Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "P"
561 to 570 of 1032 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

561
POU class 2 homeobox 1
OCT1, OTF1, Oct1Z, oct-1B

562
Pseudouridine synthase 7
IDDABS
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Intellectual developmental disorder behavioral short stature, Non-specific syndromic intellectual disability, Systemic lupus erythematosus

563
POU class 2 homeobox 2
OCT2, OTF2, Oct-2
Gastro-entero-pancreatic neuroendocrine tumor, Prostate cancer

564
POU class 3 homeobox 1
OCT6, OTF6, SCIP
Rheumatoid arthritis

565
POU class 3 homeobox 2
BRN2, N-Oct3, OCT7, OTF-7, OTF7, POUF3, brn-2, oct-7
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Cerebral amyloid angiopathy, Bipolar depression, Erectile dysfunction, Neurotic disorder, Obesity, Schizophrenia, Scoliosis, Substance abuse

566
POU class 3 homeobox 3
BRN1, OTF8, SNIBFIS, brain-1, oct-8
Neurodevelopmental disorder, Developmental disability, Intellectual developmental disorder, Intellectual developmental disorder dysmorphic, Non-specific syndromic intellectual disability, Osteoarthritis

567
POU class 3 homeobox 4
BRAIN-4, BRN-4, BRN4, DFN3, DFNX2, OCT-9, OTF-9, OTF9
Ayazi syndrome, Bipolar disorder, Choroideremia-deafness-obesity syndrome, Chromosome xq21 deletion syndrome, Deafness, nonsyndromic sensorineural, mitochondrial, Deafness, x-linked, Nonsyndromic hearing loss, Intellectual developmental disorder, Hearing loss with stapes fixation, Schizophrenia, Scoliosis, X-linked nonsyndromic hearing loss, X-linked hearing loss with perilymphatic gusher, Xq21 microdeletion syndrome

568
POU class 4 homeobox 1
ATITHS, BRN3A, Oct-T1, RDC-1, brn-3A
Ataxia with intention tremor and hypotonia, Cerebellar dysfunction with variable cognitive and behavioral abnormalities, Cervical dysplasia, Myeloid leukemia, Uterine fibroid, Uterine neoplasm

569
POU class 4 homeobox 3
BRN3C, DFNA15, DFNA42, DFNA52
Isolated sensorineural deafness, Nonsyndromic hearing loss, Bell's palsy, Deafness, Hearing impairment, Migraine, Rheumatoid arthritis, Scoliosis

570
POU class 5 homeobox 1
OCT3, OCT4, OCT4Borf1, OTF-3, OTF3, OTF4, Oct-3, Oct-4, Oct3/4
Amphetamine or related acting sympathomimetic abuse, Carcinogenesis, Congenital heart disease, Crohn disease, Giant axonal neuropathy, Glioma, Congenital heart defect, Human immunodeficiency virus infection, Inflammatory bowel disease, Membranous nephropathy, Multiple myeloma, Prostate cancer, Psoriasis, Psoriatic arthritis, Rheumatoid arthritis
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