Gene Details



SLC30A10 and homologs in 1 species are found in 102 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 786 Genes GS195226: GO:0015075 ion transmembrane transporter activity
Expand Human 236 Genes GS219717: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_SPACE
Expand Human 226 Genes GS219699: http://www.broadinstitute.org/gsea/msigdb/cards/CYTOSKELETAL_PART
Expand Human 1188 Genes GS219988: http://www.broadinstitute.org/gsea/msigdb/cards/ORGANELLE_PART
Expand Tier I Human CTD 1541 Genes GS125445: Phenobarbital interacting genes (MeSH:D010634) in CTD
Expand Human 1183 Genes GS219682: http://www.broadinstitute.org/gsea/msigdb/cards/INTRACELLULAR_ORGANELLE_PART
Expand Human 622 Genes GS219701: http://www.broadinstitute.org/gsea/msigdb/cards/NON_MEMBRANE_BOUND_ORGANELLE
Expand Tier I Human GO 497 Genes GS196432: GO:0030001 metal ion transport
Expand Tier I Human GO 21 Genes GS196362: GO:0006829 zinc ion transport
Expand Human 1188 Genes GS219681: http://www.broadinstitute.org/gsea/msigdb/cards/ORGANELLE_PART
Expand Tier I Human CTD 1601 Genes GS123916: Aflatoxin B1 interacting genes (MeSH:D016604) in CTD
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Human 143 Genes GS219925: http://www.broadinstitute.org/gsea/msigdb/cards/MICROTUBULE_CYTOSKELETON
Expand Tier I Human CTD 3171 Genes GS127127: Benzo(a)pyrene interacting genes (MeSH:D001564) in CTD
Expand Tier I Human 310 Genes GS175805: HP:0003271 Visceromegaly
Expand Tier I Human 18 Genes GS174463: HP:0001901 Polycythemia
Expand Tier I Human CTD 434 Genes GS123811: Zinc interacting genes (MeSH:D015032) in CTD
Expand Human 438 Genes GS219721: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_REGION
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
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 161 Genes GS176803: HP:0001260 Dysarthria
Expand Tier I Human GO 5436 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human GO 3318 Genes GS209452: GO:0006810 transport
Expand Human 37 Genes GS221463: http://www.broadinstitute.org/gsea/msigdb/cards/PID_PLK1_PATHWAY
Expand Human 622 Genes GS219918: http://www.broadinstitute.org/gsea/msigdb/cards/NON_MEMBRANE_BOUND_ORGANELLE
Expand Human 1183 Genes GS219899: http://www.broadinstitute.org/gsea/msigdb/cards/INTRACELLULAR_ORGANELLE_PART
Expand Human 226 Genes GS219916: http://www.broadinstitute.org/gsea/msigdb/cards/CYTOSKELETAL_PART
Expand Tier I Human GO 5320 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human GO 4371 Genes GS205500: GO:0071944 cell periphery
Expand Human 438 Genes GS219938: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_REGION
Expand Tier I Human CTD 2424 Genes GS123265: Estradiol interacting genes (MeSH:D004958) in CTD
Expand Tier I Human CTD 578 Genes GS123943: Curcumin interacting genes (MeSH:D003474) in CTD
Expand Human 143 Genes GS219708: http://www.broadinstitute.org/gsea/msigdb/cards/MICROTUBULE_CYTOSKELETON
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human GO 980 Genes GS198214: GO:0022892 substrate-specific transporter activity
Expand Human 622 Genes GS219702: http://www.broadinstitute.org/gsea/msigdb/cards/INTRACELLULAR_NON_MEMBRANE_BOUND_ORGANELLE
Expand Human 143 Genes GS219998: http://www.broadinstitute.org/gsea/msigdb/cards/MICROTUBULE_CYTOSKELETON
Expand Human 358 Genes GS219709: http://www.broadinstitute.org/gsea/msigdb/cards/CYTOSKELETON
Expand Human 622 Genes GS219997: http://www.broadinstitute.org/gsea/msigdb/cards/INTRACELLULAR_NON_MEMBRANE_BOUND_ORGANELLE
Expand Tier I Human 246 Genes GS176806: HP:0003812 Phenotypic variability
Expand Human 358 Genes GS221022: http://www.broadinstitute.org/gsea/msigdb/cards/CYTOSKELETON
Expand Human 329 Genes GS219927: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_REGION_PART
Expand Tier III Human 2430 Genes GS216491: Genes that are binding sites for CREB and zif268,transcription factors mediating nieuronal activity and plasticity, in Homo sapiens.
