GGNBP2
gametogenetin binding protein 2
Summary
Predicted to be involved in spermatogenesis. Predicted to act upstream of or within several processes, including labyrinthine layer blood vessel development; negative regulation of cell population proliferation; and negative regulation of peptidyl-tyrosine phosphorylation. Predicted to be located in cytoplasmic vesicle. Predicted to be active in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs3736166 | 17:34,900,836 | G/T | — | — |
| rs140693226 | 17:34,901,618 | C/A | — | uncertain significance |
| rs575661510 | 17:34,901,647 | A/G | — | uncertain significance |
| rs35915570 | 17:34,910,357 | C/A | — | — |
| rs1469388061 | 17:34,910,685 | G/A | — | uncertain significance |
| rs2285642 | 17:34,912,744 | G/T | — | — |
| rs771457601 | 17:34,913,122 | C/T | — | uncertain significance |
| rs2510255409 | 17:34,913,125 | G/A | — | uncertain significance |
| rs201797639 | 17:34,913,169 | G/A | — | uncertain significance |
| rs28573110 | 17:34,914,365 | A/G | intron variant | — |
| rs200365164 | 17:34,916,613 | G/A | — | likely benign |
| rs17138347 | 17:34,923,498 | G/A | — | benign |
| rs2074481734 | 17:34,923,504 | G/A | — | uncertain significance |
| rs752364975 | 17:34,923,570 | C/T | — | uncertain significance |
| rs34327767 | 17:34,929,002 | G/A | downstream gene variant | — |
| rs12951079 | 17:34,933,059 | G/A | upstream gene variant | — |
| rs2142766936 | 17:34,934,540 | C/T | — | uncertain significance |
| rs2074610284 | 17:34,934,597 | G/A | — | uncertain significance |
| rs779393330 | 17:34,934,606 | T/C | — | uncertain significance |
| rs139100369 | 17:34,935,752 | A/G | — | uncertain significance |
| rs2510291091 | 17:34,937,908 | T/G | — | uncertain significance |
| rs555095991 | 17:34,937,924 | A/G | — | likely benign |
| rs368153017 | 17:34,937,933 | C/A | — | uncertain significance |
| rs768078656 | 17:34,937,940 | C/T | — | uncertain significance |
| rs145184721 | 17:34,941,815 | A/G | — | uncertain significance |
| rs368364842 | 17:34,941,851 | A/G | — | uncertain significance |
| rs747476692 | 17:34,941,876 | G/C | — | uncertain significance |
| rs2510297800 | 17:34,942,569 | A/G | — | uncertain significance |
| rs1106908 | 17:34,942,595 | G/A | — | benign |
| rs2074708521 | 17:34,943,428 | T/C | — | uncertain significance |
| rs758346247 | 17:34,943,467 | G/A | — | uncertain significance |
| rs142994076 | 17:34,943,642 | C/T | — | likely benign |
| rs3744593 | 17:34,943,719 | C/T | upstream gene variant | — |
| rs2074735175 | 17:34,945,785 | A/C | — | uncertain significance |
| rs2510303265 | 17:34,945,822 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.