|
gptkbp:instanceOf
|
gptkb:gene
|
|
gptkbp:alternativeName
|
gptkb:HBA-T2
gptkb:alpha-globin_2
gptkb:hemoglobin_alpha_2
|
|
gptkbp:associatedWith
|
gptkb:Hb_Bart_syndrome
gptkb:hemoglobin_H_disease
gptkb:alpha-thalassemia
|
|
gptkbp:biologicalProcess
|
oxygen transport
oxygen binding
|
|
gptkbp:cellularComponent
|
gptkb:hemoglobin_complex
|
|
gptkbp:discoveredIn
|
1970s
|
|
gptkbp:encodes
|
gptkb:Hemoglobin_alpha-2_chain
|
|
gptkbp:Entrez_Gene_ID
|
gptkb:ENSG00000188536
3040
|
|
gptkbp:expressedIn
|
erythroid cells
|
|
gptkbp:fullName
|
gptkb:Hemoglobin_subunit_alpha_2
|
|
gptkbp:function
|
oxygen transport
|
|
gptkbp:geneType
|
protein-coding
|
|
gptkbp:hasParalog
|
gptkb:HBA1_gene
|
|
gptkbp:hasTranscriptVariant
|
multiple
|
|
gptkbp:HGNC_ID
|
482
|
|
gptkbp:locatedOnChromosome
|
gptkb:chromosome_16
16p13.3
|
|
gptkbp:mutationAssociatedWith
|
hemoglobinopathies
|
|
gptkbp:numberOfExons
|
3
|
|
gptkbp:OMIM
|
141850
|
|
gptkbp:organism
|
gptkb:Homo_sapiens
|
|
gptkbp:orthologInMouse
|
gptkb:Hba-a2
|
|
gptkbp:product
|
gptkb:Hemoglobin_subunit_alpha
|
|
gptkbp:proteinFamily
|
gptkb:globin_gene_family
|
|
gptkbp:sequence
|
862 bp (genomic)
|
|
gptkbp:UniProtID
|
P69905
|
|
gptkbp:bfsParent
|
gptkb:hemoglobin_alpha_chain
gptkb:Haemoglobin
gptkb:Hemoglobin_subunit_alpha
gptkb:alpha_globin
|
|
gptkbp:bfsLayer
|
8
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
HBA2 gene
|