Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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13181 to 13190 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13181
TBC1 domain family member 25
MG81, OATL1
Mood disorder

13182
TBC1 domain family member 2B
NEDSGO
Neurodevelopmental disorder, Psychiatric disorders

13183
TBC1 domain family member 31
Gm85, WDR67
Congenital anomalies of kidney and urinary tract, Diabetic neuropathy, Scoliosis

13184
TBC1 domain family member 32
ALHSA, BROMI, C6orf170, C6orf171, OFD9, RP100
Atrial fibrillation, Ciliopathy, Colorectal cancer, Hypopituitarism, Joubert syndrome, Orofaciodigital syndrome, Partial epilepsy, Retinitis pigmentosa

13185
TBC1 domain family member 4
AS160, NIDDM5
Diabetes mellitus type 2, Oligodendroglioma, Oral cavity carcinoma, Venous thromboembolism

13186
TBC1 domain family member 5
-
Anorexia nervosa, Eczema, Attention deficit hyperactivity disorder, Breast cancer, Central nervous system cancer, Diabetic neuropathy, Duchenne muscular dystrophy, Glioblastoma, Glioma, Lung cancer, Major depressive disorder, Parkinson disease, Proliferative diabetic retinopathy, Prostate cancer, Willis-ekbom disease
View all (6 more)

13187
TBC1 domain family member 7
MGCPH, PIG51, TBC7
Cardiovascular disease, Coronary artery disease

13188
-
-
Developmental and epileptic encephalopathy

13189
TBC1 domain family member 8
AD3, GRAMD8, HBLP1, TBC1D8A, VRP
Gout, Osteoporosis, Progressive supranuclear palsy, Rheumatoid arthritis

13190
TBC1 domain family member 8B
GRAMD8B, NPHS20
Idiopathic steroid-resistant nephrotic syndrome, Genetic steroid-resistant nephrotic syndrome, Hereditary steroid-resistant nephrotic syndrome, Nephrotic syndrome, Pancreatitis