Gene Details



PLA2G6 and homologs in 1 species are found in 256 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 CTD 306 Genes GS126769: Calcium interacting genes (MeSH:D002118) in CTD
Expand Tier I Human CTD 1541 Genes GS125445: Phenobarbital interacting genes (MeSH:D010634) in CTD
Expand Tier I Human 64 Genes GS174310: HP:0100705 Abnormality of the glial cells
Expand Tier I Human GO 1684 Genes GS204629: GO:1901564 organonitrogen compound metabolic process
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 71 Genes GS170917: HP:0100852 Abnormal fear/anxiety-related behavior
Expand Human 1625 Genes GS221148: http://www.broadinstitute.org/gsea/msigdb/cards/SIGNAL_TRANSDUCTION
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 414 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 1569 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 537 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Human GO 164 Genes GS201430: GO:0005516 calmodulin binding
Expand Human 1625 Genes GS221397: http://www.broadinstitute.org/gsea/msigdb/cards/SIGNAL_TRANSDUCTION
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human 282 Genes GS175900: HP:0009118 Aplasia/Hypoplasia of the mandible
Expand Tier I Human GO 1699 Genes GS203755: GO:0016265 death
Expand Tier I Human GO 112 Genes GS199036: GO:0016298 lipase activity
Expand Tier I Human CTD 148 Genes GS125688: Arachidonic Acid interacting genes (MeSH:D016718) in CTD
Expand Tier I Human 99 Genes GS175130: HP:0000750 Delayed speech and language development
Expand Tier I Human 215 Genes GS176167: HP:0001257 Spasticity
Expand Tier I Human 49 Genes GS173815: HP:0000736 Short attention span
Expand Tier I Human 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 46 Genes GS173617: HP:0011220 Prominent forehead
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 III Human 3178 Genes GS137407: Supplementary Table 2. Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Human 95 Genes GS171217: HP:0003487 Babinski sign
Expand Tier I Human GO 2368 Genes GS207365: GO:0005829 cytosol
Expand Tier I Human 107 Genes GS173786: HP:0003457 EMG abnormality
Expand Tier I Human 202 Genes GS174764: HP:0007367 Atrophy/Degeneration affecting the central nervous system
Expand Tier I Human GO 863 Genes GS209634: GO:0015630 microtubule cytoskeleton
Expand Tier I Human 246 Genes GS176806: HP:0003812 Phenotypic variability
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human GO 593 Genes GS202940: GO:0006935 chemotaxis
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 231 Genes GS202625: GO:0045017 glycerolipid biosynthetic process
Expand Tier I Human 282 Genes GS172572: HP:0000347 Micrognathia
Expand Tier I Human 185 Genes GS173065: HP:0003679 Pace of progression
Expand Tier I Human 472 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human 164 Genes GS174994: HP:0002059 Cerebral atrophy
Expand Tier I Human 491 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Human CTD 1697 Genes GS122142: Dietary Fats interacting genes (MeSH:D004041) in CTD
Expand Tier I Human 941 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
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 11 Genes GS172189: HP:0002180 Neurodegeneration
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 GO 134 Genes GS204384: GO:0006576 cellular biogenic amine metabolic process
Expand Tier I Human GO 741 Genes GS208043: GO:0016788 hydrolase activity, acting on ester bonds
Expand Tier I Human GO 2741 Genes GS195668: GO:0042221 response to chemical stimulus
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human GO 376 Genes GS208298: GO:0005813 centrosome
Expand Tier I Human 337 Genes GS174076: HP:0009122 Aplasia/Hypoplasia affecting bones of the axial skeleton
Expand Tier I Human 119 Genes GS172170: HP:0003196 Short nose
Expand Tier I Human 364 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human 786 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human GO 1287 Genes GS205610: GO:0044430 cytoskeletal part
Expand Tier I Human GO 1852 Genes GS209010: GO:1901575 organic substance catabolic process
Expand Tier I Human GO 29 Genes GS210230: GO:0004623 phospholipase A2 activity
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human 639 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human 88 Genes GS176588: HP:0001272 Cerebellar atrophy
Expand Tier I Human GO 236 Genes GS206874: GO:0006650 glycerophospholipid metabolic process
Expand Tier I Human 498 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 50 Genes GS176914: HP:0002171 Gliosis
Expand Tier I Human 699 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human 346 Genes GS172989: HP:0001324 Muscle weakness
Expand Tier I Human GO 66 Genes GS198640: GO:0046470 phosphatidylcholine metabolic process
Expand Tier I Human 8 Genes GS172192: HP:0002185 Neurofibrillary tangles
Expand Tier I Human 80 Genes GS172801: HP:0000752 Hyperactivity
Expand Tier I Human 17 Genes GS173187: HP:0007772 Impaired smooth pursuit
Expand Tier I Human 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human 28 Genes GS175193: HP:0002062 Abnormality of the pyramidal tracts
Expand Tier I Human GO 5223 Genes GS207857: GO:0009058 biosynthetic process
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 512 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Human GO 1138 Genes GS193812: GO:0006629 lipid metabolic process
Expand Tier I Human 58 Genes GS171880: HP:0003134 Abnormality of peripheral nerve conduction
