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 "A"
851 to 860 of 1165 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

851
Rho guanine nucleotide exchange factor 37
-
Asthma, Keratoconus, Major depressive disorder

852
Rho guanine nucleotide exchange factor 38
-
Autism, Breast cancer, Obstructive pulmonary disease, Cleft lip and palate, Estrogen-receptor negative breast cancer, Scoliosis, Diabetes mellitus type 2

853
Rho guanine nucleotide exchange factor 39
C9orf100, XGEF
Hepatocellular carcinoma, Diabetes mellitus type 2

854
Rho guanine nucleotide exchange factor 4
ASEF, ASEF1, GEF4, SMIM39, STM6
Congenital left-sided heart lesions, Colorectal adenoma

855
Rho guanine nucleotide exchange factor 40
SOLO
Atrial fibrillation, Neuroblastoma, Neurodevelopmental disorder

856
Rho guanine nucleotide exchange factor 5
GEF5, P60, TIM, TIM1
Breast cancer, Genetic predisposition to disease, Lung neoplasms, Ovarian cancer, Prostate cancer, Prostatic neoplasms

857
Rac/Cdc42 guanine nucleotide exchange factor 6
COOL2, Cool-2, MRX46, PIXA, alpha-PIX, alphaPIX
Autism, Congenital anomalies of the kidney and urinary tract, Childhood ataxia with cns hypomyelination, Neurodevelopmental disorder, Congenital anomalies of kidney and urinary tract, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Non-specific syndromic intellectual disability, X-linked intellectual disability

858
Rho guanine nucleotide exchange factor 7
BETA-PIX, COOL-1, COOL1, Nbla10314, P50, P50BP, P85, P85COOL1, P85SPR, PAK3, PIXB
Insomnia, Retinopathy of prematurity

859
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

860
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
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