Genes | GeDiPNet - Gene Disease Pathway & Associations

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6411 to 6420 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
6411	100505385	IQCJ-SCHIP1	IQCJ-SCHIP1 readthrough	-	Attention deficit hyperactivity disorder, B-cell acute lymphoblastic leukemia, Adrenal gland neoplasms, Asthma, Color vision deficiency, Congenital heart disease, Conotruncal cardiac defect, Diverticular disease, Obsessive-compulsive disorder, Parkinson disease, Pelvic organ prolapse, Biliary cholangitis, Scoliosis, Substance abuse, Systemic lupus erythematosus, Diabetes mellitus type 2 View all (1 more)
6412	124152	IQCK	IQ motif containing K	-	Alzheimer disease, Gastroesophageal reflux disease, Insomnia
6413	285423	IQCM	IQ motif containing M	-	Colorectal cancer, Epilepsy, Generalized epilepsy, Insomnia, Major depressive disorder, Venous thromboembolism
6414	80726	IQCN	IQ motif containing N	KIAA1683, SPGF78	Hypothyroidism, Metabolic syndrome, Spermatogenic failure, Systemic lupus erythematosus, Diabetes mellitus type 2
6415	8826	IQGAP1	IQ motif containing GTPase activating protein 1	HUMORFA01, SAR1, p195	Alzheimer disease, Androgenetic alopecia, Asthma, Eczema, Brain neoplasms, Hepatocellular carcinoma, Color vision deficiency, Multiple sclerosis, Open angle glaucoma, Rheumatoid arthritis, Seasonal allergic rhinitis
6416	10788	IQGAP2	IQ motif containing GTPase activating protein 2	-	Alzheimer disease, Angioedema, Brain neoplasms, Hepatocellular carcinoma, Color vision deficiency, Hearing loss, Ovarian cancer, Ovarian serous carcinoma, Venous thromboembolism
6417	128239	IQGAP3	IQ motif containing GTPase activating protein 3	-	Autism, Hepatocellular carcinoma
6418	9922	IQSEC1	IQ motif and Sec7 domain ArfGEF 1	ARF-GEP100, ARFGEP100, BRAG2, GEP100, IDDSSBA	Nonsyndromic intellectual disability, Central nervous system cancer, Conotruncal cardiac defect, Developmental disability, Glioblastoma, Glioma, Intellectual developmental disorder short stature behavioral, Lung neoplasms, Metabolic syndrome, Osteoarthritis, Pancreatic cancer, Peripheral arterial disease, Spondylosis, Diabetes mellitus type 2
6419	23096	IQSEC2	IQ motif and Sec7 domain ArfGEF 2	BRAG1, IQ-ArfGEF, MRX1, MRX18, MRX78, XLID1	Autism, Neurodevelopmental disorder, Epilepsy, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Developmental and epileptic encephalopathy, Non-specific syndromic intellectual disability, X-linked intellectual disability, Intellectual disability, Smith-magenis syndrome, Specific learning disability, X-linked complex neurodevelopmental disorder
6420	440073	IQSEC3	IQ motif and Sec7 domain ArfGEF 3	-	Arthrogryposis multiplex congenita, Insomnia, Pena-shokeir syndrome

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