Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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5861 to 5870 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

5861
High mobility group box 2
HMG2
Hepatocellular carcinoma, Obesity, Prostatic neoplasms

5862
High mobility group box 3
HMG-2a, HMG-4, HMG2A, HMG4
Microphthalmia, Urinary bladder neoplasms, X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome

5863
High mobility group box 4
dJ1007G16.5
Anorectal malformation

5864
3-hydroxy-3-methylglutaryl-CoA lyase
HL, HMGCL1
Hmg-coa lyase deficiency, Amino acid metabolism disorder, Hydroxymethylglutaryl-coa lyase deficiency

5865
3-hydroxy-3-methylglutaryl-CoA lyase like 1
ERCHL, bA418P12.1, er-cHL
Colorectal adenoma, Colorectal cancer, Gout, Obesity, Vesicoureteral reflux

5866
3-hydroxy-3-methylglutaryl-CoA reductase
LDLCQ3, LGMDR28, MYPLG
Alzheimer disease, Angina pectoris, Ankylosing spondylitis, Asthma, Atrial fibrillation, Attention deficit hyperactivity disorder, Autoimmune disease, Autoinflammatory syndrome, Limb girdle muscular dystrophy, Cancer, Hepatocellular carcinoma, Cardiovascular disease, Cholecystolithiasis, Ischemic heart disease, Coronary artery disease
View all (19 more)

5867
3-hydroxy-3-methylglutaryl-CoA synthase 1
HMGCS
Alzheimer disease, Eichsfeld type congenital muscular dystrophy, Rigid spine muscular dystrophy

5868
3-hydroxy-3-methylglutaryl-CoA synthase 2
-
Hmg-coa synthase deficiency, Colonic neoplasms, Congestive heart failure, Heart failure, Mouth neoplasms, Myocardial ischemia

5869
High mobility group nucleosome binding domain 1
HMG14
Alzheimer disease, Obstructive pulmonary disease, Osteoarthritis

5870
High mobility group nucleosomal binding domain 2
HMG17
Astrocytoma, Obstructive pulmonary disease