Statements (28)
Predicate | Object |
---|---|
gptkbp:instanceOf |
gptkb:gene
|
gptkbp:approvedBy |
gptkb:fibrillin_1
|
gptkbp:approvedSymbol |
gptkb:FBN1
|
gptkbp:associatedWith |
gptkb:Weill-Marchesani_syndrome
gptkb:Marfan_syndrome Acromicric dysplasia Geleophysic dysplasia |
gptkbp:Entrez_Gene_ID |
gptkb:ENSG00000166147
2200 |
gptkbp:gene_symbol_alias |
gptkb:SBB2
gptkb:ectodermal_dysplasia,_acromelic gptkb:FBN |
gptkbp:HGNC_ID |
4017
|
https://www.w3.org/2000/01/rdf-schema#label |
HGNC:4017
|
gptkbp:locatedOnChromosome |
15
15q21.1 |
gptkbp:location |
extracellular matrix
nuclear matrix |
gptkbp:locusType |
gene with protein product
|
gptkbp:OMIM |
134797
|
gptkbp:organism |
gptkb:Homo_sapiens
|
gptkbp:previousName |
fibrillin
|
gptkbp:previousSymbols |
gptkb:FBN
|
gptkbp:proteinFamily |
gptkb:fibrillin_family
|
gptkbp:RefSeq |
NM_000138
|
gptkbp:UniProtID |
gptkb:P35555
|
gptkbp:bfsParent |
gptkb:FUT1_gene
|
gptkbp:bfsLayer |
7
|