Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "T"
411 to 420 of 913 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

411
TNF receptor superfamily member 19
TAJ, TAJ-alpha, TRADE, TROY
Melanoma, Nasopharyngeal neoplasms, Nasopharyngeal cancer, Nasopharyngeal carcinoma

412
Tripartite motif containing 36
ANPH, ANPH1, HAPRIN, RBCC728, RNF98
Anencephaly, Aprosencephaly, Incomplete anencephaly, hemicrania, Spina bifida

413
Terminal nucleotidyltransferase 5A
C6orf37, FAM46A, OI18, XTP11
Breast carcinoma, Coronary artery disease, Micrognathism, Motor delay, Osteogenesis imperfecta, Osteoporosis

414
Taspase 1
C20orf13, SULEHS, dJ585I14.2
Developmental delay

415
TRNA methyltransferase 1
MRT68, TRM1, hTRM1
Developmental delay, Intellectual developmental disorder, Mental retardation, Microcephaly, Syndromic mental retardation, Synophrys

416
Tetratricopeptide repeat domain 27
-
Alopecia

417
Transmembrane protein 127
-
Adrenal gland pheochromocytoma, Aniridia, Hereditary cancer syndrome, Capillary hemangioma of retina, Carcinoid tumor of intestine, Carcinoma, Congestive heart failure, Cranial nerve compression, Endocrine gland cancer, Episodic paroxysmal anxiety, Extra-adrenal pheochromocytoma, Glomerulonephritis, Glomerulosclerosis, Hearing loss, Hemangioma
View all (16 more)

418
TRNA mitochondrial 2-thiouridylase
LCAL3, MTO2, MTU1, TRMT, TRMT1
Blood coagulation disorders, Cardiovascular abnormalities, Deafness, Developmental delay, Dysmorphic features, High palate, Hyperbilirubinemia, Liver failure, Macroglossia, Mitochondrial myopathy, Mitochondrial myopathy with reversible cytochrome c oxidase deficiency, Mitochondrial non-syndromic sensorineural deafness, Multiple congenital anomalies, Myopathy

419
Teneurin transmembrane protein 3
MCOPCB9, MCOPS15, ODZ3, TEN3, TNM3, Ten-m3, ten-3
Asthma, Microphthalmia with coloboma, Congenital coloboma of iris, Developmental delay, Esotropia, Macrotia, Mental retardation, Microcornea, Microphthalmos, Myocardial infarction, Pendular nystagmus, Ptosis, Retinal detachment, Schizophrenia, Sclerocornea

420
TBC1 domain family member 23
NS4ATP1, PCH11
Congenital clubfoot, Congenital ocular coloboma, Developmental delay, Dwarfism, Dysarthria, Dysphagia, Esotropia, Hyperopia, Hypoplasia of corpus callosum, Mental retardation, Macrotia, Microcephaly, Pontoneocerebellar hypoplasia, Pontocerebellar hypoplasia, Stereotyped behavior