GAL
galanin and GMAP prepropeptide
Summary
This gene encodes a neuroendocrine peptide that is widely expressed in the central and peripheral nervous systems and also the gastrointestinal tract, pancreas, adrenal gland and urogenital tract. The encoded protein is a precursor that is proteolytically processed to generate two mature peptides: galanin and galanin message-associated peptide (GMAP). Galanin has diverse physiological functions including nociception, feeding and energy homeostasis, osmotic regulation and water balance. GMAP has been demonstrated to possess antifungal activity and hypothesized to be part of the innate immune system. [provided by RefSeq, Jul 2015]
Known Variants54 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs948854 | 11:68,450,203 | C/A | — | — |
| rs578193461 | 11:68,452,398 | C/T | — | uncertain significance |
| rs539085763 | 11:68,452,400 | A/C | — | likely benign |
| rs749996027 | 11:68,452,404 | A/G | — | uncertain significance |
| rs760551954 | 11:68,452,407 | G/A | — | uncertain significance |
| rs766211433 | 11:68,452,419 | G/A | — | uncertain significance |
| rs956379887 | 11:68,452,428 | C/T | — | uncertain significance |
| rs1457970164 | 11:68,452,433 | C/T | — | likely benign |
| rs753843211 | 11:68,452,434 | G/A | — | uncertain significance |
| rs34725707 | 11:68,452,438 | C/T | — | benign |
| rs746008445 | 11:68,452,446 | T/C | — | uncertain significance |
| rs542684427 | 11:68,452,457 | G/A | — | likely benign |
| rs201644659 | 11:68,452,468 | C/T | — | uncertain significance |
| rs1945837611 | 11:68,452,480 | C/T | — | likely benign |
| rs1338973790 | 11:68,452,484 | G/A | — | uncertain significance |
| rs694066 | 11:68,452,985 | G/A | regulatory region variant | — |
| rs1945844204 | 11:68,453,071 | A/G | — | uncertain significance |
| rs528520052 | 11:68,453,086 | C/T | — | likely benign |
| rs1057517661 | 11:68,453,096 | C/A | missense variant | pathogenic |
| rs762777313 | 11:68,455,480 | A/G | — | uncertain significance |
| rs374472664 | 11:68,455,485 | C/T | — | uncertain significance |
| rs367644530 | 11:68,455,486 | C/T | — | likely benign |
| rs541536020 | 11:68,455,487 | G/A | — | likely benign |
| rs1238139750 | 11:68,455,492 | C/G | — | likely benign |
| rs149894151 | 11:68,455,511 | G/A | — | uncertain significance |
| rs533111349 | 11:68,455,522 | C/G | — | likely benign |
| rs527905700 | 11:68,455,523 | C/T | — | uncertain significance |
| rs372372622 | 11:68,455,536 | G/A | — | uncertain significance |
| rs200075890 | 11:68,455,544 | C/T | — | uncertain significance |
| rs768058377 | 11:68,455,545 | G/C | — | uncertain significance |
| rs1945870960 | 11:68,455,547 | C/T | — | uncertain significance |
| rs571107777 | 11:68,455,550 | G/A | — | uncertain significance |
| rs765429698 | 11:68,455,559 | A/G | — | likely benign |
| rs375393105 | 11:68,455,561 | G/A | — | uncertain significance |
| rs202155593 | 11:68,455,571 | G/A | — | uncertain significance |
| rs186840614 | 11:68,455,965 | T/G | intron variant | — |
| rs145825008 | 11:68,456,346 | A/G | — | likely benign |
| rs778530092 | 11:68,456,356 | G/A | — | uncertain significance |
| rs746920897 | 11:68,456,384 | G/T | — | uncertain significance |
| rs3136540 | 11:68,456,410 | C/T | — | benign |
| rs147122838 | 11:68,458,389 | C/T | — | likely benign |
| rs768790714 | 11:68,458,392 | T/A | — | likely benign |
| rs1186237607 | 11:68,458,394 | C/T | — | uncertain significance |
| rs748331117 | 11:68,458,398 | C/T | — | likely benign |
| rs375918368 | 11:68,458,399 | G/A | — | uncertain significance |
| rs1945899167 | 11:68,458,418 | C/G | — | uncertain significance |
| rs762637870 | 11:68,458,420 | G/A | — | uncertain significance |
| rs147742577 | 11:68,458,422 | C/T | — | likely benign |
| rs540782765 | 11:68,458,423 | G/A | — | uncertain significance |
| rs139127322 | 11:68,458,444 | G/A | — | benign |
| rs36058701 | 11:68,458,447 | C/T | — | benign |
| rs777842785 | 11:68,458,448 | G/A | — | uncertain significance |
| rs747411981 | 11:68,458,451 | C/T | — | uncertain significance |
| rs1042577 | 11:68,458,470 | T/C | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.