AADACL3
- Known as:
- AADACL3
- Catalog number:
- 000867A
- Product Quantity:
- 250ul
- Category:
- -
- Supplier:
- ABM
- Gene target:
- AADACL3
Related genes to: AADACL3
- Gene:
- AADACL3 NIH gene
- Name:
- arylacetamide deacetylase like 3
- Previous symbol:
- -
- Synonyms:
- OTTHUMG00000001887
- Chromosome:
- 1p36.21
- Locus Type:
- gene with protein product
- Date approved:
- 2006-06-30
- Date modifiied:
- 2018-05-03
Related products to: AADACL3
Related articles to: AADACL3
- Managing Ductal Carcinoma in Situ (DCIS) remains challenging due to the lack of reliable biomarkers to predict radiotherapy (RT) response, leading to both overtreatment of indolent disease and undertreatment of aggressive cases. - Source: PubMed
Publication date: 2025/07/08
Rizvi NoorMucaki Eliseos JSalmini Emily LZhang MonicaTrebinjac SabinaHahn EzraPaszat LawrenceNofech-Mozes SharonHallett Michael TRakovitch EileenDumeaux Vanessa - Russian sheep breeds represent an important economic asset by providing meat and wool, whilst being adapted to extreme climates. By resequencing two Russian breeds from Siberia: Tuva (n = 20) and Baikal (n = 20); and comparing them with a European (UK) sheep outgroup (n = 14), 41 million variants were called, and signatures of selection were identified. High-frequency missense mutations on top of selection peaks were found in genes related to immunity (LOC101109746) in the Baikal breed and wool traits (IDUA), cell differentiation (GLIS1) and fat deposition (AADACL3) in the Tuva breed. In addition, genes found under selection owing to haplotype frequency changes were related to wool traits (DSC2), parasite resistance (CLCA1), insulin receptor pathway (SOCS6) and DNA repair (DDB2) in the Baikal breed, and vision (GPR179) in the Tuva breed. Our results present candidate genes and SNPs for future selection programmes, which are necessary to maintain and increase socioeconomic gain from Siberian breeds. - Source: PubMed
Publication date: 2020/10/27
Sweet-Jones JYurchenko A AIgoshin A VYudin N SSwain M TLarkin D M - Body weight is an important economic trait for sheep and it is vital for their successful production and breeding. Therefore, identifying the genomic regions and biological pathways that contribute to understanding variability in body weight traits is significant for selection purposes. In this study, the genome-wide associations of birth, weaning, yearling, and adult weights of 460 fine-wool sheep were determined using resequencing technology. The results showed that 113 single nucleotide polymorphisms (SNPs) reached the genome-wide significance levels for the four body weight traits and 30 genes were annotated effectively, including , , , and . The genes annotated by these SNPs significantly enriched 78 gene ontology terms and 25 signaling pathways, and were found to mainly participate in skeletal muscle development and lipid metabolism. These genes can be used as candidate genes for body weight in sheep, and provide useful information for the production and genomic selection of Chinese fine-wool sheep. - Source: PubMed
Publication date: 2020/01/19
Lu ZengkuiYue YaojingYuan ChaoLiu JianbinChen ZhiqiangNiu ChuneSun XiaopingZhu ShaohuaZhao HongchangGuo TingtingYang Bohui - Many sarcoidosis-associating immunological genes have been shown to be shared between other immune-mediated diseases. In Finnish sarcoidosis patients, good prognosis subjects more commonly have * and/or ** haplotype, but no marker for persistent disease have been found. The objective was to further pinpoint genetic differences between prognosis subgroups in relation to the HLA markers. Whole-exome sequencing was conducted for 72 patients selected based on disease activity (resolved disease, = 36; persistent disease, = 36). Both groups were further divided by the HLA markers (one/both markers, = 18; neither of the markers, = 18). The Finnish exome data from the Genome Aggregation Database was used as a control population in the WES sample. Statistical analyses included single-variant analysis for common variants and gene level analysis for rare variants. We attempted to replicate associated variants in 181 Finnish sarcoidosis patients and 150 controls. An association was found in chromosome 1p36.21 (AADACL3 and C1orf158), which has recently been associated with sarcoidosis in another WES study. In our study, variations in these genes were associated with resolved disease (AADACL3, = 0.0001 and = 0.0003; C1orf158, = 7.03E-05). Another interesting chromosomal region also peaked, Leucocyte Receptor Complex in 19q13.42, but the association diminished in the replication sample. In conclusion, this WES study supports the previously found association in the region 1p36.21. Furthermore, a novel to sarcoidosis region was found, but additional studies are warranted to verify this association. - Source: PubMed
Publication date: 2019/12/24
Lahtela ElisaKankainen MattiSinisalo JuhaSelroos OlofLokki Marja-Liisa