Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "A"

861 to 870 of 1170 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
861	8874	ARHGEF7	Rho guanine nucleotide exchange factor 7	BETA-PIX, COOL-1, COOL1, Nbla10314, P50, P50BP, P85, P85COOL1, P85SPR, PAK3, PIXB	Insomnia, Retinopathy of prematurity
862	23229	ARHGEF9	Cdc42 guanine nucleotide exchange factor 9	COLLYBISTIN, DEE8, EIEE8, HPEM-2, PEM-2, PEM2	Androgenetic alopecia, Autism, Developmental and epileptic encephalopathy, Developmental disability, Epilepsy, Global developmental delay, Hyperekplexia epilepsy syndrome, Hypogonadism, Intellectual developmental disorder, X-linked complex neurodevelopmental disorder, X-linked intellectual disability
863	8289	ARID1A	AT-rich interaction domain 1A	B120, BAF250, BAF250a, BM029, C1orf4, CSS2, ELD, MRD14, OSA1, P270, SMARCF1, hELD, hOSA1	Alzheimer disease, Breast neoplasms, Burkitt lymphoma, Adenoid cystic carcinoma, Hepatocellular carcinoma, Transitional cell carcinoma, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Cholangiocarcinoma, Bronchitis, Obstructive pulmonary disease, Clonal cytopenia of undetermined significance, Coffin-siris syndrome, Colorectal neoplasms, Endometrial neoplasms, Hyperlipidemia View all (17 more)
864	57492	ARID1B	AT-rich interaction domain 1B	6A3-5, BAF250B, BRIGHT, CSS1, DAN15, ELD/OSA1, MRD12, OSA2, P250R, SMARCF2	Alzheimer disease, Asthma, Attention deficit hyperactivity disorder, Autism, Breast cancer, Hepatocellular carcinoma, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Coffin-siris syndrome, Color vision deficiency, Desbuquois syndrome, Developmental disability, Epilepsy, Global developmental delay, Hypertrichosis, Intellectual developmental disorder View all (9 more)
865	196528	ARID2	AT-rich interaction domain 2	BAF200, CSS6, SMARCF3, ZIPZAP, p200	Atrial fibrillation, Hepatocellular carcinoma, Chronic diarrhea, Coffin-siris syndrome, Neurodevelopmental disorder, Prostatic neoplasms, Thrombocytopenia, Diabetes mellitus type 2
866	1820	ARID3A	AT-rich interaction domain 3A	BRIGHT, DRIL1, DRIL3, E2FBP1	Eczema, Biliary cirrhosis, Hepatocellular carcinoma, Dermatomyositis, Biliary cholangitis, Rheumatoid arthritis, Systemic lupus erythematosus
867	10620	ARID3B	AT-rich interaction domain 3B	BDP, DRIL2	Central nervous system cancer, Craniofacial microsomia, Endometriosis, Glioblastoma, Glioma, Iga nephropathy, Nephrotic syndrome, Squamous cell carcinoma, Diabetes mellitus type 2
868	138715	ARID3C	AT-rich interaction domain 3C	-	Hypertension
869	5926	ARID4A	AT-rich interaction domain 4A	RBBP-1, RBBP1, RBP-1, RBP1	Attention deficit hyperactivity disorder, Coronary artery disease, Metabolic syndrome, Migraine, Prostatic neoplasms, Substance abuse, Diabetes mellitus type 2
870	51742	ARID4B	AT-rich interaction domain 4B	BCAA, BRCAA1, RBBP1L1, RBP1L1, SAP180	Asthma, Adenoid cystic carcinoma

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