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
11041 to 11050 of 15448 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

11041
RERG like
-
Alzheimer disease, Kidney disease, Head and neck neoplasm, Insomnia, Lung cancer, Major depressive disorder, Oropharyngeal cancer, Scoliosis, Upper aerodigestive tract neoplasm

11042
Retroelement silencing factor 1
C12orf35, GET, KIAA1551, UTA2-1
Alzheimer disease, Breast cancer, Dementia, Obesity, Ocular sarcoidosis, Testicular carcinoma, Testicular germ cell tumor

11043
Regulated endocrine specific protein 18
-
Metabolic syndrome, Diabetes mellitus type 2

11044
RE1 silencing transcription factor
DFNA27, GINGF5, HGF5, NRSF, WT6, XBR
Atrial fibrillation, Attention deficit hyperactivity disorder, Nonsyndromic hearing loss, Coronary artery disease, Deafness, Glaucoma, Major depressive disorder, Migraine, Myocardial infarction, Osteoarthritis, Schizophrenia, Seizures, Substance abuse, Wilms tumor

11045
Ret proto-oncogene
CDHF12, CDHR16, HSCR1, MEN2A, MEN2B, MTC1, PTC, RET-ELE1
Alzheimer disease, Amyloidosis, Appendicitis, Renal agenesis, Burkitt lymphoma, Congenital anomalies of the kidney and urinary tract, Medullary carcinoma, Haddad syndrome, Colorectal neoplasms, Congenital central hypoventilation syndrome, Congenital digestive system anomaly, Congenital hypoplasia of kidney, Differentiated thyroid carcinoma, Hirschsprung disease, Hypothyroidism
View all (8 more)

11046
Resistin
ADSF, FIZZ3, RENT, RETN1, RSTN, XCP1
Autism, Congestive heart failure, Diabetes mellitus type 2, Heart failure, Hypertension, Hypertrophic cardiomyopathy, Kidney failure, Promyelocytic leukemia, Metabolic syndrome, Obesity

11047
Resistin like beta
FIZZ1, FIZZ2, HXCP2, RELM-beta, RELMb, RELMbeta, XCP2
Autoimmune disease, Hypothyroidism, Major depressive disorder

11048
Reticulophagy regulator 1
FAM134B, JK-1, JK1
Charcot-marie-tooth disease, Hereditary motor and sensory neuropathies, Hereditary sensory and autonomic neuropathy, Sensory neuropathy, Hereditary spastic paraplegia, Venous thromboembolism

11049
Reticulophagy regulator family member 2
C2orf17, FAM134A, MAG-2
Schizophrenia

11050
Reticulophagy regulator family member 3
FAM134C
Colorectal cancer, Endometrial neoplasms, Parkinson disease, Diabetes mellitus type 2