Genes | GeDiPNet - Gene Disease Pathway & Associations

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1051 to 1060 of 12229 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1051	1057	CELP	Carboxyl ester lipase pseudogene	CELL, cell1, cell2, cell3	Pancreatitis
1052	10574	CCT7	Chaperonin containing TCP1 subunit 7	CCTETA, CCTH, NIP7-1, TCP1ETA	Gastric cancer, Stomach neoplasms
1053	105751187	LRP1-AS	LRP1 antisense RNA	-	Colonic neoplasms, Colorectal cancer, Colorectal neoplasms
1054	105755953	LINC02676	Long intergenic non-protein coding RNA 2676	-	Tetralogy of fallot
1055	10576	CCT2	Chaperonin containing TCP1 subunit 2	99D8.1, CCT-beta, CCTB, HEL-S-100n, PRO1633, TCP-1-beta	Myocardial infarction, Osteoporosis
1056	10577	NPC2	NPC intracellular cholesterol transporter 2	EDDM1, HE1	Alveolar proteinosis, Cataplexy, Dementia, Developmental delay, Dysarthria, Dysphagia, Fetal ascites, Mental retardation, Niemann-pick disease, Psychosis, Respiratory failure, Sea-blue histiocytosis, Stereotyped behavior, Supranuclear gaze palsy
1057	10579	TACC2	Transforming acidic coiled-coil containing protein 2	AZU-1, ECTACC	Breast cancer, Breast carcinoma, Leukemia, Myopia
1058	1058	CENPA	Centromere protein A	CENP-A, CenH3	Liver carcinoma
1059	10580	SORBS1	Sorbin and SH3 domain containing 1	CAP, FLAF2, R85FL, SH3D5, SH3P12, SORB1	Breast cancer, Cardiovascular diseases, Diabetes mellitus, Diabetic nephropathy, Leukemia
1060	10584	COLEC10	Collectin subfamily member 10	3MC3, CL-10, CL-34, CLL1	3mc syndrome, Accessory nipple, Asthma, Basal cell neoplasm, Blepharophimosis, Carcinoma, Clinodactyly, Congenital exomphalos, Craniofacial ulnar renal syndrome, Craniosynostosis, Cryptorchidism, Dwarfism, Hypospadias, Liver carcinoma, Malpuech facial clefting syndrome View all (8 more)

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