ARPP21
cAMP regulated phosphoprotein 21
Summary
This gene encodes a cAMP-regulated phosphoprotein. The encoded protein is enriched in the caudate nucleus and cerebellar cortex. A similar protein in mouse may be involved in regulating the effects of dopamine in the basal ganglia. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jun 2012]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1452243363 | 3:35,723,346 | G/T | — | uncertain significance |
| rs2081055067 | 3:35,729,240 | C/G | — | uncertain significance |
| rs745798080 | 3:35,729,249 | C/A | — | uncertain significance |
| rs2547306931 | 3:35,729,289 | G/A | — | uncertain significance |
| rs2547362561 | 3:35,731,622 | G/A | — | uncertain significance |
| rs2547381732 | 3:35,732,427 | T/C | — | uncertain significance |
| rs1054166241 | 3:35,732,476 | A/G | — | uncertain significance |
| rs1220053246 | 3:35,732,482 | C/A | — | uncertain significance |
| rs2090177468 | 3:35,750,472 | G/C | — | uncertain significance |
| rs763439655 | 3:35,756,951 | C/G | — | uncertain significance |
| rs574844611 | 3:35,758,792 | G/A | — | uncertain significance |
| rs139185498 | 3:35,758,844 | C/G | — | likely benign |
| rs1178409423 | 3:35,763,110 | G/C | — | uncertain significance |
| rs762166203 | 3:35,763,125 | T/A | — | uncertain significance |
| rs765166691 | 3:35,763,129 | G/A | — | uncertain significance |
| rs202100345 | 3:35,770,819 | G/A | — | uncertain significance |
| rs1257610844 | 3:35,770,867 | C/T | — | uncertain significance |
| rs368185215 | 3:35,770,887 | G/A | — | uncertain significance |
| rs138398652 | 3:35,770,896 | C/G | — | uncertain significance |
| rs544552101 | 3:35,770,919 | G/C | — | uncertain significance |
| rs188592147 | 3:35,770,922 | T/A | — | uncertain significance |
| rs193920911 | 3:35,770,924 | G/T | — | uncertain significance |
| rs1214649286 | 3:35,771,011 | T/G | — | uncertain significance |
| rs751772414 | 3:35,778,715 | C/T | — | uncertain significance |
| rs747895782 | 3:35,778,837 | G/A | — | uncertain significance |
| rs1456006348 | 3:35,779,759 | T/C | — | likely benign |
| rs151173813 | 3:35,780,947 | G/A | — | likely benign |
| rs371668097 | 3:35,780,954 | C/T | — | uncertain significance |
| rs754025228 | 3:35,785,334 | C/G | — | uncertain significance |
| rs778418344 | 3:35,785,424 | A/T | — | uncertain significance |
| rs747470322 | 3:35,785,443 | C/G | — | uncertain significance |
| rs56331918 | 3:35,801,168 | C/G | — | — |
| rs751398601 | 3:35,834,000 | A/G | — | uncertain significance |
| rs200410773 | 3:35,834,005 | A/G | — | uncertain significance |
| rs2470990060 | 3:35,835,231 | G/T | — | uncertain significance |
| rs1209899752 | 3:35,835,297 | G/A | — | uncertain significance |
| rs1354863652 | 3:35,835,353 | G/A | — | uncertain significance |
| rs752165990 | 3:35,835,423 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.