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"
1041 to 1050 of 1185 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1041
Tetraspanin 33
PEN, PEN., TSPAN-33
Major depressive disorder, Systemic lupus erythematosus

1042
Tetraspanin 4
NAG-2, NAG2, TETRASPAN, TM4SF7, TSPAN-4
Open angle glaucoma, Venous thromboembolism

1043
Tetraspanin 5
NET-4, NET4, TM4SF9, TSPAN-5
Dementia, Insomnia, Scoliosis, Stroke

1044
Tetraspanin 6
T245, TM4SF6, TSPAN-6
Gout

1045
Tetraspanin 7
A15, CCG-B7, CD231, DXS1692E, MRX58, MXS1, TALLA-1, TM4SF2, TM4SF2b, XLID58
Intellectual developmental disorder, x-linked, Intellectual developmental disorder, X-linked intellectual disability

1046
Tetraspanin 8
CO-029, TM4SF3
Androgenetic alopecia, Asthma, Atrial fibrillation, Bipolar disorder, Central nervous system cancer, Colorectal cancer, Creutzfeldt-jakob disease, Glioblastoma, Glioma, Intracranial hemorrhage, Metabolic syndrome, Respiratory system disease, Schizophrenia, Scoliosis, Diabetes mellitus type 2

1047
Tetraspanin 9
NET-5, NET5, PP1057
Asthma, Astrocytoma, Central nervous system cancer, Coronary artery disease, Diverticular disease, Endometriosis, Glioblastoma, Glioma, Major depressive disorder, Myocardial infarction, Oligodendroglioma, Psychiatric disorders, Amyotrophic lateral sclerosis

1048
Thrombospondin type laminin G domain and EAR repeats
C21orf29, DFNB98, ECTD14, STHAG10, TSP-EAR
Androgenetic alopecia, Nonsyndromic intellectual disability, Central nervous system cancer, Corticobasal degeneration, Deafness, Tooth agenesis, Ectodermal dysplasia, Glioblastoma, Glioma, Hearing impairment, Hearing loss, Nonsyndromic hearing loss

1049
Translocator protein
BPBS, BZRP, DBI, IBP, MBR, PBR, PBS, PKBS, PTBR, TSPO1, mDRC, pk18
Bipolar disorder, Hepatic encephalopathy

1050
TSPO associated protein 1
BZRAP1, DYT22, PBR-IP, PRAX-1, PRAX1, RIM-BP1, RIMBP1
Bardet-biedl syndrome, Cerebellar atrophy, Dementia, Dystonia, Dystonia, dopa-responsive, with or without hyperphenylalaninemia, Intellectual developmental disorder, Major depressive disorder, Multiple sclerosis, Neurodevelopmental disorder, Oligodendroglioma, , Venous thromboembolism