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
10731 to 10740 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10731
PZP alpha-2-macroglobulin like
CPAMD6
Hepatocellular carcinoma, Major depressive disorder

10732
Glutaminyl-tRNA synthetase 1
GLNRS, MSCCA, PRO2195, QARS
Attention deficit hyperactivity disorder, , Gout, Intellectual developmental disorder, Microcephaly, Prostatic neoplasms

10733
Quinoid dihydropteridine reductase
DHPR, HDHPR, PKU2, SDR33C1
Alzheimer disease, Dementia, Dihydropteridine reductase deficiency, Liver failure

10734
QKI, KH domain containing RNA binding
Hqk, QK, QK1, QK3, hqkI
Alzheimer disease, Angiocentric glioma, Cataract, Demyelinating diseases, Glioma, Insomnia, Major depressive disorder, Myocardial infarction, Osteonecrosis, Schizophrenia, Diabetes mellitus type 2, Depression

10735
Glutaminyl-peptide cyclotransferase
GCT, QC, sQC
Autism, Lymphocytic leukemia, Allergic contact dermatitis, Hodgkin lymphoma, Lymphocytic b-cell leukemia, Melanoma, Multiple myeloma, Non-hodgkins lymphoma, Schizophrenia

10736
Pyroglutamylated RFamide peptide receptor
AQ27, GPR103, SP9155
Autoimmune thyroid disease, Psoriasis, Diabetes mellitus type 1

10737
Glutamine rich 1
AB-DIP, VERBRAS
Autism, Coronary artery disease, Intellectual developmental disorder, Major depressive disorder, Intellectual disability, Schizophrenia, Ververi-brady syndrome

10738
Glutamine rich 2
SPGF35
Gout, Spermatogenic failure

10739
Glutaminyl-tRNA amidotransferase subunit QRSL1
COXPD40, GatA
Central vertigo, Combined oxidative phosphorylation deficiency, Peripheral vertigo

10740
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