Understanding the genetic basis of sheep tails is of great importance to improve sheep production and welfare. In this Comment, we discussed recent findings showing that homeobox B13 (HOXB13) is a regulator of the tail length in sheep. The revelation of the HOXB13 gene adds novel insights into the genetic determinism of the sheep tail phenotype. This new genetic highlight will lead to further advances in sheep breeding using selection-based strategies and molecular genetics-based tools.A brief background: piecing together the genetic structure of sheep tail formation The tail phenotype, an obvious body segment, has been described as a significantly divergent trait in sheep 1 , which is due to the wide phenotypic diversity of sheep tails among different breeds located within various geographical and environmental regions 2 . Several factors influence the sheep tail phenotype, including length, fat deposition level, and directionality. The overall tail length is controlled by the number and length of caudal vertebrae. On the other hand, tail fat deposition is controlled by the size and number of adipocytes. Several tail phenotypic patterns have been shown in sheep, including the thin-long tail, thin-short tail, fat-short tail, fat-long tail, and fat-rumped tail (Fig. 1, upper panel). Studies have been performed to understand the mechanistic determinism of sheep tails based on genetic basis, due to the association of sheep tails with several raising-related and welfare issues (see reviews by refs. [3][4][5][6] ). Of these issues, tail docking, as a painful practice, is the most critical 5,6 . Revealing the genetic determinism of sheep tails will help to direct the selection towards the desired phenotypes 7,8 and provide access to new biotechnological tools to directly introduce the desired variant(s) into the targeted breed 9,10 . Recently, three genes/regions were reported to be significantly associated with the sheep tail phenotype. These include the platelet derived growth factor D (PDGFD) gene 1,11,12 and the intergenic region between the bone morphogenetic protein 2 (BMP2) and hydroxyacid oxidase 1 (HAO1) genes, referred to as the IBH region [13][14][15] linked with the fat-tail phenotype, and the T-box transcription factor T (TBXT) gene [16][17][18] linked with variations in caudal vertebrae. Recent studies highlighted a new gene, HOXB13, which is highly associated with the sheep tail length [19][20][21][22][23] (Table 1). Of these studies, two independent efforts, one recently published in Communications Biology 23 and the other published as a preprint 21 , strongly highlighted a structural variation (SV) in the form of a short insertion associated with the longtail phenotype, adding a new critical member to the gene repertoire of the sheep tail configuration.