PEX5L
peroxisomal biogenesis factor 5 like
Summary
Enables peroxisome matrix targeting signal-1 binding activity and small GTPase binding activity. Predicted to be involved in protein import into peroxisome matrix, docking. Predicted to act upstream of or within maintenance of protein location and regulation of membrane potential. Located in cytosol. Part of receptor complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants24 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2545795284 | 3:179,519,692 | T/G | — | uncertain significance |
| rs2545796163 | 3:179,519,719 | G/C | — | uncertain significance |
| rs368029000 | 3:179,526,104 | T/C | — | uncertain significance |
| rs2545895513 | 3:179,526,178 | T/C | — | uncertain significance |
| rs780069829 | 3:179,527,431 | A/C | — | uncertain significance |
| rs141827659 | 3:179,529,649 | A/C | — | uncertain significance |
| rs369361167 | 3:179,537,661 | G/A | — | uncertain significance |
| rs146230186 | 3:179,537,671 | C/G | — | uncertain significance |
| rs139529181 | 3:179,537,712 | C/T | — | uncertain significance |
| rs188814073 | 3:179,576,923 | C/T | — | uncertain significance |
| rs146906651 | 3:179,592,165 | C/A | — | uncertain significance |
| rs141772500 | 3:179,593,163 | G/T | — | uncertain significance |
| rs1752016864 | 3:179,593,192 | C/T | — | uncertain significance |
| rs149599855 | 3:179,593,208 | G/T | — | uncertain significance |
| rs376209700 | 3:179,597,734 | G/C | — | uncertain significance |
| rs777000912 | 3:179,597,776 | G/A | — | uncertain significance |
| rs150573100 | 3:179,605,493 | G/A | — | uncertain significance |
| rs542977323 | 3:179,615,052 | G/A | — | — |
| rs147760601 | 3:179,615,983 | T/G | — | uncertain significance |
| rs768799147 | 3:179,615,998 | T/C | — | uncertain significance |
| rs747205183 | 3:179,626,802 | A/G | — | — |
| rs7630877 | 3:179,661,318 | G/C | — | — |
| rs9842133 | 3:179,664,102 | T/G | — | — |
| rs139944141 | 3:179,742,171 | A/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.