Name

FGQTL2 Gene

Fasting plasma glucose level QTL2

ADIPQTL5 Gene

Adiponectin, serum level of, QTL5

ADIPQTL4 Gene

Adiponectin, serum level of, QTL4

SRF Gene

serum response factor (c-fos serum response element-binding transcription factor)

This gene encodes a ubiquitous nuclear protein that stimulates both cell proliferation and differentiation. It is a member of the MADS (MCM1, Agamous, Deficiens, and SRF) box superfamily of transcription factors. This protein binds to the serum response element (SRE) in the promoter region of target genes. This protein regulates the activity of many immediate-early genes, for example c-fos, and thereby participates in cell cycle regulation, apoptosis, cell growth, and cell differentiation. This gene is the downstream target of many pathways; for example, the mitogen-activated protein kinase pathway (MAPK) that acts through the ternary complex factors (TCFs). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]

TF Gene

transferrin

This gene encodes a glycoprotein with an approximate molecular weight of 76.5 kDa. It is thought to have been created as a result of an ancient gene duplication event that led to generation of homologous C and N-terminal domains each of which binds one ion of ferric iron. The function of this protein is to transport iron from the intestine, reticuloendothelial system, and liver parenchymal cells to all proliferating cells in the body. This protein may also have a physiologic role as granulocyte/pollen-binding protein (GPBP) involved in the removal of certain organic matter and allergens from serum. [provided by RefSeq, Sep 2009]

TFRC Gene

transferrin receptor

This gene encodes a cell surface receptor necessary for cellular iron uptake by the process of receptor-mediated endocytosis. This receptor is required for erythropoiesis and neurologic development. Multiple alternatively spliced variants have been identified. [provided by RefSeq, Sep 2015]

TFR2 Gene

transferrin receptor 2

This gene encodes a single-pass type II membrane protein, which is a member of the transferrin receptor-like family. This protein mediates cellular uptake of transferrin-bound iron, and may be involved in iron metabolism, hepatocyte function and erythrocyte differentiation. Mutations in this gene have been associated with hereditary hemochromatosis type III. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, May 2011]

TFP1 Gene

transferrin pseudogene 1

AOMS2 Gene

abdominal obesity-metabolic syndrome QTL2

MENOQ2 Gene

Menopause, natural, age at, QTL2

MPVQTL2 Gene

Mean platelet volume QTL2

MENAQ2 Gene

Menarche, age at, QTL2

FGQTL4 Gene

Fasting plasma glucose level QTL 4

FGQTL6 Gene

Fasting plasma glucose level QTL 6

FGQTL1 Gene

Fasting plasma glucose level QTL 1

FGQTL3 Gene

Fasting plasma glucose level QTL3

HDLCQ6 Gene

High density lipoprotein cholesterol level QTL 6

HDLCQ1 Gene

high density lipoprotein cholesterol level QTL 1

ALPQTL3 Gene

Alkaline phosphatase, plasma level of, QTL3

ALPQTL2 Gene

Alkaline phosphatase, plasma level of, QTL 2

CLQTL2 Gene

Cholesterol level QTL 2

TSHQTL1 Gene

Thyroid-stimulating hormone level QTL 1

ALPQTL4 Gene

Alkaline phosphatase, plasma level of, QTL4

PURAQTL1 Gene

Polyunsaturated fatty acids plasma level QTL1

B6QTL1 Gene

Vitamin B6 plasma level QTL 1

HDLCQ4 Gene

High density lipoprotein cholesterol level QTL 4

HDLCQ5 Gene

High density lipoprotein cholesterol level QTL 5

HDLCQ2 Gene

High density lipoprotein cholesterol level QTL on chromosome 8

ALPQTL1 Gene

Alkaline phosphatase, plasma level of, QTL1

SXGQTL1 Gene

Sex hormone-binding blobulin circulating level QTL 1

SLEP3 Gene

Serum leptin concentration QTL 3

SLEP2 Gene

Serum leptin concentration QTL 2

SLEP1 Gene

Serum leptin concentration QTL 1

SDPR Gene

serum deprivation response

This gene encodes a calcium-independent phospholipid-binding protein whose expression increases in serum-starved cells. This protein is a substrate for protein kinase C (PKC) phosphorylation and recruits polymerase I and transcript release factor (PTRF) to caveolae. Removal of this protein causes caveolae loss and its over-expression results in caveolae deformation and membrane tubulation.[provided by RefSeq, Sep 2009]

SAAL1 Gene

serum amyloid A-like 1

Acts upstream of or within positive regulation of synoviocyte proliferation. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025]

LEPQTL1 Gene

Leptin, serum levels of

SGK2 Gene

serum/glucocorticoid regulated kinase 2

This gene encodes a serine/threonine protein kinase. Although this gene product is similar to serum- and glucocorticoid-induced protein kinase (SGK), this gene is not induced by serum or glucocorticoids. This gene is induced in response to signals that activate phosphatidylinositol 3-kinase, which is also true for SGK. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2010]

