Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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9831 to 9840 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

9831
PH domain and leucine rich repeat protein phosphatase 1
PHLPP, PLEKHE1, PPM3A, SCOP
Attention deficit hyperactivity disorder, Lymphocytic leukemia, Focal onset epileptic seizure, Hodgkin lymphoma, Multiple myeloma, Non-hodgkins lymphoma, Diabetes mellitus type 2

9832
PH domain and leucine rich repeat protein phosphatase 2
PHLPPL, PPM3B
Post-operative acute kidney injury, Prostate cancer

9833
Phosphoethanolamine/phosphocholine phosphatase 1
-
Bone disease, Metabolic bone disorder

9834
Paired like homeobox 2A
ARIX, CFEOM2, FEOM2, NCAM2, PMX2A
Congenital fibrosis of extraocular muscles

9835
Paired like homeobox 2B
CCHS, NBLST2, NBPhox, PMX2B
Haddad syndrome, Central hypoventilation syndrome, Congenital central hypoventilation syndrome, Crohn disease, Hirschsprung disease, Neuroblastoma, Schizophrenia

9836
PHD and ring finger domains 1
PPP1R125, RNF221
Hirschsprung disease, Hypothyroidism, Systemic lupus erythematosus, Rheumatoid arthritis, Systemic sclerosis

9837
Putative homeodomain transcription factor 1
PHTF
Ankylosing spondylitis, Anti-neutrophil antibody associated vasculitis, Asthma, Autoimmune disease, Autoimmune thyroid disease, Basal cell carcinoma, Celiac disease, Common variable immunodeficiency, Crohn disease, Diabetic ketoacidosis, Hyperthyroidism, Hypothyroidism, Inflammatory bowel disease, Juvenile idiopathic arthritis, Keratinocyte carcinoma
View all (17 more)

9838
Putative homeodomain transcription factor 2
-
Atrial fibrillation, Cardioembolic stroke, Dental caries, Hypertension, Major depressive disorder, Obesity

9839
Phytanoyl-CoA 2-hydroxylase
LN1, LNAP1, PAHX, PHYH1, RD
Refsum disease, Optic atrophy, Orofacial cleft, Peroxisomal disorder, Retinitis pigmentosa

9840
Phytanoyl-CoA 2-hydroxylase interacting protein
DYRK1AP3, PAHX-AP, PAHXAP1
Hypertriglyceridemia