HAPLN4
hyaluronan and proteoglycan link protein 4
Summary
Predicted to be a structural constituent of synapse-associated extracellular matrix. Predicted to be involved in GABAergic synaptic transmission; nervous system development; and skeletal system development. Predicted to be located in extracellular region. Predicted to be active in extracellular space; perineuronal net; and synapse. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs56044734 | 19:19,366,927 | G/A | coding sequence variant | — |
| rs55762233 | 19:19,367,319 | C/G | coding sequence variant | — |
| rs55765017 | 19:19,368,264 | G/A | coding sequence variant | — |
| rs56144632 | 19:19,368,310 | G/A | coding sequence variant | — |
| rs1224188534 | 19:19,368,709 | C/T | — | uncertain significance |
| rs1470707970 | 19:19,368,729 | G/A | — | uncertain significance |
| rs10425902 | 19:19,368,761 | G/A | — | benign |
| rs771786704 | 19:19,368,807 | C/T | — | uncertain significance |
| rs2512926503 | 19:19,368,904 | T/C | — | uncertain significance |
| rs374049916 | 19:19,368,951 | G/T | — | uncertain significance |
| rs146542764 | 19:19,368,990 | C/T | — | uncertain significance |
| rs1157179635 | 19:19,369,437 | T/C | — | uncertain significance |
| rs767619403 | 19:19,369,448 | C/A | — | uncertain significance |
| rs1375999173 | 19:19,369,476 | G/A | — | uncertain significance |
| rs80354663 | 19:19,369,489 | T/C | — | benign |
| rs1481185634 | 19:19,369,503 | C/T | — | uncertain significance |
| rs373269949 | 19:19,369,518 | C/G | — | uncertain significance |
| rs777095051 | 19:19,369,552 | G/T | — | uncertain significance |
| rs1326215121 | 19:19,369,587 | G/C | — | uncertain significance |
| rs770259089 | 19:19,369,590 | C/T | — | uncertain significance |
| rs764969132 | 19:19,369,620 | T/A | — | uncertain significance |
| rs1453201908 | 19:19,371,636 | T/C | — | uncertain significance |
| rs773215332 | 19:19,371,687 | C/A | — | uncertain significance |
| rs946678963 | 19:19,371,741 | C/A | — | uncertain significance |
| rs1374773629 | 19:19,371,851 | C/A | — | uncertain significance |
| rs147317504 | 19:19,371,916 | T/C | — | uncertain significance |
| rs1446821924 | 19:19,371,963 | A/G | — | uncertain significance |
| rs10422893 | 19:19,372,185 | G/T | — | — |
| rs1599833707 | 19:19,372,297 | C/T | — | uncertain significance |
| rs745547421 | 19:19,372,299 | G/A | — | uncertain significance |
| rs1242409224 | 19:19,372,362 | C/G | — | uncertain significance |
| rs10403273 | 19:19,372,968 | C/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.