Genes | GeDiPNet - Gene Disease Pathway & Associations

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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

13571 to 13580 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
13571	85013	TMEM128	Transmembrane protein 128	-	Central vertigo, Peripheral vertigo, Vestibular disease, Vitiligo
13572	23505	TMEM131	Transmembrane protein 131	CC28, PRO1048, RW1, YR-23	Autoimmune disease, Bipolar disorder, Colorectal cancer, Dyslexia, Endometriosis, Hypothyroidism, Insomnia, Scoliosis
13573	23240	TMEM131L	Transmembrane 131 like	KIAA0922	Androgenetic alopecia, Appendicitis, Asthma, Appendiceal disorder, Scoliosis
13574	114795	TMEM132B	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
13575	92293	TMEM132C	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
13576	121256	TMEM132D	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
13577	124842	TMEM132E	Transmembrane protein 132E	DFNB99	Isolated sensorineural deafness, Deafness, Glioma, Glomerulonephritis, Hearing loss, Insomnia, Amyotrophic lateral sclerosis
13578	65084	TMEM135	Transmembrane protein 135	PMP52	Bone fracture, Non-small-cell lung carcinoma, Corneal astigmatism, Glioblastoma, Intellectual developmental disorder, Neurodevelopmental disorder, Open angle glaucoma, Scoliosis
13579	51524	TMEM138	Transmembrane protein 138	HSPC196	Arima syndrome, Ciliopathy, Aplasia of the vermis, Joubert syndrome, Meckel-gruber syndrome
13580	55260	TMEM143	Transmembrane protein 143	-	Dementia

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