Gene Details



NHLRC1 and homologs in 1 species are found in 144 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 GO 10576 Genes GS203594: GO:0043226 organelle
Expand Tier I Human 11 Genes GS176288: HP:0002121 Absence seizures
Expand Human 93 Genes GS222103: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PYRIMIDINE_METABOLISM
Expand Tier I Human 877 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human GO 6743 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human GO 3108 Genes GS198685: GO:0048522 positive regulation of cellular process
Expand Human 156 Genes GS220986: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PURINE_METABOLISM
Expand Tier I Human 3 Genes GS170818: HP:0011157 Auras
Expand Tier I Human 46 Genes GS175481: HP:0000992 Cutaneous photosensitivity
Expand Tier I Human GO 3863 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier I Human GO 1839 Genes GS198572: GO:0010604 positive regulation of macromolecule metabolic process
Expand Tier I Human 829 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human GO 230 Genes GS208669: GO:0010498 proteasomal protein catabolic process
Expand Tier I Human 411 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human GO 425 Genes GS206525: GO:0044257 cellular protein catabolic process
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Human 156 Genes GS221235: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PURINE_METABOLISM
Expand Human 20 Genes GS219647: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_RNA_POLYMERASE
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human GO 167 Genes GS195031: GO:0000209 protein polyubiquitination
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 8094 Genes GS202316: GO:0050789 regulation of biological process
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 9088 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 50 Genes GS173113: HP:0002186 Apraxia
Expand Tier I Human GO 1408 Genes GS197669: GO:0051246 regulation of protein metabolic process
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 47 Genes GS171072: HP:0000572 Visual loss
Expand Tier I Human 840 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 110 Genes GS171784: HP:0001399 Hepatic failure
Expand Tier I Human 1002 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human GO 2455 Genes GS199032: GO:0036211 protein modification process
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human GO 565 Genes GS207755: GO:0032446 protein modification by small protein conjugation
Expand Tier I Human GO 7259 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human GO 534 Genes GS200344: GO:0016567 protein ubiquitination
Expand Tier I Human GO 4129 Genes GS206329: GO:0060255 regulation of macromolecule metabolic process
Expand Tier I Human GO 1974 Genes GS203688: GO:0008270 zinc ion binding
Expand Tier I Human GO 2549 Genes GS194336: GO:0043412 macromolecule modification
Expand Tier I Human GO 5908 Genes GS195199: GO:0005634 nucleus
Expand Tier I Human GO 267 Genes GS210524: GO:0019787 small conjugating protein ligase activity
Expand Tier I Human 33 Genes GS174504: HP:0000709 Psychosis
Expand Human 93 Genes GS221234: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PYRIMIDINE_METABOLISM
Expand Tier I Human 49 Genes GS173812: HP:0000738 Hallucinations
Expand Tier I Human GO 3432 Genes GS203057: GO:0048518 positive regulation of biological process
Expand Tier I Human GO 296 Genes GS208378: GO:0016881 acid-amino acid ligase activity
Expand Tier I Human GO 2216 Genes GS209291: GO:0046914 transition metal ion binding
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human GO 791 Genes GS200986: GO:0032270 positive regulation of cellular protein metabolic process
Expand Human 109 Genes GS220003: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_DNA_REPAIR
Expand Tier I Human 1046 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 131 Genes GS198239: GO:0031398 positive regulation of protein ubiquitination
Expand Tier I Human GO 5764 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human GO 890 Genes GS207863: GO:0009057 macromolecule catabolic process
Expand Tier I Human GO 252 Genes GS206483: GO:0004842 ubiquitin-protein ligase activity
Expand Human 93 Genes GS220985: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PYRIMIDINE_METABOLISM
Expand Tier I Human GO 692 Genes GS208575: GO:0044265 cellular macromolecule catabolic process
Expand Human 109 Genes GS219538: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_DNA_REPAIR
Expand Tier I Human 7 Genes GS170819: HP:0011153 Focal motor seizures
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 8645 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 135 Genes GS172857: HP:0004305 Involuntary movements
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human 2 Genes GS176064: HP:0011165 Visual auras
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human GO 1276 Genes GS196726: GO:0005783 endoplasmic reticulum
Expand Tier I Human 107 Genes GS176797: HP:0001268 Mental deterioration
Expand Tier I Human GO 1669 Genes GS202188: GO:0044248 cellular catabolic process
