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11 Possible Causes for BRCC2, human, protein

Did you mean: BRCC2, human, proteus

  • Hypoinsulinemic Hypoglycemia and Body Hemihypertrophy

    PHLPP1 - PH domain leucine-rich repeat-containing protein phosphatase 1; Protein phosphatase involved in regulation of Akt and PKC signaling.[string-db.org] FACD; FANCD; FANCD1; PNCA2; GLM3; FAD; 79184; RP11-143H17.2; BRCC3; BRCC36; C6.1A; CXorf53 79184; RP11-143H17.2; BRCC3; BRCC36; C6.1A; CXorf53; 675; RP11-298P3.4; BRCA2; BRCC2[denigma.de] Information by UniProt Functional Studies - Recombinant human AKT2 protein (ab60322) Sample Kinase Activity Plot.[abcam.com]

  • Autosomal Recessive Dyskeratosis Congenita Type 5

    Q9NZ71 Image Immunohistochemistry of paraffin-embedded human small intestine tissue using CSB-PA020563LA01HU at dilution of 1:100 Immunohistochemistry of paraffin-embedded[cusabio.com] […] early onset breast cancer 2, early-onset, included breast cancer, type 2, included fanconi anaemia, complementation group d1 fanconi anemia, complementation group d1 BRCA2 BRCC2[ukgtn.nhs.uk] The four H/ACA snoRNP proteins are also components of the telomerase complex. This gene encodes a protein related to Saccharomyces cerevisiae Nhp2p.[genecards.org]

  • Autosomal Dominant Dyskeratosis Congenita 2

    Dyskeratosis congenita, telomeres and human ageing. Trends Genet. 2000 May;16(5):193-5.[humpath.com] […] early onset breast cancer 2, early-onset, included breast cancer, type 2, included fanconi anaemia, complementation group d1 fanconi anemia, complementation group d1 BRCA2 BRCC2[ukgtn.nhs.uk] W), which is predicted to change the structure of the protein. Figure 3.[academic.oup.com]

  • Autosomal Dominant Myopia 22

    Below is a table of dominant and recessive traits shown in humans.[sciencebrainwaves.com] Broustas CG, Gokhale PC, Rahman A, Dritschilo A, Ahmad I, et al. (2004) BRCC2, a novel BH3-like domain-containing protein, induces apoptosis in a caspase-dependent manner.[journals.plos.org] Phosphoprotein Proteomic databases PTM databases Expression i Gene expression databases Organism-specific databases Interaction i Subunit structure i Binary interactions i Protein-protein[uniprot.org]

  • Pancreatic Carcinoma

    Lysosomal protein transmembrane 4 beta has two alleles designated as LAPTM4B*1 and LAPTM4B*2.[ncbi.nlm.nih.gov] C-K-RAS, K-RAS2A, K-RAS2B, K-RAS4A, K-RAS4B - KRAS and Pancreatic Cancer 421 MEN1 11q13.1 MEAI, SCG2 - MEN1 and Pancreatic Cancer 298 BRCA2 13q13.1 FAD, FACD, FAD1, GLM3, BRCC2[cancerindex.org] EA also effectively inhibit human pancreatic cancer growth in mice.[ncbi.nlm.nih.gov]

  • Homozygous 11p15-p14 Deletion Syndrome

    Overexpression of a transporter gene in a multidrug-resistant human lung cancer cell line. ‏[books.google.com] […] and Prostate Cancer 312 BRCA1 17q21 IRIS, PSCP, BRCAI, BRCC1, FANCS, PNCA4, RNF53, BROVCA1, PPP1R53 - BRCA1 and Prostate Cancer 178 BRCA2 13q12.3 FAD, FACD, FAD1, GLM3, BRCC2[cancer-genetics.org] […] not to the SUZ12 protein ( Figure 5 c).[mdpi.com]

  • Coats Plus Syndrome

    PMID 24025336, Free PMC Article Structure of the human telomeric Stn1-Ten1 capping complex. Bryan C, et al . PLoS One, 2013.[ncbi.nlm.nih.gov] […] early onset breast cancer 2, early-onset, included breast cancer, type 2, included fanconi anaemia, complementation group d1 fanconi anemia, complementation group d1 BRCA2 BRCC2[ukgtn.nhs.uk] Instead, the patients carried mutations in the gene encoding STN1, a protein that works together with CTC1 and another protein, TEN1, to maintain telomeres.[sciencedaily.com]

  • Oculootoradial Syndrome

    This information comes from a database called the Human Phenotype Ontology (HPO) .[rarediseases.info.nih.gov] […] early onset breast cancer 2, early-onset, included breast cancer, type 2, included fanconi anaemia, complementation group d1 fanconi anemia, complementation group d1 BRCA2 BRCC2[ukgtn.nhs.uk] (PMID: 23012367) Yang F … Dai W (The Journal of biological chemistry 2012) 3 4 60 A BEN-domain-containing protein associates with heterochromatin and represses transcription[genecards.org]

  • Dyskeratosis Congenita Type Scoggins

    Cell 90(4):785-95 17024208 Blackburn EH, et al. (2006) Telomeres and telomerase: the path from maize, Tetrahymena and yeast to human cancer and aging.[ppod.princeton.edu] […] early onset breast cancer 2, early-onset, included breast cancer, type 2, included fanconi anaemia, complementation group d1 fanconi anemia, complementation group d1 BRCA2 BRCC2[ukgtn.nhs.uk] Res. 94:768-775(2004)., PubMeb:14963003 DOI:10.1161/01.RES.0000121104.05977.F3 "Immunohistochemical localization of hTERT protein in human tissues."[genscript.com]

  • Jawad Syndrome

    Mol Biol Cell 16:3908–3918 PubMed CrossRef Google Scholar International Human Genome Sequence Consortium (2001) Initial sequence and analysis of the human genome.[link.springer.com] […] early onset breast cancer 2, early-onset, included breast cancer, type 2, included fanconi anaemia, complementation group d1 fanconi anemia, complementation group d1 BRCA2 BRCC2[ukgtn.nhs.uk] (PMID: 19460342) Tsang WY … Dynlacht BD (Developmental cell 2009) 3 4 22 60 Proteomic characterization of the human centrosome by protein correlation profiling.[genecards.org]