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
10091 to 10100 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10091
Prostate transmembrane protein, androgen induced 1
STAG1, TMEPAI
Congenital contractural arachnodactyly, Liver cirrhosis, Marfan syndrome, Myelodysplastic syndrome

10092
Polyamine modulated factor 1
-
Breast cancer, Clear cell renal cell carcinoma, Intracerebral hemorrhage, Kidney cancer, Myeloproliferative disorder, Small vessel stroke, Stroke

10093
PMF1-BGLAP readthrough
PMF-1, PMF1
Breast cancer, Clear cell renal cell carcinoma, Intracerebral hemorrhage, Kidney cancer, Myeloproliferative disorder, Parkinson disease, Small vessel stroke, Stroke

10094
Polyamine modulated factor 1 binding protein 1
SPGF31, STAP
Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Bronchitis, Coronary artery disease, Dementia, Dyslexia, Hyperlipidemia, Iga nephropathy, Major depressive disorder, Male infertility acephalic spermatozoa, Metabolic syndrome, Myocardial infarction, Obsessive-compulsive disorder
View all (8 more)

10095
PML nuclear body scaffold
MYL, PP8675, RNF71, TRIM19
Diabetes mellitus, Dyslipidemias, Glioblastoma, Insomnia, Promyelocytic leukemia, Liver neoplasms, Metabolic syndrome, Prostatic neoplasms, Schizophrenia, Stevens-johnson syndrome, Diabetes mellitus type 2, Uterine fibroid

10096
Phosphomannomutase 1
PMM 1, PMMH-22, Sec53
Attention deficit hyperactivity disorder, Autism, Global developmental delay

10097
Phosphomannomutase 2
CDG1, CDG1a, CDGS, PMI, PMI1, PMM 2
Breast cancer, Cerebellar ataxia, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Cerebral atrophy, Cerebral palsy, Colorectal neoplasms, Congenital disorder of glycosylation, Diabetes mellitus, Focal glomerulosclerosis, Hyperinsulinemic hypoglycemia, Intellectual developmental disorder, Muscular dystrophy, Open angle glaucoma, Premature ovarian failure, Pituitary stalk interruption syndrome

10098
Peripheral myelin protein 2
CMT1G, FABP8, M-FABP, MP2, P2
Charcot-marie-tooth disease, Cutaneous mastocytosis, Ovarian cancer, Ovarian serous carcinoma, Peripheral neuropathy, Schizophrenia, Diabetes mellitus type 2

10099
Peripheral myelin protein 22
CIDP, CMT1A, CMT1E, DSS, GAS-3, GAS3, HMSNIA, HNPP, Sp110
Charcot-marie-tooth disease, Dejerine-sottas disease, Demyelinating diseases, Developmental disability, Distal spinal muscular atrophy, Myoclonic epilepsy, Hereditary motor and sensory neuropathies, Hereditary sensory and motor neuropathy, Hypertrophic neuropathy, Hereditary, neuropathy with liability to pressure palsies, Non-neoplastic peripheral nervous system disease, Paresthesia, Peripheral nervous system disease, Peripheral neuropathy, Peroneal muscle atrophy
View all (3 more)

10100
Peptidase, mitochondrial processing subunit alpha
Alpha-MPP, CLA1, CPD3, INPP5E, MAS2, P-55, SCAR2
Cerebelloparenchymal disorder, Spinocerebellar ataxia, Ptosis, Blindness, Cerebellar ataxia, Lactic acidosis, Normal pressure hydrocephalus, Hypertrophic cardiomyopathy, Inflammatory bowel disease, Mitochondrial disease, Optic atrophy