581
|
|
|
Embigin |
GP70 |
Curated: Alzheimer disease, Breast cancer, Coronary artery disease, Allergic contact dermatitis, Diabetes mellitus, Estrogen-receptor negative breast cancer, Major depressive disorder, Mood disorder, Movement disorder, Neurotic disorder, Periodic limb movement disorder, Schizophrenia, Squamous cell carcinoma, Diabetes mellitus type 2, Upper aerodigestive tract neoplasm
Unreviewed: Anemia, Basal cell carcinoma, Breast Cancer, Breast Carcinoma, Breast neoplasm, Cardiomyopathy, Colorectal Cancer, Congestive Heart Failure, Dermatitis, Glomerulonephritis, Heart Failure, Hereditary breast and ovarian cancer syndrome, Leukemia, Liver carcinoma, Lupus Erythematosus, Lupus Nephritis, Lupus Vulgaris, Lynch Syndrome, Malignant Neoplasm, Mammary Neoplasms, Myeloid leukemia, Myocarditis, Neoplasms, Nephritis, Pancreatic adenocarcinoma, Pancreatic cancer, Pancreatic carcinoma, Pericardial effusion, Prostate cancer, Prostatic Neoplasms, Triple negative breast cancer
|
582
|
|
|
Embigin pseudogene 1 |
- |
Curated: N/A
Unreviewed: Breast Cancer, Breast Carcinoma, Breast neoplasm, Eosinophilia, Nasopharyngeal Carcinoma
|
583
|
|
|
ER membrane protein complex subunit 1 |
CAVIPMR, KIAA0090 |
Curated: 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, complex neurodevelopmental disorder with motor features
Unreviewed: Aphasia, Astigmatism, Atrophy Of Corpus Callosum, Central Visual Impairment, Cerebellar Atrophy, Visual Impairment, And Psychomotor Retardation, Cerebellar diseases, Cerebral Atrophy, Complex partial epilepsy, Congenital anomalies of kidney and urinary tract, Developmental Delay, Developmental disability, Epilepsy, Esotropia, Global Developmental Delay-Visual Anomalies-Progressive Cerebellar Atrophy-Truncal Hypotonia Syndrome, Hyperopia, Hypoplasia Of Corpus Callosum, Imperforate anus, Intellectual developmental disorder, Mental retardation, Movement Disorders, Myopia, Optic Atrophy, Scoliosis, Speech Delay, Urinary bladder neoplasms, Visual disorder
|
584
|
|
|
EMC1 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: Cerebellar atrophy, Cerebellar Atrophy, Visual Impairment, And Psychomotor Retardation, Cerebral Atrophy, Congenital anomalies of kidney and urinary tract, Imperforate anus, Movement Disorders, Scoliosis, Speech Delay
|
585
|
|
|
ER membrane protein complex subunit 10 |
C19orf63, HSM1, HSS1, NEDDFAS |
Curated: Global developmental delay, Intellectual developmental disorder, Neurodevelopmental disorder, Non-specific syndromic intellectual disability
Unreviewed: Aphasia, Arachnodactyly, Asthenozoospermia, Astrocytoma, Cerebellar diseases, Congenital abnormalities, Congestive Heart Failure, Developmental disability, Glioblastoma, Glioma, Heart Failure, Hereditary Spherocytosis, Language development disorders, Malignant Neoplasm, Myocardial Infarction, Scoliosis, Seizures, Systemic lupus erythematosus
|
586
|
|
|
ER membrane protein complex subunit 2 |
KIAA0103, TTC35 |
Curated: Androgenetic alopecia, Obstructive pulmonary disease, Dupuytren contracture, Glioma, Oligodendroglioma, Schizophrenia
Unreviewed: Alopecia, Male Pattern, Androgenetic Alopecia, Breast neoplasm, Myeloid leukemia
|
587
|
|
|
ER membrane protein complex subunit 3 |
POB, TMEM111 |
Curated: N/A
Unreviewed: Cardiomyopathy, Leigh Syndrome, Leprosy, Leukemia, Syndromic microphthalmia
|
588
|
|
|
EMC3 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
589
|
|
|
ER membrane protein complex subunit 4 |
PIG17, TMEM85 |
Curated: Corpus callosum agenesis neuronopathy syndrome
Unreviewed: N/A
|
590
|
|
|
ER membrane protein complex subunit 6 |
RAB5IFL, TMEM93 |
Curated: N/A
Unreviewed: Cervical Cancer, Cervical Intraepithelial Neoplasia, Cervical Tumor, Cervix carcinoma, Gastric Cancer, Glioblastoma, Neoplasms, Uterine disease, Uterine neoplasm
|