rs770539885

This variant is located in the PYCR1 gene.

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ClinVar annotation

Uncertain Significance★★★☆

4 submitters2 publications

not provided; Inborn genetic diseases; PYCR1-related de Barsy syndrome;Autosomal recessive cutis laxa type 2B

About PYCR1

This gene encodes an enzyme that catalyzes the NAD(P)H-dependent conversion of pyrroline-5-carboxylate to proline. This enzyme may also play a physiologic role in the generation of NADP(+) in some cell types. The protein forms a homopolymer and localizes to the mitochondrion. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]

View all PYCR1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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