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
13731 to 13740 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13731
Transmembrane protein 38A
TRIC-A, TRICA
Autism

13732
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

13733
Transmembrane protein 39A
SUSR2
Biliary cirrhosis, Biliary cholangitis, Systemic lupus erythematosus

13734
Transmembrane protein 40
-
Major depressive disorder, Mitral valve prolapse, Schizophrenia, Hypertension

13735
Transmembrane protein 41B
-
Alzheimer disease, Coronary artery disease, Insomnia

13736
Transmembrane protein 42
-
Idiopathic pulmonary fibrosis, Major depressive disorder

13737
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, Liver cirrhosis, Long qt syndrome, Xeroderma pigmentosum

13738
Transmembrane protein 45A
DERP7, DNAPTP4
Astrocytoma, Central nervous system cancer, Glioma, Lung neoplasms

13739
Transmembrane protein 45B
-
Alzheimer disease, Obesity, Oligodendroglioma, Age-related macular degeneration

13740
Transmembrane protein 47
BCMP1, TM4SF10, VAB-9
Attention deficit hyperactivity disorder, Cerebellar atrophy, Dandy-walker syndrome, Global developmental delay, Multiple sclerosis