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Browse result for Hemoglobin Creteil

※ introduction

    An alpha thalassemia that has_material_basis_in contiguous gene deletion of the hemoglobin alpha-1 (HBA1) and alpha-2 (HBA2) genes on one chromosome 16, and a defect, deletional or nondeletional, in either HBA1 or HBA2 on the other.

Reference
DiseaseOntology: Hemoglobin Creteil


PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD05927P688713043
HBB
Hemoglobin subunit beta [Cleaved into: LVV-hemorphin-7; Spinorphin]
Homo sapiens