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 "E"
91 to 100 of 465 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

91
-
-
Cataract, Gastric cancer, Glaucoma, Gout, Nonalcoholic fatty liver disease, Osteoarthritis, Parkinson disease, Systemic lupus erythematosus

92
Ephrin A5
AF1, EFL5, EPLG7, GLC1M, LERK7, RAGS
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Cataract, Color vision deficiency, Gestational diabetes, Idiopathic pulmonary fibrosis, Insomnia, Major depressive disorder, Metabolic syndrome, Myelodysplastic syndrome, Post-traumatic stress disorder, Schizophrenia, Substance abuse
View all (1 more)

93
Ephrin B1
CFND, CFNS, EFB1, EFL3, EPLG2, Elk-L, LERK2
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Craniofrontonasal dysplasia, Craniosynostosis, Desbuquois syndrome, Dysphoric mood, Frontonasal dysplasia, Major depressive disorder, Obesity, Parkinson disease, Psychiatric disorders, Schizophrenia

94
Ephrin B2
EPLG5, HTKL, Htk-L, LERK5, ephrin-B2
Pulmonary agenesis, Liver neoplasms, Lung neoplasms, Schizophrenia

95
EFR3 homolog A
-
Eczema, Cerebral amyloid angiopathy, Color vision deficiency, Colorectal cancer, Huntington disease, Metabolic syndrome, Diabetes mellitus type 2

96
EFR3 homolog B
KIAA0953
Eczema, Breast cancer, Psoriasis, Schizophrenia, Tooth disease, Diabetes mellitus type 1, Diabetes mellitus type 2, Uterine fibroid

97
Embryonal Fyn-associated substrate
CAS3, CASS3, EFS1, EFS2, HEFS, SIN
Diabetes mellitus type 1, Diabetes mellitus type 2

98
Elongation factor Tu GTP binding domain containing 2
MFDGA, MFDM, SNRNP116, Snrp116, Snu114, U5-116KD
Asthma, Desbuquois syndrome, Endometriosis, Esophageal atresia, Genetic syndromic pierre robin syndrome, Global developmental delay, Hepatitis b, Mandibulofacial dysostosis, Microcephaly, Neurodevelopmental disorder, Oligodendroglioma

99
Epidermal growth factor
HOMG4, URG
Juvenile arthritis, Autism, Breast neoplasms, Hepatocellular carcinoma, Cleft palate, Dermatitis, Disorder of magnesium metabolism, Gastric ulcer, Genetic predisposition to disease, Glioblastoma, Juvenile idiopathic arthritis, Kidney disease, Liver cirrhosis, Major depressive disorder, Obesity
View all (5 more)

100
EGF like domain multiple 6
MAEG, W80
Multiple sclerosis, Omphalocele exstrophy imperforate anus