Gene Details



GLRX5 and homologs in 1 species are found in 70 GeneSets:


- Entrez   - Ensembl   - GeneNetwork   - STRING   - Allen Brain Atlas   - Comparative Toxicogenomics Database  

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Human GO 4567 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human GO 1191 Genes GS207015: GO:0042592 homeostatic process
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 6769 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human GO 1790 Genes GS194586: GO:0002376 immune system process
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 8 Genes GS173213: HP:0003281 Increased serum ferritin
Expand Tier I Human GO 61 Genes GS209157: GO:0051536 iron-sulfur cluster binding
Expand Tier I Human CTD 4423 Genes GS123718: Ethinyl Estradiol interacting genes (MeSH:D004997) in CTD
Expand Tier I Human GO 3513 Genes GS193991: GO:0048731 system development
Expand Tier I Human 626 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human GO 27 Genes GS195476: GO:0015035 protein disulfide oxidoreductase activity
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human GO 54 Genes GS210408: GO:0016667 oxidoreductase activity, acting on a sulfur group of donors
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human 129 Genes GS174657: HP:0001425 Heterogeneous
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 32 Genes GS195844: GO:0015036 disulfide oxidoreductase activity
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 8137 Genes GS202316: GO:0050789 regulation of biological process
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human GO 3934 Genes GS198323: GO:0046872 metal ion binding
Expand Tier I Human GO 1518 Genes GS194138: GO:0005739 mitochondrion
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 57 Genes GS197968: GO:0045454 cell redox homeostasis
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human GO 561 Genes GS195206: GO:0002520 immune system development
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human 255 Genes GS176610: HP:0003593 Infantile onset
Expand Tier I Human GO 2507 Genes GS196934: GO:0065008 regulation of biological quality
Expand Tier I Human 13 Genes GS176041: HP:0011031 Abnormality of iron homeostasis
Expand Tier I Human GO 5948 Genes GS195199: GO:0005634 nucleus
Expand Tier I Human GO 2545 Genes GS203335: GO:0048513 organ development
Expand Tier I Human CTD 4389 Genes GS123768: Cyclosporine interacting genes (MeSH:D016572) in CTD
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 715 Genes GS200565: GO:0019725 cellular homeostasis
Expand Tier I Human GO 5810 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human GO 4070 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 246 Genes GS173534: HP:0001877 Abnormality of erythrocytes
Expand Tier I Human GO 4024 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 15 Genes GS176042: HP:0011030 Abnormality of transition element cation homeostasis
Expand Tier I Human GO 4034 Genes GS208978: GO:0043169 cation binding
Expand Tier I Human 223 Genes GS176632: HP:0001903 Anemia
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 117 Genes GS172364: HP:0003111 Abnormality of ion homeostasis
Expand Tier I Human GO 19 Genes GS209158: GO:0051537 2 iron, 2 sulfur cluster binding
Expand Tier I Human GO 7689 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier I Human GO 5321 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 531 Genes GS194284: GO:0048534 hematopoietic or lymphoid organ development
Expand Tier I Human GO 157 Genes GS207864: GO:0009055 electron carrier activity
Expand Tier I Human GO 8622 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human GO 61 Genes GS205357: GO:0051540 metal cluster binding
Expand Tier I Human 103 Genes GS176735: HP:0010929 Abnormality of cation homeostasis
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human GO 497 Genes GS210170: GO:0030097 hemopoiesis
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human CTD 2047 Genes GS127205: Tamoxifen interacting genes (MeSH:D013629) in CTD
Expand Tier I Human GO 709 Genes GS198755: GO:0016491 oxidoreductase activity