PADI2 Chromosome 1

Peptidyl arginine deiminase 2
4 variants 4 Health Risk

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What This Gene Does
This gene encodes a member of the peptidyl arginine deiminase family of enzymes, which catalyze the post-translational deimination of proteins by converting arginine residues into citrullines in the presence of calcium ions. The family members have distinct substrate specificities and tissue-specific expression patterns. The type II enzyme is the most widely expressed family member. Known substrates for this enzyme include myelin basic protein in the central nervous system and vimentin in skeletal muscle and macrophages. This enzyme is thought to play a role in the onset and progression of neurodegenerative human disorders, including Alzheimer disease and multiple sclerosis, and it has also been implicated in glaucoma pathogenesis. This gene exists in a cluster with four other paralogous genes. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Peptidyl arginine deiminases
Locus Type
gene with protein product
Location
1p36.13
Ensembl
ENSG00000117115
Associated Conditions (2)
Rheumatoid arthritis
Abnormal pulmonary interstitial morphology
Key Variants
All Variants (4)
RSID Category Clinical Significance Conditions
RS1005753 Health Risk association Rheumatoid arthritis, Abnormal pulmonary interstitial morphology, Rheumatoid arthritis
RS2057094 Health Risk association Rheumatoid arthritis, Abnormal pulmonary interstitial morphology, Rheumatoid arthritis
RS2076615 Health Risk association Rheumatoid arthritis, Abnormal pulmonary interstitial morphology, Rheumatoid arthritis
RS2235926 Health Risk association Rheumatoid arthritis, Abnormal pulmonary interstitial morphology, Rheumatoid arthritis
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