HNRNPUL1
heterogeneous nuclear ribonucleoprotein U like 1
Summary
This gene encodes a nuclear RNA-binding protein of the heterogeneous nuclear ribonucleoprotein (hnRNP) family. This protein binds specifically to adenovirus early-1B-55kDa oncoprotein. It may play an important role in nucleocytoplasmic RNA transport, and its function is modulated by early-1B-55kDa in adenovirus-infected cells. [provided by RefSeq, Mar 2016]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1436292174 | 19:41,770,472 | A/C | — | uncertain significance |
| rs773422950 | 19:41,770,506 | T/C | — | uncertain significance |
| rs1342419765 | 19:41,770,537 | C/G | — | uncertain significance |
| rs755807621 | 19:41,770,556 | G/A | — | uncertain significance |
| rs144715337 | 19:41,774,205 | G/A | — | uncertain significance |
| rs538705335 | 19:41,774,236 | A/C | — | uncertain significance |
| rs1454574086 | 19:41,778,032 | C/T | — | uncertain significance |
| rs1253237019 | 19:41,778,091 | T/C | — | uncertain significance |
| rs772007874 | 19:41,778,103 | C/T | — | uncertain significance |
| rs199908313 | 19:41,779,884 | C/T | — | benign |
| rs769253732 | 19:41,782,178 | G/C | — | uncertain significance |
| rs756724566 | 19:41,785,033 | C/A | — | uncertain significance |
| rs140148192 | 19:41,785,726 | A/G | intron variant | — |
| rs188910465 | 19:41,792,017 | C/T | downstream gene variant | — |
| rs778553397 | 19:41,798,378 | C/T | — | uncertain significance |
| rs528314138 | 19:41,800,476 | G/A | — | uncertain significance |
| rs866321641 | 19:41,800,499 | C/T | — | uncertain significance |
| rs148995733 | 19:41,801,801 | G/A | intron variant | — |
| rs180958600 | 19:41,806,550 | A/G | downstream gene variant | — |
| rs2122948849 | 19:41,807,444 | A/G | — | not provided |
| rs11881940 | 19:41,808,432 | A/T | regulatory region variant | — |
| rs1304955393 | 19:41,808,621 | T/C | — | uncertain significance |
| rs1310212698 | 19:41,808,633 | G/A | — | uncertain significance |
| rs1568459846 | 19:41,808,658 | G/T | — | uncertain significance |
| rs762181626 | 19:41,808,797 | C/T | — | uncertain significance |
| rs770360871 | 19:41,808,798 | G/A | — | uncertain significance |
| rs143909179 | 19:41,808,803 | G/A | — | uncertain significance |
| rs147281768 | 19:41,808,816 | G/A | — | uncertain significance |
| rs371162759 | 19:41,809,994 | C/T | — | uncertain significance |
| rs374729735 | 19:41,810,009 | C/T | — | uncertain significance |
| rs1457030852 | 19:41,810,119 | A/G | — | uncertain significance |
| rs375447450 | 19:41,810,141 | C/G | — | uncertain significance |
| rs775830164 | 19:41,812,426 | G/C | — | uncertain significance |
| rs15052 | 19:41,813,375 | T/C | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.