Cwf19l2
WebFeb 13, 2024 · The c.2288A>G (p.Q763R) alteration is located in exon 15 (coding exon 15) of the CWF19L2 gene. This alteration results from a A to G substitution at nucleotide position 2288, causing the glutamine (Q) at amino acid position 763 to be replaced by an arginine (R). Based on insufficient or conflicting evidence, the clinical significance of this ... WebOverview Product name Anti-CWF19L2 antibody Description Rabbit polyclonal to CWF19L2 Host species Rabbit Tested applications Suitable for: WB, IHC-P more details Species …
Cwf19l2
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WebCWF19L2 PATHOLOGY CANCER ANTIBODIES AND VALIDATION Dictionary Human pathology PROGNOSTIC SUMMARYi Gene product is not prognostic Show all RNA EXPRESSION OVERVIEWi TCGA dataseti RNA cancer category: Low cancer specificity PROTEIN EXPRESSIONi Colorectal cancer Breast cancer Prostate cancer Lung cancer … WebNM_152434.3(CWF19L2):c.1984A>G (p.Ile662Val) AND Inborn genetic diseases Clinical significance: Uncertain significance (Last evaluated: Aug 2, 2024) Review status: 1 star out of maximum of 4 stars
WebView Rabbit Polyclonal anti-CWF19L2 Antibody (NBP1-83533). Validated Applications: ICC/IF, IHC, IHC-P. Validated Species: Human. Sample size available. WebPanel Description. Sequence variants and/or copy number variants (deletions/duplications) within the CWF19L2 gene will be detected with >99% sensitivity. Variants classified as unknown significance (VUS), likely pathogenic, or pathogenic will be reported. Benign and likely benign variants are generally not reported.
WebCWF19L2 (COSG82496) Genomic coordinates 11:107326345..107457844 (negative strand) Synonyms FLJ32343, CCDS8336.2, Q2TBE0, ENSG00000152404.15, NM_152434.2, NP_689647 COSMIC-3D There are 2 structures for CWF19L2 . View them in COSMIC-3D . Number of samples 40544 unique samples 1024 unique samples with mutations … WebCWF19L2. General description of the gene and the encoded protein (s) using information from HGNC and Ensembl, as well as predictions made by the Human Protein Atlas …
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WebMar 21, 2024 · CWF19L2 (CWF19 Like Cell Cycle Control Factor 2) is a Protein Coding gene. Diseases associated with CWF19L2 include Bardet-Biedl Syndrome 4. Among its … cave zagaroloWebGene: Cwf19l2 MGI:1918023 Not currently registered for phenotyping at IMPC Phenotyping is currently not planned for a knockout strain of this gene. Gene Summary Name: CWF19-like 2, cell cycle control (S. pombe) Synonyms: 3230401L03Rik Order Alleles IMPC Data Collections No Body Weight Data No Embryo Imaging Data No Viability Data cave znacenjeWebFeb 13, 2024 · Description: single nucleotide variant Variant details Conditions Gene (s) Help NM_152434.3 (CWF19L2):c.2288A>G (p.Gln763Arg) Allele ID 2194817 Variant … cave zamor ruinsWebNM_152434.3(CWF19L2):c.661A>G (p.Lys221Glu) AND Inborn genetic diseases Clinical significance: Uncertain significance (Last evaluated: Dec 2, 2024) Review status: 1 star out of maximum of 4 stars cave značenjeWebNM_152434.3(CWF19L2):c.1690G>A (p.Gly564Arg) AND Inborn genetic diseases Clinical significance: Uncertain significance (Last evaluated: Jul 6, 2024) Review status: 1 star out of maximum of 4 stars cave zbWebAlternate Names for CWF19L2 Antibody CWF19-like 2, cell cycle control (S. pombe) CWF19-like protein 2 FLJ32343 Limitations This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt. Customers Who Viewed This Item Also Viewed... caveze jonesWeb cave zanzibar