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CXorf22 (chromosome X open reading frame 22) is a poorly characterized gene on the human X chromosome that encodes a protein with no clearly defined function or known domains. It is expressed in multiple tissues, and while some studies suggest possible roles in neurological processes or disease contexts, its biological significance remains largely unknown.
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: calponin homology domain-containing protein 2; Cilia- and flagella-associated protein 47; unnamed protein product
基因别名: CFAP47; CHDC2; CXorf22; CXorf30; CXorf59; SPGF52; SPGFX3
UniProt ID: (Human) Q6ZTR5
Entrez Gene ID: (Human) 286464