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. 2002 Nov 14;99(24):15524–15529. doi: 10.1073/pnas.242606799

Table 2.

Human genes with nonperfect base pairing with miR16 gene

Gene name Gene symbol Location miR16 homology
Arginyl-tRNA synthetase RARS 5pter–q11 20-nt overlap, 85%
ATP synthase, H+ transporting, mitochondrial F1 complex, epsilon subunit ATP5E 20q13.3 19-nt overlap, 89%
Bactericidal/permeability-increasing protein BPI 20q11.23–q12 19-nt overlap, 89%
DC2 protein DC2 4q25 17-nt overlap, 95%
Enhancer of polycomb 1 EPC1 10p11 18-nt overlap, 89%
Insulin-like growth factor 1 (somatomedin C) IGF1 12q22–q23 20-nt overlap, 95%
Keratin 18 KRT18 12q13 18-nt overlap, 89%
Member of the cysteine-rich secretory protein (CRISP) family TPX1, GAPDL5, CRISP-2 6p21–qter 21-nt overlap, 86%
Phosphoribosylglycinamide formyltransferase GART 21q22.11 18-nt overlap, 89%
Protein phosphatase 2, regulatory subunit A, beta isoform PPP2R1B 11q23 21-nt overlap, 81%
Slug homolog, zinc finger protein SLUG; SNAI2 8q11 21-nt overlap, 81%
Sorting nexin 2 SNX2 5q23 21-nt overlap, 81%
Spectrin, beta, nonerythrocytic 1 SPTBN1 2p21 18-nt overlap, 89%
WW domain binding protein 11 WBP11 12p13.1 21-nt overlap, 81%
HHS Vulnerability Disclosure