CKAP4
cytoskeleton associated protein 4
Summary
Enables RNA binding activity. Located in several cellular components, including lipid droplet; nuclear speck; and rough endoplasmic reticulum. Biomarker of hepatocellular carcinoma. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs118008684 | 12:106,632,873 | C/A | — | benign |
| rs1185433735 | 12:106,632,911 | A/C | — | uncertain significance |
| rs2541594536 | 12:106,632,912 | T/G | — | uncertain significance |
| rs752159289 | 12:106,633,032 | G/T | — | uncertain significance |
| rs368595011 | 12:106,633,076 | G/A | — | uncertain significance |
| rs145284636 | 12:106,633,162 | G/A | — | likely benign |
| rs200365798 | 12:106,633,178 | G/A | — | uncertain significance |
| rs749256244 | 12:106,633,251 | G/A | — | uncertain significance |
| rs761195209 | 12:106,633,271 | C/T | — | uncertain significance |
| rs112234315 | 12:106,633,279 | G/A | — | benign |
| rs773051973 | 12:106,633,355 | C/G | — | uncertain significance |
| rs139797231 | 12:106,633,365 | C/T | — | uncertain significance |
| rs147236091 | 12:106,633,430 | C/T | — | likely benign |
| rs1182130732 | 12:106,633,455 | C/T | — | likely benign |
| rs11559179 | 12:106,633,479 | G/A | — | uncertain significance |
| rs2541595738 | 12:106,633,502 | A/C | — | uncertain significance |
| rs141394460 | 12:106,633,517 | C/T | — | uncertain significance |
| rs934379141 | 12:106,633,523 | A/G | — | likely benign |
| rs370136151 | 12:106,633,535 | G/C | — | uncertain significance |
| rs200244385 | 12:106,633,553 | G/A | — | uncertain significance |
| rs567820155 | 12:106,633,580 | G/A | — | uncertain significance |
| rs2541595946 | 12:106,633,592 | T/C | — | uncertain significance |
| rs763436975 | 12:106,633,692 | T/C | — | uncertain significance |
| rs2541596156 | 12:106,633,728 | C/G | — | uncertain significance |
| rs2541596311 | 12:106,633,827 | T/C | — | uncertain significance |
| rs377084647 | 12:106,633,874 | T/C | — | uncertain significance |
| rs141436009 | 12:106,633,903 | C/T | — | benign |
| rs899320767 | 12:106,633,919 | G/A | — | uncertain significance |
| rs1375788508 | 12:106,634,016 | G/A | — | uncertain significance |
| rs183401520 | 12:106,634,026 | A/T | — | uncertain significance |
| rs200639707 | 12:106,634,030 | T/C | — | uncertain significance |
| rs1389463341 | 12:106,634,108 | G/A | — | uncertain significance |
| rs1427811118 | 12:106,634,111 | G/C | — | uncertain significance |
| rs2541601994 | 12:106,641,220 | A/T | — | uncertain significance |
| rs1258103501 | 12:106,641,380 | A/C | — | uncertain significance |
| rs1182101037 | 12:106,641,382 | G/A | — | uncertain significance |
| rs1428044617 | 12:106,641,479 | G/A | — | uncertain significance |
| rs561280299 | 12:106,641,484 | G/T | — | uncertain significance |
| rs1203205240 | 12:106,641,499 | G/A | — | uncertain significance |
| rs894435853 | 12:106,641,502 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.