Gene Details



SLC46A1 and homologs in 1 species are found in 198 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 124 Genes GS204243: GO:0006766 vitamin metabolic process
Expand Tier I Human CTD 18 Genes GS124415: 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid interacting genes (MeSH:D017878) in CTD
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human GO 1191 Genes GS207015: GO:0042592 homeostatic process
Expand Tier I Human 43 Genes GS173130: HP:0001875 Neutropenia
Expand Tier I Human 10 Genes GS176234: HP:0002305 Athetosis
Expand Tier I Human 534 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human GO 1684 Genes GS204629: GO:1901564 organonitrogen compound metabolic process
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 124 Genes GS172403: HP:0011873 Abnormal platelet count
Expand Tier I Human GO 16 Genes GS197618: GO:0005542 folic acid binding
Expand Tier I Human CTD 388 Genes GS121370: Clofibrate interacting genes (MeSH:D002994) in CTD
Expand Tier I Human 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human GO 224 Genes GS210290: GO:0016324 apical plasma membrane
Expand Tier I Human GO 1914 Genes GS198782: GO:0044459 plasma membrane part
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human GO 16 Genes GS194432: GO:0051184 cofactor transporter activity
Expand Tier I Human 537 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Human GO 129 Genes GS196969: GO:0006865 amino acid transport
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human GO 68 Genes GS201305: GO:0006879 cellular iron ion homeostasis
Expand Tier I Human 57 Genes GS174179: HP:0002514 Cerebral calcification
Expand Tier I Human GO 2511 Genes GS207903: GO:0044281 small molecule metabolic process
Expand Tier I Human GO 17 Genes GS196018: GO:0072337 modified amino acid transport
Expand Tier I Human 57 Genes GS171016: HP:0011893 Abnormal leukocyte count
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human CTD 917 Genes GS121965: Amiodarone interacting genes (MeSH:D000638) in CTD
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 5436 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human CTD 866 Genes GS126764: Calcitriol interacting genes (MeSH:D002117) in CTD
Expand Tier I Human 41 Genes GS175858: HP:0000737 Irritability
Expand Tier I Human GO 65 Genes GS204242: GO:0006767 water-soluble vitamin metabolic process
Expand Tier I Human 103 Genes GS174372: HP:0002024 Malabsorption
Expand Tier I Human GO 5320 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human GO 197 Genes GS204383: GO:0006575 cellular modified amino acid metabolic process
Expand Tier I Human 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human GO 5452 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
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 Human 255 Genes GS176610: HP:0003593 Infantile onset
Expand Tier I Human GO 649 Genes GS198498: GO:0050801 ion homeostasis
Expand Tier I Human 68 Genes GS170786: HP:0010972 Anemia of inadequate production
Expand Tier I Human 285 Genes GS175119: HP:0001881 Abnormality of leukocytes
Expand Tier I Human GO 5400 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Human GO 186 Genes GS200970: GO:0031406 carboxylic acid binding
Expand Tier I Human GO 29 Genes GS206467: GO:0042558 pteridine-containing compound metabolic process
Expand Tier I Human GO 2507 Genes GS196934: GO:0065008 regulation of biological quality
Expand Tier I Human CTD 374 Genes GS124417: Propylthiouracil interacting genes (MeSH:D011441) in CTD
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human CTD 210 Genes GS126758: Folic Acid interacting genes (MeSH:D005492) in CTD
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 715 Genes GS200565: GO:0019725 cellular homeostasis
Expand Tier I Human CTD 476 Genes GS125040: Thioacetamide interacting genes (MeSH:D013853) in CTD
Expand Tier I Human GO 4144 Genes GS200341: GO:0051179 localization
Expand Tier I Human GO 5810 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human CTD 265 Genes GS125371: Cadmium Chloride interacting genes (MeSH:D019256) in CTD
Expand Tier I Human 33 Genes GS171079: HP:0001882 Leukopenia
Expand Tier I Human 148 Genes GS173537: HP:0001872 Abnormality of thrombocytes
Expand Tier I Human 491 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Human 285 Genes GS171902: HP:0010987 Abnormality of cellular immune system
Expand Tier I Human CTD 272 Genes GS123751: Cadmium interacting genes (MeSH:D002104) in CTD
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 135 Genes GS172857: HP:0004305 Involuntary movements
