Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "G"
221 to 230 of 677 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

221
Growth hormone releasing hormone
GHRF, GRF, INN
Pulmonary edema

222
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

223
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

224
Growth hormone secretagogue receptor
GHDP, GHS-R1a, GHSR-1a
Desbuquois syndrome, Digestive system neoplasms, Growth hormone insensitivity, partial, Obesity, Pseudohypoparathyroidism

225
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

226
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

227
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
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228
GIMAP1-GIMAP5 readthrough
-
Portal hypertension

229
GTPase, IMAP family member 2
HIMAP2, IAN12, IMAP2
Multiple sclerosis

230
GTPase, IMAP family member 4
IAN-1, IAN1, IMAP4, MSTP062
Diabetes mellitus type 2