breast cancer cells identifies new target profiles for sulforaphane. James A. 55 ITPK1. Inositol-tetrakisphosphate 1-kinase. High. N. -0.02 0.76 2.11. 56 KDM3B.

564

itpk1_human

This subsection of the 'Entry information' section provides one or more accession number(s). These are stable identifiers and should be used to cite UniProtKB entries.

More information. Hallmark gene. This gene does not have a cancer hallmark. Expression of ITPK1 in cancer tissue. The cancer tissue page shows antibody staining of the protein in 20 different cancers. Expression of ITPK1 in cancer tissue.

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You can see more information about hallmarks. COSMIC gene ITPKB (COSG226) Genomic coordinates 1:226631690..226739175 Recombinant ITPK1 phosphorylated both isoforms I(1)P 1 and I(3)P 1 to IP 5 (Fig. 4B). Simultaneous expression of ITPK1 with the inositol kinase TK2285 in plc∆isc1∆ yeast strain restored the IP 6 level (Fig. 4C), which confirmed that ITPK1 can use I(3)P 1 both in vitro and in vivo. Cancer Res; 74(23); 6820–32.

Curated gene. This is NOT an expert curated gene . Mouse gene.

Gene information about ENSG00000100605 / ITPK1 - inositol-tetrakisphosphate 1-kinase We use cookies to enhance the usability of our website. If you continue, we'll assume that you are happy to receive all cookies.

1 Serologically defined breast cancer antigen 84 1 Lung cancer candidate 1 Inositol 1,3,4-triphosphate 5/6 kinase. ITPK1. Hs.6453. AA010675.

the survival of patients with GC. Furthermore, ITPK1‑AS1, KCNQ1DN, LINC00167, LINC00173 and LINC00307 may serve as biomarkers for GC pathogenesis. Introduction Gastric cancer (GC) originates from the lining of the stomach, and may metastasize to other tissues and organs, including the lungs, liver, lymph nodes and bones (1). It is estimated that

Itpk1 cancer

0.76 (0.04). 2.76E-06.

Introduction Gastric cancer (GC) originates from the lining of the stomach, and may metastasize to other tissues and organs, including the lungs, liver, lymph nodes and bones (1). It is estimated that Cell atlas. Showing subcellular location of ITPK1.
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Itpk1 cancer

We demonstrated that the RCC cell line 786-0 with mutated VHL was resistant to NK-mediated lysis as compared with the VHL-corrected cell line (WT7). ITPK1 (inositol-tetrakisphosphate 1-kinase) Non-annotated gene. Preliminary data : if you are an author. Other Solid tumors implicated (Data extracted from papers in the Atlas) [ 4 ] magnesium ion binding inositol tetrakisphosphate 6-kinase activity catalytic activity ATP binding cytoplasm cytosol signal transduction blood coagulation apical plasma ITPK1 mutation reduces labeling of InsP 6 by 50%, with concomitant accumulation of d / l ‐Ins(3,4,5,6)P 4, but because it does so without affecting the level of Ins(1,3,4,5,6)P 5 (Figures 5a and S6a) suggests that ITPK1 probably does not act as an Ins(1,3,4,5,6)P 5 1‐phosphatase. Kinase that can phosphorylate various inositol polyphosphate such as Ins (3,4,5,6)P4 or Ins (1,3,4)P3.

chr10:52561026|52561202. UCSC.
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ITPK1 is not prognostic in breast cancer Alive (n=923) Dead (n=152) Female (n=1063) Male (n=12) Stage: i (n=89) ia (n=86) ib (n=5) ii (n=6) iia (n=352) iib (n=251) iii (n=2) iiia (n=153) iiib (n=25) iiic (n=63) iv (n=20) n/a (n=11) x (n=12)

ITPK1 (Inositol-Tetrakisphosphate 1-Kinase) is a Protein Coding gene. Diseases associated with ITPK1 include Neural Tube Defects. Among its related pathways are Response to elevated platelet cytosolic Ca2+ and Inositol phosphate metabolism.


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Gene ID: 490591, updated on 3-Sep-2016. Summary Other designations. inositol-tetrakisphosphate 1-kinase, inositol 1,3,4-triphosphate 5/6 kinase, inositol 1,3,4-triphosphate 5

Cancer Gene Census 3. CancerGenes 4. Network of Cancer … Download Citation | On Jan 1, 2016, Yixing Zhou and others published ITPK1 (Inositol Tetrakisphosphate 1-Kinase) | Find, read and cite all the research you need on ResearchGate Summary of ITPK1 expression in human tissue. Moderate cytoplasmic positivity was displayed in intestinal glands, gall bladder, thyroid, renal tubules, granular layer of cerebellum and heart myocytes. Subset of gastric glands were strongly stained. Fallopian tube exhibited additional membranous staining.