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"
211 to 220 of 465 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

211
ER membrane protein complex subunit 2
KIAA0103, TTC35
Androgenetic alopecia, Obstructive pulmonary disease, Dupuytren contracture, Glioma, Oligodendroglioma, Schizophrenia

212
ER membrane protein complex subunit 4
PIG17, TMEM85
Corpus callosum agenesis neuronopathy syndrome

213
ER membrane protein complex subunit 8
C16orf2, C16orf4, COX4NB, FAM158B, NOC4
Diabetes mellitus type 2

214
Endomucin
EMCN2, MUC14
Appendicitis, Attention deficit hyperactivity disorder, Cerebral amyloid angiopathy, Eosinophilia, Insomnia, Iron metabolism disorder, Major depressive disorder, Metabolic syndrome, Colorectal adenoma, Mood disorder, Open angle glaucoma, Stroke

215
Emerin
EDMD, LEMD5, STA
Cardiomyopathy, Dilated cardiomyopathy, Emery-dreifuss muscular dystrophy, Heart disease, Hereditary motor and sensory neuropathies, Hypertrophic cardiomyopathy, Myopathy, Neuromuscular disease, X-linked emery-dreifuss muscular dystrophy

216
Essential meiotic structure-specific endonuclease subunit 2
SLX2B, gs125
Combined oxidative phosphorylation deficiency, Mitochondrial disease

217
EMG1 N1-specific pseudouridine methyltransferase
C2F, Grcc2f, NEP1
Bowen-conradi syndrome

218
EMI domain containing 1
EMI5, EMU1
Breast cancer, Clear cell renal cell carcinoma, Kidney cancer, Open angle glaucoma, Upper aerodigestive tract neoplasm

219
Elastin microfibril interfacer 1
ATBFS, EMI, EMILIN, HMN10, HMND10, gp115
Arterial tortuosity syndrome, Bone fragility with contractures, arterial rupture, and deafness, Congenital contractural arachnodactyly, Distal hereditary motor neuropathy, Osteoporosis-pseudoglioma syndrome

220
Elastin microfibril interfacer 2
EMILIN-2, FOAP-10
Atrial fibrillation, Bullous pemphigoid, Diabetes mellitus type 2