Gene Details



SLC17A5 and homologs in 1 species are found in 258 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 10 Genes GS176234: HP:0002305 Athetosis
Expand Tier I Human 10 Genes GS174959: HP:0002540 Inability to walk
Expand Tier I Human 877 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human 51 Genes GS176730: HP:0000100 Nephrotic syndrome
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 11 Genes GS170841: HP:0001107 Ocular albinism
Expand Tier I Human 231 Genes GS176771: HP:0001000 Abnormality of skin pigmentation
Expand Tier I Human 13 Genes GS172154: HP:0002679 Abnormality of the sella turcica
Expand Tier I Human 829 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
Expand Tier I Human 8 Genes GS177044: HP:0001922 Vacuolated lymphocytes
Expand Tier I Human 26 Genes GS173686: HP:0001640 Cardiomegaly
Expand Tier I Human 541 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 535 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human 100 Genes GS175101: HP:0000280 Coarse facial features
Expand Tier I Human 174 Genes GS172015: HP:0000969 Edema
Expand Tier I Human 99 Genes GS175130: HP:0000750 Delayed speech and language development
Expand Tier I Human 8 Genes GS174059: HP:0002908 Conjugated hyperbilirubinemia
Expand Tier I Human 214 Genes GS176167: HP:0001257 Spasticity
Expand Tier I Human GO 5359 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human 407 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human 50 Genes GS173113: HP:0002186 Apraxia
Expand Tier I Human 156 Genes GS174002: HP:0000189 Narrow palate
Expand Tier I Human 641 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 33 Genes GS174067: HP:0002904 Hyperbilirubinemia
Expand Tier I Human 318 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier I Human 170 Genes GS174488: HP:0000525 Abnormality of the iris
Expand Tier I Human 840 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 1002 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human GO 1 Genes GS210701: GO:0015739 sialic acid transport
Expand Tier I Human 486 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human 7 Genes GS173407: HP:0002680 J-shaped sella turcica
Expand Tier I Human 32 Genes GS174840: HP:0011358 Generalized hypopigmentation of hair
Expand Tier I Human GO 966 Genes GS209550: GO:0031982 vesicle
Expand Tier I Human 86 Genes GS174810: HP:0001635 Congestive heart failure
Expand Tier I Human 372 Genes GS175815: HP:0011025 Abnormality of cardiovascular system physiology
Expand Tier I Human 146 Genes GS170968: HP:0000156 High-arched palate
Expand Tier I Human GO 27 Genes GS198427: GO:0008028 monocarboxylic acid transmembrane transporter activity
Expand Tier I Human 66 Genes GS176153: HP:0100820 Glomerulopathy
Expand Tier I Human 489 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Human 282 Genes GS171902: HP:0010987 Abnormality of cellular immune system
Expand Tier I Human 936 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Human 262 Genes GS219934: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_SPACE
Expand Tier I Human GO 844 Genes GS198212: GO:0022891 substrate-specific transmembrane transporter activity
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 128 Genes GS207410: GO:0015293 symporter activity
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 636 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human GO 341 Genes GS197314: GO:0000323 lytic vacuole
Expand Tier I Human 222 Genes GS173995: HP:0000508 Ptosis
Expand Tier I Human GO 4250 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Human 496 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Human GO 569 Genes GS209735: GO:0008324 cation transmembrane transporter activity
Expand Tier I Human GO 6347 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human GO 39 Genes GS203887: GO:1901264 carbohydrate derivative transport
Expand Tier I Human 404 Genes GS173743: HP:0001999 Abnormal facial shape
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 187 Genes GS172471: HP:0001744 Splenomegaly
Expand Tier I Human GO 245 Genes GS195413: GO:0008509 anion transmembrane transporter activity
Expand Tier I Human 60 Genes GS172737: HP:0010991 Abnormality of the abdominal musculature
Expand Tier I Human 50 Genes GS177055: HP:0005599 Hypopigmentation of hair
Expand Tier I Human 73 Genes GS171209: HP:0000093 Proteinuria
Expand Tier I Human 413 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier I Human 10 Genes GS173408: HP:0002681 Deformed sella turcica
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 532 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Human 104 Genes GS171211: HP:0000091 Abnormality of the renal tubule
Expand Tier I Human GO 761 Genes GS209613: GO:0055085 transmembrane transport
Expand Human 195 Genes GS222320: Genes associated with high risk of intellectual disability.
