HOXA4
homeobox A4
Summary
In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. [provided by RefSeq, Jul 2008]
Known Variants57 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs4722661 | 7:27,168,512 | C/G | — | benign |
| rs1801085 | 7:27,168,590 | A/G | — | benign |
| rs4722662 | 7:27,168,719 | C/T | — | benign |
| rs201659767 | 7:27,168,882 | G/T | — | uncertain significance |
| rs766474237 | 7:27,168,887 | T/C | — | uncertain significance |
| rs753922042 | 7:27,168,888 | G/A | — | uncertain significance |
| rs139808484 | 7:27,168,896 | A/C | — | uncertain significance |
| rs776144758 | 7:27,168,920 | T/C | — | uncertain significance |
| rs200725670 | 7:27,168,927 | G/T | — | uncertain significance |
| rs1562721930 | 7:27,168,962 | C/G | — | uncertain significance |
| rs1277884800 | 7:27,168,984 | T/C | — | uncertain significance |
| rs558056484 | 7:27,169,034 | T/C | — | uncertain significance |
| rs200302499 | 7:27,169,037 | C/T | — | uncertain significance |
| rs771351849 | 7:27,169,080 | G/T | — | likely benign |
| rs2158218 | 7:27,169,093 | T/G | — | benign |
| rs774662092 | 7:27,169,137 | G/A | — | uncertain significance |
| rs765974142 | 7:27,169,155 | A/G | — | uncertain significance |
| rs145032542 | 7:27,169,157 | C/A | — | uncertain significance |
| rs1785430033 | 7:27,169,163 | G/C | — | uncertain significance |
| rs17449108 | 7:27,169,369 | T/C | — | benign |
| rs6957209 | 7:27,169,388 | A/C | — | benign |
| rs6943542 | 7:27,169,617 | T/C | — | benign |
| rs200014123 | 7:27,169,794 | G/C | — | uncertain significance |
| rs200965871 | 7:27,169,829 | C/T | — | likely benign |
| rs1159260195 | 7:27,169,928 | G/A | — | uncertain significance |
| rs10251056 | 7:27,169,934 | A/G | — | benign |
| rs540982908 | 7:27,169,939 | G/C | — | likely benign |
| rs561219190 | 7:27,169,977 | G/C | — | uncertain significance |
| rs1439072605 | 7:27,169,979 | C/A | — | uncertain significance |
| rs2534658818 | 7:27,169,991 | G/T | — | uncertain significance |
| rs1464079425 | 7:27,170,006 | G/A | — | uncertain significance |
| rs1416460786 | 7:27,170,034 | C/T | — | uncertain significance |
| rs1785489139 | 7:27,170,068 | G/A | — | likely benign |
| rs2534659351 | 7:27,170,073 | C/T | — | uncertain significance |
| rs1460926425 | 7:27,170,079 | C/G | — | uncertain significance |
| rs1348793244 | 7:27,170,085 | A/G | — | uncertain significance |
| rs761518289 | 7:27,170,110 | C/G | — | likely benign |
| rs765734275 | 7:27,170,136 | A/G | — | uncertain significance |
| rs753165957 | 7:27,170,138 | G/A | — | uncertain significance |
| rs6944345 | 7:27,170,145 | T/G | — | benign |
| rs6962314 | 7:27,170,159 | C/T | — | benign |
| rs532084815 | 7:27,170,188 | C/A | — | likely benign |
| rs1384120516 | 7:27,170,191 | C/T | — | likely benign |
| rs767129469 | 7:27,170,199 | G/A | — | uncertain significance |
| rs753251578 | 7:27,170,220 | G/C | — | uncertain significance |
| rs749207738 | 7:27,170,249 | C/T | — | uncertain significance |
| rs2534661432 | 7:27,170,251 | G/T | — | uncertain significance |
| rs2534661448 | 7:27,170,252 | C/G | — | uncertain significance |
| rs768519475 | 7:27,170,253 | C/A | — | uncertain significance |
| rs2534661497 | 7:27,170,260 | G/A | — | likely benign |
| rs1396295805 | 7:27,170,297 | G/A | — | uncertain significance |
| rs147843309 | 7:27,170,307 | T/C | — | uncertain significance |
| rs780264576 | 7:27,170,332 | C/A | — | uncertain significance |
| rs141143994 | 7:27,170,344 | C/A | — | uncertain significance |
| rs748084932 | 7:27,170,348 | G/A | — | uncertain significance |
| rs10225507 | 7:27,170,583 | C/T | — | benign |
| rs6461988 | 7:27,170,706 | G/A | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.