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Membrane-associated transporter protein

Membrane-associated transporter protein, also known as solute carrier family 45 member 2 or melanoma antigen AIM1, is a protein that in humans is encoded by the SLC45A2 gene.

Mitochondrial 2-oxoglutarate/malate carrier protein

Mitochondrial 2-oxoglutarate/malate carrier protein is a protein that in humans is encoded by the SLC25A11 gene. Inactivating mutations in this gene predispose to metastasic paraganglioma.

Mitochondrial uncoupling protein 4

Mitochondrial uncoupling protein 4 is a protein that in humans is encoded by the SLC25A27 gene. The mitochondrial uncoupling protein UCP are members of a large family of mitochondrial anion carrier proteins MACP. UCPs separate oxidative phosphory ...

Monocarboxylate transporter 1

Monocarboxylate transporter 1 is a protein that in humans is encoded by the SLC16A1 gene. It is a proton coupled monocarboxylate transporter.

Monocarboxylate transporter 2

Monocarboxylate transporter 2 also known as solute carrier family 16 member 7 is a protein that in humans is encoded by the SLC16A7 gene. MCT2 is a proton-coupled monocarboxylate transporter. It catalyzes the rapid transport across the plasma mem ...

Monocarboxylate transporter 3

Monocarboxylate transporter 3 also known as solute carrier family 16 member 8 is a protein that in humans is encoded by the SLC16A8 gene. MCT is a proton-coupled monocarboxylate transporter. It catalyzes the rapid transport across the plasma memb ...

Monocarboxylate transporter 4

Monocarboxylate transporter 4 also known as solute carrier family 16 member 3 is a protein that in humans is encoded by the SLC16A3 gene. Northern and Western Blotting is the analysis of the database showed MCT4 to be expressed especially in tiss ...

Natural resistance-associated macrophage protein 1

This gene is a member of the solute carrier family 11 proton-coupled divalent metal ion transporters family and encodes a multi-pass membrane protein. The protein functions as a divalent transition metal iron and manganese transporter involved in ...

Neutral amino acid transporter A

Neutral amino acid transporter A is a protein that in humans is encoded by the SLC1A4 gene. In melanocytic cells SLC1A4 gene expression may be regulated by MITF.

Neutral and basic amino acid transport protein rBAT

Neutral and basic amino acid transport protein rBAT is a protein that in humans is encoded by the SLC3A1 gene. Mutations in the slc3a1 gene are associated with cystinuria.

NPR1

Natriuretic peptide receptor A/guanylate cyclase A, also known as NPR1, is an atrial natriuretic peptide receptor. In humans it is encoded by the NPR1 gene.

NPR2

Natriuretic peptide receptor B/guanylate cyclase B, also known as NPR2, is an atrial natriuretic peptide receptor. In humans it is encoded by the NPR2 gene.

NPR3

Natriuretic peptide receptor C/guanylate cyclase C, also known as NPR3, is an atrial natriuretic peptide receptor. In humans it is encoded by the NPR3 gene.

NT5E

5′-nucleotidase, also known as ecto-5′-nucleotidase or CD73, is an enzyme that in humans is encoded by the NT5E gene. CD73 commonly serves to convert AMP to adenosine.

Nucleoside transporter

Nucleoside transporters are a group of membrane transport proteins which transport nucleoside substrates like adenosine across the membranes of cells and/or vesicles. There are two known types of nucleoside transporters, concentrative nucleoside ...

OX40 ligand

OX40L is the ligand for OX40 and is stably expressed on many antigen-presenting cells such as DC2s, macrophages, and activated B lymphocytes. Molecules OX40, on the other hand, is present on the surface of activated T lymphocytes, mostly T cells ...

P3 protein

P3 protein is a protein that in humans is encoded by the SLC10A3 gene. This gene maps to a GC-rich region of the X chromosome and was identified by its proximity to the CpG island. It is believed that the gene cleaning.

PDCD1LG2

Programmed cell death 1 ligand 2 is a protein that in humans is encoded by the PDCD1LG2 gene. PDCD1LG2 has also been designated as CD273.

Phosphatidylinositol transfer protein, alpha

Phosphatidylinositol transfer protein alpha isoform is a protein that in humans is encoded by the PITPNA gene. Phosphatidylinositol transfer proteins of a diverse set of cytosolic proteins transfer phospholipids, which differ in their ability to ...

Poliovirus receptor-related 1

Poliovirus receptor-related 1, also known as nectin-1 and CD111 is a human protein of the immunoglobulin superfamily, also considered a member of the nectins. It is a membrane protein with three extracellular immunoglobulin domains, a single tran ...

Poliovirus receptor-related 2

Poliovirus receptor-related 2, also known as nectin-2 and CD112, is a human plasma membrane glycoprotein.

Poliovirus receptor-related 3

Poliovirus receptor-related 3, also known as nectin-3 and CD113, is a human protein of the immunoglobulin superfamily which forms part of adherens junctions.

Potassium-dependent sodium-calcium exchanger

Potassium-dependent sodium-calcium exchanger also known as solute carrier family 24 is a type of sodium-calcium exchanger that requires potassium to function.

Proton-coupled amino acid transporter 1

Proton-coupled amino acid transporter 1 is a protein that in humans is encoded by the SLC36A1 gene. This gene encodes a member of the eukaryotic-specific amino acid / auxin permease AAAP 1 Transporter family. The encoded protein functions as a pr ...

PTGFRN

Prostaglandin F2 receptor negative regulator is a protein that in humans is encoded by the PTGFRN gene. PTGFRN has also been designated as CD315.

