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
10291 to 10300 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10291
PML-RARA regulated adaptor molecule 1
PML-RAR, PRAM-1
Heart failure

10292
PRAME nuclear receptor transcriptional regulator
CT130, MAPE, OIP-4, OIP4
Non-small-cell lung carcinoma, Renal cell carcinoma, Head and neck neoplasms, Heart failure, Leukemia, Medulloblastoma, Melanoma, Multiple myeloma, Sarcoma

10293
PRAME family member 2
DJ845O24.3
Bladder exstrophy and epispadias complex

10294
Proline rich protein BstNI subfamily 2
IB-9, PRPPRB1, Ps, cP7
Pancreatic cancer, Periodontitis

10295
Protein regulator of cytokinesis 1
ASE1, MAP65
Breast cancer, Breast neoplasms, Hepatocellular carcinoma, Diabetic neuropathy, Iga nephropathy, Migraine, Orofacial cleft, Ovarian cancer, Ovarian neoplasms, Schizophrenia, Diabetes mellitus type 2

10296
Proline rich mitotic checkpoint control factor
RCCP1, TPRC
Renal cell carcinoma, Sjogren syndrome

10297
Photoreceptor disc component
RP36
Diabetic neuropathy, Retinitis pigmentosa, Squamous cell carcinoma, Diabetes mellitus type 2

10298
Prolylcarboxypeptidase
HUMPCP, PCP
Obesity, Scoliosis

10299
PR/SET domain 1
BLIMP-1, BLIMP1, PRDI-BF1
Androgenetic alopecia, Ankylosing spondylitis, Rheumatoid arthritis, Ulcerative colitis, Colorectal cancer, Crohn disease, Inflammatory bowel disease, Insomnia, Systemic lupus erythematosus, Psoriasis, Sclerosing cholangitis, Scoliosis, Sjogren syndrome

10300
PR/SET domain 10
BHD2, PFM7, TRIS
Birt-hogg-dube syndrome, Central nervous system cancer, Color vision deficiency, Dementia, Glioblastoma, Glioma