ; NM_001362938 ; NM_001362939 ;
	NM_001362940 ; NM_001362941 ; NM_001362942 ; NM_001362943 ; NM_001362944
	NP_001153242 ; NP_631916 ; NP_001339620 ; NP_001339621 ; NP_001339622
NP_001159975 ; NP_081492 ; NP_001349866 ; NP_001349867 ; NP_001349868 ;
	NP_001349869 ; NP_001349870 ; NP_001349871 ; NP_001349872 ; NP_001349873
	Wikidata
View/Edit Human	View/Edit Mouse

Last updated September 27, 2024

Solute carrier family 39 member 11 is a protein that in humans is encoded by the SLC39A11 gene. ^[5]

Related Research Articles

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Solute carrier family 6, member 18 also known as SLC6A18 is a protein which in humans is encoded by the SLC6A18 gene.

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Solute carrier family 22 member 25 (SLC22A25), also known as organic anion transporter UST6, is a protein that in humans is encoded by the SLC22A25 gene.

Solute carrier family 12 member 8 (SLC12A8), also known as cation-chloride cotransporter 9 (CCC9), is a protein that in humans is encoded by the SLC12A8 gene.

Proton myo-inositol cotransporter, also known as solute carrier family 2 member 13 is a protein that in humans is encoded by the SLC2A13 gene.

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References

1 2 3 ENSG00000282291 GRCh38: Ensembl release 89: ENSG00000133195, ENSG00000282291 – Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000041654 – 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.
↑ "Entrez Gene: Solute carrier family 39 member 11" . Retrieved 2017-10-11.

Bagheri-Fam S, Ferraz C, Demaille J, Scherer G, Pfeifer D (2001). "Comparative genomics of the SOX9 region in human and Fugu rubripes: conservation of short regulatory sequence elements within large intergenic regions". Genomics. 78 (1–2): 73–82. doi:10.1006/geno.2001.6648. PMID 11707075.
Talmud PJ, Drenos F, Shah S, Shah T, Palmen J, Verzilli C, Gaunt TR, Pallas J, Lovering R, Li K, Casas JP, Sofat R, Kumari M, Rodriguez S, Johnson T, Newhouse SJ, Dominiczak A, Samani NJ, Caulfield M, Sever P, Stanton A, Shields DC, Padmanabhan S, Melander O, Hastie C, Delles C, Ebrahim S, Marmot MG, Smith GD, Lawlor DA, Munroe PB, Day IN, Kivimaki M, Whittaker J, Humphries SE, Hingorani AD (2009). "Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip". Am. J. Hum. Genet. 85 (5): 628–42. doi:10.1016/j.ajhg.2009.10.014. PMC 2775832 . PMID 19913121.
Rose JE, Behm FM, Drgon T, Johnson C, Uhl GR (2010). "Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score". Mol. Med. 16 (7–8): 247–53. doi:10.2119/molmed.2009.00159. PMC 2896464 . PMID 20379614.
Bailey SD, Xie C, Do R, Montpetit A, Diaz R, Mohan V, Keavney B, Yusuf S, Gerstein HC, Engert JC, Anand S (2010). "Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study". Diabetes Care. 33 (10): 2250–3. doi:10.2337/dc10-0452. PMC 2945168 . PMID 20628086.
Wu L, Chaffee KG, Parker AS, Sicotte H, Petersen GM (2015). "Zinc transporter genes and urological cancers: integrated analysis suggests a role for ZIP11 in bladder cancer". Tumour Biol. 36 (10): 7431–7. doi:10.1007/s13277-015-3459-2. PMC 4607554 . PMID 25900876.

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[refGRCh38Ensembl-1] 1 2 3 ENSG00000282291 GRCh38: Ensembl release 89: ENSG00000133195, ENSG00000282291 – Ensembl, May 2017

[refGRCm38Ensembl-2] 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000041654 – Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[entrez-5] "Entrez Gene: Solute carrier family 39 member 11" . Retrieved 2017-10-11.

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SLC39A11

Contents

See also

Related Research Articles

References

Further reading