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human 399 Genes GS171100: HP:0000759 Abnormality of the peripheral nervous system
Expand Tier I Human 246 Genes GS173534: HP:0001877 Abnormality of erythrocytes
Expand Tier I Human GO 7 Genes GS197124: GO:0015884 folic acid transport
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human GO 257 Genes GS194434: GO:0051186 cofactor metabolic process
Expand Tier I Human GO 313 Genes GS196355: GO:0006820 anion transport
Expand Tier I Human GO 4 Genes GS206557: GO:0008517 folic acid transporter activity
Expand Tier I Human GO 9 Genes GS202315: GO:0046655 folic acid metabolic process
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 353 Genes GS208526: GO:0055065 metal ion homeostasis
Expand Tier I Human CTD 14 Genes GS125801: Sulfasalazine interacting genes (MeSH:D012460) in CTD
Expand Tier I Human GO 6151 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human CTD 20 Genes GS126719: Heme interacting genes (MeSH:D006418) in CTD
Expand Tier I Human GO 631 Genes GS209611: GO:0055082 cellular chemical homeostasis
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human GO 5369 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier I Human 43 Genes GS173577: HP:0011991 Abnormal neutrophil cell number
Expand Tier I Human GO 4283 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Human 223 Genes GS176632: HP:0001903 Anemia
Expand Tier I Human GO 218 Genes GS197101: GO:0046942 carboxylic acid transport
Expand Tier I Human CTD 9 Genes GS122012: 5-methyltetrahydrofolate interacting genes (MeSH:C005984) in CTD
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human CTD 31 Genes GS124645: Leucovorin interacting genes (MeSH:D002955) in CTD
Expand Tier I Human 120 Genes GS170783: HP:0010974 Abnormality of myeloid leukocytes
Expand Tier I Human 699 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human GO 16 Genes GS194437: GO:0051183 vitamin transporter activity
Expand Tier I Human GO 971 Genes GS210163: GO:0006082 organic acid metabolic process
Expand Tier I Human 403 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Human 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human GO 837 Genes GS196920: GO:0048878 chemical homeostasis
Expand Tier I Human CTD 908 Genes GS124805: decitabine interacting genes (MeSH:C014347) in CTD
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 117 Genes GS170989: HP:0010766 Ectopic calcification
Expand Tier I Human GO 102 Genes GS197118: GO:0016597 amino acid binding
Expand Tier I Human GO 964 Genes GS209451: GO:0006811 ion transport
Expand Tier I Human CTD 303 Genes GS123351: Omeprazole interacting genes (MeSH:D009853) in CTD
Expand Tier I Human GO 215 Genes GS199314: GO:0006732 coenzyme metabolic process
Expand Tier I Human 1 Genes GS173641: HP:0004851 Folate-responsive megaloblastic anemia
Expand Tier I Human GO 8622 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human GO 294 Genes GS209721: GO:0045177 apical part of cell
Expand Tier I Human CTD 256 Genes GS126685: Methotrexate interacting genes (MeSH:D008727) in CTD
Expand Tier I Human 4 Genes GS171972: HP:0000155 Oral ulcer
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human GO 553 Genes GS201022: GO:0071705 nitrogen compound transport
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 CTD 2013 Genes GS126646: Carbon Tetrachloride interacting genes (MeSH:D002251) in CTD
Expand Tier I Human 23 Genes GS173296: HP:0011830 Abnormality of oral mucosa
Expand Tier I Human CTD 14 Genes GS125653: Sulfobromophthalein interacting genes (MeSH:D013448) in CTD
Expand Tier I Human 416 Genes GS173147: HP:0011283 Abnormality of the metencephalon
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 Human GO 20 Genes GS194436: GO:0051180 vitamin transport
Expand Tier I Human CTD 5075 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Human 473 Genes GS171893: HP:0011458 Abdominal symptom
Expand Tier I Human GO 2625 Genes GS196343: GO:0036094 small molecule binding
Expand Tier I Human CTD 281 Genes GS125104: Ethionine interacting genes (MeSH:D005001) in CTD
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 543 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human GO 263 Genes GS202551: GO:0015711 organic anion transport
Expand Tier I Human 11 Genes GS176060: HP:0002135 Basal ganglia calcification
Expand Tier I Human 534 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Human 214 Genes GS222320: Genes associated with high risk of intellectual disability.
