Genes | GeDiPNet - Gene Disease Pathway & Associations

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14171 to 14180 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
14171	158135	TTLL11	Tubulin tyrosine ligase like 11	C9orf148, C9orf20, TTLL11-IT1, bA244O19.1	Alzheimer disease, Metabolic syndrome, Periodontitis, Schizophrenia, Diabetes mellitus type 2
14172	26140	TTLL3	Tubulin tyrosine ligase like 3	HOTTL	Ocular hypertension
14173	23093	TTLL5	Tubulin tyrosine ligase like 5	CORD19, KIAA0998, STAMP	Juvenile arthritis, Carpal tunnel syndrome, Central areolar choroidal dystrophy, Central nervous system cancer, Cone-rod dystrophy, Glioblastoma, Glioma, Juvenile idiopathic arthritis, Large artery stroke, Open angle glaucoma, Optic atrophy, Oligoarticular juvenile idiopathic arthritis, Retinitis pigmentosa, Teratozoospermia
14174	284076	TTLL6	Tubulin tyrosine ligase like 6	TTL.6	Bipolar disorder, Myocardial infarction, Schizophrenia, Diabetes mellitus type 2
14175	79739	TTLL7	Tubulin tyrosine ligase like 7	-	Attention deficit hyperactivity disorder, Autism, Metabolic syndrome, Obesity, Osteoarthritis, Diabetes mellitus type 2
14176	164714	TTLL8	Tubulin tyrosine ligase like 8	-	Duodenal ulcer
14177	164395	TTLL9	Tubulin tyrosine ligase like 9	C20orf125	Liver neoplasms, Male infertility single gene azoospermia, Polycystic ovary syndrome
14178	7273	TTN	Titin	CMD1G, CMH9, CMPD4, CMYO5, CMYP5, EOMFC, HMERF, LGMD2J, LGMDR10, MYLK5, SALMY, TMD	Arrhythmogenic right ventricular cardiomyopathy, Atrial fibrillation, Atrial flutter, Centronuclear myopathy, Limb girdle muscular dystrophy, Brugada syndrome, Cardiac arrhythmia, Cardioembolic stroke, Cardiomyopathy, Dilated cardiomyopathy, Cerebral palsy, Progressive contractures limb-girdle weakness muscle dystrophy syndrome, Multiminicore myopathy, Atrioventricular block, Conduction disorder of the heart View all (29 more)
14179	7274	TTPA	Alpha tocopherol transfer protein	ATTP, AVED, TTP1, alphaTTP	Ataxia with vitamin e deficiency, Atherosclerosis, Vitamin e deficiency, Headache, Nervous system disease, Optic atrophy, Retinitis pigmentosa, Urination disorders, Visual disorder
14180	7276	TTR	Transthyretin	ATTR, CTS, CTS1, HEL111, HsT2651, PALB, TBPA, TTN	Alzheimer disease, Amyloid neuropathy, Amyloid polyneuropathy, Amyloidosis, Brugada syndrome, Cardiomyopathy, Carpal tunnel syndrome, Charcot-marie-tooth disease, Conduction disorder of the heart, Major depressive disorder, Dystransthyretinemic euthyroidal hyperthyroxinemia, Heart disease, Hyperthyroxinemia, Kidney failure, Lung neoplasms View all (3 more)

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