Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "T"

101 to 110 of 1188 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
101	128637	TBC1D20	TBC1 domain family member 20	C20orf140, WARBM4	Apert syndrome, Congenital malformation syndromes predominantly affecting facial appearance, Cryptophthalmos syndrome, Cyclocephaly, Goldenhar syndrome, Mobius syndrome, Orofaciodigital syndrome, Warburg micro syndrome
102	161514	TBC1D21	TBC1 domain family member 21	MgcRabGAP	Bipolar disorder, Kidney disease, Color vision deficiency, Conotruncal cardiac defect, Diabetic neuropathy, Insomnia, Irritable bowel syndrome, Major depressive disorder, Metabolic syndrome, Myopathy, Neurotic disorder, Oligodendroglioma, Scoliosis, Diabetes mellitus type 2
103	25771	TBC1D22A	TBC1 domain family member 22A	C22orf4, HSC79E021	Colorectal cancer, Gastroenteritis, Ovarian cancer
104	55633	TBC1D22B	TBC1 domain family member 22B	C6orf197	Central nervous system cancer, Glioblastoma, Glioma
105	55773	TBC1D23	TBC1 domain family member 23	NS4ATP1, PCH11	Central nervous system cancer, Glioma, Pontocerebellar hypoplasia
106	57465	TBC1D24	TBC1 domain family member 24	DEE16, DFNA65, DFNB86, DOORS, EIEE16, EIM, EPRPDC, FIME, TLDC6	Auditory neuropathy, Isolated sensorineural deafness, Nonsyndromic hearing loss, Nonsyndromic intellectual disability, Cerebellar atrophy, Congenital neurologic anomalies, Deafness, Deafness with congenital onychodystrophy, Deafness, onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome, Developmental and epileptic encephalopathy, Digitrenocerebral syndrome, Doors syndrome, Dysarthria, Epilepsy of infancy with migrating focal seizures, Infantile myoclonic epilepsy View all (12 more)
107	4943	TBC1D25	TBC1 domain family member 25	MG81, OATL1	Mood disorder
108	23102	TBC1D2B	TBC1 domain family member 2B	NEDSGO	Neurodevelopmental disorder, Psychiatric disorders
109	93594	TBC1D31	TBC1 domain family member 31	Gm85, WDR67	Congenital anomalies of kidney and urinary tract, Diabetic neuropathy, Scoliosis
110	221322	TBC1D32	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

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