Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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10171 to 10180 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10171
POU class 4 homeobox 2
BRN3.2, BRN3B, Brn-3b
Oligodendroglioma

10172
POU class 4 homeobox 3
BRN3C, DFNA15, DFNA42, DFNA52
Isolated sensorineural deafness, Nonsyndromic hearing loss, Bell's palsy, Congenital sensorineural hearing loss, Deafness, Hearing impairment, Hereditary hearing loss, Migraine, Rheumatoid arthritis, Scoliosis

10173
POU class 5 homeobox 1
OCT3, OCT4, OCT4Borf1, OTF-3, OTF3, OTF4, Oct-3, Oct-4, Oct3/4
Amphetamine or sympathomimetic abuse, Carcinogenesis, Congenital heart disease, Crohn disease, Gestational trophoblastic disease, Glioma, Congenital heart defect, Inflammatory bowel disease, Membranous glomerulonephritis, Multiple myeloma, Prostate cancer, Psoriasis, Psoriatic arthritis, Rheumatoid arthritis, Stevens-johnson syndrome
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10174
POU class 5 homeobox 1B
OCT4-PG1, OCT4PG1, OTF3C, OTF3P1, POU5F1P1, POU5F1P4, POU5FLC20, POU5FLC8
Neoplasms, Biliary tract cancer, Breast cancer, Cancer, Cervical cancer, Colorectal cancer, Colonic neoplasms, Colorectal adenoma, Endometrial cancer, Esophageal cancer, Estrogen-receptor negative breast cancer, Gastric cancer, Hepatocellular carcinoma, Lung cancer, Non-hodgkins lymphoma
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10175
POU domain class 5, transcription factor 2
SPRM-1
Major depressive disorder

10176
POU class 6 homeobox 2
RPF-1, WT5, WTSL
Autism, Dupuytren contracture, Dyslexia, Glaucoma, Hypogonadotropic hypogonadism, Insomnia, Metabolic syndrome, Oligodendroglioma, Open angle glaucoma, Willis-ekbom disease, Schizophrenia, Diabetes mellitus type 2, Wilms tumor

10177
Inorganic pyrophosphatase 2
HSPC124, SCFAI, SCFI, SID6-306
Attention deficit hyperactivity disorder, Autism, Breast cancer, Dilated cardiomyopathy, Insomnia, Irritable bowel syndrome

10178
Peter pan homolog
BXDC3, SSF, SSF-1, SSF1, SSF2
Cataplexy and narcolepsy, Narcolepsy

10179
PPAN-P2RY11 readthrough
BXDC3, P2RY11, P2Y11, PPAN, SSF1, Ssf-1
Cataplexy and narcolepsy, Narcolepsy

10180
Peroxisome proliferator activated receptor alpha
NR1C1, PPAR, PPAR-alpha, PPARalpha, hPPAR
Alzheimer disease, Carcinoma, Cardiomegaly, Ischemic heart disease, Coronary artery disease, Crohn disease, Atopic dermatitis, Diabetes mellitus type 2, Dyslipidemias, Fatty liver, Fatty liver, alcoholic, Hepatomegaly, Hyperlipidemia, Hyperlipoproteinemia, Hypertension
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