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BioWorld - Tuesday, February 3, 2026
Home » genetic variants

Articles Tagged with ''genetic variants''

Illustration of DNA, magnifying glass
Biomarkers

DAP3 gene behind Perrault syndrome, study finds

Jan. 23, 2025
Mitoribosomes are present in the mitochondria of all eukaryotic cells. Their function is to allow the translation of mitochondrial mRNA that exclusively encodes components of the oxidative phosphorylation complexes (OXPHOS).
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White strand of DNA
Biomarkers

Wnt/PCP signaling mediators identified as new markers in yellow nail syndrome

Jan. 20, 2025
Researchers from Tel Aviv Sourasky Medical Center presented data from a study that aimed to investigate the genetic mechanisms underlying yellow nail syndrome (YNS), a rare disorder characterized by three features, namely yellow dystrophic nails, lymphedema and chronic lung disease.
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DNA mutations or genetic disorder concept art
Biomarkers

HOXB13 gene involved in metastatic omentum carcinoma, study shows

Nov. 21, 2024
Primary tumors arising in the gastrointestinal system, ovary or pancreas may spread and lead to secondary cancers such as metastatic omentum cancer.
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Illustration of retinal detachment
Biomarkers

VSX2 variant linked to retinal detachment risk

Nov. 19, 2024
Researchers from the U.K. have analyzed whole-genome sequencing data from 7,276 cases and 236,741 controls in the UK Biobank to perform gene-level and a variant-level exome-wide association study analysis to identify variants related to retinal detachment.
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Genetic/congenital

GTF2H1 de novo genetic variants tied to developmental delay

Nov. 13, 2024
At the annual meeting of the American Society for Human Genetics, scientists presented three new cases of Kabuki syndrome presented with developmental delay, autism and myopia as the common traits.
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Biomarkers

New AIRE gene variant that causes APECED identified

Oct. 9, 2024
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) is a monogenic autoimmune disease caused by biallelic genetic variants in the AIRE gene, encoding autoimmune regulator protein.
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Biomarkers

CSNK1D variant tied to sleep-wake phase syndrome

Oct. 2, 2024
Italian researchers have presented a case study of pediatric advanced sleep-wake phase syndrome in a 4-year-old girl. Autosomal dominant forms of this syndrome due to loss-of-function mutations in the gene coding casein kinase I isoform delta (CSNK1D) have previously been described.
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Illustration of DNA composing the human body
Biomarkers

Variant in ITPR3 behind a complex multisystemic disorder

Sep. 25, 2024
The homeostasis of cytosolic calcium (Ca2+) is crucial for several physiological functions such as cell motility and neuronal transmission, among others. In this process, the inositol 1,4,5-trisphosphate receptor type 3 (ITPR3) plays a key role in the release of intracellular Ca2+.
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Biomarkers

AJAP1 de novo variants tied to epilepsy pathogenesis, study finds

July 17, 2024
Adherens junction-associated protein 1 (AJAP1) is a transmembrane protein that inhibits tumor cell migration and is a susceptibility gene for migraine. Recent hypotheses have pointed toward the potential involvement of AJAP1 in epilepsy and other neurological disorders.
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Illustration of female reproduction system
Biomarkers

Genetic variation in GEN1 predicts poor survival in epithelial ovarian cancer

July 9, 2024
Epithelial ovarian cancer (EOC) is the most predominant histologic type of ovarian cancer, with about 55% of patients at an advanced stage when diagnosed; overall survival remains poor.
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