Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "P"
661 to 670 of 1369 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

661
Pleckstrin homology and RhoGEF domain containing G3
ARHGEF43, KIAA0599
Hemolytic anemia, Scoliosis, Spherocytosis

662
Pleckstrin homology and RhoGEF domain containing G4
ARHGEF44, PRTPHN1, SCA4
Spinocerebellar ataxia

663
Pleckstrin homology and RhoGEF domain containing G4B
ARHGEF48
Alzheimer disease, Asthma, Atrial fibrillation, Hearing loss, Neurodevelopmental disorder

664
Pleckstrin homology and RhoGEF domain containing G5
ARHGEF45, CMTRIC, DSMA4, GEF720, HMNR4, Syx, Tech
Testis atrophy, Charcot-marie-tooth disease, Color vision deficiency, Dejerine-sottas disease, Distal spinal muscular atrophy, Hereditary motor and sensory neuropathies, Motor neuron disease, Hypertrophic neuropathy, Amyotrophic lateral sclerosis, Multiple sclerosis, Neuromuscular disease, Distal hereditary motor neuropathy, Peripheral neuropathy, Peroneal muscle atrophy, Polycystic ovary syndrome
View all (3 more)

665
Pleckstrin homology and RhoGEF domain containing G6
ARHGEF46, MyoGEF
Colorectal adenoma, Colorectal cancer, Lung cancer, Obesity

666
Pleckstrin homology and RhoGEF domain containing G7
C12orf74
Attention deficit hyperactivity disorder, Autism, Periodontitis, Prostate cancer

667
Pleckstrin homology, MyTH4 and FERM domain containing H1
-
Liver cirrhosis

668
Pleckstrin homology, MyTH4 and FERM domain containing H2
PLEKHH1L
Cholecystolithiasis, Coronary artery disease, Diabetes mellitus, Inflammatory bowel disease, Prostate cancer, Diabetes mellitus type 2

669
Pleckstrin homology, MyTH4 and FERM domain containing H3
-
Cataract, Tonsillitis

670
Pleckstrin homology domain containing J1
GNRPX
Atrial fibrillation, Coronary artery disease