A synthesized peptide derived from Human ALS2CR2.
A synthesized peptide derived from human ALS2CR4, corresponding to a region within the internal amino acids.
A synthesized peptide derived from human ALS2CR8, corresponding to a region within the internal amino acids.
A synthesized peptide derived from human ALS2, corresponding to a region within N-terminal amino acids.
A synthesized peptide derived from human ALX1.
A synthesized peptide derived from human ALX3, corresponding to a region within the internal amino acids.
A synthesized peptide derived from human ALX4.
A synthesized peptide derived from human AMACR, corresponding to a region within the internal amino acids.
This gene encodes a racemase. The encoded enzyme interconverts pristanoyl-CoA and C27-bile acylCoAs between their (R)- and (S)-stereoisomers. The conversion to the (S)-stereoisomers is necessary for degradation of these substrates by peroxisomal beta-oxidation. Encoded proteins from this locus localize to both mitochondria and peroxisomes. Mutations in this gene may be associated with adult-onset sensorimotor neuropathy, pigmentary retinopathy, and adrenomyeloneuropathy due to defects in bile acid synthesis. Alternatively spliced transcript variants have been described. Read-through transcription also exists between this gene and the upstream neighboring C1QTNF3 (C1q and tumor necrosis factor related protein 3) gene.
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