BAIAP3
BAI1 associated protein 3
Summary
This p53-target gene encodes a brain-specific angiogenesis inhibitor. The protein is a seven-span transmembrane protein and a member of the secretin receptor family. It interacts with the cytoplasmic region of brain-specific angiogenesis inhibitor 1. This protein also contains two C2 domains, which are often found in proteins involved in signal transduction or membrane trafficking. Its expression pattern and similarity to other proteins suggest that it may be involved in synaptic functions. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2010]
Known Variants140 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs188035944 | 16:1,382,392 | G/A | regulatory region variant | — |
| rs552188478 | 16:1,384,412 | G/T | — | — |
| rs746731178 | 16:1,384,673 | G/A | — | likely benign |
| rs768016801 | 16:1,384,676 | G/T | — | uncertain significance |
| rs367814806 | 16:1,384,735 | G/A | — | uncertain significance |
| rs200262964 | 16:1,384,741 | G/A | — | uncertain significance |
| rs199671572 | 16:1,384,746 | C/G | — | uncertain significance |
| rs778099100 | 16:1,388,576 | G/A | — | uncertain significance |
| rs148120801 | 16:1,388,581 | G/A | — | uncertain significance |
| rs761728589 | 16:1,388,628 | G/T | — | uncertain significance |
| rs761781931 | 16:1,388,668 | G/T | — | uncertain significance |
| rs116106398 | 16:1,388,672 | C/T | — | benign |
| rs753934248 | 16:1,388,907 | C/G | — | uncertain significance |
| rs149675788 | 16:1,388,919 | G/A | — | uncertain significance |
| rs145548563 | 16:1,388,959 | G/A | — | uncertain significance |
| rs1192243058 | 16:1,389,165 | G/C | — | uncertain significance |
| rs762143694 | 16:1,389,174 | C/T | — | uncertain significance |
| rs547231702 | 16:1,389,184 | C/T | — | uncertain significance |
| rs766429980 | 16:1,389,189 | G/T | — | uncertain significance |
| rs2033684371 | 16:1,389,210 | C/A | — | uncertain significance |
| rs2548157095 | 16:1,389,505 | G/A | — | uncertain significance |
| rs147709691 | 16:1,389,506 | C/T | — | uncertain significance |
| rs758903417 | 16:1,389,518 | G/A | — | uncertain significance |
| rs773881878 | 16:1,389,543 | C/T | — | uncertain significance |
| rs200855970 | 16:1,389,557 | C/G | — | uncertain significance |
| rs765556289 | 16:1,389,565 | G/C | — | uncertain significance |
| rs151334572 | 16:1,389,572 | G/A | — | uncertain significance |
| rs557488567 | 16:1,389,582 | C/T | — | uncertain significance |
| rs375520815 | 16:1,391,164 | G/A | — | uncertain significance |
| rs145056617 | 16:1,391,349 | G/A | — | uncertain significance |
| rs139469260 | 16:1,391,405 | G/A | — | likely benign |
| rs776493141 | 16:1,391,441 | G/A | — | uncertain significance |
| rs2548161967 | 16:1,391,451 | G/A | — | uncertain significance |
| rs2033923264 | 16:1,391,486 | C/G | — | uncertain significance |
| rs530843796 | 16:1,391,489 | T/C | — | uncertain significance |
| rs549602171 | 16:1,391,648 | G/C | — | — |
| rs965319193 | 16:1,392,019 | C/T | — | uncertain significance |
| rs201986231 | 16:1,392,058 | T/G | — | uncertain significance |
| rs759778890 | 16:1,392,182 | G/C | — | uncertain significance |
| rs751614665 | 16:1,392,210 | C/G | — | uncertain significance |
| rs142979816 | 16:1,392,218 | C/T | — | likely benign |
| rs151024049 | 16:1,392,220 | G/A | — | likely benign |
| rs2033977381 | 16:1,392,279 | G/A | — | likely benign |
| rs765903886 | 16:1,392,283 | G/A | — | uncertain significance |
| rs1387318282 | 16:1,392,580 | G/C | — | uncertain significance |
| rs1473216613 | 16:1,392,583 | C/T | — | uncertain significance |
