HBG2
protein-coding gene in the species Homo sapiens
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HBG2
Summary
HBG2 is a gene[1].
Key Facts
- HBG2's instance of is recorded as gene[2].
- HBG2 is a type of protein-coding gene[3].
- HBG2's HomoloGene ID is recorded as 128032[4].
- HBG2's genomic start is recorded as 5274420[5].
- HBG2's genomic start is recorded as 5253188[6].
- HBG2's genomic end is recorded as 5667019[7].
- HBG2's genomic end is recorded as 5505605[8].
- HBG2's ortholog is recorded as Hbb-y[9].
- HBG2's ortholog is recorded as Hbe1[10].
- HBG2's encodes is recorded as Hemoglobin subunit gamma 2[11].
- HBG2's found in taxon is recorded as Homo sapiens[12].
- HBG2's chromosome is recorded as human chromosome 11[13].
- HBG2's genetic association is recorded as cyanosis, transient neonatal[14].
- HBG2's strand orientation is recorded as reverse strand[15].
- HBG2's exact match is recorded as http://identifiers.org/ncbigene/3048[16].
- HBG2's cytogenetic location is recorded as 11p15.4[17].
- HBG2's expressed in is recorded as placenta[18].
- HBG2's expressed in is recorded as ganglionic eminence[19].
- HBG2's expressed in is recorded as ventricular zone[20].
- HBG2's expressed in is recorded as blood[21].
- HBG2's expressed in is recorded as monocyte[22].
- HBG2's expressed in is recorded as bone marrow[23].
- HBG2's expressed in is recorded as bone marrow cell[24].
- HBG2's expressed in is recorded as apex of heart[25].
- HBG2's expressed in is recorded as spleen[26].