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Gene Review:

C11orf21 - chromosome 11 open reading frame 21

Homo sapiens

Synonyms: Uncharacterized protein C11orf21

Zhu, X. et al.

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Disease relevance of C11orf21

C11orf21, a novel gene within the Beckwith-Wiedemann syndrome region in human chromosome 11p15.5 [1].

High impact information on C11orf21

5. C11orf21 codes a protein of 132 amino acids as proved by the expression of C11orf21-EGFP fusion protein in cultured cells [1].

References

C11orf21, a novel gene within the Beckwith-Wiedemann syndrome region in human chromosome 11p15.5. Zhu, X., Higashimoto, K., Soejima, H., Yatsuki, H., Sugihara, H., Mukai, T., Joh, K. Gene (2000) [Pubmed]

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