Gene Details



PRX and homologs in 3 species are found in 235 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 Mouse MP 331 Genes GS165366: MP:0002272 abnormal nervous system electrophysiology
Expand Tier I Human GO 33 Genes GS194804: GO:0043209 myelin sheath
Expand Tier I Mouse 973 Genes GS136900: ventral midbrain iron content 4 (Vmbic4, Published QTL Chr 7)
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Mouse GO 3706 Genes GS188641: GO:0071944 cell periphery
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 537 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Human 63 Genes GS175213: HP:0003693 Distal amyotrophy
Expand Tier I Mouse GO 8630 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse GO 8650 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse 1024 Genes GS136319: non-HDL QTL 6 (Nhdlq6, Published QTL Chr 7)
Expand Tier I Mouse MP 246 Genes GS167941: MP:0001970 abnormal pain threshold
Expand Tier I Mouse 653 Genes GS135346: Avp transcript abundance QTL 1 (Avptaq1, Published QTL Chr 7)
Expand Tier I Mouse 730 Genes GS136807: tuberculosis resistance 3 (Tbrs3, Published QTL Chr 7)
Expand Tier I Human GO 649 Genes GS198498: GO:0050801 ion homeostasis
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Human 17 Genes GS171507: HP:0002922 Increased CSF protein
Expand Tier I Human GO 2507 Genes GS196934: GO:0065008 regulation of biological quality
Expand Tier I Human GO 4070 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human 86 Genes GS172908: HP:0002450 Abnormality of the motor neurons
Expand Tier I Human 360 Genes GS172701: HP:0002650 Scoliosis
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 Tier I Mouse 958 Genes GS136745: spermatogenesis defect 3 (Spmd3, Published QTL Chr 7)
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 4024 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Mouse 653 Genes GS135679: Crhr1 transcript abundance QTL 1 (Crhr1taq1, Published QTL Chr 7)
Expand Tier I Human 8 Genes GS175478: HP:0001178 Ulnar claw
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human 18 Genes GS173678: HP:0003383 Onion bulb formation
Expand Tier I Mouse MP 14488 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Human GO 4283 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Rat DRG 4920 Genes GS86494: Table S1: Hippocampus 17 K microarray data. [DRG]
Expand Tier I Human 490 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Human GO 837 Genes GS196920: GO:0048878 chemical homeostasis
Expand Tier I Human GO 4593 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Mouse MP 70 Genes GS170583: MP:0005407 hyperalgesia
Expand Tier I Mouse MP 146 Genes GS164101: MP:0003043 hypoalgesia
Expand Tier I Mouse MP 3019 Genes GS165466: MP:0003632 abnormal nervous system morphology
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 157 Genes GS171718: HP:0002808 Kyphosis
Expand Tier I Mouse 728 Genes GS135381: bone density traits 4 (Bdt4, Published QTL Chr 7)
Expand Tier I Human 25 Genes GS173680: HP:0003380 Decreased number of peripheral myelinated nerve fibers
Expand Tier I Mouse MP 46 Genes GS170568: MP:0003998 decreased thermal nociceptive threshold
Expand Tier I Mouse MP 471 Genes GS169228: MP:0001406 abnormal gait
Expand Tier I Mouse 2087 Genes GS128573: Ethanol Induced Hypothermia Chr# 7
Expand Tier I Human 49 Genes GS173385: HP:0002751 Kyphoscoliosis
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier I Human 98 Genes GS171910: HP:0003828 Variable expressivity
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 Mouse 975 Genes GS136602: sperm beat cross frequency (Sbcf, Published QTL Chr 7)
Expand Tier I Mouse MP 221 Genes GS169362: MP:0000920 abnormal myelination
Expand Tier I Mouse MP 954 Genes GS165874: MP:0002133 abnormal respiratory system physiology
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 129 Genes GS174657: HP:0001425 Heterogeneous
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 123 Genes GS176799: HP:0001265 Hyporeflexia
Expand Tier I Mouse 973 Genes GS136531: prion resistance 2 (Prnr2, Published QTL Chr 7)
