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. Author manuscript; available in PMC: 2018 Aug 21.
Published in final edited form as: Arthritis Rheumatol. 2016 Apr;68(4):944–952. doi: 10.1002/art.39499

Table 1.

High expression of gene ontologies in podocytes after exposure to IgG from systemic lupus erythematosus patients*

Ontology Term No. of
changed genes
Total no.
of genes
Z score P
Biologic process Cellular component assembly
 involved in morphogenesis
10 (0)  257 (0) 2.787 0.01313
Biologic process Regulation of T cell activation 12 (0)  397 (8) 2.112 0.04711
Biologic process Actin filament–based process 25 (0)  945 (1) 2.353 0.02711
Cellular component Cell–substrate adherens junction 10 (0)  290 (12) 2.383 0.03349
Cellular component Focal adhesion 10 (10)  282 (282) 2.478 0.03051
Cellular component Axon part 10 (2)  281 (37) 2.49 0.03018
Cellular component I band 10 (3)  185 (28) 3.986 0.00146
Cellular component Cell–substrate junction 11 (2)  305 (12) 2.66 0.02082
Cellular component Early endosome 12 (10)  362 (256) 2.463 0.02293
Cellular component Contractile fiber part 13 (0)  290 (0) 3.761 0.00156
Cellular component Sarcomere 13 (1)  260 (33) 4.214 0.000606
Cellular component Contractile fiber 14 (0)  335 (11) 3.608 0.00196
Cellular component Myofibril 14 (1)  318 (55) 3.827 0.00123
Cellular component Endosome membrane 16 (9)  525 (282) 2.487 0.02362
Cellular component Endosomal part 17 (0)  541 (0) 2.697 0.0161
Cellular component Basolateral plasma membrane 17 (5)  585 (258) 2.357 0.032
Cellular component Endosome 27 (14)  1,040 (587) 2.361 0.02568
Cellular component Z disc  9 (9)  171 (171) 3.687 0.00294
Molecular function Cytokine receptor binding 10 (0)  303 (11) 2.234 0.03951
Molecular function Magnesium ion binding 12 (12)  368 (368) 2.403 0.03678
*

Specific ontologies with the highest Z scores were selected. Criteria for inclusion in the table were an ontology containing ≥9 genes and having a Z score of >2.0. Numbers in parentheses are the numerical value considered in the hierarchical structure of each gene ontology term.

Term selected because the genes with the highest changes included HLA–DQB1, IL10, PTPN22, CAMK4, CD80, and CD86, all of which have also been known to be linked to the pathogenesis of lupus.

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