CERS4
ceramide synthase 4
Summary
Enables sphingosine N-acyltransferase activity. Involved in ceramide biosynthetic process. Predicted to be located in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7253890 | 19:8,272,775 | T/G | — | — |
| rs62126382 | 19:8,272,916 | C/G | — | — |
| rs2336171 | 19:8,274,040 | G/C | regulatory region variant | — |
| rs922442 | 19:8,274,254 | A/C | — | — |
| rs12610250 | 19:8,277,713 | A/G | intron variant | — |
| rs2336169 | 19:8,288,298 | C/G | — | — |
| rs9749262 | 19:8,288,757 | C/G | — | — |
| rs8105664 | 19:8,290,878 | A/G | intron variant | — |
| rs8103131 | 19:8,290,909 | G/A | intron variant | — |
| rs7259572 | 19:8,291,672 | T/C | — | — |
| rs144725143 | 19:8,307,305 | A/G | upstream gene variant | — |
| rs73495427 | 19:8,311,512 | C/T | regulatory region variant | — |
| rs114171709 | 19:8,313,861 | A/G | intron variant | — |
| rs151158244 | 19:8,316,051 | C/T | — | uncertain significance |
| rs200803317 | 19:8,316,052 | G/A | — | uncertain significance |
| rs114417116 | 19:8,316,057 | T/A | — | uncertain significance |
| rs149877914 | 19:8,316,092 | C/T | — | likely benign |
| rs114701384 | 19:8,319,453 | G/A | — | likely benign |
| rs150398356 | 19:8,319,478 | C/T | — | uncertain significance |
| rs959566613 | 19:8,320,528 | C/T | — | uncertain significance |
| rs770832638 | 19:8,320,561 | G/A | — | uncertain significance |
| rs760280128 | 19:8,320,740 | G/A | — | uncertain significance |
| rs1481960818 | 19:8,321,512 | C/G | — | uncertain significance |
| rs1969398793 | 19:8,321,532 | C/G | — | uncertain significance |
| rs2288412 | 19:8,321,562 | C/T | — | benign |
| rs775358818 | 19:8,321,575 | C/G | — | uncertain significance |
| rs1163721273 | 19:8,321,843 | A/T | — | uncertain significance |
| rs746636515 | 19:8,321,847 | G/T | — | uncertain significance |
| rs777818786 | 19:8,321,908 | C/T | — | uncertain significance |
| rs775483880 | 19:8,321,912 | T/C | — | uncertain significance |
| rs141735698 | 19:8,322,734 | A/T | intron variant | — |
| rs149925061 | 19:8,322,784 | A/G | — | uncertain significance |
| rs578205747 | 19:8,322,787 | C/G | — | uncertain significance |
| rs149089779 | 19:8,322,805 | G/A | — | uncertain significance |
| rs2512553428 | 19:8,322,839 | T/C | — | uncertain significance |
| rs370319528 | 19:8,326,602 | C/G | — | uncertain significance |
| rs755418014 | 19:8,326,634 | T/C | — | uncertain significance |
| rs1191490473 | 19:8,326,820 | A/G | — | uncertain significance |
| rs763129211 | 19:8,326,857 | G/A | — | uncertain significance |
| rs199893919 | 19:8,326,894 | A/G | — | likely benign |
| rs868276266 | 19:8,326,897 | G/T | — | uncertain significance |
| rs768303981 | 19:8,326,901 | G/C | — | uncertain significance |
| rs1413247327 | 19:8,326,925 | G/A | — | uncertain significance |
| rs771355894 | 19:8,326,958 | G/A | — | uncertain significance |
| rs540801328 | 19:8,326,961 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.