Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "T"
121 to 130 of 1188 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

121
Tubulin folding cofactor D
PEBAT, SSD-1, tfcD
Astrocytoma, Central nervous system cancer, Coronary artery disease, Degenerative disorder, Developmental disability, Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome, Glioblastoma, Glioma, Intellectual developmental disorder, Cortical development malformation, Microcephaly, Neurodegenerative disorder, Optic atrophy, Seborrhea-like dermatitis with psoriasiform elements, Seborrheic keratosis
View all (3 more)

122
Tubulin folding cofactor E
HRD, KCS, KCS1, PEAMO, pac2
Kenny-caffey syndrome, Kenny caffey syndrome, Craniofacial abnormalities, Desbuquois syndrome, Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome, Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome, Obesity, Oligodendroglioma, Osteosclerosis, Pituitary stalk interruption syndrome, Sanjad-sakati syndrome, Diabetes mellitus type 2

123
Tubulin folding cofactor E like
El, LRRC35
Hearing loss

124
TBCEL-TECTA readthrough
-
Autoimmune musculoskeletal system disorder, Congenital ear anomaly, Congenital sensorineural hearing loss, Deafness, Hearing impairment, Meniere disease, Hearing loss, Nonsyndromic hearing loss, Systemic lupus erythematosus

125
TBC1 domain containing kinase
FERRY1, Fy-1, HSPC302, IHPRF3, TBCKL
Congenital neurologic anomalies, Global developmental delay, Intellectual developmental disorder, Major depressive disorder, Neurodevelopmental disorder, Oligodendroglioma, Ventricular septal defect

126
TANK binding kinase 1
AIARV, FTDALS4, IIAE8, NAK, T2K
Amyotrophic lateral sclerosis, Autoinflammation with arthritis and vasculitis, Brain disease, Corticobasal syndrome, Frontotemporal dementia with or without amyotrophic lateral sclerosis, Frontotemporal dementia with motor neuron disease, Motor neuron disease, Spastic paraplegia

127
TBK1 binding protein 1
ProSAPiP2, SINTBAD
Ankylosing spondylitis, Diverticular disease, Hypothyroidism, Multiple sclerosis

128
Transducin beta like 1 X-linked
CHNG8, EBI, SMAP55, TBL1
Autism, Breast cancer, Coronary artery disease, Dermatophytosis, Diabetes mellitus type 2, Uterine fibroid

129
TBL1X/Y related 1
C21, DC42, IRA1, MRD41, TBLR1
Alzheimer disease, Asthma, Cholesteatoma, Obstructive pulmonary disease, Neurodevelopmental disorder, Intellectual developmental disorder, Mastocytosis, Mesothelioma, Non-specific syndromic intellectual disability, Prostatic neoplasms, Respiratory system disease, Schizophrenia, Urticaria

130
Transducin beta like 1 Y-linked
DFNY2, TBL1
Autism, Deafness, y-linked