Expand Tier I Mouse GO 43 Genes GS178056: GO:0043209 myelin sheath
Expand Tier I Human 90 Genes GS172611: HP:0003474 Sensory impairment
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human 8 Genes GS174434: HP:0007107 Segmental peripheral demyelination
Expand Tier I Human CTD 1468 Genes GS125062: palm oil interacting genes (MeSH:C041786) in CTD
Expand Tier I Human GO 98 Genes GS204614: GO:0019228 regulation of action potential in neuron
Expand Tier I Mouse 831 Genes GS136728: susceptibility to lung cancer 30 (Sluc30, Published QTL Chr 7)
Expand Tier I Human 17 Genes GS174333: HP:0003376 Steppage gait
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human GO 735 Genes GS204608: GO:0019226 transmission of nerve impulse
Expand Tier I Mouse MP 80 Genes GS167104: MP:0005403 abnormal nerve conduction
Expand Tier I Mouse MP 814 Genes GS163226: MP:0003312 abnormal locomotor coordination
Expand Tier I Human GO 4371 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Mouse MP 1672 Genes GS165260: MP:0001392 abnormal locomotor behavior
Expand Tier I Mouse DRG 516 Genes provisional GS87101: Table S4: List of Saline-Treated HDAC5 KO vs. Saline-Treated WT Significantly Regulated Genes. [DRG]
Expand Tier I Mouse GO 6204 Genes GS184629: GO:0005515 protein binding
Expand Tier I Human 46 Genes GS171759: HP:0002936 Distal sensory impairment
Expand Tier I Mouse MP 2357 Genes GS163824: MP:0001259 abnormal body weight
Expand Tier I Mouse 973 Genes GS136264: modifier of mammary tumor progression 1 (Mmtp1, Published QTL Chr 7)
Expand Tier I Mouse MP 563 Genes GS168931: MP:0001431 abnormal eating behavior
Expand Tier I Human 71 Genes GS174073: HP:0009127 Abnormality of the musculature of the limbs
Expand Tier I Mouse MP 2606 Genes GS165397: MP:0001265 decreased body size
Expand Tier I Human 260 Genes GS170933: HP:0001288 Gait disturbance
Expand Tier I Human 27 Genes GS171008: HP:0011096 Peripheral demyelination
Expand Tier I Human 489 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Mouse MP 3543 Genes GS169095: MP:0004924 abnormal behavior
Expand Tier I Human GO 1236 Genes GS202899: GO:0050877 neurological system process
Expand Tier I Mouse MP 1344 Genes GS169836: MP:0005388 respiratory system phenotype
Expand Tier I Mouse 984 Genes GS135458: bone mineral density 4 (Bomd4, Published QTL Chr 7)
Expand Tier I Human GO 4567 Genes GS196806: GO:0032502 developmental process
Expand Tier I Mouse MP 83 Genes GS164054: MP:0002314 abnormal respiratory mechanics
Expand Tier I Mouse MP 33 Genes GS168940: MP:0001438 aphagia
Expand Tier I Human GO 62 Genes GS198778: GO:0021675 nerve development
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human 530 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human 21 Genes GS174332: HP:0003377 Foot drop
Expand Tier I Mouse MP 52 Genes GS167331: MP:0005498 hyporesponsive to tactile stimuli
Expand Tier I Human 10 Genes GS176338: HP:0003481 Segmental peripheral demyelination/remyelination
Expand Tier I Human 202 Genes GS175171: HP:0001315 Reduced tendon reflexes
Expand Tier I Mouse 2121 Genes GS128593: Average rotarod training latency Chr# 7
Expand Tier I Mouse MP 722 Genes GS169396: MP:0002069 abnormal eating/drinking behavior
Expand Tier I Human 6 Genes GS173675: HP:0003382 Hypertrophic nerve changes
Expand Tier I Mouse 730 Genes GS136966: weight loss response 4 (Wtlr4, Published QTL Chr 7)
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Mouse 831 Genes GS136263: modifier of mammary tumor growth 3 (Mmtg3, Published QTL Chr 7)
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Human GO 1693 Genes GS209960: GO:0003008 system process
Expand Tier I Human GO 751 Genes GS202715: GO:0035637 multicellular organismal signaling
Expand Tier I Mouse MP 3543 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier I Mouse MP 875 Genes GS168958: MP:0003492 abnormal involuntary movement
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 Human 25 Genes GS171767: HP:0003431 Decreased motor nerve conduction velocity
Expand Tier III Mouse 8003 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampal tissue
