Gene Details



CDAN1 and homologs in 1 species are found in 51 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 877 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human 1 Genes GS175190: HP:0005532 Macrocytic dyserythropoietic anemia
Expand Tier I Human 621 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human 32 Genes GS171831: HP:0001972 Macrocytic anemia
Expand Tier III Human 721 Genes GS218676: Differentially expressed in hippocampus of chronic alcoholics.
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human 3 Genes GS172794: HP:0001530 Mild postnatal growth retardation
Expand Tier I Human 213 Genes GS176040: HP:0011032 Abnormality of fluid regulation
Expand Tier I Human 2 Genes GS173943: HP:0003655 Reduced activity of N-acetylglucosaminyltransferase II
Expand Tier I Human 174 Genes GS172015: HP:0000969 Edema
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 99 Genes GS176774: HP:0001005 Dermatological manifestations of systemic disorders
Expand Tier I Human GO 5359 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Human 1470 Genes GS219947: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier I Human 81 Genes GS171786: HP:0001396 Cholestasis
Expand Tier I Human 51 Genes GS171296: HP:0008897 Postnatal growth retardation
Expand Tier I Human 641 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human GO 5243 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human 840 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 15 Genes GS175977: HP:0006579 Prolonged neonatal jaundice
Expand Tier I Human 32 Genes GS176141: HP:0001789 Hydrops fetalis
Expand Tier I Human 108 Genes GS175595: HP:0011017 Abnormality of cell physiology
Expand Tier I Human 66 Genes GS170786: HP:0010972 Anemia of inadequate production
Expand Human 2063 Genes GS219980: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human 257 Genes GS172272: HP:0001197 Abnormality of prenatal development or birth
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 2 Genes GS173851: HP:0003352 Endopolyploidy on chromosome studies of bone marrow
Expand Tier I Human 3 Genes GS173331: HP:0004367 Abnormality of glycoprotein metabolism
Expand Tier I Human 243 Genes GS173534: HP:0001877 Abnormality of erythrocytes
Expand Human 282 Genes GS222704: test
Expand Tier I Human 62 Genes GS174527: HP:0000952 Jaundice
Expand Human 1470 Genes GS219983: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier I Human GO 6073 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 483 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Human 220 Genes GS176632: HP:0001903 Anemia
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 1068 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 19 Genes GS173827: HP:0002916 Abnormality of chromosome segregation
Expand Human 2063 Genes GS219986: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 128 Genes GS171905: HP:0004297 Abnormality of the biliary system
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Human 2063 Genes GS219964: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human CTD 5081 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Human 2063 Genes GS219747: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 736 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Human 1470 Genes GS219730: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Human 1470 Genes GS219977: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE