Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11361 to 11370 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11361
Ras related GTP binding C
GTR2, LNGODS, LNGOS, RAGC, TIB929
Alzheimer disease, Lymphoma

11362
Ras related GTP binding D
HOMG7, RAGD, bA11D8.2.1
Gout, Heart failure, Nephrolithiasis

11363
RAS related
R-Ras, RRAS1
Desbuquois syndrome, Hypertension, Myelomonocytic leukemia, Noonan syndrome, Prostatic neoplasms

11364
RAS related 2
NS12, TC21
Desbuquois syndrome, Hypertrophic cardiomyopathy, Multiple sclerosis, Noonan syndrome

11365
Ribosome binding protein 1
ES/130, ES130, RRp, hES, p180
Coronary artery disease, Frontotemporal dementia, Migraine, Tooth disease

11366
Ras responsive element binding protein 1
FINB, HNT, LZ321, RREB-1, Zep-1
22q11.2 deletion syndrome, Alzheimer disease, Androgenetic alopecia, Atrial fibrillation, Breast cancer, Cancer, Central nervous system cancer, Kidney disease, Lymphocytic leukemia, Obstructive pulmonary disease, Colorectal cancer, Neurodevelopmental disorder, Melanoma, Desbuquois syndrome, Diabetes mellitus
View all (28 more)

11367
Retinal pigment epithelium-derived rhodopsin homolog
-
Color vision deficiency

11368
Ribonucleotide reductase catalytic subunit M1
PEOB6, R1, RIR1, RR1
Progressive external ophthalmoplegia, Hepatocellular carcinoma, Non-small-cell lung carcinoma, Central nervous system cancer, Glioblastoma, Glioma, Neural tube defect, Neural tube defects, x-linked

11369
Ribonucleotide reductase regulatory subunit M2
C2orf48, R2, RR2, RR2M
Hepatocellular carcinoma, Kidney disease, Color vision deficiency, Colorectal neoplasms, Polycystic ovary syndrome

11370
Ribonucleotide reductase regulatory TP53 inducible subunit M2B
MTDPS8A, MTDPS8B, P53R2, RCDFRD
Chronic progressive external ophthalmoplegia, Progressive external ophthalmoplegia, Camptocormia, Obstructive pulmonary disease, Mitochondrial dna depletion syndrome, Kidney disease, Mitochondrial disease, Mitochondrial myopathy, Rod-cone dystrophy, Rod-cone dystrophy, sensorineural deafness, and fanconi-type renal dysfunction, Hearing loss, Visceral neuropathy