SLC35D2
solute carrier family 35 member D2
Summary
Nucleotide sugars, which are synthesized in the cytosol or the nucleus, are high-energy donor substrates for glycosyltransferases located in the lumen of the endoplasmic reticulum and Golgi apparatus. Translocation of nucleotide sugars from the cytosol into the lumen compartment is mediated by specific nucleotide sugar transporters, such as SLC35D2 (Suda et al., 2004 [PubMed 15082721]).[supplied by OMIM, Mar 2008]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1387327309 | 9:99,083,581 | G/C | — | uncertain significance |
| rs16910750 | 9:99,084,471 | G/C | intron variant | — |
| rs111821073 | 9:99,084,793 | C/T | intron variant | — |
| rs2489979752 | 9:99,086,439 | C/T | — | uncertain significance |
| rs58088508 | 9:99,087,217 | G/A | — | — |
| rs12375999 | 9:99,087,796 | C/T | intron variant | — |
| rs10820383 | 9:99,095,694 | C/T | intron variant | — |
| rs6479272 | 9:99,097,527 | T/C | intron variant | — |
| rs757347905 | 9:99,099,023 | T/C | — | uncertain significance |
| rs1321558520 | 9:99,099,039 | C/T | — | uncertain significance |
| rs150233547 | 9:99,099,063 | T/C | — | uncertain significance |
| rs80024379 | 9:99,100,250 | C/T | intron variant | — |
| rs1296856552 | 9:99,106,235 | A/G | — | uncertain significance |
| rs141277502 | 9:99,107,592 | T/C | — | uncertain significance |
| rs755225551 | 9:99,107,654 | T/G | — | uncertain significance |
| rs1316209370 | 9:99,113,423 | A/C | — | uncertain significance |
| rs139645246 | 9:99,114,386 | G/A | — | uncertain significance |
| rs10990682 | 9:99,116,620 | C/A | — | — |
| rs11794772 | 9:99,118,445 | G/A | regulatory region variant | — |
| rs758307618 | 9:99,122,471 | G/T | — | uncertain significance |
| rs200009581 | 9:99,122,481 | T/C | — | uncertain significance |
| rs756304198 | 9:99,122,482 | A/T | — | uncertain significance |
| rs74699469 | 9:99,125,313 | T/C | intron variant | — |
| rs76756213 | 9:99,125,315 | A/G | intron variant | — |
| rs10820447 | 9:99,132,044 | C/T | intron variant | — |
| rs117509987 | 9:99,143,192 | G/A | intron variant | — |
| rs571683940 | 9:99,145,762 | T/C | — | uncertain significance |
| rs762591752 | 9:99,145,780 | T/C | — | uncertain significance |
| rs766207755 | 9:99,145,781 | T/C | — | uncertain significance |
| rs1016485263 | 9:99,145,783 | T/C | — | uncertain significance |
| rs757349758 | 9:99,145,810 | G/T | — | uncertain significance |
| rs1564135385 | 9:99,145,885 | C/T | — | uncertain significance |
| rs6479295 | 9:99,147,180 | A/T | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.