Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4211 to 4220 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4211
Glutamyl-prolyl-tRNA synthetase 1
EARS, EPRS, GLUPRORS, HLD15, PARS, PIG32, QARS, QPRS
Alzheimer disease, Global developmental delay, Intellectual developmental disorder, Hypomyelinating leukodystrophy

4212
Epidermal growth factor receptor pathway substrate 15
AF-1P, AF1P, MLLT5
Cardioembolic stroke, Color vision deficiency, Seasonal allergic rhinitis

4213
Epidermal growth factor receptor pathway substrate 15 like 1
EPS15R
Asthma, Ectrodactyly, Multiple sclerosis, Split hand-foot malformation, Systemic lupus erythematosus

4214
EGFR pathway substrate 8, signaling adaptor
DFNB102
Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Hearing loss

4215
EPS8 signaling adaptor L2
DFNB106, EPS8R2
Isolated sensorineural deafness, Deafness, Hearing loss, Meniere disease

4216
EPS8 signaling adaptor L3
EPS8R3, HYPT5, MUHH2
Hepatocellular carcinoma, Hypotrichosis, Multiple sclerosis, Prostatic neoplasms

4217
Epithelial stromal interaction 1
BRESI1
Alzheimer disease, Breast cancer, Irritable bowel syndrome, Obesity

4218
Epiphycan
DSPG3, PGLB, Pg-Lb, SLRR3B
Central nervous system cancer, Glioblastoma, Glioma, Schizophrenia

4219
Equatorin
AFAF, C9orf11, SPACA8
Asthma, Hemolytic anemia, Major depressive disorder, Obesity, Osteoarthritis

4220
Era like 12S mitochondrial rRNA chaperone 1
CEGA, ERA, ERA-W, ERAL1A, ERAL1B, H-ERA, HERA-A, HERA-B, PRLTS6
Gonadal dysgenesis, Hearing impairment, Perrault syndrome, Xx gonadal dysgenesis syndrome