SLC2A4RG
SLC2A4 regulator
Summary
The protein encoded by this gene is a nuclear transcription factor involved in the activation of the solute carrier family 2 member 4 gene. The encoded protein interacts with another transcription factor, myocyte enhancer factor 2, to activate transcription of this gene. [provided by RefSeq, Jul 2008]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1015743280 | 20:62,371,329 | T/A | — | uncertain significance |
| rs1200532060 | 20:62,371,381 | C/A | — | uncertain significance |
| rs1034754109 | 20:62,371,736 | T/A | — | uncertain significance |
| rs1379753904 | 20:62,371,737 | C/A | — | uncertain significance |
| rs2517505829 | 20:62,371,826 | A/C | — | uncertain significance |
| rs2517505897 | 20:62,371,848 | G/C | — | likely benign |
| rs2145721336 | 20:62,371,850 | A/C | — | uncertain significance |
| rs2092036346 | 20:62,371,871 | G/A | — | uncertain significance |
| rs6062510 | 20:62,372,148 | G/C | regulatory region variant | — |
| rs4809221 | 20:62,372,706 | G/C | — | — |
| rs1601366086 | 20:62,372,728 | C/A | — | uncertain significance |
| rs2517506995 | 20:62,372,733 | G/A | — | uncertain significance |
| rs767965534 | 20:62,372,766 | G/A | — | uncertain significance |
| rs375432430 | 20:62,372,809 | C/A | — | uncertain significance |
| rs1171112636 | 20:62,372,830 | C/T | — | uncertain significance |
| rs2253829 | 20:62,373,079 | G/C | regulatory region variant | — |
| rs1404026636 | 20:62,373,236 | C/T | — | uncertain significance |
| rs2092043632 | 20:62,373,249 | C/T | — | uncertain significance |
| rs2517508072 | 20:62,373,351 | C/T | — | uncertain significance |
| rs1241803581 | 20:62,373,506 | G/C | — | uncertain significance |
| rs1392978870 | 20:62,373,552 | A/G | — | uncertain significance |
| rs767215066 | 20:62,373,697 | C/A | — | uncertain significance |
| rs750390729 | 20:62,373,817 | C/T | — | uncertain significance |
| rs748366261 | 20:62,373,825 | T/A | — | uncertain significance |
| rs749266529 | 20:62,373,832 | G/T | — | uncertain significance |
| rs1206025913 | 20:62,373,834 | C/G | — | uncertain significance |
| rs199721279 | 20:62,373,838 | A/G | — | likely benign |
| rs760172544 | 20:62,373,853 | T/C | — | uncertain significance |
| rs377712823 | 20:62,373,864 | G/T | — | uncertain significance |
| rs371300112 | 20:62,373,876 | C/T | — | uncertain significance |
| rs761270964 | 20:62,373,882 | C/T | — | uncertain significance |
| rs764747858 | 20:62,373,883 | G/A | — | likely benign |
| rs1338270383 | 20:62,373,888 | C/T | — | uncertain significance |
| rs757393986 | 20:62,373,907 | C/T | — | uncertain significance |
| rs370931422 | 20:62,373,957 | C/T | — | uncertain significance |
| rs537149520 | 20:62,373,958 | G/A | — | likely benign |
| rs2256814 | 20:62,373,983 | G/A | regulatory region variant | — |
| rs752597447 | 20:62,374,062 | C/T | — | uncertain significance |
| rs1223467180 | 20:62,374,063 | G/T | — | likely benign |
| rs372238748 | 20:62,374,071 | G/A | — | likely benign |
| rs368418225 | 20:62,374,081 | G/A | — | benign |
| rs549920642 | 20:62,374,110 | C/T | — | uncertain significance |
| rs61736645 | 20:62,374,112 | G/C | — | benign |
| rs1169390440 | 20:62,374,130 | G/A | — | uncertain significance |
| rs193920971 | 20:62,374,239 | C/A | — | uncertain significance |
| rs2517509971 | 20:62,374,293 | T/C | — | uncertain significance |
| rs746457946 | 20:62,374,308 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.