Genes | GeDiPNet - Gene Disease Pathway & Associations

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3501 to 3510 of 12229 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
3501	23212	RRS1	Regulator of ribosome synthesis 1	-	Lung adenocarcinoma
3502	23213	SULF1	Sulfatase 1	SULF-1	Mesomelia-synostoses syndrome, Ovarian neoplasm, Ovarian cancer
3503	23215	PRRC2C	Proline rich coiled-coil 2C	BAT2-iso, BAT2D1, BAT2L2, XTP2	Alzheimer disease
3504	23216	TBC1D1	TBC1 domain family member 1	TBC, TBC1	Arthritis, Congenital anomalies of kidney and urinary tract, Obesity
3505	23217	ZFR2	Zinc finger RNA binding protein 2	KIAA1086	Obesity
3506	23218	NBEAL2	Neurobeachin like 2	BDPLT4, GPS	Gray platelet syndrome, Myelodysplasia, Myelodysplastic syndrome, Platelet alpha-granule deficiency, Myelofibrosis
3507	2322	FLT3	Fms related receptor tyrosine kinase 3	CD135, FLK-2, FLK2, STK1	Autoimmune diseases, Burkitt`s lymphoma, Csf pleocytosis, Erythroleukemia, Hypothyroidism, Lymphoblastic leukemia, Leukemia, Lymphocytic leukemia, Mixed phenotype leukemia, Myeloblastic leukemia with maturation, Myeloblastic leukemia without maturation, Myeloid leukemia, Myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22), Myeloid leukemia with t(8;21)(q22;q22) translocation, Myelomonocytic leukemia View all (2 more)
3508	23220	DTX4	Deltex E3 ubiquitin ligase 4	RNF155	Adenocarcinoma, Pancreatic ductal carcinoma
3509	23221	RHOBTB2	Rho related BTB domain containing 2	DBC2, DEE64, EIEE64, p83	Cerebellar hypoplasia, Cerebral cortical atrophy, Congenital epicanthus, Developmental delay, Developmental regression, Epileptic encephalopathy, Hypoplasia of corpus callosum, Macrotia, Mental retardation, Micrognathism, Movement disorders, Nervous system diseases, Phakomatosis pigmentovascularis, Renal carcinoma, Rett syndrome View all (2 more)
3510	23224	SYNE2	Spectrin repeat containing nuclear envelope protein 2	EDMD5, KASH2, NUA, NUANCE, Nesp2, Nesprin-2, SYNE-2, TROPH	Amyotrophy, Atrial fibrillation, Atrioventricular block, Autism, Breast cancer, Cardiomyopathy, Chromophobe carcinoma, Congenital muscular dystrophy, Congenital pectus excavatum, Elbow flexion contracture, Emery-dreifuss muscular dystrophy, Emery-dreifuss muscular dystrophy, x-linked, Hypertrophic cardiomyopathy, Ichthyosis, Kidney disease View all (16 more)

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