NECAB2
N-terminal EF-hand calcium binding protein 2
Summary
The protein encoded by this gene is a neuronal calcium-binding protein that binds to and modulates the function of at least two receptors, adenosine A(2A) receptor and metabotropic glutamate receptor type 5. [provided by RefSeq, Jul 2016]
Known Variants54 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1348419648 | 16:84,002,264 | G/C | — | uncertain significance |
| rs866329316 | 16:84,002,285 | C/T | — | uncertain significance |
| rs2507478775 | 16:84,002,312 | C/A | — | uncertain significance |
| rs2507478800 | 16:84,002,318 | A/C | — | uncertain significance |
| rs2507478994 | 16:84,002,381 | A/C | — | uncertain significance |
| rs2151082537 | 16:84,002,383 | T/C | — | likely benign |
| rs1379842105 | 16:84,002,404 | G/C | — | uncertain significance |
| rs2507479144 | 16:84,002,408 | A/C | — | uncertain significance |
| rs2507479285 | 16:84,002,437 | A/C | — | uncertain significance |
| rs768200680 | 16:84,005,765 | C/T | — | uncertain significance |
| rs376943166 | 16:84,012,132 | C/G | — | uncertain significance |
| rs138901077 | 16:84,012,136 | C/T | — | uncertain significance |
| rs779931609 | 16:84,014,676 | G/C | — | uncertain significance |
| rs150547119 | 16:84,014,682 | C/G | — | uncertain significance |
| rs770058947 | 16:84,024,127 | A/G | — | uncertain significance |
| rs763808340 | 16:84,024,136 | C/T | — | uncertain significance |
| rs757750776 | 16:84,024,157 | C/T | — | uncertain significance |
| rs149674637 | 16:84,024,163 | A/G | — | uncertain significance |
| rs2084610046 | 16:84,024,165 | C/G | — | uncertain significance |
| rs771970941 | 16:84,024,196 | G/A | — | uncertain significance |
| rs1331499950 | 16:84,024,220 | A/T | — | uncertain significance |
| rs781071263 | 16:84,027,908 | C/G | — | uncertain significance |
| rs778491123 | 16:84,027,919 | C/G | — | uncertain significance |
| rs367651817 | 16:84,027,939 | C/T | — | likely benign |
| rs778437927 | 16:84,027,959 | C/A | — | uncertain significance |
| rs746174813 | 16:84,027,963 | C/T | — | uncertain significance |
| rs373972239 | 16:84,027,984 | A/G | — | uncertain significance |
| rs147022655 | 16:84,027,985 | C/G | — | uncertain significance |
| rs765680439 | 16:84,028,214 | C/A | — | uncertain significance |
| rs753066050 | 16:84,028,217 | C/T | — | uncertain significance |
| rs148631295 | 16:84,028,264 | G/A | — | uncertain significance |
| rs139095086 | 16:84,030,846 | G/A | — | uncertain significance |
| rs764346302 | 16:84,030,867 | C/G | — | uncertain significance |
| rs139863929 | 16:84,030,873 | T/A | — | uncertain significance |
| rs777877025 | 16:84,031,819 | C/G | — | uncertain significance |
| rs368505537 | 16:84,031,825 | C/T | — | uncertain significance |
| rs1314103607 | 16:84,031,836 | G/A | — | uncertain significance |
| rs759775850 | 16:84,031,838 | C/A | — | uncertain significance |
| rs147666898 | 16:84,031,849 | G/A | — | uncertain significance |
| rs377652406 | 16:84,031,891 | C/T | — | uncertain significance |
| rs369982409 | 16:84,031,892 | G/A | — | uncertain significance |
| rs746473427 | 16:84,031,906 | G/A | — | uncertain significance |
| rs372410814 | 16:84,034,348 | T/A | — | uncertain significance |
| rs151288264 | 16:84,034,355 | G/C | — | uncertain significance |
| rs539453642 | 16:84,034,386 | G/C | — | uncertain significance |
| rs4997522 | 16:84,035,098 | G/C | intron variant | — |
| rs1293508742 | 16:84,035,443 | C/T | — | uncertain significance |
| rs757877432 | 16:84,035,459 | T/G | — | uncertain significance |
| rs577359018 | 16:84,035,461 | C/T | — | uncertain significance |
| rs376727485 | 16:84,035,462 | G/A | — | uncertain significance |
| rs547664063 | 16:84,035,467 | G/A | — | uncertain significance |
| rs542133378 | 16:84,035,498 | C/A | — | uncertain significance |
| rs774895031 | 16:84,035,504 | C/G | — | uncertain significance |
| rs199676132 | 16:84,035,944 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.