Truncated NUS1 variant causes MRD55
收藏NIAID Data Ecosystem2026-03-13 收录
下载链接：
https://www.ncbi.nlm.nih.gov/sra/SRP331549
下载链接
链接失效反馈官方服务：
资源简介：
Sequence of a novle NUS1 variant identified in a Chinese patient with MRD55
应用场景：
创建时间：
2022-09-01
相关数据集
SFARI Gene
SFARI Gene（神经发育障碍基因数据库）是一个专注于自闭症谱系障碍（ASD）相关基因的在线数据库。它由西蒙斯基金会自闭症研究计划（SFARI）所有，旨在为自闭症研究社区提供关于人类基因、基因评分、拷贝数变异和动物模型的最新信息。该数据库持续更新，并包含来自西蒙斯单纯形收集等资源的数据。
知名数据库1700
SARS-CoV-2 Delta variant genomic variation associated with breakthrough infection in Northern California: A retrospective cohort study
To characterize the genomic variation within a circulating variant and identifying potential mutations associated with breakthrough infection among persons with Delta variant SARS-CoV-2 infection
DataCite Commons2023-09-19 更新80
NCBP2 modulates neurodevelopmental defects of the 3q29 deletion in Drosophila and Xenopus laevis models
The 1.6 Mbp deletion on chromosome 3q29 is associated with a range of neurodevelopmental disorders, including schizophrenia, autism, microcephaly, and intellectual disability. Despite its importance t
NIAID Data Ecosystem70
HCMV UL97 phosphotransferase gene mutations may be associated with antiviral resistance in immunocompromised patients in Belém, PA, Northern Brazil
Abstract INTRODUCTION: Human cytomegalovirus is one of the causes of opportunist infections in immunocompromised patients, and is triggered by factors such as state of viral latency, weakened immune r
DataCite Commons2020-08-29 更新100
Additional file 7 of The 29-nucleotide deletion in SARS-CoV: truncated versions of ORF8 are under purifying selection
Additional file 2: Python script for extraction of mutations from BLASTN multiple alignments (ZIP file).
DataCite Commons2023-07-11 更新80
