Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4101 to 4110 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4101
Embigin
GP70
Alzheimer disease, Breast cancer, Coronary artery disease, Allergic contact dermatitis, Diabetes mellitus, Estrogen-receptor negative breast cancer, Liver cirrhosis, Major depressive disorder, Mood disorder, Movement disorder, Neurotic disorder, Periodic limb movement disorder, Schizophrenia, Squamous cell carcinoma, Diabetes mellitus type 2
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4102
ER membrane protein complex subunit 1
CAVIPMR, KIAA0090
Retinitis pigmentosa, Congenital anomalies of the kidney and urinary tract, Cerebellar atrophy, Cerebellar atrophy with seizures and variable developmental delay, Neurodevelopmental disorder, Global developmental delay, Obesity

4103
ER membrane protein complex subunit 10
C19orf63, HSM1, HSS1, NEDDFAS
Global developmental delay, Intellectual developmental disorder, Neurodevelopmental disorder, Non-specific syndromic intellectual disability

4104
ER membrane protein complex subunit 2
KIAA0103, TTC35
Androgenetic alopecia, Obstructive pulmonary disease, Dupuytren contracture, Glioma, Oligodendroglioma, Schizophrenia

4105
ER membrane protein complex subunit 4
PIG17, TMEM85
Corpus callosum agenesis neuronopathy syndrome

4106
ER membrane protein complex subunit 8
C16orf2, C16orf4, COX4NB, FAM158B, NOC4
Diabetes mellitus type 2

4107
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

4108
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

4109
Essential meiotic structure-specific endonuclease subunit 2
SLX2B, gs125
Combined oxidative phosphorylation deficiency, Mitochondrial disease

4110
EMG1 N1-specific pseudouridine methyltransferase
C2F, Grcc2f, NEP1
Bowen-conradi syndrome