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human 361 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human GO 1853 Genes GS209010: GO:1901575 organic substance catabolic process
Expand Tier I Human GO 632 Genes GS208919: GO:0070647 protein modification by small protein conjugation or removal
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human GO 4003 Genes GS208978: GO:0043169 cation binding
Expand Tier I Human 483 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Human GO 410 Genes GS209989: GO:0051603 proteolysis involved in cellular protein catabolic process
Expand Tier I Human 260 Genes GS170933: HP:0001288 Gait disturbance
Expand Tier I Human GO 535 Genes GS194735: GO:0030163 protein catabolic process
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human GO 385 Genes GS195019: GO:0006511 ubiquitin-dependent protein catabolic process
Expand Tier I Human GO 222 Genes GS206741: GO:0043161 proteasomal ubiquitin-dependent protein catabolic process
Expand Tier I Human 1068 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human 19 Genes GS171042: HP:0002344 Progressive neurologic deterioration
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 15 Genes GS171025: HP:0011146 Dialeptic seizures
Expand Tier I Human 469 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human GO 862 Genes GS197670: GO:0051247 positive regulation of protein metabolic process
Expand Tier I Human GO 391 Genes GS200003: GO:0019941 modification-dependent protein catabolic process
Expand Tier I Human GO 7650 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier I Human GO 5280 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 3239 Genes GS200602: GO:0044267 cellular protein metabolic process
Expand Tier I Human 15 Genes GS175448: HP:0007359 Focal seizures
Expand Tier I Human GO 328 Genes GS208535: GO:0016879 ligase activity, forming carbon-nitrogen bonds
Expand Tier I Human GO 4354 Genes GS210182: GO:0031323 regulation of cellular metabolic process
Expand Tier I Human GO 940 Genes GS199468: GO:0006508 proteolysis
Expand Tier I Human GO 1245 Genes GS195710: GO:0032268 regulation of cellular protein metabolic process
Expand Tier I Human GO 8578 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human GO 1001 Genes GS198240: GO:0031399 regulation of protein modification process
Expand Tier I Human 62 Genes GS174055: HP:0000726 Dementia
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 27 Genes GS175187: HP:0002069 Generalized tonic-clonic seizures
Expand Human 109 Genes GS222142: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_DNA_REPAIR
Expand Tier I Human 124 Genes GS174854: HP:0001410 Decreased liver function
Expand Human 156 Genes GS222102: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PURINE_METABOLISM
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 394 Genes GS204468: GO:0043632 modification-dependent macromolecule catabolic process
Expand Human 109 Genes GS221099: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_DNA_REPAIR
Expand Tier I Human GO 2455 Genes GS196595: GO:0006464 cellular protein modification process
Expand Tier I Human 614 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Human 109 Genes GS221348: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_DNA_REPAIR
Expand Tier I Human GO 481 Genes GS195244: GO:0016874 ligase activity
Expand Tier I Human GO 6605 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 542 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human 53 Genes GS173243: HP:0001336 Myoclonus
Expand Tier I Human 26 Genes GS176290: HP:0002123 Generalized myoclonic seizures
Expand Tier I Human 736 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human GO 4292 Genes GS204746: GO:0080090 regulation of primary metabolic process
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 1876 Genes GS210181: GO:0031325 positive regulation of cellular metabolic process
Expand Tier I Human GO 4787 Genes GS204612: GO:0019222 regulation of metabolic process
Expand Tier I Human GO 467 Genes GS209583: GO:0048471 perinuclear region of cytoplasm
Expand Human 156 Genes GS219668: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PURINE_METABOLISM
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier III Human 721 Genes GS218676: Differentially expressed in hippocampus of chronic alcoholics.
Expand Tier I Human 7 Genes GS176257: HP:0002367 Visual hallucinations
Expand Tier I Human 128 Genes GS174657: HP:0001425 Heterogeneous
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human 4 Genes GS174104: HP:0007334 Bilateral convulsive seizures
Expand Human 93 Genes GS219656: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PYRIMIDINE_METABOLISM
Expand Tier I Human 50 Genes GS172258: HP:0002197 Generalized seizures
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 708 Genes GS203147: GO:0031401 positive regulation of protein modification process
Expand Tier I Human GO 1977 Genes GS204568: GO:0009893 positive regulation of metabolic process
Expand Tier I Human GO 3902 Genes GS198323: GO:0046872 metal ion binding
Expand Tier I Human GO 177 Genes GS198241: GO:0031396 regulation of protein ubiquitination
Expand Tier I Human GO 1994 Genes GS207862: GO:0009056 catabolic process