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 10 Genes GS174508: HP:0100710 Impulsivity
Expand Tier I Human GO 12 Genes GS206869: GO:0006655 phosphatidylglycerol biosynthetic process
Expand Tier I Human CTD 3 Genes GS121755: 2,2',4,6-tetrachlorobiphenyl interacting genes (MeSH:C447028) in CTD
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 27 Genes GS176808: HP:0002067 Bradykinesia
Expand Tier I Human 106 Genes GS173246: HP:0001332 Dystonia
Expand Tier I Human GO 7 Genes GS206284: GO:0035965 cardiolipin acyl-chain remodeling
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 Human 258 Genes GS222192: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_MAPK_SIGNALING_PATHWAY
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 435 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
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 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 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 41 Genes GS174305: HP:0000712 Emotional lability
Expand Tier I Human CTD 18 Genes GS123058: KT 5720 interacting genes (MeSH:C057416) in CTD
Expand Tier I Human 534 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Human GO 193 Genes GS198636: GO:0046474 glycerophospholipid biosynthetic process
Expand Tier I Human 92 Genes GS173061: HP:0003676 Progressive disorder
Expand Tier I Human 316 Genes GS170825: HP:0002167 Neurological speech impairment
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 192 Genes GS174579: HP:0002031 Abnormality of the esophagus
Expand Tier I Human GO 1789 Genes GS208893: GO:0005856 cytoskeleton
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human 174 Genes GS171148: HP:0011218 Abnormal shape of the frontal region
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human 173 Genes GS175117: HP:0001883 Talipes
Expand Tier I Human GO 216 Genes GS196055: GO:0008654 phospholipid biosynthetic process
Expand Tier I Human CTD 277 Genes GS125409: Triiodothyronine interacting genes (MeSH:D014284) in CTD
Expand Human 1625 Genes GS219769: http://www.broadinstitute.org/gsea/msigdb/cards/SIGNAL_TRANSDUCTION
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human 302 Genes GS176029: HP:0009116 Aplasia/Hypoplasia involving bones of the skull
Expand Tier I Human GO 5601 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Human 261 Genes GS176172: HP:0001251 Ataxia
Expand Tier I Human 84 Genes GS174760: HP:0002376 Developmental regression
Expand Tier I Human CTD 191 Genes GS125390: Aspirin interacting genes (MeSH:D001241) in CTD
Expand Tier I Human 21 Genes GS175360: HP:0002529 Neuronal loss in central nervous system
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human GO 6 Genes GS209623: GO:0032049 cardiolipin biosynthetic process
Expand Tier I Human 19 Genes GS171721: HP:0003445 EMG: neuropathic changes
Expand Tier I Human 7 Genes GS175124: HP:0001884 Talipes calcaneovalgus
Expand Tier I Human 416 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Human 23 Genes GS172373: HP:0000649 Abnormality of vision evoked potentials
Expand Tier I Human GO 1180 Genes GS195151: GO:0019637 organophosphate metabolic process
Expand Tier I Human CTD 355 Genes GS123990: perfluorooctanoic acid interacting genes (MeSH:C023036) in CTD
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human GO 33 Genes GS198639: GO:0046471 phosphatidylglycerol metabolic process
Expand Tier I Human CTD 453 Genes GS125669: Phenylephrine interacting genes (MeSH:D010656) in CTD
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human CTD 1468 Genes GS125062: palm oil interacting genes (MeSH:C041786) in CTD
Expand Tier I Human GO 3125 Genes GS199272: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Human GO 198 Genes GS210666: GO:0044106 cellular amine metabolic process
Expand Tier I Human 96 Genes GS174135: HP:0002015 Dysphagia
Expand Tier I Human 161 Genes GS176803: HP:0001260 Dysarthria
Expand Tier I Human GO 2353 Genes GS208037: GO:0016787 hydrolase activity
Expand Tier I Human 174 Genes GS171806: HP:0005656 Positional foot deformities
Expand Tier I Human GO 2494 Genes GS209235: GO:0006793 phosphorus metabolic process
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human GO 315 Genes GS201237: GO:0046486 glycerolipid metabolic process
Expand Tier I Human 273 Genes GS172516: HP:0001347 Hyperreflexia
Expand Human 438 Genes GS219938: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_REGION
Expand Tier I Human GO 1993 Genes GS207862: GO:0009056 catabolic process
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 5962 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human GO 486 Genes GS208302: GO:0005815 microtubule organizing center
Expand Tier I Human GO 5047 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Tier I Human 65 Genes GS170884: HP:0006919 Abnormal aggressive, impulsive or violent behavior
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 5 Genes GS195332: GO:0047499 calcium-independent phospholipase A2 activity
Expand Tier I Human GO 6585 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 515 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human GO 321 Genes GS200827: GO:0006066 alcohol metabolic process
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human 4 Genes GS171307: HP:0003444 EMG: chronic denervation signs
Expand Tier I Human GO 87 Genes GS198072: GO:0042439 ethanolamine-containing compound metabolic process
