Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4091 to 4100 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4091
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

4092
Essential meiotic structure-specific endonuclease subunit 2
SLX2B, gs125
Combined oxidative phosphorylation deficiency, Mitochondrial disease

4093
EMG1 N1-specific pseudouridine methyltransferase
C2F, Grcc2f, NEP1
Bowen-conradi syndrome

4094
EMI domain containing 1
EMI5, EMU1
Breast cancer, Clear cell renal cell carcinoma, Kidney cancer, Open angle glaucoma, Upper aerodigestive tract neoplasm

4095
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

4096
Elastin microfibril interfacer 2
EMILIN-2, FOAP-10
Atrial fibrillation, Bullous pemphigoid, Diabetes mellitus type 2

4097
Elastin microfibril interfacer 3
C20orf130, EMILIN5, dJ620E11.4
Bipolar disorder, Diabetes mellitus, Major depressive disorder

4098
EMAP like 1
BH, ELP79, EMAP, EMAP-1, EMAPL
Atrial fibrillation, Color vision deficiency, Coronary artery disease, Major depressive disorder

4099
EMAP like 2
ELP70, EMAP-2, EMAP2
Diabetes mellitus, Metabolic syndrome, Diabetes mellitus type 2

4100
EMAP like 3
ELP95, EMAP3, EMAP95
Retinitis pigmentosa