HGNC:3821

URI: https://gptkb.org/entity/HGNC:3821

GPTKB entity

Predicate	Object
gptkbp:instanceOf	gptkb:gene
gptkbp:alias	gptkb:SBB2 gptkb:ectodermal_dysplasia,_acromelic gptkb:FBN
gptkbp:approvedBy	gptkb:fibrillin_1
gptkbp:approvedSymbol	gptkb:FBN1
gptkbp:associatedWith	gptkb:Ectopia_lentis gptkb:Familial_thoracic_aortic_aneurysm gptkb:Weill-Marchesani_syndrome gptkb:Marfan_syndrome
gptkbp:Entrez_Gene_ID	gptkb:ENSG00000166147 2200
gptkbp:HGNC_ID	gptkb:HGNC:3821
https://www.w3.org/2000/01/rdf-schema#label	HGNC:3821
gptkbp:locatedOnChromosome	15
gptkbp:location	15q21.1
gptkbp:locusType	gptkb:gene gene with protein product
gptkbp:OMIM	134797
gptkbp:organism	gptkb:Homo_sapiens
gptkbp:previousSymbols	gptkb:FBN
gptkbp:proteinFamily	gptkb:fibrillin_family extracellular matrix glycoproteins
gptkbp:RefSeq	NM_000138
gptkbp:symbol	approved
gptkbp:UniProtID	gptkb:P35555
gptkbp:bfsParent	gptkb:FOXO3
gptkbp:bfsLayer	7