Gene Details



SLC25A15 and homologs in 1 species are found in 203 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 739 Genes GS201250: GO:0044429 mitochondrial part
Expand Human 1375 Genes GS219728: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_MEMBRANE
Expand Human 1375 Genes GS219978: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_MEMBRANE
Expand Tier I Human GO 380 Genes GS196559: GO:0019866 organelle inner membrane
Expand Human 1733 Genes GS219955: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE_PART
Expand Tier I Human CTD 1541 Genes GS125445: Phenobarbital interacting genes (MeSH:D010634) in CTD
Expand Tier I Human GO 1682 Genes GS204629: GO:1901564 organonitrogen compound metabolic process
Expand Human 1003 Genes GS219719: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_PLASMA_MEMBRANE
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
Expand Tier I Human 36 Genes GS171040: HP:0002157 Azotemia
Expand Tier I Human 81 Genes GS171773: HP:0000532 Chorioretinal abnormality
Expand Tier I Human 92 Genes GS171656: HP:0000610 Abnormality of the choroid
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 56 Genes GS174922: HP:0000762 Decreased nerve conduction velocity
Expand Tier I Human GO 525 Genes GS198059: GO:0005740 mitochondrial envelope
Expand Tier I Human 168 Genes GS175668: HP:0007369 Atrophy/Degeneration affecting the cerebrum
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 129 Genes GS196969: GO:0006865 amino acid transport
Expand Human 1393 Genes GS219979: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_MEMBRANE
Expand Human 1197 Genes GS219982: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE_PART
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human GO 2509 Genes GS207903: GO:0044281 small molecule metabolic process
Expand Tier I Human GO 6256 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human 37 Genes GS173012: HP:0004364 Abnormality of nitrogen compound homeostasis
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 214 Genes GS176167: HP:0001257 Spasticity
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 GO 5359 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Human 1470 Genes GS219947: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Human 1197 Genes GS219942: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE_PART
Expand Tier I Human GO 5243 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human GO 1965 Genes GS210586: GO:0051641 cellular localization
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 840 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human CTD 200 Genes GS125369: Lamivudine interacting genes (MeSH:D019259) in CTD
Expand Tier I Human 825 Genes GS175525: HP:0000004 Onset and clinical course
Expand Human 1733 Genes GS219981: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE_PART
Expand Tier I Human 201 Genes GS171631: HP:0008051 Abnormality of the retinal pigment epithelium
Expand Tier I Human 341 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Human CTD 377 Genes GS121976: Zidovudine interacting genes (MeSH:D015215) in CTD
Expand Tier I Human GO 830 Genes GS194556: GO:0031975 envelope
Expand Human 1197 Genes GS219725: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE_PART
Expand Human 2063 Genes GS219980: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human GO 67 Genes GS199184: GO:0015171 amino acid transmembrane transporter activity
Expand Tier I Human 21 Genes GS170830: HP:0002169 Clonus
Expand Tier I Human 202 Genes GS174764: HP:0007367 Atrophy/Degeneration affecting the central nervous system
Expand Tier I Human 59 Genes GS176175: HP:0001259 Coma
Expand Tier I Human 245 Genes GS176806: HP:0003812 Phenotypic variability
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
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 1 Genes GS175232: HP:0012026 Hyperornithinemia
Expand Tier I Human GO 4 Genes GS199344: GO:0000064 L-ornithine transmembrane transporter activity
Expand Tier I Human GO 4134 Genes GS200341: GO:0051179 localization
Expand Tier I Human GO 1123 Genes GS196794: GO:0046907 intracellular transport
Expand Tier I Human GO 50 Genes GS200161: GO:0043604 amide biosynthetic process
Expand Tier I Human GO 924 Genes GS197610: GO:0022857 transmembrane transporter activity
Expand Tier I Human GO 13 Genes GS207622: GO:0019627 urea metabolic process
Expand Tier I Human 164 Genes GS174994: HP:0002059 Cerebral atrophy
Expand Tier I Human 5 Genes GS172162: HP:0002038 Protein avoidance
