APBB1IP
amyloid beta precursor protein binding family B member 1 interacting protein
Summary
Predicted to be involved in signal transduction. Predicted to act upstream of or within T cell activation via T cell receptor contact with antigen bound to MHC molecule on antigen presenting cell and positive regulation of cell adhesion. Located in cytosol and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants56 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1335552 | 10:26,725,355 | T/G | — | — |
| rs1335540 | 10:26,727,238 | T/G | — | — |
| rs4749125 | 10:26,727,636 | G/C | regulatory region variant | — |
| rs2992335 | 10:26,727,934 | C/T | — | — |
| rs11591540 | 10:26,734,517 | G/A | intron variant | — |
| rs2992257 | 10:26,734,587 | C/T | intron variant | — |
| rs7098710 | 10:26,734,987 | C/T | intron variant | — |
| rs4747560 | 10:26,736,214 | G/A | regulatory region variant | — |
| rs3006802 | 10:26,736,240 | T/G | — | — |
| rs11015114 | 10:26,736,478 | C/T | regulatory region variant | — |
| rs10829001 | 10:26,737,945 | G/C | — | — |
| rs12770943 | 10:26,740,256 | A/C | intron variant | — |
| rs4749142 | 10:26,743,851 | A/G | intron variant | — |
| rs786870 | 10:26,774,694 | T/C | regulatory region variant | — |
| rs146489691 | 10:26,781,288 | G/A | — | uncertain significance |
| rs201471966 | 10:26,785,258 | C/T | — | uncertain significance |
| rs2494639979 | 10:26,785,281 | G/A | — | uncertain significance |
| rs748677908 | 10:26,785,287 | T/C | — | uncertain significance |
| rs2494646029 | 10:26,789,807 | G/A | — | uncertain significance |
| rs775214385 | 10:26,789,836 | C/G | — | uncertain significance |
| rs148086849 | 10:26,789,894 | A/G | — | uncertain significance |
| rs113442503 | 10:26,792,144 | G/A | missense variant | — |
| rs117705625 | 10:26,792,170 | G/A | — | likely benign |
| rs1397190214 | 10:26,800,695 | T/C | — | uncertain significance |
| rs149483004 | 10:26,800,768 | C/T | — | benign |
| rs780615541 | 10:26,800,821 | C/T | — | uncertain significance |
| rs755589060 | 10:26,802,473 | T/C | — | uncertain significance |
| rs763282951 | 10:26,822,427 | T/G | — | uncertain significance |
| rs1354534151 | 10:26,825,025 | T/C | — | uncertain significance |
| rs777167702 | 10:26,830,527 | C/T | — | uncertain significance |
| rs372662729 | 10:26,830,545 | A/C | — | uncertain significance |
| rs756030620 | 10:26,830,605 | A/G | — | uncertain significance |
| rs143061604 | 10:26,849,689 | C/T | — | benign |
| rs148216770 | 10:26,849,744 | A/G | — | uncertain significance |
| rs762738139 | 10:26,849,765 | C/T | — | uncertain significance |
| rs747691466 | 10:26,851,267 | G/A | — | uncertain significance |
| rs756893811 | 10:26,855,927 | C/T | — | uncertain significance |
| rs768737682 | 10:26,855,945 | A/C | — | uncertain significance |
| rs759985543 | 10:26,855,978 | C/T | — | uncertain significance |
| rs2132489160 | 10:26,855,999 | C/T | — | uncertain significance |
| rs2494743162 | 10:26,856,010 | C/T | — | uncertain significance |
| rs1837057689 | 10:26,856,070 | G/C | — | uncertain significance |
| rs1225077094 | 10:26,856,073 | T/A | — | uncertain significance |
| rs781009429 | 10:26,856,074 | T/C | — | uncertain significance |
| rs925580313 | 10:26,856,118 | C/T | — | uncertain significance |
| rs1164039719 | 10:26,856,121 | C/T | — | uncertain significance |
| rs1157471172 | 10:26,856,143 | T/C | — | uncertain significance |
| rs949838125 | 10:26,856,208 | C/G | — | uncertain significance |
| rs1045509412 | 10:26,856,209 | T/G | — | uncertain significance |
| rs1407937540 | 10:26,856,224 | C/T | — | uncertain significance |
| rs7903226 | 10:26,856,265 | G/A | — | benign |
| rs200114349 | 10:26,856,281 | C/T | — | benign |
| rs771072897 | 10:26,856,307 | C/G | — | uncertain significance |
| rs746218305 | 10:26,856,308 | C/A | — | uncertain significance |
| rs374621872 | 10:26,856,337 | G/A | — | likely benign |
| rs150768801 | 10:26,856,414 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.