Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11651 to 11660 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11651
SEC23 homolog A, COPII component
CLSD, hSec23A
Craniolenticulosutural dysplasia, Insomnia, Osteoarthritis

11652
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

11653
SEC23 interacting protein
MSTP053, P125, P125A, iPLA1A, iPLA1beta
Lymphocytic leukemia, Parkinson disease, Diabetes mellitus type 2

11654
SEC24 homolog A, COPII component
-
Schizophrenia

11655
SEC24 homolog B, COPII component
SEC24
Alzheimer disease

11656
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

11657
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

11658
SEC31 homolog A, COPII component
ABP125, ABP130, HPBKS, HSPC275, HSPC334, NEDSOSB, SEC31L1
Asthma, Diffuse large b-cell lymphoma, Neurodevelopmental disorder, Oligodendroglioma

11659
SEC61 translocon subunit alpha 1
ADTKD5, CVID15, HNFJ4, HSEC61, SEC61, SEC61A
Tubulointerstitial kidney disease, Common variable immunodeficiency, Craniofacial abnormalities, Hyperuricemic nephropathy, Neutropenia, Severe congenital neutropenia, Polycystic liver disease, Prostate cancer, Congenital neutropenia

11660
SEC61 translocon subunit alpha 2
-
Prostate cancer, Diabetes mellitus type 2