Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14181 to 14190 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14181
Tetraspanin 6
T245, TM4SF6, TSPAN-6
Gout

14182
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

14183
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, Liver cirrhosis, Metabolic syndrome, Respiratory system disease, Schizophrenia, Scoliosis
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14184
Tetraspanin 9
NET-5, NET5, PP1057
Asthma, Astrocytoma, Central nervous system cancer, Coronary artery disease, Cutaneous leishmaniasis, Diverticular disease, Endometriosis, Glioblastoma, Glioma, Major depressive disorder, Myocardial infarction, Oligodendroglioma, Psychiatric disorders, Amyotrophic lateral sclerosis

14185
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

14186
Translocator protein
BPBS, BZRP, DBI, IBP, MBR, PBR, PBS, PKBS, PTBR, TSPO1, mDRC, pk18
Bipolar disorder, Hepatic encephalopathy, Liver cirrhosis

14187
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

14188
Testis specific protein Y-linked 1
CT78, DYS14, TSPY, pJA923
Chromosome y microdeletion syndrome, Male infertility y chromosome microdeletion

14189
TSPY like 1
TSPYL
Gonadal dysgenesis

14190
TSPY like 2
CDA1, CINAP, CTCL, DENTT, HRIHFB2216, NP79, SE204, TSPX
Endometrial neoplasms