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. 2004 Sep;113(1):99–105. doi: 10.1111/j.1365-2567.2004.01929.x

Table 1.

Accession number, chromosome location and possible role in the pathogenesis of SLE of selected genes whose expression was repressed when untreated patients were compared to healthy individuals, and genes whose expression was induced when untreated patients were compared to treated ones

(’000 MW) Accession no. Location Associations with SLE pathogenesis *Fold change q-value
Repressed genes
Small nuclear ribonucleoprotein (70) R02346 19q13.3 SLE autoantigen −7·812 23·91
Splicing factor 3a, subunit 3 (60) R43015 1p34.2 SLE autoantigen −2·153 23·91
Nucleolar autoantigen (55) W81191 17q21.2 Autoantigen, interstitial cystitis −3·175 23·91
Tetranectin (plasminogen-binding protein) W73889 3p21 Plasminogen activation −1·748 23·91
TNF (ligand), member 9 AA778663 19p13.3 SLE nephritis development −3·958 23·91
CD22 antigen N53534 19q13.1 B-cell receptor regulation −2·387 30·26
Zinc finger protein 74 AA629838 22q11.21 Not yet associated to SLE −3·149 23·91
Phosphonoformate immuno-associated protein 5 W80632 13 Not yet associated to SLE −1·912 30·26
E1b (55) associated protein 5 AA464198 19q13.13 Not yet associated to SLE −1·807 23·91
Sema domain, Ig domain AA454570 3p21.3 Not yet associated to SLE −8·387 23·91
Induced genes
Fc fragment of IgG, receptor for CD32 R68106 1q23 Antibody modulation  7·876 38·31
Apoptotic protease activating factor N51014 12q21 Apoptosis  2·437 38·31
Cytochrome-c oxidase subunity VIc AA456931 8q22 Apoptosis  3·318 38·31
Cytochrome-c oxidase subunity VIII AA862813 11q13 Apoptosis  1·921 38·31
Complement component 5 (C5) N53664 9q32 Complement system pathway  2·591 38·31
MHC, class II, DR α (HLA-DRA) R47979 6p21.3 Susceptibility to SLE 148·387 38·31
MHC, class II, DP β 1 (HLA-DPB1) AA486532 6p21.3 Susceptibility to SLE  19·630 38·31
TGF-β R II AA487034 3p22 Cell growth and differentiation  62·562 38·31
Thyroid autoantigen (70) (Ku antigen) AA486207 22q13 SLE autoantigen  2·842 38·31
Small nuclear ribonucleoprotein (SNRPN) T54926 15q12 SLE autoantigen  3·369 38·31
Heterogeneous nuclear RNP-C (HRNPC) H05899 14q11.1 mRNA processing and splicing  1·523 38·31
Splicing factor arg/ser rich 9 (SFRS9) AA491213 12q24.31 mRNA processing and splicing  1·623 38·31
Argininosuccinate lyase (ASL) AA486741 7cen-q11.2 NO production  5·056 38·31
Tumour protein p53 (TP53) R39356 17p13.1 Tumour suppressor  4·676 38·31
Mannosidase-α, class 1A, member 1 T91261 6p22 Mannose removal  10·825 38·31
TNF (ligand), member 9 AA778663 19p13.3 SLE nephritis development  3·512 38·31
CD22 antigen N53534 19q13.1 B-cell receptor regulation  91·725 38·31
Zinc finger protein 74 AA629838 22q11.21 Not yet associated to SLE  3·872 38·31
Phosphonoformate immuno-associated protein 5 W80632 13 Not yet associated to SLE  2·878 38·31
Elb (55) associated protein 5 AA464198 19q13.13 Not yet associated to SLE  1·366 38·31
Sema domain, Ig domain AA454570 3p21.3 Not yet associated to SLE  8·764 38·31
*

Fold change is the variability in the gene expression between patient and normal individuals or treated and untreated patients (negative values correspond to repressed and positive values to induced genes).

q-value is a P-value adapted for multiple testing to measure the difference in the expression of each gene.

Ig, immunoglobulin; TNF, tumour necrosis factor.