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
10681 to 10690 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10681
PIGY upstream open reading frame
NDUFAFQ, PREY
Central nervous system cancer, Glioblastoma, Glioma, Hyperphosphatasia with intellectual disability syndrome, Mitochondrial disease

10682
Peptide YY
PYY-I, PYY1
Alzheimer disease, Anorexia, Major depressive disorder, Diverticular disease, Hyperammonemia, Neural tube defect, Neural tube defects, x-linked, Obesity

10683
PZP alpha-2-macroglobulin like
CPAMD6
Hepatocellular carcinoma, Major depressive disorder

10684
Glutaminyl-tRNA synthetase 1
GLNRS, MSCCA, PRO2195, QARS
Attention deficit hyperactivity disorder, , Gout, Intellectual developmental disorder, Microcephaly, Prostatic neoplasms

10685
Quinoid dihydropteridine reductase
DHPR, HDHPR, PKU2, SDR33C1
Alzheimer disease, Dementia, Dihydropteridine reductase deficiency, Liver failure

10686
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

10687
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

10688
Pyroglutamylated RFamide peptide receptor
AQ27, GPR103, SP9155
Autoimmune thyroid disease, Psoriasis, Diabetes mellitus type 1

10689
Glutamine rich 1
AB-DIP, VERBRAS
Autism, Coronary artery disease, Intellectual developmental disorder, Major depressive disorder, Intellectual disability, Schizophrenia, Ververi-brady syndrome

10690
Glutamine rich 2
SPGF35
Gout, Spermatogenic failure