Hemoglobin subunit beta

HBB
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesHBB, CD113t-C, beta-globin, hemoglobin subunit beta, ECYT6
External IDsOMIM: 141900; MGI: 5474850; HomoloGene: 68066; GeneCards: HBB; OMA:HBB - orthologs
Orthologs
SpeciesHumanMouse
Entrez

3043

101488143

Ensembl

ENSG00000244734

ENSMUSG00000073940

UniProt

P68871

P02088

RefSeq (mRNA)

NM_000518

NM_008220

RefSeq (protein)

NP_000509

NP_032246
NP_001188320
NP_001265090

Location (UCSC)Chr 11: 5.23 – 5.23 MbChr 7: 103.46 – 103.46 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Hemoglobin subunit beta (beta globin, β-globin, haemoglobin beta, hemoglobin beta) is a globin protein, coded for by the HBB gene, which along with alpha globin (HBA), makes up the most common form of haemoglobin in adult humans, hemoglobin A (HbA). It is 147 amino acids long and has a molecular weight of 15,867 Da. Normal adult human HbA is a heterotetramer consisting of two alpha chains and two beta chains.

β-globin is encoded by the HBB gene on human chromosome 11. Mutations in the gene produce several variants of the proteins which are implicated with genetic disorders such as sickle-cell disease and beta thalassemia, as well as beneficial traits such as genetic resistance to malaria. At least 50 disease-causing mutations in this gene have been discovered.