ITGB2
protein-coding gene in the species Homo sapiens
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ITGB2
Summary
ITGB2 is a gene[1].
Key Facts
- ITGB2's instance of is recorded as gene[2].
- ITGB2 is a type of protein-coding gene[3].
- ITGB2's HomoloGene ID is recorded as 20092[4].
- ITGB2's genomic start is recorded as 44885953[5].
- ITGB2's genomic start is recorded as 46305868[6].
- ITGB2's genomic end is recorded as 44931989[7].
- ITGB2's genomic end is recorded as 46351904[8].
- ITGB2's ortholog is recorded as Itgb2[9].
- ITGB2's ortholog is recorded as Itgb2[10].
- ITGB2's ortholog is recorded as itgb2[11].
- ITGB2's encodes is recorded as integrin subunit beta 2[12].
- ITGB2's encodes is recorded as Integrin beta[13].
- ITGB2's found in taxon is recorded as Homo sapiens[14].
- ITGB2's chromosome is recorded as human chromosome 21[15].
- ITGB2's genetic association is recorded as leukocyte adhesion deficiency-1[16].
- ITGB2's strand orientation is recorded as reverse strand[17].
- ITGB2's exact match is recorded as http://identifiers.org/ncbigene/3689[18].
- ITGB2's cytogenetic location is recorded as 21q22.3[19].
- ITGB2's expressed in is recorded as granulocyte[20].
- ITGB2's expressed in is recorded as monocyte[21].
- ITGB2's expressed in is recorded as blood[22].
- ITGB2's expressed in is recorded as spleen[23].
- ITGB2's expressed in is recorded as bone marrow cell[24].
- ITGB2's expressed in is recorded as appendix[25].
- ITGB2's expressed in is recorded as trabecular bone[26].