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
9391 to 9400 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

9391
Phosphatase domain containing paladin 1
KIAA1274, PALD
Basal cell carcinoma, Bone fracture, Carpal tunnel syndrome, Lymphocytic leukemia, Lymphoid leukemia, Narcolepsy, Obesity, Squamous cell carcinoma, Diabetes mellitus type 1, Diabetes mellitus type 2

9392
Palladin, cytoskeletal associated protein
CGI-151, CGI151, MYN, PNCA1, SIH002
Central nervous system cancer, Colorectal cancer, Coronary artery disease, Coronary thrombosis, Pancreatic cancer, Glioblastoma, Glioma, Lung cancer, Pancreatic neoplasms, Psoriasis, Scoliosis, Squamous cell carcinoma, Diabetes mellitus type 2

9393
Paralemmin
PALM1
Basal cell carcinoma, Lung cancer

9394
PALM2 and AKAP2 fusion
AKAP-KL, AKAP2, AKAPKL, MISP2, PALM2, PALM2-AKAP2, PRKA2
Thyroid gland neoplasms, Cardiovascular disease, Cholecystolithiasis, Clear cell renal cell carcinoma, Colorectal cancer, Diabetic retinopathy, Frontotemporal dementia, Obesity, Diabetes mellitus type 2, Vascular brain injury

9395
Palmdelphin
C1orf11, PALML
Atrial fibrillation, Ocular hypertension

9396
Protein associated with LIN7 1, MAGUK p55 family member
MPP5
Anxiety disorder, Arachnoid cysts, Cerebral palsy, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Rett syndrome

9397
Protein associated with LIN7 2, MAGUK p55 family member
MPP6, VAM-1, VAM1, p55T
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Gout, Major depressive disorder, Major salivary gland carcinoma, Neurotic disorder, Post-traumatic stress disorder, Schizophrenia

9398
Peptidylglycine alpha-amidating monooxygenase
PAL, PAM-1, PHM
Androgenetic alopecia, Anxiety disorder, Diabetes mellitus, Diabetes mellitus type 2, Diabetic retinopathy, Insomnia, Osteoarthritis, Parkinson disease, Willis-ekbom disease, Schizophrenia, Seizures

9399
Presequence translocase associated motor 16
CGI-136, MAGMAS, SMDMDM, TIM16, TIMM16
Androgenetic alopecia, Spondylometaphyseal dysplasia, Chondrodysplasia, Desbuquois syndrome, Duodenitis

9400
Peptidase domain containing associated with muscle regeneration 1
DKFZP586H2123, FP938, RAMP
Bronchopulmonary dysplasia, Hepatocellular carcinoma, Congestive heart failure, Heart failure, Hypertrophy, Left ventricular disease, Ocular sarcoidosis