Search Thermo Fisher Scientific
Deletions of the 22q11.2 have been associated with a wide range of developmental defects (notably DiGeorge syndrome, velocardiofacial syndrome, conotruncal anomaly face syndrome and isolated conotruncal cardiac defects) classified under the acronym CATCH 22. The DGCR2 gene encodes a novel putative adhesion receptor protein, which could play a role in neural crest cells migration, a process which has been proposed to be altered in DiGeorge syndrome.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: DiGeorge syndrome critical region protein 2; DiGeorge syndrome gene c; DiGeorge syndrome protein C; integral membrane protein deleted in DiGeorge syndrome; Integral membrane protein DGCR2/IDD; Seizure-related membrane-bound adhesion protein
基因别名: 9930034O06Rik; DGCR2; DGS-C; Dgsc; IDD; KIAA0163; LAN; mKIAA0163; SEZ-12; Sez12
UniProt ID: (Human) P98153, (Mouse) P98154
Entrez Gene ID: (Human) 9993, (Rat) 360742, (Mouse) 13356
分子生物学功能:
apolipoprotein