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
13691 to 13700 of 15380 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

13691
Transmembrane protein 63C
C14orf171, CSC1, SPG87, hTMEM63C, hsCSC1
Spastic paraplegia, Bipolar disorder, Large artery stroke

13692
Transmembrane protein 64
-
Insomnia

13693
Transmembrane protein 65
-
Color vision deficiency, Mitochondrial disease

13694
Transmembrane protein 67
JBTS6, MECKELIN, MKS3, NPHP11, TNEM67
Anhydramnios, Hemolytic uremic syndrome, Bardet-biedl syndrome, Boichis syndrome, Cerebellar malformation, Ciliopathy, Coach syndrome, Congenital neurologic anomalies, Congenital ocular coloboma, Cystic kidney disease, Desbuquois syndrome, Aplasia of the vermis, Global developmental delay, Insomnia, Intellectual developmental disorder
View all (13 more)

13695
Transmembrane protein 68
DIESL, MGAT/DGAT
Migraine

13696
Transmembrane protein 69
C1orf154
Breast cancer

13697
Transmembrane protein 70
MC5DN2
Hepatocellular carcinoma, Cardiomyopathy, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial encephalocardiomyopathy, Mitochondrial encephalomyopathy, Neurodevelopmental disorder

13698
Transmembrane protein 71
-
Astrocytoma, Attention deficit hyperactivity disorder, Congestive heart failure, Heart failure, Hyperthyroidism, Substance abuse

13699
Transmembrane protein 72
C10orf127, KSP37
Pernicious anemia

13700
Transmembrane protein 74
NET36
Androgenetic alopecia, Obstructive pulmonary disease, Corneal neovascularization, Coronary artery disease, Dupuytren contracture, Female infertility, Myoclonic epilepsy, Keratitis, Metabolic syndrome, Oligodendroglioma, Diabetes mellitus type 2