LPIN2, lipin 2, 9663

N. diseases: 81; N. variants: 10
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0151825
Disease: Bone pain
Bone pain 		0.100 Biomarker phenotype HPO
CUI: C0231528
Disease: Myalgia
Myalgia 		0.100 Biomarker phenotype HPO
CUI: C0235896
Disease: Pulmonary Infiltrate
Pulmonary Infiltrate 		0.100 Biomarker phenotype HPO
CUI: C0239937
Disease: Microscopic hematuria
Microscopic hematuria 		0.100 Biomarker phenotype HPO
CUI: C0241157
Disease: pustule
pustule 		0.100 Biomarker phenotype HPO
CUI: C0268731
Disease: Renal glomerular disease
Renal glomerular disease 		0.100 Biomarker group HPO
CUI: C0271901
Disease: Microcytic hypochromic anemia (disorder)
Microcytic hypochromic anemia (disorder) 		0.100 Biomarker disease HPO
CUI: C0332563
Disease: Papule
Papule 		0.100 Biomarker phenotype HPO
CUI: C0333068
Disease: Flexion contracture
Flexion contracture 		0.100 Biomarker disease HPO
CUI: C0456070
Disease: Growth delay
Growth delay 		0.100 Biomarker phenotype HPO
CUI: C0702166
Disease: Acne
Acne 		0.100 Biomarker disease HPO
CUI: C0949116
Disease: Congenital hypoplastic anemia
Congenital hypoplastic anemia 		0.100 Biomarker disease HPO
CUI: C1390474
Disease: Increased susceptibility to fractures
Increased susceptibility to fractures 		0.100 Biomarker phenotype HPO
CUI: C1519353
Disease: Skin Papule
Skin Papule 		0.100 Biomarker phenotype HPO
CUI: C1838662
Disease: Metaphyseal irregularity
Metaphyseal irregularity 		0.100 Biomarker phenotype HPO
CUI: C1963077
Disease: Bone Pain, CTCAE 3.0
Bone Pain, CTCAE 3.0 		0.100 Biomarker phenotype HPO
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE 		0.100 Biomarker phenotype HPO
CUI: C3714745
Disease: Malabsorption
Malabsorption 		0.100 Biomarker phenotype HPO
CUI: C3875321
Disease: Inflammatory dermatosis
Inflammatory dermatosis 		0.100 Biomarker disease HPO
CUI: C4021634
Disease: Abnormality of bone marrow cell morphology
Abnormality of bone marrow cell morphology 		0.100 Biomarker disease HPO
CUI: C4521256
Disease: Glomerulopathy Assessment
Glomerulopathy Assessment 		0.100 Biomarker phenotype HPO
CUI: C4554063
Disease: Bone Pain, CTCAE 5.0
Bone Pain, CTCAE 5.0 		0.100 Biomarker phenotype HPO
CUI: C0028754
Disease: Obesity
Obesity 		0.030 Biomarker disease BEFREE The data provide new insights into the role of lipin-2 in human and murine macrophage biology and may open new avenues for controlling the fatty acid-related low grade inflammation that constitutes the sine qua non of obesity and associated metabolic disorders. 22334674 2012
CUI: C0028754
Disease: Obesity
Obesity 		0.030 Biomarker disease BEFREE Another member of the lipin family (lipin 2) is enriched in liver, and hepatic lipin 2 protein content was markedly increased by lipin 1 deficiency, food deprivation, and obesity, often independent of changes in steady-state mRNA levels. 19136718 2009
CUI: C0028754
Disease: Obesity
Obesity 		0.030 GeneticVariation disease BEFREE This SNP is located at the 3' untranslated region of the LPIN2 gene, which is a plausible candidate for type 2 diabetes and obesity. 17804763 2007