SAA3P Gene

serum amyloid A3 pseudogene

Predicted to enable Toll-like receptor 4 binding activity and chemoattractant activity. Predicted to be involved in response to stilbenoid. Predicted to act upstream of or within several processes, including I-kappaB phosphorylation; cell chemotaxis; and cellular response to interleukin-1. Predicted to be located in extracellular space. [provided by Alliance of Genome Resources, Mar 2025]

IGES Gene

immunoglobulin E concentration, serum

UAQTL6 Gene

Uric acid concentration, serum, QTL6

UAQTL5 Gene

Uric acid concentration, serum, QTL5

UAQTL4 Gene

Uric acid concentration, serum, QTL4

UAQTL3 Gene

Uric acid concentration, serum, QTL3

F7 Gene

coagulation factor VII (serum prothrombin conversion accelerator)

This gene encodes coagulation factor VII which is a vitamin K-dependent factor essential for hemostasis. This factor circulates in the blood in a zymogen form, and is converted to an active form by either factor IXa, factor Xa, factor XIIa, or thrombin by minor proteolysis. Upon activation of the factor VII, a heavy chain containing a catalytic domain and a light chain containing 2 EGF-like domains are generated, and two chains are held together by a disulfide bond. In the presence of factor III and calcium ions, the activated factor then further activates the coagulation cascade by converting factor IX to factor IXa and/or factor X to factor Xa. Defects in this gene can cause coagulopathy. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing to generate mature polypeptides. [provided by RefSeq, Aug 2015]

SGK3 Gene

serum/glucocorticoid regulated kinase family, member 3

This gene is a member of the Ser/Thr protein kinase family and encodes a phosphoprotein with a PX (phox homology) domain. The protein phosphorylates several target proteins and has a role in neutral amino acid transport and activation of potassium and chloride channels. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]

SRFBP1 Gene

serum response factor binding protein 1

Enables RNA binding activity. Predicted to be involved in maturation of SSU-rRNA. Predicted to be located in perinuclear region of cytoplasm. Predicted to be part of 90S preribosome. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025]

APCS Gene

amyloid P component, serum

The protein encoded by this gene is a glycoprotein, belonging to the pentraxin family of proteins, which has a characteristic pentameric organization. These family members have considerable sequence homology which is thought to be the result of gene duplication. The binding of the encoded protein to proteins in the pathological amyloid cross-beta fold suggests its possible role as a chaperone. This protein is also thought to control the degradation of chromatin. It has been demonstrated that this protein binds to apoptotic cells at an early stage, which raises the possibility that it is involved in dealing with apoptotic cells in vivo. [provided by RefSeq, Sep 2008]

LOC646430 Gene

amyloid P component, serum pseudogene

SGK1 Gene

serum/glucocorticoid regulated kinase 1

This gene encodes a serine/threonine protein kinase that plays an important role in cellular stress response. This kinase activates certain potassium, sodium, and chloride channels, suggesting an involvement in the regulation of processes such as cell survival, neuronal excitability, and renal sodium excretion. High levels of expression of this gene may contribute to conditions such as hypertension and diabetic nephropathy. Several alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jan 2009]

SAA4 Gene

serum amyloid A4, constitutive

Predicted to be involved in acute-phase response. Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025]

SAA2 Gene

serum amyloid A2

This gene encodes a member of the serum amyloid A family of apolipoproteins. The encoded preproprotein is proteolytically processed to generate the mature protein. This protein is a major acute phase protein that is highly expressed in response to inflammation and tissue injury. This protein also plays an important role in HDL metabolism and cholesterol homeostasis. High levels of this protein are associated with chronic inflammatory diseases including atherosclerosis, rheumatoid arthritis, Alzheimer's disease and Crohn's disease. This protein may also be a potential biomarker for certain tumors. Finally, antimicrobial activity against S. aureus and E. coli resides in the N-terminal portion of the mature protein. [provided by RefSeq, Jul 2020]

SAA1 Gene

serum amyloid A1

This gene encodes a member of the serum amyloid A family of apolipoproteins. The encoded preproprotein is proteolytically processed to generate the mature protein. This protein is a major acute phase protein that is highly expressed in response to inflammation and tissue injury. This protein also plays an important role in HDL metabolism and cholesterol homeostasis. High levels of this protein are associated with chronic inflammatory diseases including atherosclerosis, rheumatoid arthritis, Alzheimer's disease and Crohn's disease. This protein may also be a potential biomarker for certain tumors. Finally, antimicrobial activity against S. aureus and E. coli resides in the N-terminal portion of the mature protein. Alternate splicing results in multiple transcript variants that encode the same protein. A pseudogene of this gene is found on chromosome 11. [provided by RefSeq, Jul 2020]

SAA@ Gene

serum amyloid A1 cluster

HDLC3 Gene

High density lipoprotein cholesterol, low serum, 3