Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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10811 to 10820 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10811
RAB GTPase activating protein 1 like
HHL, TBC1D18
Asthma, Cholesteatoma, Obstructive pulmonary disease, Diverticular disease, Endometriosis, Gastroesophageal reflux disease, Liver cirrhosis, Major depressive disorder, Metabolic syndrome, Migraine, Mood disorder, Neurotic disorder, Osteoarthritis, Psychiatric disorders, Schizophrenia
View all (2 more)

10812
RAB guanine nucleotide exchange factor 1
RABEX5, RAP1, rabex-5
Alzheimer disease, Color vision deficiency, Multiple system atrophy, Stroke

10813
RAB, member of RAS oncogene family like 3
PNCA5
Pancreatic cancer, Obesity, Pancreatic neoplasms

10814
RAB, member RAS oncogene family like 6
C9orf86, PARF, RBEL1, pp8875
Intellectual developmental disorder, Meniere disease, Neurodevelopmental disorder

10815
Rac family small GTPase 1
MIG5, MRD48, Rac-1, TC-25, p21-Rac1
Alzheimer disease, Basal cell carcinoma, Hepatocellular carcinoma, Dilated cardiomyopathy, Congestive heart failure, Coronary artery disease, Major depressive disorder, Diabetes mellitus, Global developmental delay, Heart failure, Intellectual developmental disorder, Keratinocyte carcinoma, Liver disease, Melanoma, Metabolic syndrome
View all (4 more)

10816
Rac family small GTPase 2
EN-7, Gx, HSPC022, IMD73A, IMD73B, IMD73C, p21-Rac2
Celiac disease, Heart disease, Immunodeficiency, Myeloid leukemia, Liver cirrhosis, Lymphoma, Melanoma

10817
Rac family small GTPase 3
-
Basal cell carcinoma, Desbuquois syndrome, Facial dysmorphism syndrome, Intellectual developmental disorder, Myeloid leukemia, Neurodevelopmental disorder, Non-specific syndromic intellectual disability

10818
Rac GTPase activating protein 1
CDAN3B, CYK4, HsCYK-4, ID-GAP, MgcRacGAP, RCGAP1
Congenital dyserythropoietic anemia, Hepatocellular carcinoma, Polycystic ovary syndrome

10819
Receptor for activated C kinase 1
GNB2L1, Gnb2-rs1, H12.3, HLC-7, PIG21
Alzheimer disease, Bipolar disorder, Squamous cell carcinoma, Tourette syndrome, Mouth neoplasms, Neurodevelopmental disorder

10820
RAD17 checkpoint clamp loader component
CCYC, HRAD17, R24L, RAD17SP, RAD24
Multiple sclerosis