Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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10161 to 10170 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10161
POU class 2 homeobox associating factor 1
BOB1, OBF-1, OBF1, OCAB
Agammaglobulinemia, Biliary cirrhosis, Colorectal cancer, Diverticular disease, Hodgkin lymphoma, Ovarian epithelial cancer, Multiple sclerosis, Nephrolithiasis, Ovarian cancer, Biliary cholangitis, Vascular dementia

10162
POU class 2 homeobox associating factor 2
C11orf53, OCA-T1, OCAT1
Colorectal adenoma, Colorectal cancer

10163
POU class 2 homeobox associating factor 3
C11orf93, CASC13, COLCA2, LOH11CR1G, OCA-T2
Neoplasms, Biliary tract cancer, Breast cancer, Cancer, Celiac disease, Cervical cancer, Colorectal cancer, Endometrial cancer, Esophageal cancer, Estrogen-receptor negative breast cancer, Gastric cancer, Hepatocellular carcinoma, Lung cancer, Non-hodgkins lymphoma, Ovarian cancer
View all (4 more)

10164
POU class 2 homeobox 2
OCT2, OTF2, Oct-2
Gastro-entero-pancreatic neuroendocrine tumor, Prostate cancer

10165
POU class 2 homeobox 3
Epoc-1, OCT-11, OCT11, OTF-11, PLA-1, PLA1, Skn-1a
Melanoma, Pernicious anemia, Psoriasis, Seborrheic keratosis, Skin disease

10166
POU class 3 homeobox 1
OCT6, OTF6, SCIP
Rheumatoid arthritis

10167
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

10168
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

10169
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, Congenital ear anomaly, Deafness, nonsyndromic sensorineural, mitochondrial, Deafness, x-linked, Hereditary hearing loss, Major depressive disorder, Hearing loss with stapes fixation, Schizophrenia, Scoliosis, X-linked nonsyndromic hearing loss, X-linked hearing loss with perilymphatic gusher, Xq21 microdeletion syndrome

10170
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 disease, Uterine neoplasms