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
10151 to 10160 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10151
DNA polymerase eta
RAD30, RAD30A, XP-V, XPV
Eosinophilia, Xeroderma pigmentosum

10152
DNA polymerase iota
RAD30B, RAD3OB, eta2
Asthma, Eczema, Erythematosquamous dermatosis, Inflammatory skin disease, Oligodendroglioma, Prostate cancer, Psoriasis, Psoriasis vulgaris, Seborrheic dermatitis

10153
DNA polymerase kappa
DINB1, DINP, POLQ
Atrial fibrillation, Cancer, Coronary artery disease, Diabetes mellitus, Glioblastoma, Heart failure, Intellectual developmental disorder, Prostatic neoplasms, Stroke, Diabetes mellitus type 2

10154
DNA polymerase lambda
BETAN, POLKAPPA
Desbuquois syndrome, Insomnia

10155
DNA polymerase nu
POL4P
Alzheimer disease

10156
DNA polymerase theta
PRO0327
Cutaneous mastocytosis, Multiple myeloma

10157
RNA polymerase I subunit A
A190, AFDCIN, HLD27, RPA1, RPA190, RPA194, RPO1-4, RPO14
Acrofacial dysostosis, Burn-mckeown syndrome, Cardiovascular disease, Choanal atresia syndrome, Desbuquois syndrome, Hypomyelinating leukodystrophy, Hypertension

10158
RNA polymerase I subunit B
A135, RPA135, RPA2, Rpo1-2, TCS4
Mandibulofacial dysostosis, Treacher collins syndrome

10159
RNA polymerase I and III subunit C
AC40, HLD11, RPA39, RPA40, RPA5, RPAC1, RPC40, TCS3
Cerebellar ataxia, Desbuquois syndrome, Hearing impairment, Hypomyelinating leukodystrophy, Mandibulofacial dysostosis, Treacher collins syndrome

10160
RNA polymerase I and III subunit D
AC19, POLR1C, RPA16, RPA9, RPAC2, RPC16, RPO1-3, TCS2
Desbuquois syndrome, Diffuse large b-cell lymphoma, Hearing impairment, Mandibulofacial dysostosis, Sialolithiasis, Treacher collins syndrome, Diabetes mellitus type 2