NPNT
nephronectin
Summary
Predicted to enable integrin binding activity. Predicted to be involved in several processes, including cell-cell adhesion mediated by integrin; positive regulation of ERK1 and ERK2 cascade; and positive regulation of alkaline phosphatase activity. Predicted to act upstream of or within positive regulation of transforming growth factor beta receptor signaling pathway. Located in collagen-containing extracellular matrix and extracellular exosome. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs59462153 | 4:106,815,088 | T/G | — | — |
| rs1013127198 | 4:106,816,816 | T/G | — | uncertain significance |
| rs535893355 | 4:106,816,837 | G/A | — | uncertain significance |
| rs765331387 | 4:106,816,868 | A/G | — | uncertain significance |
| rs961789836 | 4:106,816,874 | A/T | — | uncertain significance |
| rs147630398 | 4:106,819,089 | C/T | — | likely benign |
| rs372304586 | 4:106,819,095 | C/T | — | uncertain significance |
| rs374634164 | 4:106,819,096 | G/A | — | uncertain significance |
| rs1024999103 | 4:106,819,111 | T/C | — | uncertain significance |
| rs747884992 | 4:106,819,135 | G/A | — | uncertain significance |
| rs1006316084 | 4:106,848,574 | C/T | — | uncertain significance |
| rs184432546 | 4:106,852,425 | A/G | intron variant | — |
| rs371961951 | 4:106,858,170 | A/C | — | likely benign |
| rs751397823 | 4:106,859,475 | A/G | — | uncertain significance |
| rs116477289 | 4:106,859,539 | C/T | — | likely benign |
| rs775325362 | 4:106,859,541 | G/A | — | uncertain significance |
| rs138345254 | 4:106,861,246 | G/A | — | uncertain significance |
| rs144069851 | 4:106,861,316 | G/A | — | uncertain significance |
| rs199598735 | 4:106,861,330 | G/A | — | uncertain significance |
| rs746827166 | 4:106,861,338 | G/A | — | uncertain significance |
| rs143168697 | 4:106,861,719 | G/A | — | uncertain significance |
| rs756047160 | 4:106,861,728 | A/G | — | uncertain significance |
| rs774330718 | 4:106,861,744 | C/G | — | uncertain significance |
| rs577538073 | 4:106,863,544 | G/A | — | uncertain significance |
| rs541585826 | 4:106,863,575 | G/A | — | uncertain significance |
| rs773876234 | 4:106,863,604 | A/G | — | uncertain significance |
| rs781283871 | 4:106,863,664 | C/G | — | uncertain significance |
| rs750276514 | 4:106,863,737 | C/T | — | uncertain significance |
| rs756406157 | 4:106,863,757 | G/A | — | likely benign |
| rs373315142 | 4:106,863,788 | C/T | — | uncertain significance |
| rs143758714 | 4:106,863,842 | C/T | — | likely benign |
| rs771871394 | 4:106,880,212 | A/G | — | uncertain significance |
| rs970022875 | 4:106,880,220 | C/G | — | uncertain significance |
| rs774753922 | 4:106,880,268 | A/G | — | likely benign |
| rs1178238208 | 4:106,888,353 | T/C | — | uncertain significance |
| rs754853674 | 4:106,888,359 | A/T | — | uncertain significance |
| rs35613262 | 4:106,888,416 | G/A | missense variant | — |
| rs201656446 | 4:106,888,420 | G/A | — | likely benign |
| rs375878808 | 4:106,888,429 | A/G | — | uncertain significance |
| rs369844601 | 4:106,888,512 | G/A | — | likely benign |
| rs1359908292 | 4:106,888,521 | G/A | — | uncertain significance |
| rs1560547736 | 4:106,888,543 | A/T | — | uncertain significance |
| rs780136006 | 4:106,888,546 | G/T | — | uncertain significance |
| rs199795974 | 4:106,888,582 | G/A | — | uncertain significance |
| rs753058987 | 4:106,890,073 | A/G | — | uncertain significance |
| rs139540458 | 4:106,890,076 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.