Gene Details



MFSD8 and homologs in 5 species are found in 147 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 II Mouse 452 Genes GS34322: Hippocampus Gene expression correlates of Cocaine TOTAL locomotion (activity beam breaks) in Males BXD
Expand Tier III Mouse 77 Genes GS216888: Co-expression cluster of haloperidol-induced catalepsy genes in striatum of HS mice short term selected lines. Light cyan Cluster
Expand Tier II Mouse 459 Genes GS34005: Hippocampus Gene expression correlates of Open Field locomotion 15-30 min post cocaine in Males BXD
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
Expand Tier I Human 414 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human 97 Genes GS175976: HP:0003621 Juvenile onset
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human GO 1699 Genes GS203755: GO:0016265 death
Expand Tier I Mouse 200 Genes GS135753: experimental allergic encephalomyelitis susceptibility 20 (Eae20, Published QTL Chr 3)
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Mouse GO 5588 Genes GS193061: GO:0044444 cytoplasmic part
Expand Tier I Mouse 178 Genes GS135998: HIV-associated nephropathy 1 (Hivan1, Published QTL Chr 3)
Expand Tier I Mouse GO 8630 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 99 Genes GS175130: HP:0000750 Delayed speech and language development
Expand Tier I Human 109 Genes GS176899: HP:0002353 EEG abnormality
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Mouse GO 8650 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 5436 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Mouse GO 5247 Genes GS178448: GO:0005634 nucleus
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier III Human 3178 Genes GS137407: Supplementary Table 2. Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Mouse 350 Genes GS135597: cholesterol and HDL QTL 2 (Chldq2, Published QTL Chr 3)
Expand Tier III Mouse 8107 Genes GS213076: Genes with suggestive difference in (B6) vs (B6PF1 + PB6F1 + PWD) comparison
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 11 Genes GS172189: HP:0002180 Neurodegeneration
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier II Mouse 262 Genes GS84145: high-dose ethanol actions (Published QTL, Chr 3)
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Mouse GO 5734 Genes GS190713: GO:0016021 integral to membrane
Expand Tier I Human GO 344 Genes GS197314: GO:0000323 lytic vacuole
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier II Mouse 454 Genes GS35748: Hippocampus Gene expression correlates of Open Field locomotion (activity beam breaks) 0-15 min post 2nd cocaine in Males BXD
Expand Tier III Fly 2671 Genes GS213271: Head and thorax heatmapping of Canton-S fruit flies with dietary restrictions
Expand Tier I Human 416 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier I Human GO 761 Genes GS209613: GO:0055085 transmembrane transport
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier I Mouse GO 8406 Genes GS177404: GO:0005737 cytoplasm
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human 261 Genes GS176172: HP:0001251 Ataxia
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Mouse GO 4001 Genes GS183543: GO:0051179 localization
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Mouse 244 Genes GS136077: inspiratory timing at baseline QTL 1 (Itbq1, Published QTL Chr 3)
Expand Tier III Fly 2674 Genes GS213272: Head and thorax heatmapping of reservatrol treated Canton-S fruit flies
Expand Tier I Human GO 3318 Genes GS209452: GO:0006810 transport
Expand Tier I Mouse 242 Genes GS135413: bar holding four paws (Bh4p, Published QTL Chr 3)
Expand Tier I Mouse 178 Genes GS136829: thymocyte proliferative response 3 (Thypr3, Published QTL Chr 3)
Expand Tier I Human GO 344 Genes GS207982: GO:0005764 lysosome
Expand Tier II Mouse 150 Genes GS26244: Cerebellum Gene expression correlates of Mechanical Nociception - Tail Clip Test in Females BXD
Expand Tier I Human GO 407 Genes GS209163: GO:0005773 vacuole
Expand Tier II Mouse 255 Genes GS84148: ethanol withdrawal (Published QTL, Chr 3)
Expand Tier I Mouse 230 Genes GS136047: insulin dependent diabetes susceptibility 3 (Idd3, Published QTL Chr 3)
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human CTD 5725 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Human 416 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Human GO 3372 Genes GS194459: GO:0051234 establishment of localization
Expand Tier II Mouse 255 Genes GS84147: ethanol conditioned taste aversion (Published QTL, Chr 3)
Expand Tier I Mouse GO 324 Genes GS192230: GO:0005773 vacuole
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Mouse GO 888 Genes GS192671: GO:0055085 transmembrane transport
Expand Tier I Human GO 253 Genes GS205611: GO:0044437 vacuolar part
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Mouse 224 Genes GS135545: CD4 T cell subset 1 (Cd4ts1, Published QTL Chr 3)
Expand Tier I Mouse 175 Genes GS135878: femur geometry 2 (Fmgty2, Published QTL Chr 3)
