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 **31 - 37** of 37 in total

« First

‹ Prev

1

2

3

4
Gene ID	Gene Symbol	Description	Source
9126	SMC3	structural maintenance of chromosomes 3	DisGeNET
9365	KL	klotho	DisGeNET
11285	B4GALT7	beta-1,4-galactosyltransferase 7	DisGeNET
56994	CHPT1	choline phosphotransferase 1	DisGeNET
64132	XYLT2	xylosyltransferase 2	DisGeNET
79623	GALNT14	polypeptide N-acetylgalactosaminyltransferase 14	DisGeNET
79947	DHDDS	dehydrodolichyl diphosphate synthase subunit	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