PID1
phosphotyrosine interaction domain containing 1
Summary
Involved in several processes, including negative regulation of ATP biosynthetic process; negative regulation of D-glucose import; and positive regulation of metabolic process. Located in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs544315038 | 2:229,890,386 | C/T | — | uncertain significance |
| rs751961969 | 2:229,890,410 | G/A | — | uncertain significance |
| rs375488219 | 2:229,890,416 | C/T | — | likely pathogenic |
| rs754405826 | 2:229,890,428 | T/C | — | uncertain significance |
| rs1693401654 | 2:229,890,457 | A/G | — | uncertain significance |
| rs147401384 | 2:229,890,514 | T/A | — | uncertain significance |
| rs914655421 | 2:229,890,520 | T/C | — | uncertain significance |
| rs143934715 | 2:229,890,626 | C/G | — | uncertain significance |
| rs116780832 | 2:229,890,733 | G/A | — | likely benign |
| rs369664470 | 2:229,890,741 | C/A | — | uncertain significance |
| rs746316153 | 2:229,890,824 | C/T | — | uncertain significance |
| rs56192920 | 2:229,941,644 | G/A | intron variant | — |
| rs183393710 | 2:229,949,195 | G/A | intron variant | — |
| rs6436839 | 2:229,969,798 | A/G | intron variant | — |
| rs143078898 | 2:229,994,086 | C/T | intron variant | — |
| rs4140748 | 2:230,005,505 | A/G | intron variant | — |
| rs13411207 | 2:230,007,119 | G/A | intron variant | — |
| rs11691714 | 2:230,012,076 | T/A | intron variant | — |
| rs6738438 | 2:230,020,220 | C/G | — | — |
| rs6738548 | 2:230,020,298 | C/G | — | — |
| rs6738549 | 2:230,020,304 | C/A | — | — |
| rs554571331 | 2:230,020,605 | G/A | — | uncertain significance |
| rs775616491 | 2:230,020,666 | C/T | — | uncertain significance |
| rs4973180 | 2:230,101,512 | T/C | upstream gene variant | — |
| rs77623237 | 2:230,114,499 | T/C | intron variant | — |
| rs7596814 | 2:230,128,204 | G/T | intron variant | — |
| rs35519782 | 2:230,128,720 | T/G | — | — |
| rs564647280 | 2:230,135,744 | T/C | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.