FSTL5
follistatin like 5
Summary
Predicted to enable calcium ion binding activity. Predicted to be involved in cell differentiation and regulation of BMP signaling pathway. Predicted to be active in extracellular region. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1473277955 | 4:162,306,904 | C/T | — | uncertain significance |
| rs933767663 | 4:162,307,012 | T/A | — | uncertain significance |
| rs2477083155 | 4:162,307,052 | G/C | — | uncertain significance |
| rs370765604 | 4:162,307,185 | T/C | — | uncertain significance |
| rs1445115464 | 4:162,307,329 | T/C | — | uncertain significance |
| rs370951713 | 4:162,307,350 | T/C | — | uncertain significance |
| rs371506767 | 4:162,307,409 | C/T | — | uncertain significance |
| rs2477086603 | 4:162,307,465 | A/G | — | uncertain significance |
| rs201627637 | 4:162,307,509 | T/C | — | uncertain significance |
| rs750641663 | 4:162,307,541 | C/G | — | uncertain significance |
| rs181527249 | 4:162,307,557 | A/G | — | uncertain significance |
| rs71610959 | 4:162,332,652 | G/A | intron variant | — |
| rs375309884 | 4:162,376,181 | T/G | — | uncertain significance |
| rs2476918599 | 4:162,402,321 | C/G | — | uncertain significance |
| rs115809651 | 4:162,414,623 | G/A | intron variant | — |
| rs1026348227 | 4:162,421,211 | A/C | — | uncertain significance |
| rs2476974957 | 4:162,421,226 | G/A | — | uncertain significance |
| rs768436797 | 4:162,421,250 | T/C | — | uncertain significance |
| rs1296829269 | 4:162,459,330 | C/T | — | uncertain significance |
| rs779562211 | 4:162,459,416 | T/C | — | uncertain significance |
| rs1407579471 | 4:162,463,764 | C/A | — | uncertain significance |
| rs1298654277 | 4:162,508,622 | T/C | — | uncertain significance |
| rs2477253636 | 4:162,508,629 | C/G | — | uncertain significance |
| rs1355399137 | 4:162,508,702 | T/C | — | uncertain significance |
| rs183247057 | 4:162,508,720 | C/T | — | uncertain significance |
| rs182601174 | 4:162,577,520 | T/C | — | uncertain significance |
| rs2477033348 | 4:162,577,575 | C/A | — | uncertain significance |
| rs202160962 | 4:162,577,589 | A/G | — | uncertain significance |
| rs17638464 | 4:162,602,209 | G/A | intron variant | — |
| rs140734017 | 4:162,642,863 | A/C | intron variant | — |
| rs745326447 | 4:162,680,652 | A/G | — | uncertain significance |
| rs199944647 | 4:162,680,682 | A/G | — | uncertain significance |
| rs373181331 | 4:162,697,047 | T/C | — | uncertain significance |
| rs2476828325 | 4:162,697,064 | C/T | — | uncertain significance |
| rs2476828425 | 4:162,697,086 | A/G | — | uncertain significance |
| rs201030606 | 4:162,697,125 | C/T | — | uncertain significance |
| rs908657429 | 4:162,697,214 | T/A | — | uncertain significance |
| rs1481787026 | 4:162,841,598 | G/T | — | uncertain significance |
| rs769789513 | 4:162,841,615 | G/T | — | uncertain significance |
| rs148666972 | 4:162,841,652 | C/T | — | uncertain significance |
| rs773942489 | 4:162,841,657 | G/T | — | uncertain significance |
| rs148108933 | 4:162,841,799 | T/C | — | uncertain significance |
| rs182769441 | 4:162,954,807 | C/T | — | uncertain significance |
| rs72693248 | 4:162,991,714 | G/A | intron variant | — |
| rs2111407159 | 4:163,032,440 | T/A | — | uncertain significance |
| rs780936186 | 4:163,032,445 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.