Expand Tier I Human 886 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human GO 1193 Genes GS196168: GO:0005215 transporter activity
Expand Tier I Human 315 Genes GS170825: HP:0002167 Neurological speech impairment
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 Tier I Human 209 Genes GS175990: HP:0000463 Anteverted nares
Expand Tier I Human 36 Genes GS171175: HP:0001541 Ascites
Expand Tier I Human 263 Genes GS172415: HP:0002240 Hepatomegaly
Expand Tier I Human GO 924 Genes GS205321: GO:0031410 cytoplasmic vesicle
Expand Tier I Human 77 Genes GS172699: HP:0002652 Skeletal dysplasia
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human 282 Genes GS172060: HP:0001508 Failure to thrive
Expand Tier I Human GO 1925 Genes GS201025: GO:0071702 organic substance transport
Expand Tier I Human 418 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human 621 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human 259 Genes GS176172: HP:0001251 Ataxia
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human GO 9 Genes GS207379: GO:0005402 cation:sugar symporter activity
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 48 Genes GS176364: HP:0008034 Abnormal iris pigmentation
Expand Tier I Human 49 Genes GS173667: HP:0010318 Aplasia/Hypoplasia of the abdominal wall musculature
Expand Tier I Human GO 24 Genes GS208177: GO:0051119 sugar transmembrane transporter activity
Expand Tier I Human 213 Genes GS176040: HP:0011032 Abnormality of fluid regulation
Expand Tier I Human 484 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human 307 Genes GS175805: HP:0003271 Visceromegaly
Expand Tier I Human 269 Genes GS174948: HP:0100763 Abnormality of the lymphatic system
Expand Tier I Human 413 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Human GO 311 Genes GS209586: GO:0022804 active transmembrane transporter activity
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 273 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 99 Genes GS202545: GO:0015718 monocarboxylic acid transport
Expand Tier I Human 181 Genes GS175907: HP:0004349 Reduced bone mineral density
Expand Tier I Human 160 Genes GS176803: HP:0001260 Dysarthria
Expand Tier I Human GO 3310 Genes GS209452: GO:0006810 transport
Expand Tier I Human 267 Genes GS172365: HP:0003110 Abnormality of urine homeostasis
Expand Tier I Human GO 112 Genes GS195933: GO:0008514 organic anion transmembrane transporter activity
Expand Tier I Human GO 220 Genes GS200204: GO:0015849 organic acid transport
Expand Tier I Human 20 Genes GS171252: HP:0003819 Death in childhood
Expand Tier I Human GO 4338 Genes GS205500: GO:0071944 cell periphery
Expand Human 474 Genes GS219938: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_REGION
Expand Tier I Human 542 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human GO 9 Genes GS195044: GO:0005351 sugar:hydrogen symporter activity
Expand Tier I Human GO 95 Genes GS198238: GO:0046943 carboxylic acid transmembrane transporter activity
Expand Tier I Human 159 Genes GS175096: HP:0000286 Epicanthus
Expand Tier I Human GO 341 Genes GS207982: GO:0005764 lysosome
Expand Tier I Human GO 182 Genes GS209175: GO:0005774 vacuolar membrane
Expand Tier I Human 394 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human 32 Genes GS176141: HP:0001789 Hydrops fetalis
Expand Tier I Human 393 Genes GS172362: HP:0004325 Decreased body weight
Expand Tier I Human 450 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human 203 Genes GS174706: HP:0000553 Abnormality of the uvea
Expand Tier I Human 513 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human GO 404 Genes GS209163: GO:0005773 vacuole
Expand Tier I Human 733 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human GO 978 Genes GS198214: GO:0022892 substrate-specific transporter activity
Expand Tier I Human 454 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Human 607 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human 19 Genes GS175116: HP:0000577 Exotropia
Expand Tier I Human 33 Genes GS172620: HP:0000657 Oculomotor apraxia
Expand Tier I Human 159 Genes GS176900: HP:0000218 High palate
Expand Human 360 Genes GS219927: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_REGION_PART
Expand Tier III Human 2161 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 1046 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human CTD 5732 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Human 413 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Human 242 Genes GS175909: HP:0004348 Abnormality of bone mineral density
Expand Tier I Human GO 3364 Genes GS194459: GO:0051234 establishment of localization
Expand Tier I Human 917 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 604 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human GO 878 Genes GS209555: GO:0031988 membrane-bounded vesicle
Expand Tier I Human GO 2361 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human GO 192 Genes GS207409: GO:0015291 secondary active transmembrane transporter activity
Expand Tier I Human 186 Genes GS173355: HP:0002205 Recurrent respiratory infections
Expand Tier I Human GO 138 Genes GS206073: GO:0005765 lysosomal membrane
Expand Tier I Human 985 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human 97 Genes GS176756: HP:0011420 Death
Expand Tier I Human 313 Genes GS176568: HP:0000486 Strabismus
Expand Tier I Human 469 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Human GO 313 Genes GS196355: GO:0006820 anion transport
Expand Tier I Human 397 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
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 170 Genes GS173476: HP:0002311 Incoordination
Expand Tier I Human 11 Genes GS175233: HP:0002286 Fair hair
Expand Tier I Human 53 Genes GS175407: HP:0002072 Chorea
Expand Tier I Human 483 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Human 737 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 260 Genes GS170933: HP:0001288 Gait disturbance
Expand Tier I Human 487 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human GO 218 Genes GS197101: GO:0046942 carboxylic acid transport
