DisGeNET - a database of gene-disease associations

Source: ALL

Gene: AGPAT2 ×

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Gene Full Name

DSI _g

DPI _g

pLI

Disease

Type

Score _gda

EL_gda

EI _gda

N.PMIDs

N.SNPs _gda

First Ref.

LastRef.

Entrez Id:	10555
Gene Symbol:	AGPAT2

AGPAT2

1-acylglycerol-3-phosphate O-acyltransferase 2

0.585

0.654

1.2E-07

CUI:	C0235986
Disease:	Growth hormone excess

Growth hormone excess

phenotype

0.100

None

Entrez Id:	10555
Gene Symbol:	AGPAT2

AGPAT2

1-acylglycerol-3-phosphate O-acyltransferase 2

0.585

0.654

1.2E-07

CUI:	C0545053
Disease:	Advanced bone age

Advanced bone age

phenotype

0.100

None

Entrez Id:	10555
Gene Symbol:	AGPAT2

AGPAT2

1-acylglycerol-3-phosphate O-acyltransferase 2

0.585

0.654

1.2E-07

CUI:	C0576225
Disease:	Long foot

Long foot

phenotype

0.100

None

Entrez Id:	10555
Gene Symbol:	AGPAT2

AGPAT2

1-acylglycerol-3-phosphate O-acyltransferase 2

0.585

0.654

1.2E-07

CUI:	C1260926
Disease:	Abnormal pigmentation

Abnormal pigmentation

phenotype

0.100

None

Entrez Id:	10555
Gene Symbol:	AGPAT2

AGPAT2

1-acylglycerol-3-phosphate O-acyltransferase 2

0.585

0.654

1.2E-07

CUI:	C1306503
Disease:	Congenital exomphalos

Congenital exomphalos

disease

0.100

None

Entrez Id:	10555
Gene Symbol:	AGPAT2

AGPAT2

1-acylglycerol-3-phosphate O-acyltransferase 2

0.585

0.654

1.2E-07

CUI:	C1531647
Disease:	Cerebral ventriculomegaly

Cerebral ventriculomegaly

phenotype

0.100

None

Entrez Id:	10555
Gene Symbol:	AGPAT2

AGPAT2

1-acylglycerol-3-phosphate O-acyltransferase 2

0.585

0.654

1.2E-07

CUI:	C1560305
Disease:	Prolonged QTc interval

Prolonged QTc interval

phenotype

0.100

None

Entrez Id:	10555
Gene Symbol:	AGPAT2

AGPAT2

1-acylglycerol-3-phosphate O-acyltransferase 2

0.585

0.654

1.2E-07

CUI:	C1565489
Disease:	Renal Insufficiency

Renal Insufficiency

disease

0.100

None

Entrez Id:	10555
Gene Symbol:	AGPAT2

AGPAT2

1-acylglycerol-3-phosphate O-acyltransferase 2

0.585

0.654

1.2E-07

CUI:	C1623038
Disease:	Cirrhosis

Cirrhosis

disease

0.100

None

Entrez Id:	10555
Gene Symbol:	AGPAT2

AGPAT2

1-acylglycerol-3-phosphate O-acyltransferase 2

0.585

0.654

1.2E-07

CUI:	C1835884
Disease:	Triangular face

Triangular face

phenotype

0.100

None

Entrez Id:	10555
Gene Symbol:	AGPAT2

AGPAT2

1-acylglycerol-3-phosphate O-acyltransferase 2

0.585

0.654

1.2E-07

CUI:	C1836156
Disease:	Progressive proximal muscle weakness

Progressive proximal muscle weakness

phenotype

0.100

None

Entrez Id:	10555
Gene Symbol:	AGPAT2

AGPAT2

1-acylglycerol-3-phosphate O-acyltransferase 2

0.585

0.654

1.2E-07

CUI:	C1837764
Disease:	Loss of subcutaneous adipose tissue in limbs

