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FANCD2(Phospho Ser222) Polyclonal Antibody, 50ul Cell Culture Plates This gene functions as a

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FANCD2(Phospho Ser222) Polyclonal Antibody, 50ul Cell Culture Plates This gene functions as aThe Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal

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Description

This gene functions as a tumor suppressor

Epidermodysplasia verruciformis (EV) is an autosomal recessive dermatosis characterized by abnormal susceptibility to human papillomaviruses (HPVs) and a high rate of progression to squamous cell carcinoma on sun-exposed skin

Alternative splicing results in multiple transcript variants and pseudogenes have been identified on chromosomes 9 and 12

This gene is closely linked to related family member T-box 3 (ulnar mammary syndrome) on human chromosome 12

NMDA receptor channels are heteromers composed of three different subunits: NR1 (GRIN1)

FANCD2(Phospho Ser222) Polyclonal Antibody, 50ul Cell Culture Plates This gene functions as aThe Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal

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