Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11701 to 11710 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11701
SEC16 homolog A, endoplasmic reticulum export factor
KIAA0310, SEC16L, p250
Basal cell carcinoma, Cutaneous squamous cell carcinoma, Inflammatory bowel disease, Non-small cell lung carcinoma, Squamous cell carcinoma, Diabetes mellitus type 2

11702
SEC16 homolog B, endoplasmic reticulum export factor
LZTR2, PGPR-p117, RGPR, RGPR-p117, SEC16S
Amyotrophic lateral sclerosis, Attention deficit hyperactivity disorder, Polycystic liver disease, Body weight, Bone fragility with contractures, arterial rupture, and deafness, Breast cancer, Color vision deficiency, Gout, Metabolic syndrome, Obesity, Osteoarthritis, Osteoporosis-pseudoglioma syndrome, Schizoaffective disorder, Schizophrenia, Scoliosis
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11703
SEC22 homolog A, vesicle trafficking protein
SEC22L2
Diabetes mellitus type 2

11704
SEC23 homolog A, COPII component
CLSD, hSec23A
Craniolenticulosutural dysplasia, Insomnia, Osteoarthritis

11705
SEC23 homolog B, COPII component
CDA-II, CDAII, CDAN2, CWS7, HEMPAS, hSec23B
Congenital dyserythropoietic anemia, Central nervous system cancer, Cowden disease, Glioblastoma, Glioma, Neurotic disorder

11706
SEC23 interacting protein
MSTP053, P125, P125A, iPLA1A, iPLA1beta
Lymphocytic leukemia, Parkinson disease, Diabetes mellitus type 2

11707
SEC24 homolog A, COPII component
-
Schizophrenia

11708
SEC24 homolog B, COPII component
SEC24
Alzheimer disease

11709
SEC24 homolog C, COPII component
-
22q11.2 deletion syndrome, Bipolar disorder, Developmental and epileptic encephalopathy, Digeorge syndrome, Major depressive disorder, Metabolic syndrome, Diabetes mellitus type 2, Depression

11710
SEC24 homolog D, COPII component
CLCRP2
Bone fragility with contractures, arterial rupture, and deafness, Cole-carpenter syndrome, Desbuquois syndrome, Epilepsy, Intellectual developmental disorder, Myocardial infarction, Osteogenesis imperfecta, Osteoporosis-pseudoglioma syndrome, Hypertension