HOXD3
homeobox D3
Summary
This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located at 2q31-2q37 chromosome regions. Deletions that removed the entire HOXD gene cluster or 5' end of this cluster have been associated with severe limb and genital abnormalities. The protein encoded by this gene may play a role in the regulation of cell adhesion processes. [provided by RefSeq, Jul 2008]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs13418078 | 2:177,015,815 | C/T | upstream gene variant | — |
| rs104893636 | 2:177,016,603 | A/T | missense variant | uncertain significance |
| rs4972504 | 2:177,018,726 | T/G | — | — |
| rs2551802 | 2:177,022,158 | C/G | regulatory region variant | — |
| rs34720456 | 2:177,027,292 | G/A | regulatory region variant | — |
| rs2857532 | 2:177,033,283 | A/T | — | — |
| rs774465493 | 2:177,033,910 | A/G | — | uncertain significance |
| rs143404265 | 2:177,033,993 | C/A | — | uncertain significance |
| rs141168805 | 2:177,033,995 | A/C | — | benign |
| rs145664108 | 2:177,034,115 | G/A | — | uncertain significance |
| rs751122506 | 2:177,034,117 | G/A | — | uncertain significance |
| rs34729309 | 2:177,034,121 | G/A | synonymous variant | — |
| rs747140540 | 2:177,034,143 | G/C | — | uncertain significance |
| rs2468275577 | 2:177,034,152 | G/A | — | likely benign |
| rs773686530 | 2:177,034,200 | C/G | — | uncertain significance |
| rs140883088 | 2:177,034,213 | C/T | — | uncertain significance |
| rs2468275890 | 2:177,034,215 | A/C | — | uncertain significance |
| rs749119115 | 2:177,034,275 | G/A | — | uncertain significance |
| rs774350237 | 2:177,034,297 | C/G | — | uncertain significance |
| rs2105452090 | 2:177,034,381 | C/A | — | uncertain significance |
| rs2468282068 | 2:177,036,262 | A/C | — | uncertain significance |
| rs1448683845 | 2:177,036,353 | G/C | — | uncertain significance |
| rs2468283260 | 2:177,036,496 | C/G | — | uncertain significance |
| rs748868145 | 2:177,036,541 | G/C | — | uncertain significance |
| rs1462673039 | 2:177,036,554 | G/A | — | uncertain significance |
| rs1180468526 | 2:177,036,590 | C/A | — | uncertain significance |
| rs2468283959 | 2:177,036,593 | C/A | — | uncertain significance |
| rs2468283982 | 2:177,036,595 | T/C | — | uncertain significance |
| rs374139731 | 2:177,036,662 | G/A | — | uncertain significance |
| rs199832736 | 2:177,036,682 | A/G | — | uncertain significance |
| rs755289780 | 2:177,036,691 | G/A | — | uncertain significance |
| rs2468284755 | 2:177,036,713 | A/C | — | uncertain significance |
| rs1051929 | 2:177,036,754 | T/C | synonymous variant | — |
| rs372195235 | 2:177,036,786 | C/G | — | uncertain significance |
| rs747257402 | 2:177,036,878 | C/T | — | uncertain significance |
| rs966801 | 2:177,037,827 | G/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.