Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "I"
421 to 430 of 438 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

421
Inositol-trisphosphate 3-kinase B
IP3-3KB, IP3K, IP3K-B, IP3KB, PIG37
Alzheimer disease, Asthma, Colonic neoplasms, Dental caries, Tourette syndrome, Hyperopia, Major depressive disorder, Parkinson disease, Respiratory system disease, Urticaria

422
Inositol-trisphosphate 3-kinase C
IP3-3KC, IP3KC
Coronary aneurysm, Kawasaki disease

423
Inositol 1,4,5-trisphosphate receptor type 1
ACV, CLA4, INSP3R1, IP3R, IP3R1, PPP1R94, SCA15, SCA16, SCA29
Androgenetic alopecia, Aniridia-cerebellar ataxia-intellectual disability syndrome, Anterior segment mesenchymal dysgenesis, Cerebellar ataxia, Bilateral congenital mydriasis, Bipolar disorder, Breast cancer, Diabetic neuropathy, Gastric cancer, Gillespie syndrome, Intellectual developmental disorder, Movement disorder, Multiple sclerosis, Neurodevelopmental disorder, Obesity
View all (8 more)

424
Inositol 1,4,5-trisphosphate receptor type 2
ANHD, CFAP48, INSP3R2, IP3R2
Amyotrophic lateral sclerosis, Isolated anhidrosis, Asthma, Atrial fibrillation, Breast cancer, Cardiomegaly, Clonal hematopoiesis, Digestive system disease, Endometriosis, Hodgkin lymphoma, Intellectual developmental disorder, Kidney cancer, Major depressive disorder, Open angle glaucoma, Peripheral arterial disease
View all (2 more)

425
Inositol 1,4,5-trisphosphate receptor type 3
CMT1J, IMD132, IMD133, IP3R, IP3R-3, IP3R3
Asthma, Attention deficit hyperactivity disorder, Autism, Celiac disease, Charcot-marie-tooth disease, Diabetes mellitus type 1, Long qt syndrome, Graves disease, Immunodeficiency, Insomnia, Major depressive disorder, Metabolic syndrome, Multiple sclerosis, Obesity, Osteoarthritis
View all (7 more)

426
ITPR interacting domain containing 1
CCDC129
Cadasil, Dementia, Psoriasis

427
ITPR interacting domain containing 2
CS-1, CS1, KRAP, SPAG13, SSFA2
Central nervous system cancer, Glioblastoma, Glioma

428
Inositol 1,4,5-trisphosphate receptor interacting protein
D1A, DANGER, KIAA1754, bA127L20, bA127L20.2
Uterine fibroid

429
ITPRIP like 2
D1C
Color vision deficiency

430
Intersectin 1
ITSN, SH3D1A, SH3P17
Autism, Nonsyndromic intellectual disability, Central nervous system cancer, Seizure, Glioblastoma, Glioma, Intellectual developmental disorder, Nephrotic syndrome, Neurodevelopmental disorder, Prostatic neoplasms, Schizophrenia