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Antibody detects endogenous levels of total LHX3.
This gene encodes a member a large protein family which carry the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein is a transcription factor that is required for pituitary development and motor neuron specification. Mutations in this gene have been associated with a syndrome of combined pituitary hormone deficiency and rigid cervical spine. Two transcripts variants encoding distinct isoforms have been identified for this gene.
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Protein Aliases: DKFZp762A2013; Homeobox protein LIM-3; Homeobox protein P-LIM; LIM homeo box protein 3; LIM homeobox protein 3; LIM/homeobox protein Lhx3; LIM/homeodomain protein LHX3
Gene Aliases: CPHD3; LHX3; Lim-3; LIM3; M2-LHX3; mLim-3; mLIM3; P-LIM; Plim
UniProt ID: (Human) Q9UBR4, (Mouse) P50481
Entrez Gene ID: (Human) 8022, (Rat) 170671, (Mouse) 16871
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