BEGAIN
brain enriched guanylate kinase associated
Summary
Predicted to enable kinase activity. Predicted to be involved in evoked excitatory postsynaptic potential and regulation of postsynaptic neurotransmitter receptor activity. Predicted to be located in dendrite; nucleus; and presynapse. Predicted to be active in glutamatergic synapse and postsynapse. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs758663053 | 14:101,004,380 | G/C | — | uncertain significance |
| rs781500772 | 14:101,004,433 | G/C | — | uncertain significance |
| rs1346352608 | 14:101,004,515 | C/T | — | uncertain significance |
| rs780718553 | 14:101,004,535 | C/G | — | uncertain significance |
| rs112914069 | 14:101,004,555 | G/A | — | benign |
| rs764209715 | 14:101,004,574 | C/T | — | uncertain significance |
| rs1276491455 | 14:101,004,596 | C/T | — | uncertain significance |
| rs2030938843 | 14:101,004,734 | C/G | — | uncertain significance |
| rs772257897 | 14:101,004,739 | C/A | — | uncertain significance |
| rs759826863 | 14:101,004,776 | G/A | — | uncertain significance |
| rs1192852960 | 14:101,004,904 | G/T | — | uncertain significance |
| rs2549436475 | 14:101,004,908 | G/A | — | uncertain significance |
| rs2549436782 | 14:101,004,971 | A/T | — | uncertain significance |
| rs775701649 | 14:101,004,980 | G/A | — | uncertain significance |
| rs370537162 | 14:101,004,983 | C/T | — | uncertain significance |
| rs774868143 | 14:101,005,001 | C/T | — | uncertain significance |
| rs369893698 | 14:101,005,291 | G/C | — | uncertain significance |
| rs1309360763 | 14:101,005,366 | C/G | — | uncertain significance |
| rs146033303 | 14:101,005,435 | T/G | — | benign |
| rs530174214 | 14:101,005,483 | G/C | — | uncertain significance |
| rs180737404 | 14:101,005,487 | C/T | — | uncertain significance |
| rs749342655 | 14:101,005,544 | C/T | — | uncertain significance |
| rs35286207 | 14:101,005,562 | C/T | — | benign |
| rs2549439569 | 14:101,005,616 | T/A | — | uncertain significance |
| rs2549462512 | 14:101,011,345 | A/G | — | uncertain significance |
| rs571419037 | 14:101,011,385 | C/G | — | uncertain significance |
| rs6575793 | 14:101,032,217 | T/G | — | — |
| rs8006543 | 14:101,033,420 | C/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.