Genes | GeDiPNet - Gene Disease Pathway & Associations

Dataset:

All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

13431 to 13440 of 15448 Genes

Show

	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
13431	7032	TFF2	Trefoil factor 2	SML1, SP	Color vision deficiency, Pancreatic cancer
13432	7033	TFF3	Trefoil factor 3	ITF, P1B, TFI	Color vision deficiency, Hepatitis animal, Kidney disease, Kidney failure, Mucositis
13433	10342	TFG	Trafficking from ER to golgi regulator	HMSNP, SPG57, TF6, TRKT3	Charcot-marie-tooth disease, Spastic paraplegia, Differentiated thyroid carcinoma, Extraskeletal myxoid chondrosarcoma, Hereditary motor and sensory neuropathies, Hereditary motor and sensory neuropathy, Hereditary spastic paraplegia
13434	24144	TFIP11	Tuftelin interacting protein 11	NTR1, STIP, STIP-1, Spp382, TIP39, bK445C9.6	Hypertension
13435	7035	TFPI	Tissue factor pathway inhibitor	EPI, LACI, TFI, TFPI1	Juvenile arthritis, Osteonecrosis of the femoral head, Avascular necrosis of bone, Basal cell carcinoma, Color vision deficiency, Coronary artery disease, Disseminated intravascular coagulation, Endometriosis, Hemophilia a, Hypoxia, Juvenile idiopathic arthritis, Liver cirrhosis, Lung cancer, Myocardial infarction, Osteonecrosis of medial femoral condyle View all (6 more)
13436	7980	TFPI2	Tissue factor pathway inhibitor 2	PP5, REF1, TFPI-2	Rheumatoid arthritis, Breast neoplasms, Hepatocellular carcinoma, Colorectal neoplasms, Liver cirrhosis, Melanoma, Osteoarthritis, Pancreatic neoplasms
13437	29844	TFPT	TCF3 fusion partner	FB1, INO80F, amida	Obesity, Retinitis pigmentosa
13438	7036	TFR2	Transferrin receptor 2	HFE3, TFRC2	Alzheimer disease, Beta thalassemia, Digenic hemochromatosis, Gastroesophageal reflux disease, Hemochromatosis, Hereditary hemochromatosis, Schizophrenia
13439	7037	TFRC	Transferrin receptor	CD71, IMD46, T9, TFR, TFR1, TR, TRFR, p90	Iron deficiency anemia, Asthma, Autism, Beta thalassemia, Breast neoplasms, Colorectal neoplasms, Combined immunodeficiency disease, Diabetes mellitus, Glioma, Immunodeficiency, Iron metabolism disorder, Lymphocytic b-cell leukemia, Lung neoplasms, Myocardial ischemia, Obesity View all (6 more)
13440	7038	TG	Thyroglobulin	AITD3, TGN	Ankylosing spondylitis, Anxiety disorder, Astrocytoma, Autoimmune disease, Autoimmune thyroid disease, B-cell acute lymphoblastic leukemia, Color vision deficiency, Major depressive disorder, Dwarfism, Thyroid dyshormonogenesis, Graves disease, Hashimoto disease, Hyperthyroidism, Hypothyroidism, Liver cirrhosis View all (10 more)

«««...1342 134313441345 1346...»»»