ABHD17C
abhydrolase domain containing 17C, depalmitoylase
Summary
Enables palmitoyl-(protein) hydrolase activity. Involved in protein depalmitoylation. Predicted to be located in dendritic spine; postsynaptic density membrane; and recycling endosome membrane. Predicted to be active in endosome membrane; glutamatergic synapse; and plasma membrane. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants24 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs117959127 | 15:80,987,675 | G/C | — | — |
| rs1245250165 | 15:80,987,850 | G/C | — | uncertain significance |
| rs1234745828 | 15:80,987,909 | C/G | — | uncertain significance |
| rs1356243140 | 15:80,987,930 | G/A | — | uncertain significance |
| rs1007271041 | 15:80,987,945 | C/T | — | uncertain significance |
| rs1467693359 | 15:80,987,949 | C/T | — | uncertain significance |
| rs1270696234 | 15:80,987,955 | C/G | — | uncertain significance |
| rs2505348304 | 15:80,988,114 | C/T | — | uncertain significance |
| rs2505348335 | 15:80,988,126 | G/C | — | uncertain significance |
| rs2505348678 | 15:80,988,297 | G/A | — | uncertain significance |
| rs1441095750 | 15:80,988,348 | C/A | — | uncertain significance |
| rs34769775 | 15:80,989,172 | C/T | upstream gene variant | — |
| rs12148329 | 15:81,001,278 | T/G | intron variant | — |
| rs7171632 | 15:81,003,816 | G/C | regulatory region variant | — |
| rs2759315 | 15:81,009,646 | C/T | — | — |
| rs2062316 | 15:81,010,249 | A/G | intron variant | — |
| rs35199222 | 15:81,013,037 | G/A | intron variant | — |
| rs2627308 | 15:81,015,427 | C/A | intron variant | — |
| rs7174222 | 15:81,018,543 | C/T | intron variant | — |
| rs7174250 | 15:81,018,587 | C/T | intron variant | — |
| rs12708529 | 15:81,022,364 | A/G | intron variant | — |
| rs11634851 | 15:81,028,965 | C/A | — | — |
| rs374695794 | 15:81,041,861 | G/A | — | uncertain significance |
| rs1895404884 | 15:81,046,599 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.