KLHL38
kelch like family member 38
Summary
Predicted to enable ubiquitin-like ligase-substrate adaptor activity. Predicted to be involved in proteasome-mediated ubiquitin-dependent protein catabolic process. Predicted to be part of Cul3-RING ubiquitin ligase complex. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants60 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs758719041 | 8:124,657,999 | G/A | — | uncertain significance |
| rs375307692 | 8:124,658,104 | C/T | — | uncertain significance |
| rs1818653938 | 8:124,658,110 | C/T | — | uncertain significance |
| rs532668897 | 8:124,658,136 | C/T | — | uncertain significance |
| rs753483963 | 8:124,658,137 | G/A | — | uncertain significance |
| rs376576295 | 8:124,658,152 | C/T | — | uncertain significance |
| rs201599108 | 8:124,658,193 | C/A | — | uncertain significance |
| rs1328447683 | 8:124,658,239 | G/T | — | uncertain significance |
| rs773078118 | 8:124,659,167 | G/A | — | uncertain significance |
| rs1302297374 | 8:124,659,221 | T/G | — | uncertain significance |
| rs16898685 | 8:124,662,660 | C/T | — | — |
| rs375302916 | 8:124,663,834 | G/A | — | uncertain significance |
| rs200289283 | 8:124,663,857 | C/T | — | uncertain significance |
| rs2488597688 | 8:124,663,867 | A/G | — | uncertain significance |
| rs769828904 | 8:124,663,880 | T/A | — | uncertain significance |
| rs374238365 | 8:124,663,888 | C/A | — | uncertain significance |
| rs202094935 | 8:124,663,931 | C/A | — | uncertain significance |
| rs1203393099 | 8:124,663,945 | A/G | — | uncertain significance |
| rs1250369617 | 8:124,663,949 | G/T | — | uncertain significance |
| rs2488598018 | 8:124,663,972 | C/T | — | uncertain significance |
| rs750103081 | 8:124,663,981 | C/G | — | uncertain significance |
| rs16898691 | 8:124,663,987 | C/G | — | benign |
| rs151241896 | 8:124,663,995 | A/G | — | uncertain significance |
| rs370038628 | 8:124,664,002 | C/T | — | uncertain significance |
| rs1158771409 | 8:124,664,011 | A/G | — | uncertain significance |
| rs371021488 | 8:124,664,050 | G/A | — | uncertain significance |
| rs935161929 | 8:124,664,068 | C/T | — | uncertain significance |
| rs373810829 | 8:124,664,099 | G/C | — | uncertain significance |
| rs762318828 | 8:124,664,122 | C/G | — | uncertain significance |
| rs368547076 | 8:124,664,172 | C/T | — | uncertain significance |
| rs992338801 | 8:124,664,185 | T/C | — | likely benign |
| rs1354922694 | 8:124,664,241 | G/T | — | uncertain significance |
| rs750210063 | 8:124,664,263 | C/T | — | uncertain significance |
| rs376377773 | 8:124,664,391 | A/G | — | uncertain significance |
| rs147114029 | 8:124,664,404 | C/T | — | uncertain significance |
| rs370989857 | 8:124,664,448 | G/T | — | uncertain significance |
| rs544443097 | 8:124,664,458 | C/G | — | uncertain significance |
| rs2488599420 | 8:124,664,461 | T/C | — | uncertain significance |
| rs764060753 | 8:124,664,467 | G/A | — | uncertain significance |
| rs74884256 | 8:124,664,572 | C/T | — | benign |
| rs746461027 | 8:124,664,627 | C/G | — | uncertain significance |
| rs28742115 | 8:124,664,657 | G/A | — | benign |
| rs144002487 | 8:124,664,708 | C/T | — | benign |
| rs546545268 | 8:124,664,713 | T/C | — | uncertain significance |
| rs747146077 | 8:124,664,719 | T/C | — | uncertain significance |
| rs759773974 | 8:124,664,748 | A/G | — | uncertain significance |
| rs200378303 | 8:124,664,772 | G/A | — | uncertain significance |
| rs199973284 | 8:124,664,798 | G/C | — | uncertain significance |
| rs1812674052 | 8:124,664,800 | A/G | — | uncertain significance |
| rs201098575 | 8:124,664,836 | C/T | — | uncertain significance |
| rs201057767 | 8:124,664,860 | T/C | — | uncertain significance |
| rs200205923 | 8:124,664,893 | C/T | — | uncertain significance |
| rs1812676786 | 8:124,664,910 | T/C | — | uncertain significance |
| rs1229837043 | 8:124,664,917 | T/C | — | uncertain significance |
| rs1004864714 | 8:124,664,923 | G/C | — | uncertain significance |
| rs372548823 | 8:124,664,964 | C/T | — | uncertain significance |
| rs369592276 | 8:124,665,022 | G/T | — | uncertain significance |
| rs199511281 | 8:124,665,046 | C/T | — | uncertain significance |
| rs2488601161 | 8:124,665,055 | T/C | — | uncertain significance |
| rs1296454210 | 8:124,665,127 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.