GlyCosmos Portal

Noonan syndrome 1

Synonym

Definition

A Noonan syndrome that has_material_basis_in the PTPN11 gene on chromosome 12q24.

Super Class

Noonan syndrome autosomal dominant disease

Disease Ontology

DOID:0060578

Mondo Disease Ontology

OMIM

MGI genotype (from TogoID)

Related Genes

Displaying entries **1 - 10** of 37 in total

1

2

3

4

Next ›

Last »
Gene ID	Gene Symbol	Description	Source
35	ACADS	acyl-CoA dehydrogenase short chain	DisGeNET
43	ACHE	acetylcholinesterase (Yt blood group)	DisGeNET
142	PARP1	poly(ADP-ribose) polymerase 1	DisGeNET
275	AMT	aminomethyltransferase	DisGeNET
410	ARSA	arylsulfatase A	DisGeNET
412	STS	steroid sulfatase	DisGeNET
414	ARSD	arylsulfatase D	DisGeNET DisGeNET
570	BAAT	bile acid-CoA:amino acid N-acyltransferase	DisGeNET
847	CAT	catalase	DisGeNET
1583	CYP11A1	cytochrome P450 family 11 subfamily A member 1	DisGeNET

Related Glycoprotein

Displaying entries **11 - 20** of 27 in total

« First

‹ Prev

1

2

3

Next ›

Last »
UniProt ID	Protein Name	Source
P15289	Arylsulfatase A	DisGeNET
P15328	Folate receptor alpha	DisGeNET
P16278	Beta-galactosidase	DisGeNET
P22303	Acetylcholinesterase	DisGeNET
P23434	Glycine cleavage system H protein, mitochondrial	DisGeNET
P42338	Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform	DisGeNET DisGeNET
P48736	Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform	DisGeNET DisGeNET
P51689	Arylsulfatase D	DisGeNET DisGeNET
P60484	Phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN	DisGeNET
P98160	Basement membrane-specific heparan sulfate proteoglycan core protein	DisGeNET