ANHX
anomalous homeobox
Summary
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of skeletal muscle cell proliferation; regulation of transcription by RNA polymerase II; and skeletal muscle fiber development. Predicted to be part of transcription regulator complex. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2500812820 | 12:133,795,547 | G/C | — | uncertain significance |
| rs2500814082 | 12:133,795,915 | C/A | — | uncertain significance |
| rs549420372 | 12:133,795,916 | C/A | — | uncertain significance |
| rs1054886305 | 12:133,795,918 | G/C | — | uncertain significance |
| rs948731144 | 12:133,797,801 | G/C | — | uncertain significance |
| rs1029538221 | 12:133,797,908 | T/G | — | uncertain significance |
| rs1317128641 | 12:133,802,908 | C/G | — | uncertain significance |
| rs570549152 | 12:133,802,949 | G/A | — | uncertain significance |
| rs375664171 | 12:133,803,019 | G/A | — | uncertain significance |
| rs36146434 | 12:133,803,551 | G/C | — | benign |
| rs1041520136 | 12:133,803,560 | C/T | — | likely benign |
| rs777636956 | 12:133,803,602 | C/T | — | uncertain significance |
| rs1032664607 | 12:133,803,645 | T/C | — | uncertain significance |
| rs762774820 | 12:133,803,668 | C/T | — | uncertain significance |
| rs745417751 | 12:133,803,719 | G/A | — | uncertain significance |
| rs754252966 | 12:133,804,435 | T/C | — | likely benign |
| rs1215951789 | 12:133,804,492 | C/T | — | uncertain significance |
| rs1170778051 | 12:133,804,526 | G/C | — | uncertain significance |
| rs890990385 | 12:133,808,128 | C/A | — | uncertain significance |
| rs761611199 | 12:133,808,146 | C/T | — | uncertain significance |
| rs756419511 | 12:133,808,169 | C/T | — | likely benign |
| rs2500852784 | 12:133,808,184 | T/C | — | uncertain significance |
| rs1489908882 | 12:133,810,708 | A/C | — | uncertain significance |
| rs971327129 | 12:133,810,747 | C/T | — | uncertain significance |
| rs746038900 | 12:133,810,752 | G/A | — | likely benign |
| rs748018873 | 12:133,810,788 | C/T | — | uncertain significance |
| rs568867315 | 12:133,810,794 | T/C | — | uncertain significance |
| rs760700021 | 12:133,810,869 | G/C | — | uncertain significance |
| rs555648876 | 12:133,810,926 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.