Expand Tier I Human 62 Genes GS171488: HP:0002921 Abnormality of the cerebrospinal fluid
Expand Tier I Human 579 Genes GS171253: HP:0002817 Abnormality of the upper limb
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 Mouse 1023 Genes GS136742: Streptococcus pneumoniae infection resistance 1 (Spir1, Published QTL Chr 7)
Expand Tier I Human GO 248 Genes GS194078: GO:0042391 regulation of membrane potential
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Mouse MP 638 Genes GS167656: MP:0001943 abnormal respiration
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 398 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human 255 Genes GS176610: HP:0003593 Infantile onset
Expand Tier I Human 263 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier I Human GO 5948 Genes GS195199: GO:0005634 nucleus
Expand Tier I Mouse 910 Genes GS135938: HDL level 38 (Hdl38, Published QTL Chr 7)
Expand Tier I Mouse 910 Genes GS135746: experimental allergic encephalomyelitis susceptibility 12 (Eae12, Published QTL Chr 7)
Expand Tier I Human 82 Genes GS172000: HP:0001761 Pes cavus
Expand Tier I Human 246 Genes GS176806: HP:0003812 Phenotypic variability
Expand Tier I Mouse MP 3716 Genes GS163803: MP:0003631 nervous system phenotype
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 Mouse MP 1856 Genes GS165386: MP:0001262 decreased body weight
Expand Tier I Mouse 1027 Genes GS128580: BECs at LORR Recovery Chr# 7
Expand Tier I Human 38 Genes GS174443: HP:0001437 Abnormality of the musculature of the lower limbs
Expand Tier I Mouse MP 506 Genes GS168592: MP:0003634 abnormal glial cell morphology
Expand Tier I Human 399 Genes GS171100: HP:0000759 Abnormality of the peripheral nervous system
Expand Tier I Mouse MP 291 Genes GS164046: MP:0001968 abnormal touch/ nociception
Expand Tier I Mouse 973 Genes GS135988: Hfe modifier 1 (Hfem1, Published QTL Chr 7)
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Mouse MP 2406 Genes GS169391: MP:0002066 abnormal motor capabilities/coordination/movement
Expand Tier I Human CTD 765 Genes GS123769: 2-(1'H-indolo-3'-carbonyl)thiazole-4-carboxylic acid methyl ester interacting genes (MeSH:C548651) in CTD
Expand Tier I Mouse MP 64 Genes GS166076: MP:0001105 abnormal PNS glial cell morphology
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Mouse MP 898 Genes GS169390: MP:0002067 abnormal sensory capabilities/reflexes/nociception
Expand Tier I Human 346 Genes GS172989: HP:0001324 Muscle weakness
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Mouse MP 1825 Genes GS168956: MP:0003491 abnormal voluntary movement
Expand Tier I Human GO 8622 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Mouse GO 8145 Genes GS190714: GO:0016020 membrane
Expand Tier I Mouse DRG 178 Genes provisional GS87379: Table S2: The data provided represent genes showing differential expression using ANOVA. (Whole Table) [DRG]
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
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 GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse GO 3614 Genes GS180229: GO:0005886 plasma membrane
Expand Tier I Human GO 1724 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Human 143 Genes GS176586: HP:0001270 Motor delay
Expand Tier I Human 543 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Mouse 940 Genes GS135417: beta-carboline induced seizures 4 (Bis4, Published QTL Chr 7)
Expand Tier I Human 534 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Mouse MP 497 Genes GS165388: MP:0001263 weight loss
Expand Tier I Mouse MP 3437 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Human GO 83 Genes GS207579: GO:0007272 ensheathment of neurons
Expand Tier I Human GO 3513 Genes GS193991: GO:0048731 system development
Expand Tier I Mouse MP 90 Genes GS167227: MP:0005316 abnormal response to tactile stimuli
Expand Tier I Human GO 136 Genes GS201741: GO:0001508 regulation of action potential
Expand Tier I Mouse MP 648 Genes GS164023: MP:0001961 abnormal reflex
Expand Tier II Mouse 104 Genes GS36473: Cerebellum Gene expression correlates of Morphine - Severity of ptosis in Females BXD
