BTNL2

Summary

BTNL2 is a gene^[1]. BTNL2 ranks in the top 2% of gene entities by monthly Wikipedia readership (3 views/month).^[2]

Key Facts

• BTNL2's instance of is recorded as gene^[3].
• BTNL2 is a type of protein-coding gene^[4].
• BTNL2's HomoloGene ID is recorded as 10482^[5].
• BTNL2's genomic start is recorded as 32361740^[6].
• BTNL2's genomic start is recorded as 32393339^[7].
• BTNL2's genomic end is recorded as 32374905^[8].
• BTNL2's genomic end is recorded as 32407181^[9].
• BTNL2's ortholog is recorded as Btnl2^[10].
• BTNL2's ortholog is recorded as Btnl2^[11].
• BTNL2's encodes is recorded as Butyrophilin like 2^[12].
• BTNL2's found in taxon is recorded as Homo sapiens^[13].
• BTNL2's chromosome is recorded as human chromosome 6^[14].
• BTNL2's genetic association is recorded as multiple sclerosis^[15].
• BTNL2's genetic association is recorded as hepatitis C^[16].
• BTNL2's genetic association is recorded as liver cirrhosis^[17].
• BTNL2's genetic association is recorded as sarcoidosis^[18].
• BTNL2's genetic association is recorded as adenocarcinoma of the lung^[19].
• BTNL2's genetic association is recorded as ulcerative colitis^[20].
• BTNL2's strand orientation is recorded as reverse strand^[21].

Why It Matters

BTNL2 ranks in the top 2% of gene entities by monthly Wikipedia readership (3 views/month).^[2] BTNL2 is known by 6 alternative names across languages and contexts.^[22]