NOC3L
NOC3 like DNA replication regulator
Summary
Enables RNA binding activity. Predicted to be involved in DNA replication initiation. Predicted to act upstream of or within fat cell differentiation. Located in mitochondrion; nucleolus; and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs373890811 | 10:96,093,995 | C/T | — | likely benign |
| rs375381157 | 10:96,094,444 | T/C | — | uncertain significance |
| rs200196729 | 10:96,094,458 | A/G | — | uncertain significance |
| rs201691751 | 10:96,094,473 | G/A | — | uncertain significance |
| rs775786615 | 10:96,097,537 | C/T | — | uncertain significance |
| rs17109928 | 10:96,098,093 | T/C | — | — |
| rs938866977 | 10:96,098,388 | G/T | — | uncertain significance |
| rs766551564 | 10:96,098,433 | G/T | — | uncertain significance |
| rs1043911414 | 10:96,099,585 | C/T | — | uncertain significance |
| rs2497854294 | 10:96,100,036 | C/T | — | uncertain significance |
| rs533523491 | 10:96,104,206 | G/A | — | uncertain significance |
| rs2497866747 | 10:96,104,266 | C/G | — | uncertain significance |
| rs911141850 | 10:96,109,119 | C/T | — | uncertain significance |
| rs756990751 | 10:96,109,960 | C/G | — | uncertain significance |
| rs749860528 | 10:96,109,988 | C/A | — | uncertain significance |
| rs147826125 | 10:96,112,157 | G/C | — | uncertain significance |
| rs746433275 | 10:96,112,160 | T/A | — | uncertain significance |
| rs376369982 | 10:96,112,705 | A/G | — | uncertain significance |
| rs758954884 | 10:96,112,720 | T/A | — | uncertain significance |
| rs1291650074 | 10:96,112,778 | C/T | — | uncertain significance |
| rs2497892455 | 10:96,112,782 | C/G | — | uncertain significance |
| rs773976870 | 10:96,112,787 | T/C | — | uncertain significance |
| rs150224263 | 10:96,112,799 | C/G | — | uncertain significance |
| rs368362912 | 10:96,114,780 | C/G | — | uncertain significance |
| rs764714535 | 10:96,114,793 | T/C | — | uncertain significance |
| rs2497903056 | 10:96,116,327 | T/A | — | uncertain significance |
| rs2497903059 | 10:96,116,328 | C/T | — | uncertain significance |
| rs759218090 | 10:96,116,330 | T/C | — | uncertain significance |
| rs12771562 | 10:96,116,419 | G/A | intron variant | — |
| rs12771055 | 10:96,116,420 | A/G | intron variant | — |
| rs746293694 | 10:96,117,054 | G/A | — | uncertain significance |
| rs771279495 | 10:96,117,871 | C/T | — | uncertain significance |
| rs148216421 | 10:96,117,876 | T/C | — | uncertain significance |
| rs201542910 | 10:96,117,924 | A/G | — | uncertain significance |
| rs2054509932 | 10:96,117,933 | G/C | — | uncertain significance |
| rs71482305 | 10:96,119,130 | C/A | — | — |
| rs759225017 | 10:96,121,427 | C/T | — | uncertain significance |
| rs2054552644 | 10:96,121,434 | C/G | — | uncertain significance |
| rs545895087 | 10:96,121,587 | T/G | — | uncertain significance |
| rs781574865 | 10:96,121,598 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.