CNKSR2

Summary

CNKSR2 is a gene^[1]. CNKSR2 ranks in the top 2% of gene entities by monthly Wikipedia readership (7 views/month).^[2]

Key Facts

• CNKSR2's instance of is recorded as gene^[3].
• CNKSR2 is a type of protein-coding gene^[4].
• CNKSR2's HomoloGene ID is recorded as 8956^[5].
• CNKSR2's genomic start is recorded as 21392536^[6].
• CNKSR2's genomic start is recorded as 21372801^[7].
• CNKSR2's genomic end is recorded as 21654695^[8].
• CNKSR2's genomic end is recorded as 21672813^[9].
• CNKSR2's ortholog is recorded as Cnksr2^[10].
• CNKSR2's ortholog is recorded as Cnksr2^[11].
• CNKSR2's ortholog is recorded as cnksr2a^[12].
• CNKSR2's encodes is recorded as Connector enhancer of kinase suppressor of Ras 2^[13].
• CNKSR2's found in taxon is recorded as Homo sapiens^[14].
• CNKSR2's chromosome is recorded as human X chromosome^[15].
• CNKSR2's genetic association is recorded as syndromic X-linked mental retardation Hough type^[16].
• CNKSR2's genetic association is recorded as X-linked dominant intellectual disability-epilepsy syndrome^[17].
• CNKSR2's strand orientation is recorded as forward strand^[18].
• CNKSR2's exact match is recorded as http://identifiers.org/ncbigene/22866^[19].
• CNKSR2's cytogenetic location is recorded as Xp22.12^[20].
• CNKSR2's expressed in is recorded as Brodmann area 23^[21].
• CNKSR2's expressed in is recorded as cerebellar cortex^[22].

Why It Matters

CNKSR2 ranks in the top 2% of gene entities by monthly Wikipedia readership (7 views/month).^[2]