HBB
protein-coding gene in the species Homo sapiens
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HBB
Summary
HBB is a gene[1].
Key Facts
- HBB's instance of is recorded as gene[2].
- HBB is a type of protein-coding gene[3].
- HBB's Commons category is recorded as Hemoglobin, beta-chain[4].
- HBB's HomoloGene ID is recorded as 68066[5].
- HBB's genomic start is recorded as 5225464[6].
- HBB's genomic start is recorded as 5246694[7].
- HBB's genomic end is recorded as 5229395[8].
- HBB's genomic end is recorded as 5250625[9].
- HBB's ortholog is recorded as Hbb-bt[10].
- HBB's ortholog is recorded as Hbb-b1[11].
- HBB's ortholog is recorded as Hbb-bs[12].
- HBB's ortholog is recorded as Hbb-bs[13].
- HBB's ortholog is recorded as Hbb[14].
- HBB's ortholog is recorded as LOC100134871[15].
- HBB's encodes is recorded as Hemoglobin subunit beta[16].
- HBB's found in taxon is recorded as Homo sapiens[17].
- HBB's chromosome is recorded as human chromosome 11[18].
- HBB's genetic association is recorded as Heinz body anemia[19].
- HBB's genetic association is recorded as dominant beta-thalassemia[20].
- HBB's genetic association is recorded as beta-thalassemia HBB/LCRB[21].
- HBB's genetic association is recorded as hereditary persistence of fetal hemoglobin-sickle cell disease syndrome[22].
- HBB's genetic association is recorded as hemoglobin M disease[23].
- HBB's genetic association is recorded as beta thalassemia[24].
- HBB's strand orientation is recorded as reverse strand[25].
- HBB's exact match is recorded as http://identifiers.org/ncbigene/3043[26].