Expand Tier I Human GO 2 Genes GS199345: GO:0000066 mitochondrial ornithine transport
Expand Human 1197 Genes GS219976: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE_PART
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
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 396 Genes GS171100: HP:0000759 Abnormality of the peripheral nervous system
Expand Human 1733 Genes GS219987: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE_PART
Expand Tier I Human 93 Genes GS176289: HP:0002120 Cerebral cortical atrophy
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human GO 817 Genes GS198970: GO:0031967 organelle envelope
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 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human GO 6347 Genes GS201256: GO:0044422 organelle part
Expand Human 2063 Genes GS219986: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human 27 Genes GS175193: HP:0002062 Abnormality of the pyramidal tracts
Expand Tier I Human 42 Genes GS176071: HP:0010551 Paraplegia/paraparesis
Expand Tier I Human GO 5190 Genes GS207857: GO:0009058 biosynthetic process
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 510 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Human 58 Genes GS171880: HP:0003134 Abnormality of peripheral nerve conduction
Expand Tier I Human 4 Genes GS174284: HP:0002572 Episodic vomiting
Expand Tier I Human GO 245 Genes GS195413: GO:0008509 anion transmembrane transporter activity
Expand Tier I Human GO 550 Genes GS201022: GO:0071705 nitrogen compound transport
Expand Tier I Human GO 632 Genes GS209450: GO:0006812 cation transport
Expand Tier I Human 124 Genes GS174854: HP:0001410 Decreased liver function
Expand Tier I Human 50 Genes GS177002: HP:0001298 Encephalopathy
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
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 105 Genes GS174133: HP:0002013 Vomiting
Expand Tier I Human 43 Genes GS171083: HP:0001328 Specific learning disability
Expand Tier I Human 130 Genes GS174137: HP:0002017 Nausea and vomiting
Expand Tier I Human 614 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Human 1003 Genes GS219975: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_PLASMA_MEMBRANE
Expand Tier I Human 8 Genes GS171975: HP:0000533 Chorioretinal atrophy
Expand Tier I Human CTD 5081 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Human 472 Genes GS171893: HP:0011458 Abdominal symptom
Expand Tier I Human GO 140 Genes GS200166: GO:0043603 cellular amide metabolic process
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
Expand Tier I Human 26 Genes GS176290: HP:0002123 Generalized myoclonic seizures
Expand Human 195 Genes GS222320: Genes associated with high risk of intellectual disability.
Expand Human 2063 Genes GS219747: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human 25 Genes GS171234: HP:0002495 Impaired vibratory sensation
Expand Tier I Human GO 1193 Genes GS196168: GO:0005215 transporter activity
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 121 Genes GS172672: HP:0004337 Abnormality of amino acid metabolism
Expand Human 1470 Genes GS219730: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier I Human 263 Genes GS172415: HP:0002240 Hepatomegaly
Expand Tier I Human GO 503 Genes GS198971: GO:0031966 mitochondrial membrane
Expand Tier I Human GO 339 Genes GS195494: GO:0006520 cellular amino acid metabolic process
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Human 1470 Genes GS219977: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
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 GO 5567 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human GO 43 Genes GS200763: GO:0015179 L-amino acid transmembrane transporter activity
Expand Tier I Human 50 Genes GS172258: HP:0002197 Generalized seizures
Expand Human 1733 Genes GS219738: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE_PART
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human GO 350 Genes GS198058: GO:0005743 mitochondrial inner membrane
Expand Tier I Human 307 Genes GS175805: HP:0003271 Visceromegaly
Expand Tier I Human GO 14 Genes GS205503: GO:0071941 nitrogen cycle metabolic process
Expand Tier I Human 90 Genes GS172611: HP:0003474 Sensory impairment
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 140 Genes GS174860: HP:0010549 Paralysis due to lesions of the principle motor tracts
Expand Tier I Human GO 110 Genes GS200733: GO:0006839 mitochondrial transport
