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
9981 to 9990 of 15380 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

9981
Pleckstrin homology and RhoGEF domain containing G2
ARHGEF42, CLG, CTB-60E11.4, LDAMD
Epilepsy, Jarcho-levin syndrome

9982
Pleckstrin homology and RhoGEF domain containing G3
ARHGEF43, KIAA0599
Hemolytic anemia, Scoliosis, Spherocytosis

9983
Pleckstrin homology and RhoGEF domain containing G4
ARHGEF44, PRTPHN1, SCA4
Spinocerebellar ataxia

9984
Pleckstrin homology and RhoGEF domain containing G4B
ARHGEF48
Alzheimer disease, Asthma, Atrial fibrillation, Hearing loss, Neurodevelopmental disorder

9985
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, Odontochondrodysplasia 2 with hearing loss and diabetes, Neuromuscular disease, Distal hereditary motor neuropathy, Peripheral neuropathy, Peroneal muscle atrophy
View all (4 more)

9986
Pleckstrin homology and RhoGEF domain containing G6
ARHGEF46, MyoGEF
Colorectal adenoma, Colorectal cancer, Lung cancer, Obesity

9987
Pleckstrin homology and RhoGEF domain containing G7
C12orf74
Attention deficit hyperactivity disorder, Autism, Periodontitis, Prostate cancer

9988
Pleckstrin homology, MyTH4 and FERM domain containing H2
PLEKHH1L
Cholecystolithiasis, Coronary artery disease, Diabetes mellitus, Inflammatory bowel disease, Prostate cancer, Diabetes mellitus type 2

9989
Pleckstrin homology, MyTH4 and FERM domain containing H3
-
Cataract

9990
Pleckstrin homology domain containing J1
GNRPX
Atrial fibrillation, Coronary artery disease