Expand Tier I Human GO 761 Genes GS209613: GO:0055085 transmembrane transport
Expand Tier I Human GO 1195 Genes GS196168: GO:0005215 transporter activity
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human GO 339 Genes GS195494: GO:0006520 cellular amino acid metabolic process
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 82 Genes GS199560: GO:0043648 dicarboxylic acid metabolic process
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 5379 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Human 283 Genes GS172060: HP:0001508 Failure to thrive
Expand Tier I Human GO 63 Genes GS200729: GO:0006835 dicarboxylic acid transport
Expand Tier I Human GO 1929 Genes GS201025: GO:0071702 organic substance transport
Expand Tier I Human 626 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human 261 Genes GS176172: HP:0001251 Ataxia
Expand Tier I Human 33 Genes GS171831: HP:0001972 Macrocytic anemia
Expand Tier I Human 303 Genes GS172416: HP:0002242 Abnormality of the intestine
Expand Tier I Human GO 48 Genes GS199797: GO:0072341 modified amino acid binding
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human 104 Genes GS173535: HP:0001874 Abnormality of neutrophils
Expand Tier I Human 114 Genes GS176840: HP:0001911 Abnormality of granulocytes
Expand Human 43 Genes GS222176: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_STARCH_AND_SUCROSE_METABOLISM
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human GO 5558 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human 416 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Human GO 586 Genes GS201310: GO:0006873 cellular ion homeostasis
Expand Tier I Human GO 87 Genes GS205838: GO:0055072 iron ion homeostasis
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human 275 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 23 Genes GS204244: GO:0006760 folic acid-containing compound metabolic process
Expand Tier I Human 207 Genes GS176283: HP:0009830 Peripheral neuropathy
Expand Tier I Human GO 137 Genes GS205251: GO:0019842 vitamin binding
Expand Tier I Human GO 3318 Genes GS209452: GO:0006810 transport
Expand Tier I Human GO 220 Genes GS200204: GO:0015849 organic acid transport
Expand Tier I Human GO 846 Genes GS204326: GO:0019752 carboxylic acid metabolic process
Expand Tier I Human GO 327 Genes GS201306: GO:0006875 cellular metal ion homeostasis
Expand Tier I Human GO 4371 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Human 26 Genes GS176059: HP:0002134 Abnormality of the basal ganglia
Expand Tier I Human GO 2392 Genes GS206737: GO:0043168 anion binding
Expand Tier I Human GO 8 Genes GS194794: GO:0015232 heme transporter activity
Expand Tier I Human GO 5962 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human 215 Genes GS172139: HP:0010993 Abnormality of the cerebral subcortex
Expand Tier I Human 394 Genes GS172362: HP:0004325 Decreased body weight
Expand Tier I Human 237 Genes GS174292: HP:0011968 Feeding difficulties
Expand Tier I Human GO 953 Genes GS202555: GO:0043436 oxoacid metabolic process
Expand Tier I Human 109 Genes GS174136: HP:0002014 Diarrhea
Expand Tier I Human 121 Genes GS173538: HP:0001873 Thrombocytopenia
Expand Tier I Human GO 367 Genes GS196433: GO:0030003 cellular cation homeostasis
Expand Tier I Human CTD 281 Genes GS121771: Benzbromarone interacting genes (MeSH:D001553) in CTD
Expand Tier I Human 199 Genes GS171637: HP:0008872 Feeding difficulties in infancy
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human GO 20 Genes GS194435: GO:0051181 cofactor transport
Expand Tier I Human CTD 4389 Genes GS123768: Cyclosporine interacting genes (MeSH:D016572) in CTD
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 203 Genes GS171621: HP:0100851 Abnormal emotion/affect behavior
Expand Tier I Human GO 3372 Genes GS194459: GO:0051234 establishment of localization
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 GO 428 Genes GS209609: GO:0055080 cation homeostasis
Expand Tier I Human 16 Genes GS175112: HP:0001889 Megaloblastic anemia
Expand Tier I Human GO 8702 Genes GS205255: GO:0044238 primary metabolic process