Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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13751 to 13760 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13751
Transmembrane protein 63B
C6orf110, DEE118, hTMEM63B
Neurodevelopmental disorder, Developmental and epileptic encephalopathy, Non-specific syndromic intellectual disability

13752
Transmembrane protein 63C
C14orf171, CSC1, SPG87, hTMEM63C, hsCSC1
Spastic paraplegia, Bipolar disorder, Large artery stroke

13753
Transmembrane protein 64
-
Insomnia

13754
Transmembrane protein 65
-
Color vision deficiency, Liver cirrhosis, Mitochondrial disease

13755
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)

13756
Transmembrane protein 68
DIESL, MGAT/DGAT
Migraine

13757
Transmembrane protein 69
C1orf154
Breast cancer

13758
Transmembrane protein 70
MC5DN2
Hepatocellular carcinoma, Cardiomyopathy, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial encephalocardiomyopathy, Mitochondrial encephalomyopathy, Neurodevelopmental disorder

13759
Transmembrane protein 71
-
Astrocytoma, Attention deficit hyperactivity disorder, Congestive heart failure, Heart failure, Hyperthyroidism, Substance abuse

13760
Transmembrane protein 72
C10orf127, KSP37
Pernicious anemia