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
10991 to 11000 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10991
RERG like
-
Alzheimer disease, Kidney disease, Head and neck neoplasm, Insomnia, Lung cancer, Major depressive disorder, Oropharyngeal cancer, Scoliosis, Upper aerodigestive tract neoplasm

10992
Retroelement silencing factor 1
C12orf35, GET, KIAA1551, UTA2-1
Alzheimer disease, Breast cancer, Dementia, Obesity, Ocular sarcoidosis, Testicular carcinoma, Testicular germ cell tumor

10993
Regulated endocrine specific protein 18
-
Metabolic syndrome, Diabetes mellitus type 2

10994
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

10995
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)

10996
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

10997
Resistin like beta
FIZZ1, FIZZ2, HXCP2, RELM-beta, RELMb, RELMbeta, XCP2
Autoimmune disease, Hypothyroidism, Major depressive disorder

10998
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

10999
Reticulophagy regulator family member 2
C2orf17, FAM134A, MAG-2
Schizophrenia

11000
Reticulophagy regulator family member 3
FAM134C
Colorectal cancer, Endometrial neoplasms, Parkinson disease, Diabetes mellitus type 2