Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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10961 to 10970 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10961
Radixin
DFNB24
Ankylosing spondylitis, Isolated sensorineural deafness, Nonsyndromic hearing loss, Cholelithiasis, Corneal ulcer, Crohn disease, Deafness, Diabetic neuropathy, Eye disease, Hearing impairment, Hearing loss, Hereditary hearing loss, Alzheimer disease, Major depressive disorder, Nonalcoholic fatty liver disease
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10962
REC114 meiotic recombination protein
C15orf60, CT147, OOMD10, OZEMA10
Atrial fibrillation, Atrial flutter, Cardiac arrhythmia, Cardioembolic stroke, Insomnia, Oocyte maturation defect, Stevens-johnson syndrome, Toxic epidermal necrolysis

10963
REC8 meiotic recombination protein
HR21spB, REC8L1, Rec8p
Alzheimer disease, Azoospermia, Focal segmental glomerulosclerosis, Melanoma, Premature ovarian failure, Prostatic neoplasms, Testicular azoospermia

10964
Reversion inducing cysteine rich protein with kazal motifs
ST15
Non-small-cell lung carcinoma, Colonic neoplasms, Glioblastoma, Sensory peripheral neuropathy

10965
RecQ like helicase
RECON, RECQL1, RecQ1
Breast neoplasms, Hereditary breast cancer

10966
RecQ like helicase 4
RECQ4
Congenital heart disease, Craniosynostosis, Desbuquois syndrome, Osteosarcoma, Rothmund-thomson syndrome

10967
RecQ like helicase 5
RECQ5
Breast cancer, Coronary artery disease, Prostate cancer

10968
Regulator of DNA class I crossover intermediates 1
C12orf40, HEIP1, HEL-206, HEL-S-94
Alzheimer disease, Colorectal cancer

10969
Reeler domain containing 1
-
Atrial fibrillation

10970
Receptor accessory protein 1
C2orf23, DSMA6, HMN5B, HMND12, HMNR6, SPG31, Yip2a
Atrial fibrillation, Spastic paraplegia, Charcot-marie-tooth disease, Distal hereditary motor neuropathy, Oropharyngeal cancer, Polyneuropathy, Hereditary spastic paraplegia, Spinal muscular atrophy