Genes | GeDiPNet - Gene Disease Pathway & Associations

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13231 to 13240 of 15448 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
13231	64786	TBC1D15	TBC1 domain family member 15	RAB7-GAP	Alzheimer disease, Schizophrenia
13232	125058	TBC1D16	TBC1 domain family member 16	-	Color vision deficiency, Major depressive disorder, Migraine
13233	55296	TBC1D19	TBC1 domain family member 19	-	Cardiovascular disease, Coronary artery disease, Heart failure, Hypertension, Myocardial infarction, Schizophrenia
13234	55357	TBC1D2	TBC1 domain family member 2	PARIS-1, PARIS1, TBC1D2A	Duodenitis, Gastroenteritis, Hypertrophic cardiomyopathy, Post-traumatic stress disorder, Prostatic neoplasms
13235	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
13236	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
13237	25771	TBC1D22A	TBC1 domain family member 22A	C22orf4, HSC79E021	Colorectal cancer, Gastroenteritis, Ovarian cancer
13238	55633	TBC1D22B	TBC1 domain family member 22B	C6orf197	Central nervous system cancer, Glioblastoma, Glioma
13239	55773	TBC1D23	TBC1 domain family member 23	NS4ATP1, PCH11	Central nervous system cancer, Glioma, Pontocerebellar hypoplasia
13240	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)

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