C2orf72 (Chromosome 2, Open Reading Frame 72) is a gene in humans (Homo sapiens) that encodes a protein currently named after its gene, C2orf72. It is also designated LOC257407 and can be found under GenBank accession code NM_001144994.2. The protein can be found under UniProt accession code A6NCS6. WebC2orf72. 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 project. Official gene symbol, which is typically a short form of the gene name, according to HGNC. Full gene name according to HGNC.

PrEST Antigen C2orf72 [Catalog No.: ATL-APrEST79249]

WebAug 15, 2024 · Hexanucleotide (GGGGCC) repeat expansions in C9orf72 are the leading genetic cause of frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS). WebPrimePCR™ Template for Probe Assay: C2orf72, Human Reaction: 200 x 20 µl reactions Gene-specific synthetic DNA template designed to give a positive real-time PCR result … bophelowater gmail.com

Addgene: Plasmids related to C9orf72

WebNov 1, 2014 · C2orf72. LOCATION. 2q37.1. LOCUSID. 257407. ALIAS-FUSION GENES. Show Gene Fusions . Non-annotated gene. Preliminary data : if you are an author who … WebC2orf72. 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 project. … WebGene ID: 106002993, updated on 10-May-2024. Summary Other designations. LOW QUALITY PROTEIN: uncharacterized protein C2orf72 homolog hauling receipt