Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
10721 to 10730 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10721
RAB27A, member RAS oncogene family
GS2, HsT18676, RAB27, RAM
Autoinflammatory syndrome, Central nervous system cancer, Glioma, Griscelli syndrome, Melanoma, Urinary bladder neoplasms

10722
RAB27B, member RAS oncogene family
C25KG
Anxiety disorder, Asthma, Bipolar disorder, Gestational diabetes, Major depressive disorder, Metabolic syndrome, Mood disorder, Neurotic disorder, Obesity, Oligodendroglioma, Schizophrenia, Diabetes mellitus type 2, Urinary bladder neoplasms, Uveal melanoma

10723
RAB28, member RAS oncogene family
CORD18
Basal cell carcinoma, Cone dystrophy, Cone-rod dystrophy, Optic atrophy, Retinitis pigmentosa

10724
RAB29, member RAS oncogene family
RAB7L, RAB7L1
Atrial fibrillation, Essential tremor, Hearing loss, Metabolic syndrome, Nephrolithiasis, Parkinson disease, Prostate cancer, Diabetes mellitus type 2

10725
RAB2A, member RAS oncogene family
LHX, RAB2
Autoimmune thyroid disease, Hypothyroidism, Major depressive disorder, Polycystic ovary syndrome, Systemic sclerosis

10726
RAB31, member RAS oncogene family
Rab22B
Alzheimer disease, Bone fracture, Colorectal cancer, Dupuytren contracture, Lung cancer

10727
RAB32, member RAS oncogene family
PARK26
Allergic contact dermatitis, Differentiated thyroid carcinoma, Parkinson disease

10728
RAB33A, member RAS oncogene family
RabS10
Auditory neuropathy, Autism, Beta-hydroxyisobutyryl-coa deacylase deficiency, Charcot-marie-tooth disease, Combined oxidative phosphorylation deficiency, Congenital ear anomaly, Cowchock syndrome, Deafness, x-linked, Leukodystrophy, Peripheral neuropathy, Hearing loss, Spondyloepimetaphyseal dysplasia

10729
RAB33B, member RAS oncogene family
SMC2
Desbuquois syndrome, Smith-mccort dysplasia

10730
RAB34, member RAS oncogene family
NARR, OFD20, RAB39, RAH
Jeune thoracic dystrophy, Orofaciodigital syndrome