VNN2
protein-coding gene in the species Homo sapiens
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VNN2
Summary
VNN2 is a gene[1]. VNN2 is known by 4 alternative names across languages and contexts.[2]
Key Facts
- VNN2's instance of is recorded as gene[3].
- VNN2 is a type of protein-coding gene[4].
- VNN2's HomoloGene ID is recorded as 130041[5].
- VNN2's genomic start is recorded as 132743870[6].
- VNN2's genomic start is recorded as 133065009[7].
- VNN2's genomic end is recorded as 132763459[8].
- VNN2's genomic end is recorded as 133084598[9].
- VNN2's ortholog is recorded as Btnd[10].
- VNN2's encodes is recorded as Vanin 2[11].
- VNN2's found in taxon is recorded as Homo sapiens[12].
- VNN2's chromosome is recorded as human chromosome 6[13].
- VNN2's strand orientation is recorded as reverse strand[14].
- VNN2's exact match is recorded as http://identifiers.org/ncbigene/8875[15].
- VNN2's cytogenetic location is recorded as 6q23.2[16].
- VNN2's expressed in is recorded as blood[17].
- VNN2's expressed in is recorded as monocyte[18].
- VNN2's expressed in is recorded as granulocyte[19].
- VNN2's expressed in is recorded as palpebral conjunctiva[20].
- VNN2's expressed in is recorded as periodontal fiber[21].
- VNN2's expressed in is recorded as trabecular bone[22].
- VNN2's expressed in is recorded as right lung[23].
- VNN2's expressed in is recorded as spleen[24].
- VNN2's expressed in is recorded as bone marrow[25].
- VNN2's expressed in is recorded as gallbladder[26].
Why It Matters
VNN2 is known by 4 alternative names across languages and contexts.[2]