DMRT3 antibody - middle region (ARP33210_P050)
- Known as:
- DMRT3 (anti-) - middle region (ARP33210_P050)
- Catalog number:
- arp33210_p050
- Product Quantity:
- USD
- Category:
- -
- Supplier:
- Aviva Systems Biology
- Gene target:
- DMRT3 antibody - middle region (ARP33210_P050)
Related genes to: DMRT3 antibody - middle region (ARP33210_P050)
- Gene:
- DMRT3 NIH gene
- Name:
- doublesex and mab-3 related transcription factor 3
- Previous symbol:
- DMRTA3
- Synonyms:
- -
- Chromosome:
- 9p24.3
- Locus Type:
- gene with protein product
- Date approved:
- 2000-11-24
- Date modifiied:
- 2014-11-19
Related products to: DMRT3 antibody - middle region (ARP33210_P050)
Related articles to: DMRT3 antibody - middle region (ARP33210_P050)
- The DMRT3 gene, often referred to as the "gait keeper," plays a key role in controlling alternative gaits in horses, such as tölt and pace. This study aimed to determine the frequency of known and to screen for potential novel polymorphisms within the second exon of the DMRT3 gene. - Source: PubMed
Publication date: 2026/04/03
Ropka-Molik KatarzynaMusiał Adrianna DMajtyka AnnaBieniek AgnieszkaAyad AbdelhanineMuszyński SiemowitStefaniuk-Szmukier Monika - The Miyako horse is one of the eight Japanese native horse breeds and is scarce in terms of population size. Japanese native horses are believed to be descended from Mongolian horses and represent a precious lineage that has preserved its traits for over a thousand years in Japan. Genetic analysis of the endangered Miyako horse is useful for preserving its original phenotypic traits. This study analysed the genetic variation in trait-related genes for coat colour (), body composition (), gait (), and temperament () in 46 extant Miyako horses. In addition, because numerous Miyako horses have vertical stripes on their backs, we analysed the genes associated with the dorsal stripe (), a characteristic of primitive horses. Until now, Miyako horses were believed to comprise only bays and chestnuts, but genetic analysis revealed that two individuals were black. No mutations were detected in g.66619237delinsSINE, , or , whereas polymorphisms were observed in g.66608679T>C and . Furthermore, analysis suggested that the patterns observed on the backs of Miyako horses could be genetically classified as dorsal stripes. Using the information on trait-related genes obtained in this study as a foundation for breeding plans is expected to contribute significantly to the production of individuals that maintain the phenotype traditionally preserved in Miyako horses. Furthermore, genetic confirmation of the Miyako horse dorsal stripe pattern could provide significant clues regarding similar markings in other Japanese native horses. - Source: PubMed
Publication date: 2026/03/14
Masuda MiokoTozaki TeruakiKawate KokiFurukawa RisakoKikuchi MioIshige TaichiroKakoi Hironaga - Plectropomus leopardus is a hermaphrodite fish with a unique pattern of gonadal development. However, the molecular mechanism of sexual differentiation in this species remains unclear. The Doublesex and Mab-3 related transcription factor (dmrt) gene family are known to play a crucial role in gonad differentiation and development. Notably, systematic investigations into the composition and function of the dmrt gene family in this hermaphrodite fish remain conspicuously lacking. - Source: PubMed
Publication date: 2025/10/29
Ding HuiLi PeiyuWang JingwenYin ChenlinWu JiayiLi JiahangGuo QingranBao ZhenminWang BoHu Jingjie - Previous genomic efforts on chromosome 9p deletion and duplication syndromes have utilized low-resolution strategies (i.e., karyotypes, chromosome microarrays). These studies have provided important initial insights into these syndromes. This current study is the first large-scale whole-genome sequencing (WGS) study of 100 individuals from families with chromosome 9p syndromes. - Source: PubMed
Publication date: 2025/10/24
Wang YingxiSams Eleanor ISlaugh RachelCrocker SandraHurtado Emily CordovaTracy SophiaHou Ying-Chen ClaireMarkovic ChristopherValle KostandinTate VictoriaBelhassan KhadijaAppelbaum ElizabethAkinwe TitilopeStarosta Rodrigo TCao YangNeilson AmberLiu YuJensen NathanielGhasemi RezaLindsay TinaManuel JuanaCouteranis SophiaKremitzki MilinnUstanik JackAntonacci ThomasNg Jeffrey KEmory AndrewMetz LauraDeLuca TracieLyons Katherine NSinnwell ToniThomeczek BrianneWang KymmeSisneros NickMuraleedharan MeghaKethireddy AnanthaCorbo MarcoGowda HarshaKing Katherine AGurnett Christina ADutcher Susan KGooch CatherineLi Yang EMitchell Matthew WPeterson Kevin AHorani AmjadRosenfeld Jill ABi WeiminStankiewicz PawelChao Hsiao-TuanPosey Jennifer EGrochowski Christopher MDardas ZainPuffenberger Erik GPearson Christopher EKooy FrankAnnear DaleInnes A MicheilHeinz MichaelHead RichardFulton RobertToutain Stephan Antonacci-Fulton LucindaCui XiaoxiaMitra Robi DCole F SessionsNeidich JulieDickson Patricia IMilbrandt JeffreyTurner Tychele N - We report a rare case involving a 22-year-old phenotypically female patient who presented to our care with primary amenorrhea and spontaneous breast development. Hormonal analysis indicated hypergonadotropic hypogonadism, and imaging revealed a hypoplastic uterus and calcified ovaries. Karyotyping was 46, XY and the presence of the SRY gene was confirmed. The patient underwent laparoscopic bilateral salpingo-oophorectomy due to the high risk of malignancy development. Histopathological analysis revealed bilateral Sertoli cell tumors and a sex cord tumor with annular tubules in the right gonad. Next generation sequencing genetic testing identified a 1.24 Mb deletion on chromosome 9p24.3, which included the DMRT1, DMRT2, and DMRT3 genes, as well as a partial deletion of KANK1. Hormonal replacement therapy was not initiated due to the potential risk of tumor recurrence, and follow-up imaging was scheduled every 6 months for the first 2 years and then annually. No recurrence was observed at 24 months. - Source: PubMed
Petrillo TabathaBattipaglia ChristianSemprini ElisaBaldessari CinziaPirola MartaCalabrese OlgaFarulla AntoninoTernelli GilianaEccher AlbinoBotticelli LauraGenazzani Alessandro D