Expand Tier I Mouse 641 Genes GS136214: lupus BXSB x NZW 6 (Lxw6, Published QTL Chr 7)
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier III Rat 3441 Genes GS135132: bHR vs bLR genes different in Nucleus Acumbens
Expand Tier I Rat DRG 4920 Genes GS86932: Table S3: CORTEX 17K MICROARRAY [DRG]
Expand Tier I Human GO 4593 Genes GS206355: GO:0023052 signaling
Expand Tier I Human GO 586 Genes GS201310: GO:0006873 cellular ion homeostasis
Expand Tier I Mouse MP 4173 Genes GS165527: MP:0005378 growth/size phenotype
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human 6 Genes GS171284: HP:0010871 Sensory ataxia
Expand Tier I Mouse MP 142 Genes GS165726: MP:0002733 abnormal thermal nociception
Expand Tier I Human 207 Genes GS176283: HP:0009830 Peripheral neuropathy
Expand Tier III Rat 3441 Genes GS135133: bHR vs bLR genes different in Hippocampus
Expand Tier I Human GO 4719 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human 913 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Mouse 593 Genes GS136894: ventricular size 3 (Vent3, Published QTL Chr 7)
Expand Tier I Mouse MP 111 Genes GS169364: MP:0005402 abnormal action potential
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Mouse 1024 Genes GS136253: modifier of Dlk1 (mdlk1, Published QTL Chr 7)
Expand Tier I Human GO 83 Genes GS209121: GO:0008366 axon ensheathment
Expand Tier I Human CTD 1522 Genes GS124579: Selenium interacting genes (MeSH:D012643) in CTD
Expand Tier I Human 49 Genes GS171306: HP:0003130 Abnormal peripheral myelination
Expand Tier I Mouse 940 Genes GS136189: lipoprotein QTL 5 (Lprq5, Published QTL Chr 7)
Expand Tier II Mouse 929 Genes GS84191: alcohol preference 7 QTL (Ap7q, Published QTL, Chr 7)
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier III Human 2430 Genes GS216491: Genes that are binding sites for CREB and zif268,transcription factors mediating nieuronal activity and plasticity, in Homo sapiens.
Expand Tier III Mouse 659 Genes GS874: Differential expression in Meander-tail (mea) vs. BLKS controls.
Expand Tier I Mouse 730 Genes GS136592: reactive oxygen species QTL 1 (Rosq1, Published QTL Chr 7)
Expand Tier I Mouse MP 255 Genes GS166583: MP:0001513 limb grasping
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human 13 Genes GS171058: HP:0010831 Impaired proprioception
Expand Tier II Mouse 61 Genes GS36468: Cerebellum Gene expression correlates of Morphine - Severity of ptosis in Females & Males BXD
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 Mouse MP 2200 Genes GS165465: MP:0003633 abnormal nervous system physiology
Expand Tier I Human 62 Genes GS172355: HP:0002460 Distal muscle weakness
Expand Tier I Human 229 Genes GS175577: HP:0003202 Amyotrophy
Expand Tier I Human 95 Genes GS170930: HP:0001284 Areflexia
Expand Tier I Mouse DRG 178 Genes provisional GS87119: Table S2: The data provided represent genes showing differential expression using ANOVA. B. Genes showing main effect of treatment. [DRG]
Expand Tier I Human GO 1191 Genes GS207015: GO:0042592 homeostatic process
Expand Tier I Human CTD 1245 Genes GS123554: vinclozolin interacting genes (MeSH:C025643) in CTD
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
Expand Tier I Mouse 901 Genes GS135415: bronchial hyperresponsiveness 6 (Bhr6, Published QTL Chr 7)
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 Mouse MP 3110 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Human 23 Genes GS174442: HP:0001436 Abnormality of the foot musculature
Expand Tier I Mouse MP 63 Genes GS166079: MP:0001106 abnormal Schwann cell morphology
Expand Tier I Mouse MP 419 Genes GS163888: MP:0005449 abnormal food intake
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Human 553 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Mouse GO 5247 Genes GS178448: GO:0005634 nucleus
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 22 Genes GS171996: HP:0001765 Hammertoe
Expand Tier I Human CTD 1697 Genes GS122142: Dietary Fats interacting genes (MeSH:D004041) in CTD
Expand Tier I Mouse MP 2199 Genes GS165244: MP:0010771 integument phenotype