Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
13671 to 13680 of 15380 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

13671
Transmembrane protein 38B
C9orf87, D4Ertd89e, OI14, TRIC-B, TRICB, bA219P18.1
Atypical femoral fracture, Autism, Bone fragility with contractures, arterial rupture, and deafness, Desbuquois syndrome, Osteogenesis imperfecta, Osteoporosis-pseudoglioma syndrome, Schizophrenia

13672
Transmembrane protein 39A
SUSR2
Biliary cirrhosis, Biliary cholangitis, Systemic lupus erythematosus

13673
Transmembrane protein 40
-
Major depressive disorder, Mitral valve prolapse, Schizophrenia, Hypertension

13674
Transmembrane protein 41B
-
Alzheimer disease, Coronary artery disease, Insomnia

13675
Transmembrane protein 42
-
Idiopathic pulmonary fibrosis, Major depressive disorder

13676
Transmembrane protein 43
ARVC5, ARVD5, AUNA3, EDMD7, EDMD7; AUNA2, LUMA
Arrhythmogenic right ventricular cardiomyopathy, Auditory neuropathy, Emery-dreifuss muscular dystrophy, Cardiomyopathy, Dilated cardiomyopathy, Arrhythmogenic right ventricular dysplasia, Hypertrophic cardiomyopathy, Left ventricular noncompaction cardiomyopathy, Long qt syndrome, Xeroderma pigmentosum

13677
Transmembrane protein 45A
DERP7, DNAPTP4
Astrocytoma, Central nervous system cancer, Glioma, Lung neoplasms

13678
Transmembrane protein 45B
-
Alzheimer disease, Obesity, Oligodendroglioma, Age-related macular degeneration

13679
Transmembrane protein 47
BCMP1, TM4SF10, VAB-9
Attention deficit hyperactivity disorder, Cerebellar atrophy, Dandy-walker syndrome, Global developmental delay, Multiple sclerosis

13680
Transmembrane protein 50A
IFNRC, SMP1
Autoimmune neurological syndrome