Expand Tier I Mouse 210 Genes GS136404: organ weight QTL 4 (Orgwq4, Published QTL Chr 3)
Expand Tier I Human GO 6769 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Mouse 148 Genes GS129078: autoimmune ovarian dysgenesis 2 (Aod2 Published QTL Chr 3)
Expand Tier I Human 274 Genes GS172372: HP:0000648 Optic atrophy
Expand Tier I Human 168 Genes GS175668: HP:0007369 Atrophy/Degeneration affecting the cerebrum
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse GO 274 Genes GS191074: GO:0005764 lysosome
Expand Tier II Mouse 238 Genes GS84144: METH responses for home cage activity (Published QTL, Chr 3)
Expand Tier III Mouse 6105 Genes GS213074: Genes with suggestive difference in (B6PF1) vs (PB6F1 + B6 + PWD) comparison
Expand Tier III Mouse 8003 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampal tissue
Expand Tier I Mouse GO 5859 Genes GS182404: GO:0031224 intrinsic to membrane
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 123 Genes GS175588: HP:0001311 Neurophysiological abnormality
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
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 III Mouse 124 Genes GS26275: Hippocampus Gene expression correlates of Mechanical Sensitivity-Von Frey Threshold [Pain] in Males BXD
Expand Tier I Human 47 Genes GS171072: HP:0000572 Visual loss
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 344 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Mouse GO 6473 Genes GS184448: GO:0044425 membrane part
Expand Tier I Human GO 5948 Genes GS195199: GO:0005634 nucleus
Expand Tier I Human 202 Genes GS174764: HP:0007367 Atrophy/Degeneration affecting the central nervous system
Expand Tier I Mouse GO 274 Genes GS180521: GO:0000323 lytic vacuole
Expand Tier I Mouse DRG 1187 Genes provisional GS87137: Table S2: List of probe-sets of genes differentially expressed among the four inbred strains of mice. Gene Ranks [DRG]
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 4144 Genes GS200341: GO:0051179 localization
Expand Tier I Human 164 Genes GS174994: HP:0002059 Cerebral atrophy
Expand Tier III Fly 2280 Genes GS75562: Differentially expressed alcohol sensitivity in Drosophila melanogaster (line)
Expand Tier II Mouse 465 Genes GS35733: Hippocampus Gene expression correlates of Open Field locomotion (cm) 0-15 min post cocaine in Males BXD
Expand Tier I Mouse 224 Genes GS135610: circulating hormone level QTL 2 (Chlq2, Published QTL Chr 3)
Expand Tier I Mouse 229 Genes GS136352: novelty/stress induced locomotor activation 2 (Nsila2, Published QTL Chr 3)
Expand Tier I Mouse GO 3211 Genes GS192509: GO:0006810 transport
Expand Tier I Human 364 Genes GS173991: HP:0000505 Visual impairment
Expand Tier II Mouse 464 Genes GS35718: Hippocampus Gene expression correlates of Open Field locomotion 0-15 min post cocaine in Males BXD
Expand Tier I Human 88 Genes GS176588: HP:0001272 Cerebellar atrophy
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 699 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 512 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Mouse GO 8145 Genes GS190714: GO:0016020 membrane
Expand Tier II Mouse 124 Genes GS35392: Hippocampus Gene expression correlates of Mechanical Sensitivity-Von Frey Threshold in Males BXD
Expand Tier I Human 77 Genes GS171254: HP:0002360 Sleep disturbance
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 35 Genes GS172848: HP:0000488 Retinopathy
Expand Tier I Human 616 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse 244 Genes GS136625: Stem cell proliferation 6 (Scpro6, Published QTL Chr 3)
Expand Tier I Human 26 Genes GS176290: HP:0002123 Generalized myoclonic seizures
Expand Tier I Human 50 Genes GS172258: HP:0002197 Generalized seizures
Expand Tier I Human 416 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Human 308 Genes GS172100: HP:0000587 Abnormality of the optic nerve
Expand Tier I Human GO 1697 Genes GS194905: GO:0008219 cell death
Expand Tier I Human GO 184 Genes GS209175: GO:0005774 vacuolar membrane
Expand Tier I Human 515 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier II Mouse 256 Genes GS84146: METH responses for home cage activity (Published QTL, Chr 3)
Expand Tier I Mouse 230 Genes GS136420: platelet activation 1 (Pact1, Published QTL Chr 3)
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human 65 Genes GS171651: HP:0000618 Blindness
Expand Tier I Human GO 2373 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human GO 140 Genes GS206073: GO:0005765 lysosomal membrane
Expand Tier I Human 108 Genes GS176797: HP:0001268 Mental deterioration
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 Mouse 229 Genes GS135328: arthropathy in MRL and DBA/1 mice 2 (Artmd2, Published QTL Chr 3)
Expand Tier I Mouse GO 3268 Genes GS177721: GO:0051234 establishment of localization
Expand Tier I Human 388 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier II Mouse 361 Genes GS26280: Hippocampus Gene expression correlates of Mechanical Sensitivity-Von Frey Threshold in Females & Males BXD