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Human 358 Genes GS221271: http://www.broadinstitute.org/gsea/msigdb/cards/CYTOSKELETON
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 4144 Genes GS200341: GO:0051179 localization
Expand Human 1188 Genes GS219898: http://www.broadinstitute.org/gsea/msigdb/cards/ORGANELLE_PART
Expand Tier I Human GO 925 Genes GS197610: GO:0022857 transmembrane transporter activity
Expand Tier I Human GO 3372 Genes GS194459: GO:0051234 establishment of localization
Expand Tier I Human CTD 26 Genes GS124625: methylmercuric chloride interacting genes (MeSH:C004925) in CTD
Expand Tier I Human 38 Genes GS173459: HP:0001300 Parkinsonism
Expand Tier I Human 123 Genes GS173242: HP:0001337 Tremor
Expand Human 622 Genes GS219919: http://www.broadinstitute.org/gsea/msigdb/cards/INTRACELLULAR_NON_MEMBRANE_BOUND_ORGANELLE
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Human 236 Genes GS219934: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_SPACE
Expand Tier I Human CTD 217 Genes GS124987: Trinitrobenzenesulfonic Acid interacting genes (MeSH:D014302) in CTD
Expand Tier I Human GO 845 Genes GS198212: GO:0022891 substrate-specific transmembrane transporter activity
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human 246 Genes GS173534: HP:0001877 Abnormality of erythrocytes
Expand Human 1183 Genes GS219989: http://www.broadinstitute.org/gsea/msigdb/cards/INTRACELLULAR_ORGANELLE_PART
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human 12 Genes GS176911: HP:0002172 Postural instability
Expand Tier I Human GO 244 Genes GS205653: GO:0070838 divalent metal ion transport
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 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 67 Genes GS171788: HP:0001394 Cirrhosis
Expand Tier I Human 73 Genes GS175408: HP:0002071 Abnormality of extrapyramidal motor function
Expand Human 622 Genes GS219996: http://www.broadinstitute.org/gsea/msigdb/cards/NON_MEMBRANE_BOUND_ORGANELLE
Expand Tier I Human 487 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Human GO 4283 Genes GS197009: GO:0005886 plasma membrane
Expand Human 358 Genes GS219926: http://www.broadinstitute.org/gsea/msigdb/cards/CYTOSKELETON
Expand Tier I Human GO 569 Genes GS209735: GO:0008324 cation transmembrane transporter activity
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Human 1183 Genes GS221019: http://www.broadinstitute.org/gsea/msigdb/cards/INTRACELLULAR_ORGANELLE_PART
Expand Tier I Human 699 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Human 358 Genes GS219999: http://www.broadinstitute.org/gsea/msigdb/cards/CYTOSKELETON
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Human 37 Genes GS221501: http://www.broadinstitute.org/gsea/msigdb/cards/PID_PLK1_PATHWAY
Expand Tier I Human GO 964 Genes GS209451: GO:0006811 ion transport
Expand Tier I Human 68 Genes GS175906: HP:0002910 Elevated hepatic transaminases
Expand Human 329 Genes GS219710: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_REGION_PART
Expand Tier I Human GO 247 Genes GS206031: GO:0072511 divalent inorganic cation transport
Expand Tier I Human 27 Genes GS176808: HP:0002067 Bradykinesia
Expand Tier I Human GO 632 Genes GS209450: GO:0006812 cation transport
Expand Tier I Human 125 Genes GS174854: HP:0001410 Decreased liver function
Expand Tier I Human 106 Genes GS173246: HP:0001332 Dystonia
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Human CTD 5075 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Human 543 Genes GS175673: HP:0100022 Abnormality of movement
Expand Human 1183 Genes GS221268: http://www.broadinstitute.org/gsea/msigdb/cards/INTRACELLULAR_ORGANELLE_PART
Expand Tier I Human GO 1195 Genes GS196168: GO:0005215 transporter activity
Expand Tier I Human 316 Genes GS170825: HP:0002167 Neurological speech impairment
Expand Tier I Human 98 Genes GS171910: HP:0003828 Variable expressivity
Expand Tier I Human 266 Genes GS172415: HP:0002240 Hepatomegaly
Expand Tier I Human 626 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human 40 Genes GS175194: HP:0002063 Rigidity
Expand Tier I Human GO 90 Genes GS207399: GO:0000041 transition metal ion transport