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
13631 to 13640 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13631
Transmembrane protein 127
-
Clear cell papillary renal cell carcinoma, Pheochromocytoma, Diabetes mellitus type 2

13632
Transmembrane protein 128
-
Central vertigo, Peripheral vertigo, Vestibular disease, Vitiligo

13633
Transmembrane protein 131
CC28, PRO1048, RW1, YR-23
Autoimmune disease, Bipolar disorder, Colorectal cancer, Dyslexia, Endometriosis, Hypothyroidism, Insomnia, Scoliosis

13634
Transmembrane 131 like
KIAA0922
Androgenetic alopecia, Appendicitis, Asthma, Disorder of appendix, Scoliosis

13635
Transmembrane protein 132B
-
Alzheimer disease, Attention deficit hyperactivity disorder, Bipolar disorder, Dementia, Major depressive disorder, Melanoma, Nonalcoholic fatty liver disease, Obstructive sleep apnea syndrome, Psychiatric disorders, Amyotrophic lateral sclerosis, Substance abuse, Diabetes mellitus type 2

13636
Transmembrane protein 132C
PPP1R152
Alzheimer disease, Anxiety disorder, Cholecystitis, Cholecystolithiasis, Color vision deficiency, Lung cancer, Ocular hypertension, Scoliosis, Systemic lupus erythematosus, Upper extremity fracture, Uterine fibroid

13637
Transmembrane protein 132D
MOLT, PPP1R153
Anxiety disorder, Asthma, B-cell acute lymphoblastic leukemia, Color vision deficiency, Colorectal cancer, Coronary artery disease, Dementia, Intellectual developmental disorder, Liver neoplasms, Major depressive disorder, Obesity, Schizophrenia, Small cell lung carcinoma, Hypertension, Diabetes mellitus type 2

13638
Transmembrane protein 132E
DFNB99
Isolated sensorineural deafness, Deafness, Glioma, Glomerulonephritis, Hearing loss, Insomnia, Amyotrophic lateral sclerosis

13639
Transmembrane protein 135
PMP52
Bone fracture, Non-small-cell lung carcinoma, Corneal astigmatism, Glioblastoma, Intellectual developmental disorder, Neurodevelopmental disorder, Open angle glaucoma, Scoliosis

13640
Transmembrane protein 138
HSPC196
Arima syndrome, Ciliopathy, Aplasia of the vermis, Joubert syndrome, Meckel-gruber syndrome