The HUGO Gene Nomenclature Committee (HGNC) provides a list of genes in the PTP family
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Genetics Home Reference summarizes the normal function and health implications of these genes in the PTP gene family:
- EPM2A: epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
- EYA1: eyes absent homolog 1 (Drosophila)
- EYA4: eyes absent homolog 4 (Drosophila)
- MTM1: myotubularin 1
- MTMR2: myotubularin related protein 2
- PTEN: phosphatase and tensin homolog
- PTPN11: protein tyrosine phosphatase, non-receptor type 11
- PTPN22: protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
- SBF2: SET binding factor 2
