HLX
H2.0 like homeobox
Summary
Enables sequence-specific DNA binding activity. Predicted to be involved in signal transduction. Predicted to act upstream of or within several processes, including embryonic digestive tract morphogenesis; enteric nervous system development; and regulation of T-helper cell differentiation. Predicted to be located in chromatin. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2738751 | 1:221,051,713 | C/G | 5 prime UTR variant | — |
| rs3806325 | 1:221,051,792 | C/T | regulatory region variant | — |
| rs2184658 | 1:221,052,457 | C/T | — | — |
| rs2738752 | 1:221,052,765 | A/G | regulatory region variant | — |
| rs771705333 | 1:221,053,227 | T/A | — | uncertain significance |
| rs764903919 | 1:221,053,257 | G/T | — | uncertain significance |
| rs2464375727 | 1:221,053,332 | T/A | — | uncertain significance |
| rs1674387596 | 1:221,053,350 | C/T | — | uncertain significance |
| rs2464375803 | 1:221,053,360 | T/G | — | uncertain significance |
| rs374220349 | 1:221,053,491 | G/C | — | uncertain significance |
| rs2464376484 | 1:221,053,501 | C/T | — | uncertain significance |
| rs757089301 | 1:221,053,531 | G/A | — | uncertain significance |
| rs1571711852 | 1:221,053,681 | A/C | — | uncertain significance |
| rs201755479 | 1:221,053,698 | C/T | — | likely benign |
| rs2464377451 | 1:221,053,701 | G/C | — | uncertain significance |
| rs149312492 | 1:221,053,733 | T/C | — | likely benign |
| rs373398191 | 1:221,054,571 | G/A | — | uncertain significance |
| rs1674432040 | 1:221,054,602 | C/T | — | uncertain significance |
| rs375880001 | 1:221,054,631 | A/G | — | uncertain significance |
| rs140376930 | 1:221,054,647 | C/T | — | benign |
| rs1297023453 | 1:221,055,599 | A/C | — | uncertain significance |
| rs34180575 | 1:221,057,173 | C/T | upstream gene variant | — |
| rs149152615 | 1:221,057,528 | G/A | — | benign |
| rs199521070 | 1:221,057,751 | C/A | — | uncertain significance |
| rs371016648 | 1:221,057,775 | G/A | — | uncertain significance |
| rs370407346 | 1:221,057,819 | G/A | — | uncertain significance |
| rs751147381 | 1:221,057,834 | A/C | — | uncertain significance |
| rs748250119 | 1:221,057,849 | G/A | — | uncertain significance |
| rs763478463 | 1:221,057,904 | T/A | — | uncertain significance |
| rs756876388 | 1:221,057,928 | G/T | — | uncertain significance |
| rs370523363 | 1:221,057,978 | A/G | — | uncertain significance |
| rs11588625 | 1:221,058,846 | T/C | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.