Expand Human 329 Genes GS219927: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_REGION_PART
Expand Tier I Human 11 Genes GS172944: HP:0100314 Cerebral inclusion bodies
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
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 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 520 Genes GS194460: GO:0090407 organophosphate biosynthetic process
Expand Tier I Human 348 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier I Human 123 Genes GS173242: HP:0001337 Tremor
Expand Tier I Human GO 8702 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human CTD 358 Genes GS124286: Benzene interacting genes (MeSH:D001554) in CTD
Expand Tier I Human CTD 4 Genes GS122489: 6-(bromomethylene)tetrahydro-3-(1-naphthaleneyl)-2H-pyran-2-one interacting genes (MeSH:C068314) in CTD
Expand Tier I Human 315 Genes GS176568: HP:0000486 Strabismus
Expand Tier I Human GO 25 Genes GS194017: GO:0036151 phosphatidylcholine acyl-chain remodeling
Expand Tier I Human 21 Genes GS171661: HP:0000617 Abnormality of ocular smooth pursuit
Expand Tier I Human 27 Genes GS175179: HP:0001310 Dysmetria
Expand Tier I Human 319 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Human 108 Genes GS176797: HP:0001268 Mental deterioration
Expand Tier I Human 397 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier I Human 398 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Human 13 Genes GS175404: HP:0002075 Dysdiadochokinesis
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 2431 Genes GS209232: GO:0006796 phosphate-containing compound metabolic process
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human CTD 79 Genes GS122552: Thapsigargin interacting genes (MeSH:D019284) in CTD
Expand Tier I Human 73 Genes GS175408: HP:0002071 Abnormality of extrapyramidal motor function
Expand Tier I Human 53 Genes GS175407: HP:0002072 Chorea
Expand Tier I Human 260 Genes GS170933: HP:0001288 Gait disturbance
Expand Tier I Human 489 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human GO 541 Genes GS196667: GO:0008610 lipid biosynthetic process
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 23 Genes GS194019: GO:0036152 phosphatidylethanolamine acyl-chain remodeling
Expand Tier I Human GO 5321 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human CTD 627 Genes GS122305: resveratrol interacting genes (MeSH:C059514) in CTD
Expand Tier I Human 578 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human GO 346 Genes GS202602: GO:0006644 phospholipid metabolic process
Expand Human 367 Genes GS222195: http://www.broadinstitute.org/gsea/msigdb/cards/ANATOMICAL_STRUCTURE_MORPHOGENESIS
Expand Tier I Human 34 Genes GS171944: HP:0003324 Generalized muscle weakness
Expand Human 329 Genes GS219710: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_REGION_PART
Expand Tier I Human GO 12 Genes GS209624: GO:0032048 cardiolipin metabolic process
Expand Tier I Human 95 Genes GS170930: HP:0001284 Areflexia
Expand Tier I Human 174 Genes GS173901: HP:0002007 Frontal bossing
Expand Tier I Human GO 1244 Genes GS196080: GO:0040011 locomotion
Expand Tier I Human 25 Genes GS175552: HP:0002510 Spastic tetraplegia
Expand Tier I Human 319 Genes GS176591: HP:0001276 Hypertonia
Expand Human 236 Genes GS219717: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_SPACE
Expand Tier I Human GO 1319 Genes GS208126: GO:0009605 response to external stimulus
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 110 Genes GS197967: GO:0052689 carboxylic ester hydrolase activity
Expand Tier I Human GO 229 Genes GS203381: GO:0009308 amine metabolic process
Expand Tier I Human 534 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human 403 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human GO 3125 Genes GS197892: GO:0043228 non-membrane-bounded organelle
Expand Tier I Human GO 6769 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human GO 5152 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier I Human 202 Genes GS175171: HP:0001315 Reduced tendon reflexes
Expand Tier I Human 41 Genes GS175197: HP:0002066 Gait ataxia
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human 17 Genes GS176018: HP:0002317 Unsteady gait
Expand Tier I Human GO 252 Genes GS194309: GO:0016042 lipid catabolic process
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 Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human GO 593 Genes GS201060: GO:0042330 taxis
Expand Tier I Human GO 2511 Genes GS207903: GO:0044281 small molecule metabolic process
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
Expand Human 438 Genes GS219721: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_REGION
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 GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 599 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human 324 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Human 16 Genes GS174368: HP:0002080 Intention tremor
Expand Human 1625 Genes GS222093: http://www.broadinstitute.org/gsea/msigdb/cards/SIGNAL_TRANSDUCTION
Expand Tier I Human GO 95 Genes GS210231: GO:0004620 phospholipase activity
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 47 Genes GS171072: HP:0000572 Visual loss
Expand Tier I Human 403 Genes GS174217: HP:0005105 Abnormal nasal morphology
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 810 Genes GS195897: GO:0044255 cellular lipid metabolic process