Expand Tier I Human 54 Genes GS175220: HP:0009887 Abnormality of hair pigmentation
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 857 Genes GS207614: GO:0016023 cytoplasmic membrane-bounded vesicle
Expand Tier I Human 564 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human 532 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human 33 Genes GS176924: HP:0000212 Gingival overgrowth
Expand Tier I Human GO 964 Genes GS209451: GO:0006811 ion transport
Expand Human 360 Genes GS219710: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_REGION_PART
Expand Tier I Human CTD 1556 Genes GS125506: Valproic Acid interacting genes (MeSH:D014635) in CTD
Expand Tier I Human 17 Genes GS175565: HP:0003025 Irregular metaphyses
Expand Tier I Human GO 251 Genes GS205611: GO:0044437 vacuolar part
Expand Tier I Human GO 785 Genes GS195226: GO:0015075 ion transmembrane transporter activity
Expand Tier I Human 317 Genes GS176591: HP:0001276 Hypertonia
Expand Human 262 Genes GS219717: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_SPACE
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human 278 Genes GS171204: HP:0011314 Abnormality of long bone morphology
Expand Tier I Human GO 1 Genes GS198403: GO:0015136 sialic acid transmembrane transporter activity
Expand Tier I Human GO 10576 Genes GS203594: GO:0043226 organelle
Expand Tier I Human 532 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human 401 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 196 Genes GS174756: HP:0011947 Respiratory tract infection
Expand Tier I Human GO 82 Genes GS207406: GO:0015294 solute:cation symporter activity
Expand Tier I Human GO 6743 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 228 Genes GS171908: HP:0004298 Abnormality of the abdominal wall
Expand Tier I Human GO 29 Genes GS210107: GO:1901476 carbohydrate transporter activity
Expand Tier I Human 676 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human GO 1905 Genes GS198782: GO:0044459 plasma membrane part
Expand Tier I Human 168 Genes GS175668: HP:0007369 Atrophy/Degeneration affecting the cerebrum
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human 142 Genes GS171178: HP:0000238 Hydrocephalus
Expand Tier I Human 248 Genes GS176844: HP:0000429 Abnormality of the nasal alae
Expand Tier I Human GO 6256 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human 576 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human 121 Genes GS176672: HP:0000980 Pallor
Expand Human 474 Genes GS219721: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_REGION
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
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 596 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human 280 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human 75 Genes GS175692: HP:0200042 Skin ulcer
Expand Tier I Human GO 5243 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 232 Genes GS170999: HP:0000082 Abnormality of renal physiology
Expand Tier I Human 401 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Human 310 Genes GS176642: HP:0011355 Localized skin lesion
Expand Tier I Human 825 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 341 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Human 282 Genes GS175119: HP:0001881 Abnormality of leukocytes
Expand Tier I Human 257 Genes GS172272: HP:0001197 Abnormality of prenatal development or birth
Expand Tier I Human 64 Genes GS175020: HP:0001622 Premature birth
Expand Tier I Human 54 Genes GS175896: HP:0000938 Osteopenia
Expand Tier I Human 14 Genes GS173223: HP:0007730 Iris hypopigmentation
Expand Tier I Human 202 Genes GS174764: HP:0007367 Atrophy/Degeneration affecting the central nervous system
Expand Tier I Human GO 1254 Genes GS199199: GO:0031226 intrinsic to plasma membrane
Expand Tier I Human GO 98 Genes GS207551: GO:0005342 organic acid transmembrane transporter activity
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 4134 Genes GS200341: GO:0051179 localization
Expand Tier I Human GO 924 Genes GS197610: GO:0022857 transmembrane transporter activity
Expand Tier I Human 471 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human 164 Genes GS174994: HP:0002059 Cerebral atrophy
Expand Tier I Human 70 Genes GS171600: HP:0000168 Abnormality of the gingiva
Expand Tier I Human 135 Genes GS172857: HP:0004305 Involuntary movements
Expand Tier I Human 390 Genes GS175537: HP:0011277 Abnormality of the urinary system physiology
Expand Tier I Human GO 14 Genes GS207405: GO:0015295 solute:hydrogen symporter activity
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 108 Genes GS172118: HP:0004332 Abnormality of lymphocytes
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human 401 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Human 541 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 94 Genes GS176560: HP:0001010 Hypopigmentation of the skin
Expand Tier I Human 96 Genes GS174851: HP:0000944 Abnormality of the metaphyses
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 1210 Genes GS197008: GO:0005887 integral to plasma membrane
Expand Tier I Human 510 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Human 226 Genes GS172470: HP:0001743 Abnormality of the spleen
Expand Tier I Human 263 Genes GS176477: HP:0002118 Abnormality of the cerebral ventricles
Expand Tier I Human 220 Genes GS171139: HP:0005288 Abnormality of the nares
Expand Tier I Human 583 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 776 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 780 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human GO 29 Genes GS196398: GO:0015144 carbohydrate transmembrane transporter activity
Expand Tier I Human 614 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human GO 28 Genes GS195328: GO:1901505 carbohydrate derivative transporter activity
Expand Tier I Human 18 Genes GS173403: HP:0002684 Thickened calvaria
Expand Tier I Human 542 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human GO 263 Genes GS202551: GO:0015711 organic anion transport