NEGR1
neuronal growth regulator 1
Summary
Predicted to be involved in cell adhesion and regulation of synapse assembly. Predicted to act upstream of or within several processes, including cholesterol homeostasis; lipid droplet formation; and nervous system development. Predicted to be located in extracellular region and plasma membrane. Predicted to be active in postsynaptic density. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants52 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs748454918 | 1:71,873,145 | T/G | — | uncertain significance |
| rs144477627 | 1:71,873,219 | G/A | — | benign |
| rs138963902 | 1:72,058,610 | C/T | — | likely benign |
| rs6424434 | 1:72,062,963 | A/G | intron variant | — |
| rs10493485 | 1:72,071,129 | A/C | — | — |
| rs2523301834 | 1:72,076,757 | C/G | — | uncertain significance |
| rs545038964 | 1:72,076,790 | G/A | — | uncertain significance |
| rs61729931 | 1:72,076,795 | G/T | — | benign |
| rs778071072 | 1:72,076,799 | C/A | — | uncertain significance |
| rs954299 | 1:72,121,585 | C/G | — | — |
| rs2422021 | 1:72,130,161 | C/T | intron variant | — |
| rs201170592 | 1:72,163,761 | C/T | — | likely benign |
| rs11209828 | 1:72,175,700 | A/T | intron variant | — |
| rs10789322 | 1:72,178,928 | G/T | — | — |
| rs76099857 | 1:72,192,616 | A/G | intron variant | — |
| rs12740031 | 1:72,222,487 | G/A | intron variant | — |
| rs2523733206 | 1:72,241,884 | G/C | — | uncertain significance |
| rs12141391 | 1:72,274,473 | C/A | intron variant | — |
| rs140524673 | 1:72,285,187 | G/T | intron variant | — |
| rs6659202 | 1:72,307,420 | T/A | upstream gene variant | — |
| rs591540 | 1:72,331,815 | T/A | — | — |
| rs140517365 | 1:72,400,878 | T/C | — | uncertain significance |
| rs369949208 | 1:72,400,939 | T/G | — | uncertain significance |
| rs11209896 | 1:72,512,988 | G/A | intron variant | — |
| rs12564163 | 1:72,513,121 | T/G | intron variant | — |
| rs2422134 | 1:72,514,701 | G/T | — | — |
| rs1026997 | 1:72,516,287 | T/C | regulatory region variant | — |
| rs11209909 | 1:72,553,122 | A/C | — | — |
| rs12085418 | 1:72,553,891 | G/C | — | — |
| rs2821260 | 1:72,554,093 | C/T | intron variant | — |
| rs7541651 | 1:72,554,833 | T/A | intron variant | — |
| rs2016698 | 1:72,562,478 | G/A | intron variant | — |
| rs114887144 | 1:72,563,122 | C/T | intron variant | — |
| rs2220253 | 1:72,565,460 | C/T | intron variant | — |
| rs67474621 | 1:72,577,950 | A/G | — | — |
| rs12402629 | 1:72,578,709 | T/C | intron variant | — |
| rs12133604 | 1:72,610,879 | G/C | — | — |
| rs11587895 | 1:72,612,615 | T/C | intron variant | — |
| rs11209928 | 1:72,627,031 | G/A | intron variant | — |
| rs34691764 | 1:72,641,334 | T/G | intron variant | — |
| rs12725081 | 1:72,682,718 | T/A | intron variant | — |
| rs34940719 | 1:72,693,786 | G/A | intron variant | — |
| rs1194282 | 1:72,713,559 | T/C | intron variant | — |
| rs1194281 | 1:72,714,003 | T/C | intron variant | — |
| rs1194278 | 1:72,714,220 | C/T | intron variant | — |
| rs12137936 | 1:72,720,357 | C/G | intron variant | — |
| rs61765646 | 1:72,723,211 | T/A | intron variant | — |
| rs12737564 | 1:72,739,527 | A/C | upstream gene variant | — |
| rs151324323 | 1:72,748,011 | G/A | — | uncertain significance |
| rs142674139 | 1:72,748,084 | G/C | — | benign |
| rs1570224157 | 1:72,748,118 | C/A | — | likely benign |
| rs3101339 | 1:72,748,669 | A/C | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.