Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
10691 to 10700 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10691
Glutaminyl-tRNA amidotransferase subunit QRSL1
COXPD40, GatA
Central vertigo, Combined oxidative phosphorylation deficiency, Peripheral vertigo

10692
Glutamine and serine rich 1
-
Atrial fibrillation, Obstructive pulmonary disease, Coronary artery disease, Major depressive disorder, Parkinson disease, Prostate cancer, Sarcoidosis, Diabetes mellitus type 2, Uterine fibroid

10693
Quiescin sulfhydryl oxidase 1
Q6, QSCN6
Anorexia nervosa, Eating disorder

10694
Quiescin sulfhydryl oxidase 2
QSCN6L1, SOXN
Gout, Insomnia, Diabetes mellitus type 2

10695
Queuosine-tRNA mannosyltransferase
GTDC1, Hmat-Xa, mat-Xa
Neurodevelopmental disorder

10696
Queuine tRNA-ribosyltransferase catalytic subunit 1
FP3235, TGT, TGUT
Eczema, Inflammatory skin disease, Osteoarthritis, Psoriasis, Psoriasis vulgaris

10697
R3H domain and coiled-coil containing 1
-
Alzheimer disease, Systemic lupus erythematosus

10698
R3H domain and coiled-coil containing 1 like
C10orf28, GIDRP86, GIDRP88, PSORT
Eczema, Carpal tunnel syndrome, Central nervous system cancer, Coronary artery disease, Digestive system disease, Dry eye syndrome, Dyslexia, Glioblastoma, Glioma, Inflammatory skin disease, Metabolic syndrome, Myocardial infarction, Psoriasis, Willis-ekbom disease, Diabetes mellitus type 2

10699
R3H domain containing 1
R3HDM
Colorectal cancer, Metabolic syndrome, Obstructive sleep apnea syndrome, Diabetes mellitus type 2, Uterine fibroid

10700
R3H domain containing 2
CAG6, PR01365
Juvenile arthritis, Coronary artery disease, Gout, Insomnia, Juvenile idiopathic arthritis, Metabolic syndrome, Oligoarticular juvenile idiopathic arthritis, Schizophrenia, Diabetes mellitus type 2