Loss of subcutaneous adipose tissue in limbs

phenotype

0.100

None

Entrez Id:	10555
Gene Symbol:	AGPAT2

AGPAT2

1-acylglycerol-3-phosphate O-acyltransferase 2

0.585

0.654

1.2E-07

CUI:	C0541764
Disease:	Delayed bone age

Delayed bone age

phenotype

0.100

None

Entrez Id:	10555
Gene Symbol:	AGPAT2

AGPAT2

1-acylglycerol-3-phosphate O-acyltransferase 2

0.585

0.654

1.2E-07

CUI:	C0428977
Disease:	Bradycardia

Bradycardia

phenotype

0.100

None

Entrez Id:	10555
Gene Symbol:	AGPAT2

AGPAT2

1-acylglycerol-3-phosphate O-acyltransferase 2

0.585

0.654

1.2E-07

CUI:	C0239998
Disease:	Recurrent infections

Recurrent infections

phenotype

0.100

None

Entrez Id:	10555
Gene Symbol:	AGPAT2

AGPAT2

1-acylglycerol-3-phosphate O-acyltransferase 2

0.585

0.654

1.2E-07

CUI:	C0241240
Disease:	Tall stature

Tall stature

phenotype

0.100

None

Entrez Id:	10555
Gene Symbol:	AGPAT2

AGPAT2

1-acylglycerol-3-phosphate O-acyltransferase 2

0.585

0.654

1.2E-07

CUI:	C0268731
Disease:	Renal glomerular disease

Renal glomerular disease

group

0.100

None

Entrez Id:	10555
Gene Symbol:	AGPAT2

AGPAT2

1-acylglycerol-3-phosphate O-acyltransferase 2

0.585

0.654

1.2E-07

CUI:	C0271561
Disease:	Somatotropin deficiency

Somatotropin deficiency

disease

0.100

None

Entrez Id:	10555
Gene Symbol:	AGPAT2

AGPAT2

1-acylglycerol-3-phosphate O-acyltransferase 2

0.585

0.654

1.2E-07

CUI:	C0333068
Disease:	Flexion contracture

Flexion contracture

disease

0.100

None

Entrez Id:	10555
Gene Symbol:	AGPAT2

AGPAT2

1-acylglycerol-3-phosphate O-acyltransferase 2

0.585

0.654

1.2E-07

CUI:	C0340279
Disease:	Ventricular hypertrophy

Ventricular hypertrophy

disease

0.100

None

Entrez Id:	10555
Gene Symbol:	AGPAT2

AGPAT2

1-acylglycerol-3-phosphate O-acyltransferase 2

0.585

0.654

1.2E-07

CUI:	C0392525
Disease:	Nephrolithiasis

Nephrolithiasis

disease

0.100

None

Entrez Id:	10555
Gene Symbol:	AGPAT2

AGPAT2

1-acylglycerol-3-phosphate O-acyltransferase 2

0.585

0.654

1.2E-07

CUI:	C0399526
Disease:	Class III malocclusion

Class III malocclusion

disease

0.100

None

Entrez Id:	10555
Gene Symbol:	AGPAT2

AGPAT2

1-acylglycerol-3-phosphate O-acyltransferase 2

0.585

0.654

1.2E-07

CUI:	C0404531
Disease:	Hypertrophy of labia

Hypertrophy of labia

phenotype

0.100

None

Entrez Id:	10555
Gene Symbol:	AGPAT2

AGPAT2

1-acylglycerol-3-phosphate O-acyltransferase 2

0.585

0.654

1.2E-07

CUI:	C0425957
Disease:	Secondary amenorrhea

Secondary amenorrhea

phenotype

0.100

None

Entrez Id:	10555
Gene Symbol:	AGPAT2

AGPAT2

1-acylglycerol-3-phosphate O-acyltransferase 2

0.585

0.654

1.2E-07

CUI:	C0426870
Disease:	Large hand

Large hand

phenotype

0.100

None