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CHX10 encodes a homeobox protein originally described as a retina-specific transcription factor. Mutations in this gene are associated with microphthalmia, cataracts and iris abnormalities.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: C. elegans ceh-10 homeo domain containing homolog; ceh-10 homeo domain containing homolog; Ceh-10 homeodomain-containing homolog; Homeobox protein CHX10; ocular retardation; Visual system homeobox 2
Gene Aliases: CHX10; Hox-10; HOX10; MCOP2; MCOPCB3; or; RET1; VSX2
UniProt ID: (Human) A1A4X6, (Mouse) Q61412
Entrez Gene ID: (Human) 338917, (Mouse) 12677, (Rat) 171360
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