FANCG Products

Description

The Fanconi anemia group subunit G protein (FANCG) confers resistance to both hygromycin and mitomycin C. Defects in FANCG cause the autosomal recessive disorder, Fanconi anemia, with diverse clinical symptoms.

FANCG antibodies are useful for DNA repair studies and cell cycle research.

Bioinformatics

Entrez	2189 Human
Uniprot	AAH11623 Human NM_004629 Human NP_004620 Human NP_004620.1 Human O15287 Human
Product By Gene ID	2189
Alternate Names	DNA repair protein XRCC9 FAG Fanconi anemia group G protein Fanconi anemia, complementation group G Protein FACG X-ray repair, complementing defective, in Chinese hamster, 9 XRCC9X-ray repair complementing defective repair in Chinese hamster cells 9

Research Areas for FANCG

Find related products by research area and learn more about each of the different research areas below.

Breast Cancer
Cancer
Chromatin Research
DNA Double Strand Break Repair
DNA Repair
Genes Sensitive to DNA Damaging Agents
Phospho-Specific

Related FANCG Blog Posts

Check out the latest blog posts on FANCG.

Fanconi Antibodies and Cancer Research We at Novus Biologicals have an extensive antibody databasedevoted to the 13 Fanconi anaemia complementation (FANC) genes, which are involved in the recognition and repair of damaged DNA.The core complex of 8 proteins (FANCA, B, C, E, F, G, L and M)...    Read more.

Read more FANCG related blogs.