Gene Details



PIGO and homologs in 1 species are found in 127 GeneSets:


- Entrez   - GeneNetwork   - 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 387 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 1771 Genes GS196284: GO:0012505 endomembrane system
Expand Tier I Human 51 Genes GS177034: HP:0000436 Abnormality of the nasal tip
Expand Tier I Human GO 4713 Genes GS205364: GO:0010467 gene expression
Expand Tier I Human GO 1736 Genes GS208734: GO:0016740 transferase activity
Expand Tier I Human GO 6769 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human GO 3885 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier I Human GO 5152 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier I Human 15 Genes GS173040: HP:0010804 Tented upper lip vermilion
Expand Tier I Human 275 Genes GS170962: HP:0000159 Abnormality of the lip
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human GO 137 Genes GS201235: GO:0046488 phosphatidylinositol metabolic process
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
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 34 Genes GS174820: HP:0002023 Anal atresia
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human GO 1205 Genes GS194505: GO:1901135 carbohydrate derivative metabolic process
Expand Tier I Human 249 Genes GS176844: HP:0000429 Abnormality of the nasal alae
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human 99 Genes GS175130: HP:0000750 Delayed speech and language development
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
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 101 Genes GS196261: GO:0042157 lipoprotein metabolic process
Expand Tier I Human 281 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human GO 5436 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human GO 97 Genes GS194400: GO:0006661 phosphatidylinositol biosynthetic process
Expand Tier I Human GO 5320 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human GO 2464 Genes GS199032: GO:0036211 protein modification process
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 403 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 27 Genes GS171442: HP:0003155 Elevated alkaline phosphatase
Expand Tier I Human GO 810 Genes GS195897: GO:0044255 cellular lipid metabolic process
Expand Tier I Human GO 98 Genes GS194244: GO:0046467 membrane lipid biosynthetic process
Expand Tier I Human GO 36 Genes GS199463: GO:0006505 GPI anchor metabolic process
Expand Tier I Human GO 196 Genes GS201308: GO:0043687 post-translational protein modification
Expand Tier I Human GO 2558 Genes GS194336: GO:0043412 macromolecule modification
Expand Tier I Human 31 Genes GS171610: HP:0004379 Abnormality of alkaline phosphatase activity
Expand Tier I Human GO 102 Genes GS194403: GO:0006664 glycolipid metabolic process
Expand Tier I Human GO 52 Genes GS196318: GO:0009247 glycolipid biosynthetic process
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 139 Genes GS171397: HP:0000177 Abnormality of upper lip
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 231 Genes GS202625: GO:0045017 glycerolipid biosynthetic process
Expand Tier I Human GO 520 Genes GS194460: GO:0090407 organophosphate biosynthetic process
Expand Tier I Human 61 Genes GS171609: HP:0011339 Abnormality of upper lip vermillion
Expand Tier I Human GO 2373 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 8702 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 60 Genes GS196262: GO:0042158 lipoprotein biosynthetic process
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human GO 1281 Genes GS196726: GO:0005783 endoplasmic reticulum
Expand Tier I Human GO 4276 Genes GS207858: GO:0009059 macromolecule biosynthetic process
Expand Tier I Human CTD 1587 Genes GS124695: arsenic trioxide interacting genes (MeSH:C006632) in CTD
Expand Tier I Human 119 Genes GS172170: HP:0003196 Short nose
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 6151 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human GO 835 Genes GS210330: GO:0006412 translation
Expand Tier I Human 639 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human GO 2431 Genes GS209232: GO:0006796 phosphate-containing compound metabolic process
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human GO 236 Genes GS206874: GO:0006650 glycerophospholipid metabolic process
Expand Tier I Human GO 551 Genes GS194503: GO:1901137 carbohydrate derivative biosynthetic process
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human GO 541 Genes GS196667: GO:0008610 lipid biosynthetic process
Expand Tier I Human GO 30 Genes GS196964: GO:0018410 C-terminal protein amino acid modification
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 5223 Genes GS207857: GO:0009058 biosynthetic process
Expand Tier I Human GO 55 Genes GS194544: GO:0006497 protein lipidation
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 525 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Human GO 1138 Genes GS193812: GO:0006629 lipid metabolic process
Expand Tier I Human GO 3254 Genes GS200602: GO:0044267 cellular protein metabolic process
Expand Tier I Human GO 346 Genes GS202602: GO:0006644 phospholipid metabolic process
Expand Tier I Human 48 Genes GS173103: HP:0004378 Abnormality of the anus
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 221 Genes GS171139: HP:0005288 Abnormality of the nares
Expand Tier I Human 588 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Human GO 34 Genes GS199466: GO:0006506 GPI anchor biosynthetic process
Expand Tier I Human GO 2464 Genes GS196595: GO:0006464 cellular protein modification process
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human 232 Genes GS173288: HP:0000316 Hypertelorism
Expand Tier I Human CTD 5075 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Human GO 6651 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human GO 193 Genes GS198636: GO:0046474 glycerophospholipid biosynthetic process
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 210 Genes GS175990: HP:0000463 Anteverted nares
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 4169 Genes GS207925: GO:0034645 cellular macromolecule biosynthetic process
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 216 Genes GS196055: GO:0008654 phospholipid biosynthetic process
Expand Tier I Human 15 Genes GS176629: HP:0000455 Broad nasal tip
Expand Tier I Human GO 772 Genes GS196729: GO:0005789 endoplasmic reticulum membrane
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 311 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier I Human GO 164 Genes GS202605: GO:0006643 membrane lipid metabolic process
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human GO 1180 Genes GS195151: GO:0019637 organophosphate metabolic process
Expand Tier I Human 15 Genes GS175229: HP:0002025 Anal stenosis
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human 183 Genes GS176955: HP:0000431 Wide nasal bridge
Expand Tier I Human GO 919 Genes GS197025: GO:0044432 endoplasmic reticulum part
Expand Tier I Human GO 2494 Genes GS209235: GO:0006793 phosphorus metabolic process
Expand Tier I Human GO 789 Genes GS204928: GO:0042175 nuclear outer membrane-endoplasmic reticulum membrane network
Expand Tier I Human 98 Genes GS176867: HP:0003577 Congenital onset
Expand Tier I Human GO 315 Genes GS201237: GO:0046486 glycerolipid metabolic process
Expand Tier I Human 358 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Human GO 7311 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human GO 25 Genes GS199461: GO:0006501 C-terminal protein lipidation
Expand Tier I Human GO 5047 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Tier I Human GO 16 Genes GS208105: GO:0016254 preassembly of GPI anchor in ER membrane