| rs369551612 | 16:1,392,724 | A/G | — | uncertain significance |
| rs374500322 | 16:1,392,736 | G/A | — | uncertain significance |
| rs34598300 | 16:1,392,745 | G/C | — | benign |
| rs748675139 | 16:1,392,992 | C/G | — | uncertain significance |
| rs2235632 | 16:1,393,020 | G/A | splice region variant | — |
| rs576394425 | 16:1,393,413 | C/A | — | uncertain significance |
| rs749521546 | 16:1,393,432 | C/T | — | uncertain significance |
| rs374677667 | 16:1,393,440 | T/G | — | uncertain significance |
| rs2034132487 | 16:1,394,086 | C/T | — | uncertain significance |
| rs765199494 | 16:1,394,119 | G/A | — | uncertain significance |
| rs2141598224 | 16:1,394,125 | C/T | — | likely benign |
| rs201916316 | 16:1,394,132 | T/C | — | uncertain significance |
| rs905558185 | 16:1,394,137 | C/A | — | uncertain significance |
| rs2548168972 | 16:1,394,146 | A/C | — | uncertain significance |
| rs767326712 | 16:1,394,272 | G/A | — | uncertain significance |
| rs758083375 | 16:1,394,296 | T/C | — | uncertain significance |
| rs372851721 | 16:1,394,473 | G/A | — | uncertain significance |
| rs114280977 | 16:1,394,491 | G/A | — | benign |
| rs748620008 | 16:1,394,515 | C/T | — | uncertain significance |
| rs777857668 | 16:1,394,519 | G/A | — | uncertain significance |
| rs74710678 | 16:1,394,606 | G/A | — | uncertain significance |
| rs772645664 | 16:1,394,656 | G/A | — | uncertain significance |
| rs1385938640 | 16:1,394,675 | G/A | — | uncertain significance |
| rs2548170614 | 16:1,394,810 | T/C | — | uncertain significance |
| rs371042943 | 16:1,394,815 | G/A | — | uncertain significance |
| rs376716419 | 16:1,394,834 | G/A | — | uncertain significance |
| rs373118062 | 16:1,394,846 | G/A | — | uncertain significance |
| rs138220444 | 16:1,395,045 | G/C | — | uncertain significance |
| rs747262689 | 16:1,395,251 | G/A | — | uncertain significance |
| rs370188967 | 16:1,395,285 | C/T | — | uncertain significance |
| rs574407537 | 16:1,395,297 | C/T | — | uncertain significance |
| rs144507024 | 16:1,395,331 | C/T | — | benign |
| rs1308572785 | 16:1,395,341 | T/C | — | uncertain significance |
| rs1229091042 | 16:1,395,363 | A/G | — | uncertain significance |
| rs148131174 | 16:1,395,372 | C/T | — | uncertain significance |
| rs763266737 | 16:1,395,757 | G/C | — | uncertain significance |
| rs1012208598 | 16:1,395,758 | T/G | — | uncertain significance |
| rs2548173208 | 16:1,395,766 | T/C | — | uncertain significance |
| rs762351761 | 16:1,395,773 | G/C | — | uncertain significance |
| rs1051934143 | 16:1,395,776 | A/G | — | uncertain significance |
| rs768443365 | 16:1,395,991 | T/C | — | uncertain significance |
| rs746363437 | 16:1,396,023 | C/T | — | uncertain significance |
| rs143578932 | 16:1,396,026 | C/T | — | uncertain significance |
| rs1482003920 | 16:1,396,074 | G/A | — | uncertain significance |
| rs768238384 | 16:1,396,189 | A/G | — | likely benign |
| rs147638428 | 16:1,396,197 | G/C | — | uncertain significance |
| rs754353782 | 16:1,396,201 | G/A | — | uncertain significance |
| rs2034353810 | 16:1,396,232 | G/C | — | uncertain significance |
| rs142229314 | 16:1,396,256 | C/T | — | benign |
| rs751837612 | 16:1,396,279 | C/T | — | uncertain significance |
| rs772048317 | 16:1,396,506 | G/A | — | uncertain significance |
| rs796052185 | 16:1,396,606 | G/C | — | likely benign |
| rs749171942 | 16:1,396,661 | C/T | — | uncertain significance |
| rs2548175999 | 16:1,396,859 | C/T | — | uncertain significance |
Showing 100 of 140 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.