Induced > 3x by LPS @ 1h 445 A B C D E F G H I J K L M N O P Q

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2021-03-02 · ITPKC inositol-trisphosphate 3-kinase C [ (human)] Our findings suggest that ITPKC is a susceptibility gene for bone mineral density (BMD), and rs2607420 may play an important role in the regulation of this gene. This study identified several important polymorphisms in the ITPKC and SLC11A1 genes in Koreans. The gene view histogram is a graphical view of mutations across ITPKC. These mutations are displayed at the amino acid level across the full length of the gene by default.

Itpkc gene

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Results: The GC and CC genotypes of ITPKC gene SNP rs28493229 were overrepresented in KD patients (GG:GC:CC was 236:43:1, C allele frequency: 8.04%) than those in the controls (GG:GC:CC was … 2019-12-07 ITPKC Antibodies Inositol 1, 4, 5-trisphosphate 3-kinase (ITPK) catalyzes the phosphorylation of Ins(1, 4, 5)P3 to Ins(1, 3, 4, 5)P4, both of which are modulators of calcium homeostasis. ITPK isoforms include ITPKA, ITPKB, and ITPKC, all of which contain a conserved catalytic unit in their C termini, but have unique N-terminal sequences and tissue distributions. This gene plays a role in both second messenger metabolism and calcium homeostasis. Skip to search form Skip to main content > Semantic Scholar's Logo. Search.

Gene ID Unique ID sequence Mouse GeCKOv2 A number

Among its related pathways are superpathway of inositol phosphate compounds and Metabolism . Gene name: ITPKC (HGNC Symbol) Synonyms: IP3-3KC, IP3KC: Description: Inositol-trisphosphate 3-kinase C (HGNC Symbol) Chromosome: 19: Cytoband: q13.2: Chromosome location (bp) 40717103 - 40740860: Number of transcripts i HGNC:14897, ITPKC: MIM i: 606476, gene: neXtProt i: NX_Q96DU7: VEuPathDB i: HostDB:ENSG00000086544.2 We investigated the association between KD and single nucleotide polymorphisms (SNPs) in two candidate genes: inositol 1,4,5-triphosphate 3-kinase (ITPKC), a well-studied KD-associated gene, and solute carrier 11a1 (SLC11A1), which is associated with the hypersensitive reaction to the BCG strain in Koreans.

Casp3-gen-enkel-nukleotidpolymorfism rs72689236 och

Itpkc gene

The encoded protein is localized to the nucleus and cytoplasm and has both nuclear import and nuclear export activity. The ITPKC gene was expressed in the mammary gland, but its expression was highest in breast cancer cells among other stromal cells in a bulk tumor.

The product SIRGT45481WQ is a type of small interfering RNA (siRNA) that targets ITPKC gene and regulates the expression of gene.
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Itpkc gene

ITPKC gene. Properties. ITPKC gene products (24): 3'UTR GoClone (1), Antibodies (5), Custom CRISPR Plasmid (1), Proteins (4), SYBR Green Primers (2), , shRNA Products (6), siRNA Products (5) Peer-Reviewed Papers. Related Gene Products. The ITPKC gene provides instructions for making an enzyme called inositol 1,4,5-trisphosphate 3-kinase C. This enzyme helps limit the activity of immune system cells called T cells.

Inmunógeno, ITPKC Fusion Protein Ag5583. Isotipo, IgG. Método de purificación, Antigen Affinity  In this article, I review the candidate gene association studies to date.
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En enda nukleotidpolymorfism rs4236480 i trpv5 kalciumkanalgen

This gene that has been associated with Kawasaki disease. Kawasaki disease is an acute febrile illness that involves the inflammation of blood vessels throughout the body. The majority of cases that have been diagnosed involve children under the age of 5.


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Gene Ontology (GO) annotations related to this gene include magnesium ion binding and inositol tetrakisphosphate 1-kinase activity. UniProtKB/Swiss-Prot Summary for ITPK1 Gene Kinase that can phosphorylate various inositol polyphosphate such as Ins(3,4,5,6)P4 or Ins(1,3,4)P3. 2021-03-02 · ITPKC inositol-trisphosphate 3-kinase C [ (human)] Our findings suggest that ITPKC is a susceptibility gene for bone mineral density (BMD), and rs2607420 may play an important role in the regulation of this gene. This study identified several important polymorphisms in the ITPKC and SLC11A1 genes in Koreans. The gene view histogram is a graphical view of mutations across ITPKC.