Expand Human 1016 Genes GS219939: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_PLASMA_MEMBRANE
Expand Tier I Human 205 Genes GS176283: HP:0009830 Peripheral neuropathy
Expand Tier I Human GO 3310 Genes GS209452: GO:0006810 transport
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 GO 1515 Genes GS194138: GO:0005739 mitochondrion
Expand Tier I Human GO 11 Genes GS194879: GO:0000050 urea cycle
Expand Tier I Human GO 845 Genes GS204326: GO:0019752 carboxylic acid metabolic process
Expand Tier I Human 273 Genes GS172516: HP:0001347 Hyperreflexia
Expand Tier I Human GO 2 Genes GS207654: GO:0015822 ornithine transport
Expand Tier I Human CTD 102 Genes GS123157: Carbamazepine interacting genes (MeSH:D002220) in CTD
Expand Tier I Human GO 95 Genes GS198238: GO:0046943 carboxylic acid transmembrane transporter activity
Expand Tier I Human GO 5928 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human GO 5014 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Human 1375 Genes GS219945: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_MEMBRANE
Expand Tier I Human 393 Genes GS172362: HP:0004325 Decreased body weight
Expand Tier I Human GO 952 Genes GS202555: GO:0043436 oxoacid metabolic process
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 Human 1375 Genes GS219984: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_MEMBRANE
Expand Tier I Human GO 978 Genes GS198214: GO:0022892 substrate-specific transporter activity
Expand Tier I Human 607 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human 17 Genes GS174555: HP:0002385 Paraparesis
Expand Tier I Human 134 Genes GS175172: HP:0004354 Abnormality of carboxylic acid metabolism
Expand Tier I Human 1046 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human GO 3697 Genes GS194499: GO:0044271 cellular nitrogen compound biosynthetic process
Expand Tier I Human CTD 4391 Genes GS123768: Cyclosporine interacting genes (MeSH:D016572) in CTD
Expand Human 1393 Genes GS219948: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_MEMBRANE
Expand Tier I Human 1 Genes GS174767: HP:0012025 Abnormality of ornithine metabolism
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 71 Genes GS176168: HP:0001254 Lethargy
Expand Tier I Human GO 2361 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human 20 Genes GS172877: HP:0002370 Poor coordination
Expand Tier I Human GO 8645 Genes GS205255: GO:0044238 primary metabolic process
Expand Human 1016 Genes GS219722: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_PLASMA_MEMBRANE
Expand Tier I Human GO 313 Genes GS196355: GO:0006820 anion transport
Expand Human 1470 Genes GS219983: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier I Human 20 Genes GS173676: HP:0006846 Acute encephalopathy
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 Human 1393 Genes GS219985: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_MEMBRANE
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 483 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Human GO 218 Genes GS197101: GO:0046942 carboxylic acid transport
Expand Tier I Human 14 Genes GS176517: HP:0007894 Hypopigmentation of the fundus
Expand Tier I Human GO 970 Genes GS210163: GO:0006082 organic acid metabolic process
Expand Tier I Human 386 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 29 Genes GS172066: HP:0001987 Hyperammonemia
Expand Tier I Human 532 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human GO 964 Genes GS209451: GO:0006811 ion transport
Expand Tier I Human 9 Genes GS176731: HP:0002313 Spastic paraparesis
Expand Human 1393 Genes GS219731: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_MEMBRANE
Expand Human 1003 Genes GS219936: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_PLASMA_MEMBRANE
Expand Tier I Human GO 785 Genes GS195226: GO:0015075 ion transmembrane transporter activity
Expand Tier I Human 41 Genes GS175192: HP:0002061 Lower limb spasticity
Expand Tier I Human 317 Genes GS176591: HP:0001276 Hypertonia
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 GO 6743 Genes GS210002: GO:0044444 cytoplasmic part
Expand Human 1003 Genes GS221018: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_PLASMA_MEMBRANE
Expand Tier I Human GO 5120 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Human 1003 Genes GS221267: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_PLASMA_MEMBRANE
Expand Tier I Human 128 Genes GS173093: HP:0004372 Reduced consciousness/confusion
Expand Tier I Human GO 1745 Genes GS210579: GO:0051649 establishment of localization in cell