Rap GTP-binding protein

Rap GTP-binding protein also known as Ras-related proteins or simply RAP is a type of small GTPase, similar in structure to Ras. These proteins share approximately 50% identity of amino acids with the classical RAS proteins and have numerous stru ...

RHBG

RHBG and RHCG are non-erythroid members of the Rhesus Rh protein family that are mainly expressed in the kidney and belong to the methylammonium-ammonium permease/ammonia transporters superfamily. Rh family proteins are all predicted to be transm ...

RHCE (gene)

Blood group Rh polypeptide is a protein that in humans is encoded by the RHCE gene. RHCE has also recently been designated CD240CE. System the RH blood group is the second most clinically significant of the blood groups second only to ABO. It is ...

RHCG

RHCG plays a critical role in ammonium handling and pH homeostasis in the kidney. The structure of the RHCG protein indicates that it has a hydrophobic ammonia-conducting channel and shows that it shares a common fold with the ammonia transporter ...

SEMA4D

Semaphorin-4D also known as C luster of D ifferentiation 100, is a protein of the semaphorin family that in humans is encoded by the SEMA4D gene.

Sialin

A deficiency of this protein causes Salla disease. and Infantile Sialic Acid Storage Disease ISSD. HP59 gene contains, entirely within the coding, the Sialin gene SLC17A5. Member 5, also known as or SLC17A5 sialin is a lysosomal membrane sialic a ...

Sialoadhesin

Sialoadhesin is a cell adhesion molecule found on the surface of macrophages. It is found in especially high amounts on macrophages of the spleen, liver, lymph node, bone marrow, colon, and lungs. Also, in patients suffering from rheumatoid arthr ...

SIGLEC5

Sialic acid-binding Ig-like lectin 5 is a protein that in humans is encoded by the SIGLEC5 gene. SIGLEC5 has also been designated CD170.

SIGLEC7

Sialic acid-binding Ig-like lectin 7 is a protein that in humans is encoded by the SIGLEC7 gene. SIGLEC7 has also been designated as CD328.

Signal-regulatory protein

A Signal-regulatory protein is one of a family of transmembrane glycoproteins involved in immunological signalling, expressed mainly by myeloid cells. Includes: SIRPB1. SIRPG, ligand=CD47. (SIRPG, лиганд=CD47) Signal-regulatory protein alpha, lig ...

SIRPG

Signal-regulatory protein gamma is a protein that in humans is encoded by the SIRPG gene. SIRPG has also recently been designated CD172G. The protein encoded by this gene is a member of the signal regulatory protein family MRE and belongs to the ...

SLAMF1

Signaling lymphocytic activation molecule 1 is a protein that in humans is encoded by the SLAMF1 gene. Recently SLAMF1 has also been designated CD150. SLAMF1 signaling lymphocytic belongs to the family molecule activation. Interaction SLAMF1 prom ...

SLC2A6

Hexose transport into mammalian cells is catalyzed by a family of membrane proteins, including SLC2A6, that contain 12 transmembrane domains and a number of critical conserved residues.

SLC2A9

Solute carrier family 2, facilitated glucose transporter member 9 is a protein that in humans is encoded by the SLC2A9 gene. This gene encodes a member of the SLC2A Transporter family the facilitative glucose. The members of this family play an i ...

SLC2A10

Solute carrier family 2, facilitated glucose transporter member 10 is a protein that in humans is encoded by the SLC2A10 gene. SLC2A10 is a member of the family to stimulate the glucose Transporter that plays an important role in maintaining gluc ...

SLC2A14

Solute carrier family 2, member 14 is a protein that in humans is encoded by the SLC2A14 gene. Family members of the glut Transporter of glucose, including SLC2A14, are highly conserved integral membrane proteins that transport hexoses such as gl ...

SLC12A6

Solute carrier family 12 member 6 is a protein that in humans is encoded by the SLC12A6 gene. This gene is a member of the K-CL family cotransporter KCC. K-CL cotransporters are integral membrane proteins that decrease intracellular chloride conc ...

SLC13A3

Solute carrier family 13 member 3 also called sodium-dependent dicarboxylate transporter is a protein that in humans is encoded by the SLC13A3 gene. Mammalian sodium-dicarboxylate cotransporters transport succinate and other intermediates of the ...

SLC20A1

Sodium-dependent phosphate transporter 1 is a protein that in humans is encoded by the SLC20A1 gene. Retrovirus receptors allow infection of human and murine cells of various retroviruses. Receptors that have been identified at the molecular leve ...

SLC20A2

This gene is found on the short arm of chromosome 8 8p12-p11 on the minus Crick strand. It is 123.077 bases in length. The encoded protein has 652 amino acids and the predicted molecular weight of the protein is 70.392 kiloDaltons.

SLC22A2

Solute carrier family 22 member 2 is a protein that in humans is encoded by the SLC22A2 gene. Polyspecificity organic cation transporters in the liver, kidneys, intestines, and other organs are critical for elimination of many endogenous small or ...

SLC22A4

The encoded protein is an integral protein of the plasma membrane containing 12 transmembrane segments. The first functional designation of this protein was OCTN1, but efficiency of transport for organic cations e.g., tetraethylammonium is very l ...

SLC22A7

Solute carrier family 22 member 7 is a protein that in humans is encoded by the gene SLC22A7. The protein encoded by this gene, is involved in sodium-independent transport and excretion of organic anions, some of which are potentially toxic. The ...

SLC22A10

Solute carrier family 22 member 10, also known as organic anion transporter 5, is a protein that in humans is encoded by the SLC22A10 gene.

SLC22A11

Solute carrier family 22 member 11 is a protein that in humans is encoded by the SLC22A11 gene. The protein encoded by this gene, is involved in sodium-independent transport and excretion of organic anions, some of which are potentially toxic. Th ...