Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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5651 to 5660 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

5651
Hyaluronan binding protein 2
FSAP, HABP, HGFAL, NMTC5, PHBP, PHBSP
Breast cancer, Colorectal cancer, Thyroid cancer, Gout, Thrombophilia, Nonmedullary thyroid cancer, Diabetes mellitus type 2

5652
3-hydroxyacyl-CoA dehydratase 1
CAP, CMYO11, CMYP11, MYONP, PTPLA
Congenital fiber type disproportion myopathy, Congenital myopathy, Polycystic ovary syndrome, Triple negative breast cancer

5653
3-hydroxyacyl-CoA dehydratase 2
PTPLB
Kidney disease, Metabolic syndrome, Polycystic ovary syndrome, Diabetes mellitus type 2

5654
3-hydroxyacyl-CoA dehydratase 3
B-IND1, BIND1, HSPC121, PTPLAD1
Astrocytoma, Central nervous system cancer, Color vision deficiency, Glioma

5655
3-hydroxyacyl-CoA dehydratase 4
PTPLAD2
Erectile dysfunction

5656
HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1
SPPRS
Alzheimer disease, Aortic valve stenosis, Attention deficit hyperactivity disorder, Bipolar disorder, Central nervous system cancer, Epilepsy, Glioblastoma, Glioma, Global developmental delay, Major salivary gland carcinoma, Major depressive disorder, Metabolic syndrome, Multiple sclerosis, Neuroblastoma, Obsessive-compulsive disorder
View all (6 more)

5657
2-hydroxyacyl-CoA lyase 1
2-HPCL, HPCL, HPCL2, PHYH2
Alzheimer disease, Cholelithiasis

5658
Hydroxyacyl-CoA dehydrogenase
HAD, HADH1, HADHSC, HCDH, HHF4, MSCHAD, SCHAD
3-hydroxyacyl-coa dehydrogenase deficiency, Congenital hyperinsulinism, Hyperinsulinemic hypoglycemia, Hyperinsulinism, Obesity, Amyotrophic lateral sclerosis

5659
Hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha
ECHA, GBP, HADH, LCEH, LCHAD, MLCL AT, MTPA, TP-ALPHA
Alzheimer disease, Fatty liver, Fatty liver, alcoholic, Myocardial ischemia, Osteoarthritis, Trifunctional protein deficiency

5660
Hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta
ECHB, MSTP029, MTPB, MTPD, MTPD2, TP-BETA
Breast neoplasms, Charcot-marie-tooth disease, Fatty liver, Fatty liver, alcoholic, Heart disease, Mitochondrial disease, Non-small cell lung carcinoma, Oligodendroglioma, Rickets, Trifunctional protein deficiency