Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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6211 to 6220 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

6211
Immunoglobulin superfamily member 9B
LINC00947, MIR4697HG
Anorexia nervosa, Anxiety disorder, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Cardiomyopathy, Color vision deficiency, Generalized anxiety disorder, Insomnia, Major depressive disorder, Migraine, Neurotic disorder, Obesity, Obsessive-compulsive disorder, Parkinson disease
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6212
Indian hedgehog signaling molecule
BDA1, HHG2
Acrocapitofemoral dysplasia, Brachydactyly, Desbuquois syndrome, Endometriosis, Gastrointestinal stromal tumor, Osteoarthritis, Ovarian cysts, Retinopathy of prematurity, Syndactyly

6213
Interactor of HORMAD1 1
CCDC36, CT74, LELA1
Anorexia nervosa, Anxiety disorder, Attention deficit hyperactivity disorder, Insomnia, Major depressive disorder, Neurotic disorder, Obesity, Schizophrenia

6214
IKBKB interacting protein
IKIP
Barrett esophagus

6215
Inhibitor of nuclear factor kappa B kinase subunit beta
IKK-2, IKK-beta, IKK2, IKKB, IMD15, IMD15A, IMD15B, NFKBIKB
Combined immunodeficiency disease, Dermatitis, Desbuquois syndrome, Diabetes mellitus type 2, Hirschsprung disease, Hyperbilirubinemia, Hypertension, Immunodeficiency, Osteoarthritis, Severe combined immunodeficiency, Systemic lupus erythematosus, Vascular disease

6216
Inhibitor of nuclear factor kappa B kinase subunit epsilon
IKK-E, IKK-i, IKKE, IKKI
Asthma, Iga nephropathy, Major depressive disorder, Psoriasis, Systemic lupus erythematosus, Depression

6217
Inhibitor of nuclear factor kappa B kinase regulatory subunit gamma
AMCBX1, EDAID1, FIP-3, FIP3, Fip3p, IKK-gamma, IKKAP1, IKKG, IMD33, IP, IP1, IP2, IPD2, NEMO, SAIDX, ZC2HC9
Congenital nonspherocytic hemolytic anemia, Anhidrotic ectodermal dysplasia with immunodeficiency, osteopetrosis, and lymphedema, Anophthalmia/microphthalmia-esophageal atresia syndrome, Autoinflammatory disease, systemic, x-linked, Behcet disease, Bloch sulzberger syndrome, Common variable immunodeficiency, Glucose-6-phosphate dehydrogenase deficiency, Desbuquois syndrome, Ectodermal dysplasia, Hyper-igm immunodeficiency syndrome, Immunodeficiency, Learning disorders, Lung neoplasms, Nonalcoholic fatty liver disease

6218
IKAROS family zinc finger 1
CVID13, Hs.54452, IK1, IKAROS, LYF1, LyF-1, PPP1R92, PRO0758, ZNFN1A1
Alzheimer disease, Ankylosing spondylitis, Asthma, Eczema, Autoimmune disease, B-cell acute lymphoblastic leukemia, B-lymphoblastic leukemia/lymphoma, Lymphoblastic leukemia, Ulcerative colitis, Color vision deficiency, Combined immunodeficiency disease, Common variable immunodeficiency, Crohn disease, Diamond-blackfan anemia, Pharyngeal disorder
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6219
IKAROS family zinc finger 2
ANF1A2, HELIOS, ICHAD, IMDIA, ZNF1A2, ZNFN1A2
Attention deficit hyperactivity disorder, Combined immunodeficiency disease, Hearing impairment, Hearing loss, T-cell leukemia-lymphoma, Multiple sclerosis, Prostate cancer, Squamous cell carcinoma, Substance abuse, Systemic lupus erythematosus, Systemic sclerosis, Hypertension, Diabetes mellitus type 2

6220
IKAROS family zinc finger 3
AIO, AIOLOS, IMD84, ZNFN1A3
Rheumatoid arthritis, Asthma, Eczema, Atrial fibrillation, Atrial flutter, B-cell acute lymphoblastic leukemia, B-cell chronic lymphocytic leukemia, Biliary cirrhosis, Cardiovascular disease, Cervical cancer, Combined immunodeficiency-lymphopenia-cancer predisposing syndrome due to aiolos deficiency, Crohn disease, Gastro-entero-pancreatic neuroendocrine tumor, Hypothyroidism, Immune system disease
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