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

5161 to 5170 of 15448 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
5161	27069	GHITM	Growth hormone inducible transmembrane protein	DERP2, HSPC282, MICS1, My021, PTD010, TMBIM5	Sleep apnea
5162	2690	GHR	Growth hormone receptor	GHBP, GHIP	Alzheimer disease, Atrial fibrillation, Autism, Hepatocellular carcinoma, Central nervous system infection, Colonic disease, Desbuquois syndrome, Diabetes mellitus type 2, Growth hormone insensitivity, partial, Growth hormone insensitivity syndrome, Hypercholesterolemia, Hyperlipoproteinemia, Insomnia, Liver cirrhosis, Myocardial ischemia View all (6 more)
5163	2691	GHRH	Growth hormone releasing hormone	GHRF, GRF, INN	Pulmonary edema
5164	2692	GHRHR	Growth hormone releasing hormone receptor	GHRFR, GRFR, IGHD1B, IGHD4	Congenital isolated growth hormone deficiency, Congenital left-sided heart lesions, Desbuquois syndrome, Hypogonadotropic hypogonadism, Hypopituitarism, Growth hormone deficiency, Kallmann syndrome, Panhypopituitarism, Pituitary dwarfism, Pituitary short stature, Schizophrenia, Scoliosis, Sheehan syndrome
5165	51738	GHRL	Ghrelin and obestatin prepropeptide	MTLRP	Bone resorption, Cachexia, Ulcerative colitis, Colitis, Congestive heart failure, Major depressive disorder, Diabetes mellitus type 2, Diabetic neuropathy, Esophageal neoplasms, Gastric ulcer, Heart failure, Obesity, Neural tube defect, Neural tube defects, x-linked, Seizures
5166	2693	GHSR	Growth hormone secretagogue receptor	GHDP, GHS-R1a, GHSR-1a	Desbuquois syndrome, Digestive system neoplasms, Growth hormone insensitivity, partial, Obesity, Pseudohypoparathyroidism
5167	79018	GID4	GID complex subunit 4 homolog	C17orf39, VID2, VID24	Alzheimer disease, Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Breast cancer, Major depressive disorder, Myocardial infarction, Nonalcoholic fatty liver disease, Obsessive-compulsive disorder, Schizophrenia, Tourette syndrome, Diabetes mellitus type 2
5168	64599	GIGYF1	GRB10 interacting GYF protein 1	GYF1, PERQ1	Alzheimer disease, Autism, Autoimmune disease, Autoimmune thyroid disease, Coffin-siris syndrome, Neurodevelopmental disorder, Hypothyroidism, Non-specific syndromic intellectual disability, Schizophrenia
5169	26058	GIGYF2	GRB10 interacting GYF protein 2	GYF2, PARK11, PERQ2, PERQ3, TNRC15	Anorexia nervosa, Anxiety disorder, Asthma, Attention deficit hyperactivity disorder, Autism, Coronary artery disease, Gastroesophageal reflux disease, Hereditary parkinson disease, Leber congenital amaurosis, Major depressive disorder, Myocardial infarction, Nasal polyp, Neurodevelopmental disorder, Obesity, Parkinson disease View all (3 more)
5170	100527949	GIMAP1-GIMAP5	GIMAP1-GIMAP5 readthrough	-	Portal hypertension

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