FNDC3B
fibronectin type III domain containing 3B
Summary
Enables RNA binding activity. Predicted to act upstream of or within several processes, including negative regulation of osteoblast differentiation; substrate adhesion-dependent cell spreading; and type II pneumocyte differentiation. Predicted to be located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants95 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs8179884 | 3:171,781,535 | C/G | intron variant | — |
| rs9647379 | 3:171,785,168 | G/T | — | — |
| rs62283793 | 3:171,817,325 | C/T | intron variant | — |
| rs62283814 | 3:171,821,556 | C/T | regulatory region variant | — |
| rs4308305 | 3:171,831,116 | T/C | intron variant | — |
| rs546985029 | 3:171,881,986 | A/G | — | — |
| rs4894525 | 3:171,897,975 | C/T | — | — |
| rs28731496 | 3:171,910,970 | T/G | — | — |
| rs4639001 | 3:171,919,214 | G/T | — | — |
| rs368064533 | 3:171,924,885 | G/A | — | — |
| rs4535251 | 3:171,926,373 | T/C | intron variant | — |
| rs12492846 | 3:171,926,691 | C/T | intron variant | — |
| rs34770855 | 3:171,940,305 | A/G | downstream gene variant | — |
| rs4423796 | 3:171,943,511 | C/T | coding sequence variant | — |
| rs35898760 | 3:171,950,181 | C/T | upstream gene variant | — |
| rs59976239 | 3:171,956,651 | A/T | — | — |
| rs4894529 | 3:171,959,684 | A/T | — | — |
| rs1874259 | 3:171,963,717 | C/T | intron variant | — |
| rs149331185 | 3:171,965,405 | C/T | — | uncertain significance |
| rs2475194391 | 3:171,965,482 | T/C | — | uncertain significance |
| rs750254687 | 3:171,965,501 | C/A | — | uncertain significance |
| rs778699186 | 3:171,965,552 | T/C | — | uncertain significance |
| rs7652177 | 3:171,969,077 | C/G | missense variant | benign |
| rs745636990 | 3:171,969,215 | A/G | — | uncertain significance |
| rs774975615 | 3:171,969,217 | G/C | — | uncertain significance |
| rs768433890 | 3:171,969,226 | C/T | — | uncertain significance |
| rs35366330 | 3:171,969,228 | T/C | — | benign |
| rs2475214398 | 3:171,969,229 | A/G | — | uncertain significance |
| rs768417527 | 3:171,969,311 | C/T | — | uncertain significance |
| rs34553291 | 3:171,969,312 | G/C | — | benign |
| rs4894533 | 3:171,974,969 | G/T | — | — |
| rs9290448 | 3:171,984,405 | T/A | intron variant | — |
| rs59540498 | 3:171,987,748 | T/C | intron variant | — |
| rs4894535 | 3:171,995,605 | C/T | intron variant | — |
| rs12639337 | 3:171,996,939 | G/C | intron variant | — |
| rs4894537 | 3:171,998,829 | C/A | — | — |
| rs150452141 | 3:171,999,047 | A/G | intron variant | — |
| rs374959823 | 3:172,013,259 | C/T | — | uncertain significance |
| rs577979739 | 3:172,015,556 | G/A | — | — |
| rs17521583 | 3:172,022,842 | A/G | upstream gene variant | — |
| rs531768294 | 3:172,025,175 | G/A | — | uncertain significance |
| rs36032820 | 3:172,025,228 | C/T | — | benign |
| rs111698934 | 3:172,033,011 | C/G | upstream gene variant | — |
| rs372880783 | 3:172,046,816 | G/A | — | likely benign |
| rs35409041 | 3:172,046,841 | G/T | — | benign |
| rs1208849040 | 3:172,046,856 | A/G | — | uncertain significance |
| rs2270568 | 3:172,046,861 | T/C | — | benign |
| rs147159768 | 3:172,048,499 | T/A | — | uncertain significance |
| rs768743506 | 3:172,048,504 | A/G | — | uncertain significance |
| rs139505585 | 3:172,052,790 | G/A | — | likely benign |
| rs148414755 | 3:172,052,861 | G/C | — | uncertain significance |
| rs773263646 | 3:172,055,122 | C/G | — | uncertain significance |
| rs756041159 | 3:172,055,131 | G/T | — | uncertain significance |
| rs749330093 | 3:172,058,941 | G/A | — | uncertain significance |
| rs145680877 | 3:172,058,948 | C/T | — | uncertain significance |
| rs373844597 | 3:172,058,951 | T/G | — | uncertain significance |
| rs112342266 | 3:172,059,031 | G/A | — | benign |
| rs759424206 | 3:172,060,825 | A/G | — | uncertain significance |
| rs371188009 | 3:172,060,853 | G/A | — | uncertain significance |
| rs1471068373 | 3:172,060,859 | C/T | — | uncertain significance |
| rs943382723 | 3:172,061,011 | C/T | — | — |
| rs750889128 | 3:172,061,881 | C/G | — | uncertain significance |
| rs751773331 | 3:172,061,969 | C/T | — | uncertain significance |
| rs138991587 | 3:172,061,986 | G/A | — | uncertain significance |
| rs376295496 | 3:172,062,010 | G/A | — | uncertain significance |
| rs142366050 | 3:172,062,017 | G/A | — | uncertain significance |
| rs1294695831 | 3:172,062,022 | C/T | — | uncertain significance |
| rs753919960 | 3:172,062,023 | G/T | — | uncertain significance |
| rs144543240 | 3:172,064,180 | G/A | — | uncertain significance |
| rs779461095 | 3:172,064,199 | C/T | — | uncertain significance |
| rs1040335747 | 3:172,065,003 | G/A | — | uncertain significance |
| rs1733656373 | 3:172,065,030 | C/T | — | uncertain significance |
| rs781409204 | 3:172,065,099 | G/A | — | uncertain significance |
| rs113522210 | 3:172,065,148 | A/G | — | likely benign |
| rs181124723 | 3:172,068,242 | C/G | intron variant | — |
| rs201224311 | 3:172,070,611 | G/A | — | uncertain significance |
| rs776658202 | 3:172,070,618 | C/T | — | uncertain significance |
| rs202127932 | 3:172,070,645 | C/T | — | uncertain significance |
| rs113685139 | 3:172,070,646 | G/T | — | likely benign |
| rs143064249 | 3:172,070,668 | G/A | — | benign |
| rs747129199 | 3:172,070,809 | A/T | — | uncertain significance |
| rs61734221 | 3:172,080,594 | G/C | — | benign |
| rs145935144 | 3:172,096,113 | C/T | — | uncertain significance |
| rs779511731 | 3:172,096,206 | G/A | — | uncertain significance |
| rs111462932 | 3:172,104,549 | G/C | — | — |
| rs1264405629 | 3:172,114,961 | A/G | — | uncertain significance |
| rs2473504929 | 3:172,114,970 | A/C | — | uncertain significance |
| rs774307921 | 3:172,115,039 | G/A | — | uncertain significance |
| rs772878434 | 3:172,115,080 | C/T | — | uncertain significance |
| rs1361288526 | 3:172,115,095 | G/A | — | uncertain significance |
| rs779045906 | 3:172,115,157 | G/A | — | uncertain significance |
| rs2473505824 | 3:172,115,219 | T/C | — | uncertain significance |
| rs1261516222 | 3:172,115,257 | A/G | — | uncertain significance |
| rs2431 | 3:172,117,107 | A/T | — | — |
| rs9859248 | 3:172,118,857 | T/C | 3 prime UTR variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.