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

2821 to 2830 of 12229 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
2821	192668	CYS1	Cystin 1	-	Chronic obstructive pulmonary disease, Bronchitis
2822	192669	AGO3	Argonaute RISC catalytic component 3	EIF2C3	Barrett esophagus
2823	192683	SCAMP5	Secretory carrier membrane protein 5	-	Autism, Developmental delay, Lupus erythematosus, Mental retardation
2824	1933	EEF1B2	Eukaryotic translation elongation factor 1 beta 2	EEF1B, EEF1B1, EF1B	Breast cancer, Mammary neoplasms, Breast carcinoma, Mental retardation, Marfan syndrome
2825	1936	EEF1D	Eukaryotic translation elongation factor 1 delta	EF-1D, EF1D, FP1047, NEDTCHAL	Acne
2826	1938	EEF2	Eukaryotic translation elongation factor 2	EEF-2, EF-2, EF2, SCA26	Adenocarcinoma, Arthritis, Breast cancer, Mammary neoplasms, Breast carcinoma, Carcinoma, Cerebellar ataxia, Cerebellar atrophy, Chromophobe carcinoma, Dysarthria, Lung neoplasms, Lung cancer, Marfan syndrome, Nystagmus, Osteoarthrosis deformans View all (3 more)
2827	1942	EFNA1	Ephrin A1	B61, ECKLG, EFL1, EPLG1, GMAN, LERK-1, LERK1, TNFAIP4	Breast cancer, Mammary neoplasms, Breast carcinoma, Marfan syndrome
2828	1946	EFNA5	Ephrin A5	AF1, EFL5, EPLG7, GLC1M, LERK7, RAGS	Schizophrenia
2829	1947	EFNB1	Ephrin B1	CFND, CFNS, EFB1, EFL3, EPLG2, Elk-L, LERK2	Acrocephaly, Agenesis of corpus callosum, Brachycephaly, Brachydactyly, Camptodactyly of fingers, Congenital diaphragmatic hernia, Congenital exomphalos, Breast hypoplasia, Congenital pectus excavatum, Coronal craniosynostosis, Craniofrontonasal dysplasia, Craniosynostosis, Cryptorchidism, Developmental delay, Dwarfism View all (23 more)
2830	1948	EFNB2	Ephrin B2	EPLG5, HTKL, Htk-L, LERK5, ephrin-B2	Congenital lung agenesis, Liver neoplasms, Liver cancer, Lung agenesis, Lung neoplasms, Lung cancer, Pulmonary hypoplasia, Schizophrenia, Unilateral lobar pulmonary agenesis

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