Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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13251 to 13260 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13251
TBC1 domain family member 9
GRAMD9, MDR1
Alzheimer disease, Attention deficit hyperactivity disorder, Liver cirrhosis, Prostate cancer

13252
Tubulin folding cofactor A
-
Cardiomyopathy, Hypertrophic cardiomyopathy, Multiple myeloma, Pelvic organ prolapse, Psychiatric disorders

13253
Tubulin folding cofactor C
CFC
Bipolar disorder, Stroke

13254
TBCC domain containing 1
-
Male infertility single gene azoospermia

13255
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)

13256
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

13257
Tubulin folding cofactor E like
El, LRRC35
Hearing loss

13258
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

13259
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

13260
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