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"
901 to 910 of 1185 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

901
Tripartite motif containing 24
PTC6, RNF82, TF1A, TIF1, TIF1A, TIF1ALPHA, hTIF1
Hepatocellular carcinoma, Differentiated thyroid carcinoma, Prostatic neoplasms

902
Tripartite motif containing 25
EFP, RNF147, Z147, ZNF147
Osteoarthritis, Diabetes mellitus type 2

903
Tripartite motif containing 26
AFP, RNF95, ZNF173
Asthma, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Obstructive pulmonary disease, Hypothyroidism, Lung cancer, Major depressive disorder, Psoriatic arthritis, Rheumatoid arthritis, Sarcoidosis, Schizophrenia, Squamous cell carcinoma, Ulcerative colitis, Upper aerodigestive tract neoplasm

904
Tripartite motif containing 27
RFP, RNF76
Differentiated thyroid carcinoma, Hyperthyroidism, Lung cancer, Psoriasis, Schizophrenia

905
Tripartite motif containing 28
KAP1, PPP1R157, RNF96, TF1B, TIF1B, TIF1beta
Atherosclerosis, Childhood kidney wilms tumor, Colorectal neoplasms, Wilms tumor

906
Tripartite motif containing 29
ATDC
Glioma, Gout, Metabolic syndrome, Retinal detachment, Stroke, Diabetes mellitus type 2, Uveal melanoma, Vascular dementia

907
Tripartite motif containing 3
BERP, HAC1, RNF22, RNF97
Autism

908
Tripartite motif containing 31
C6orf13, HCG1, HCGI, RNF
Asthma, Autism, Autoimmune thyroid disease, Breast cancer, Obstructive pulmonary disease, Irritant dermatitis, Hepatocellular carcinoma, Insomnia, Major depressive disorder, Non-melanoma skin carcinoma, Prostate cancer, Psoriasis, Schizophrenia, Systemic lupus erythematosus, Diabetes mellitus type 1

909
Tripartite motif containing 32
BBS11, HT2A, LGMD2H, LGMDR8, TATIP
Limb girdle muscular dystrophy, Bardet-biedl syndrome, Limb-girdle muscular dystrophy, Muscular dystrophy, Myopathy, Retinitis pigmentosa, Sarcotubular myopathy

910
Tripartite motif containing 33
DDH4, ECTO, PTC7, RFG7, TF1G, TIF1G, TIF1GAMMA, TIFGAMMA
Anorexia nervosa, Autism, Color vision deficiency, Congenital hip dysplasia, Developmental dysplasia of the hip, Differentiated thyroid carcinoma, Hip dislocation-facial dysmorphism syndrome, Schizophrenia