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
13651 to 13660 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13651
Transmembrane protein 161B
FLB3342, PRO1313
Hypertension, Insomnia, Irritable bowel syndrome, Major depressive disorder, Neurodevelopmental disorder, Neurotic disorder, Psychiatric disorders, Schizophrenia, Tourette syndrome

13652
Transmembrane protein 163
DC29, HLD25, SLC30A11, SV31
Alzheimer disease, Asthma, Attention deficit hyperactivity disorder, Biliary cirrhosis, Melanoma, Endocrine neoplasms, Kidney cancer, Large artery stroke, Leukodystrophy, Hypomyelinating leukodystrophy, Neurotic disorder, Obstructive sleep apnea syndrome, Pancreatic cancer, Parkinson disease, Biliary cholangitis
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13653
Transmembrane protein 164
bB360B22.3
Scoliosis

13654
Transmembrane protein 165
CDG2K, FT27, GDT1, SLC64A1, TMPT27, TPARL
Carbohydrate deficient glycoprotein syndrome, Congenital disorder of glycosylation, Coronary artery disease, Desbuquois syndrome, Hirschsprung disease, Liver cirrhosis

13655
Transmembrane protein 167A
TMEM167, kish
Androgenetic alopecia, Colorectal cancer, Gastric cancer, Neonatal diabetes mellitus

13656
Transmembrane protein 169
-
Hodgkin lymphoma

13657
Transmembrane protein 17
-
Central nervous system cancer, Aplasia of the vermis, Gastrointestinal stromal tumor, Glioblastoma, Glioma, Meckel-gruber syndrome, Orofaciodigital syndrome, Prostate cancer, Schizophrenia

13658
Transmembrane protein 170A
TMEM170
Aortic stenosis, Aortic valve disease, Basal cell carcinoma, Obstructive pulmonary disease, Coronary artery disease, Crohn disease, Inflammatory bowel disease, Moyamoya disease, Diabetes mellitus type 2, Ulcerative colitis

13659
Transmembrane protein 170B
-
Attention deficit hyperactivity disorder, Autism, Melanoma, Schizophrenia, Stroke, Venous thromboembolism

13660
Transmembrane protein 171
PRP2
Cholecystolithiasis, Color vision deficiency, Coronary artery disease, Gout, Hyperuricemia, Nephrolithiasis, Orofacial cleft, Venous thromboembolism