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
9821 to 9830 of 15448 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

9821
Phosphorylase kinase regulatory subunit alpha 2
GSD9A, PHK, PYK, PYKL, XLG, XLG2
Glycogen phosphorylase kinase deficiency, Glycogen storage disease, Ocular albinism

9822
Phosphorylase kinase regulatory subunit beta
-
Glycogen phosphorylase kinase deficiency, Glycogen storage disease

9823
Phosphorylase kinase catalytic subunit gamma 1
PHKG
Glycogen storage disease, Multiple sclerosis

9824
Phosphorylase kinase catalytic subunit gamma 2
GSD9C
Glycogen phosphorylase kinase deficiency, Glycogen storage disease, Liver cirrhosis

9825
Pleckstrin homology like domain family A member 1
DT1P1B11, PHRIP, TDAG51
Atrial fibrillation, Hepatocellular carcinoma, Cognition disorder, Delirium, dementia, and cognitive disorders, Allergic contact dermatitis

9826
Pleckstrin homology like domain family A member 2
BRW1C, BWR1C, HLDA2, IPL, TSSC3
Non-small-cell lung carcinoma, Gout, Osteosarcoma

9827
Pleckstrin homology like domain family A member 3
TIH1
Androgenetic alopecia, Breast cancer, Myocardial infarction

9828
Pleckstrin homology like domain family B member 1
LL5A, LL5alpha, OI23
Bardet-biedl syndrome, Bone fragility with contractures, arterial rupture, and deafness, Celiac disease, Central nervous system cancer, Glioma, Hearing loss, Lung cancer, Multiple sclerosis, Non-small cell lung carcinoma, Osteogenesis imperfecta, Osteoporosis-pseudoglioma syndrome, Systemic lupus erythematosus

9829
Pleckstrin homology like domain family B member 2
LL5b, LL5beta
Atrial fibrillation, Atrial flutter, Crohn disease, Hemorrhoid, Ileocolitis, Nonalcoholic fatty liver disease, Diabetes mellitus type 1, Diabetes mellitus type 2

9830
Pleckstrin homology like domain family B member 3
-
Breast cancer, Oligodendroglioma