RPL9
ribosomal protein L9
Summary
Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L6P family of ribosomal proteins. It is located in the cytoplasm. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]
Known Variants59 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2474974257 | 4:39,456,164 | T/C | — | likely benign |
| rs374515136 | 4:39,456,167 | T/C | — | uncertain significance |
| rs779414751 | 4:39,456,172 | A/G | — | likely benign |
| rs1453715995 | 4:39,456,174 | C/A | — | uncertain significance |
| rs748195496 | 4:39,456,178 | C/A | — | uncertain significance |
| rs758145477 | 4:39,456,251 | G/A | — | uncertain significance |
| rs1744016653 | 4:39,456,278 | G/A | — | likely benign |
| rs1463478 | 4:39,456,392 | G/A | — | benign |
| rs1469388210 | 4:39,456,468 | T/C | — | likely benign |
| rs1412359099 | 4:39,456,494 | A/C | — | likely benign |
| rs193055808 | 4:39,456,533 | T/C | — | likely benign |
| rs200690365 | 4:39,456,542 | T/G | — | uncertain significance |
| rs372055477 | 4:39,456,551 | T/C | — | likely benign |
| rs778833788 | 4:39,456,576 | G/A | — | likely benign |
| rs10025155 | 4:39,456,635 | C/T | — | benign |
| rs536484014 | 4:39,457,263 | C/T | — | — |
| rs13103023 | 4:39,457,617 | G/A | regulatory region variant | — |
| rs1015450 | 4:39,457,857 | T/C | — | benign |
| rs28688785 | 4:39,458,010 | G/A | — | likely benign |
| rs114111678 | 4:39,458,018 | G/A | — | likely benign |
| rs1345812176 | 4:39,458,037 | C/T | — | uncertain significance |
| rs202000648 | 4:39,458,038 | G/A | — | uncertain significance |
| rs145459909 | 4:39,458,042 | C/G | — | uncertain significance |
| rs2125313 | 4:39,458,051 | A/G | — | benign |
| rs1019586152 | 4:39,458,082 | A/G | — | uncertain significance |
| rs757203996 | 4:39,458,087 | A/C | — | likely benign |
| rs372498694 | 4:39,458,134 | C/G | — | uncertain significance |
| rs768417540 | 4:39,458,147 | G/A | — | likely benign |
| rs200276230 | 4:39,458,152 | G/A | — | uncertain significance |
| rs745731738 | 4:39,458,163 | G/A | — | likely benign |
| rs1430628276 | 4:39,458,172 | A/G | — | likely benign |
| rs2687957 | 4:39,459,031 | T/C | — | benign |
| rs2608830 | 4:39,459,154 | G/A | — | benign |
| rs2474980166 | 4:39,459,186 | A/C | — | likely benign |
| rs1197389980 | 4:39,459,190 | T/C | — | likely benign |
| rs2474980219 | 4:39,459,219 | T/C | — | uncertain significance |
| rs748553586 | 4:39,459,245 | A/G | — | likely benign |
| rs1744160516 | 4:39,459,252 | C/G | — | uncertain significance |
| rs1331263882 | 4:39,459,253 | G/T | — | uncertain significance |
| rs747523284 | 4:39,459,257 | G/A | — | likely benign |
| rs1744161626 | 4:39,459,265 | G/A | — | likely benign |
| rs571555380 | 4:39,459,297 | C/T | — | uncertain significance |
| rs775733169 | 4:39,459,309 | A/G | — | likely benign |
| rs2474980339 | 4:39,459,310 | G/C | — | likely benign |
| rs2687958 | 4:39,459,724 | T/C | — | benign |
| rs200724499 | 4:39,459,795 | T/C | — | likely benign |
| rs2474981633 | 4:39,459,811 | C/T | — | uncertain significance |
| rs761909586 | 4:39,459,816 | T/C | — | uncertain significance |
| rs756847748 | 4:39,459,860 | T/C | — | uncertain significance |
| rs147466054 | 4:39,459,862 | G/T | — | uncertain significance |
| rs772175387 | 4:39,459,904 | T/C | — | likely benign |
| rs201850421 | 4:39,459,905 | G/A | — | uncertain significance |
| rs141176319 | 4:39,459,917 | A/G | — | uncertain significance |
| rs767101796 | 4:39,459,928 | G/A | — | likely benign |
| rs754417283 | 4:39,459,940 | G/A | — | likely benign |
| rs777980650 | 4:39,460,005 | G/A | — | likely benign |
| rs146928803 | 4:39,460,040 | T/C | — | uncertain significance |
| rs771618498 | 4:39,460,050 | T/C | — | uncertain significance |
| rs192165699 | 4:39,460,507 | T/C | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.