Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4121 to 4130 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4121
Epithelial membrane protein 1
CL-20, EMP-1, TMP
Alzheimer disease, Coronary artery disease, Liver cirrhosis, Major depressive disorder, Neuroblastoma, Prostatic neoplasms, Depression

4122
Epithelial membrane protein 2
XMP
Attention deficit hyperactivity disorder, Breast cancer, Obstructive pulmonary disease, Coronary artery disease, Eating disorder, Idiopathic steroid-resistant nephrotic syndrome, Genetic steroid-resistant nephrotic syndrome, Hereditary steroid-resistant nephrotic syndrome, Major depressive disorder, Nephrotic syndrome

4123
Epithelial membrane protein 3 (MAM blood group)
YMP
Dermatomyositis, Prostatic neoplasms

4124
EMSY transcriptional repressor, BRCA2 interacting
C11orf30, GL002
Alzheimer disease, Ankylosing spondylitis, Asthma, Eczema, Basal cell carcinoma, Breast neoplasms, Obstructive pulmonary disease, Crohn disease, Dementia, Dermatitis, Atopic dermatitis, Eosinophilia, Inflammatory bowel disease, Inflammatory skin disease, Irritable bowel syndrome
View all (16 more)

4125
Empty spiracles homeobox 1
-
Schizoaffective disorder, Schizophrenia

4126
Empty spiracles homeobox 2
-
Aortic stenosis, Aortic valve disease, Conduct disorder, Congenital hypogonadotropic hypogonadism, Endometriosis, Female infertility, Gout, Lung neoplasms, Obesity, Schizencephaly, Schizophrenia, Scoliosis

4127
Engrailed homeobox 1
ENDOVESLB
Adenoid cystic carcinoma, Intestinal infectious disease, Nervous system disease, Parkinson disease, Salivary gland neoplasms, Schizophrenia

4128
Engrailed homeobox 2
-
Autism, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Schizophrenia

4129
ENAH actin regulator
ENA, MENA, NDPP1
Color vision deficiency, Myeloid leukemia, Major depressive disorder, Neurotic disorder, Obesity

4130
Enamelin
ADAI, AI1C, AIH2
Amelogenesis imperfecta, Coronary artery disease, Dentin dysplasia, Dentinogenesis imperfecta