Gene Details



OPA3 and homologs in 5 species are found in 261 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 1350 Genes GS165707: MP:0000428 abnormal craniofacial morphology
Expand Tier I Mouse GO 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Mouse MP 1724 Genes GS164220: MP:0002882 abnormal neuron morphology
Expand Tier I Mouse MP 215 Genes GS168129: MP:0010025 decreased total body fat amount
Expand Tier I Mouse 973 Genes GS136900: ventral midbrain iron content 4 (Vmbic4, Published QTL Chr 7)
Expand Tier I Mouse MP 1055 Genes GS166120: MP:0002106 abnormal muscle physiology
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Mouse MP 246 Genes GS170738: MP:0001056 abnormal cranial nerve morphology
Expand Tier II Mouse 78 Genes GS36017: Striatum Gene expression correlates of Light-Dark Box Total seconds spent in dark compartment in Females & Males BXD
Expand Tier I Human 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier II Mouse 91 Genes GS35311: Striatum Gene expression correlates of Acoustic Startle Response Percentage of maximum response at 85 db in Females BXD
Expand Tier I Mouse GO 5588 Genes GS193061: GO:0044444 cytoplasmic part
Expand Tier I Mouse GO 8630 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse MP 224 Genes GS167702: MP:0003141 cardiac fibrosis
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 3631 Genes GS169830: MP:0005384 cellular phenotype
Expand Tier II Mouse 362 Genes GS35306: Striatum Gene expression correlates of Acoustic Startle Response Percentage of maximum startle response at 80 db in Females & Males BXD
Expand Tier I Mouse MP 396 Genes GS170108: MP:0003727 abnormal retinal layer morphology
Expand Tier I Mouse 653 Genes GS135346: Avp transcript abundance QTL 1 (Avptaq1, Published QTL Chr 7)
Expand Tier I Mouse MP 71 Genes GS169907: MP:0002090 abnormal vision
Expand Tier I Mouse MP 128 Genes GS169978: MP:0006035 abnormal mitochondrion morphology
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 Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Mouse GO 123 Genes GS193046: GO:0050953 sensory perception of light stimulus
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 Mouse MP 1628 Genes GS163852: MP:0001544 abnormal cardiovascular system physiology
Expand Tier II Mouse 39 Genes GS34260: Cerebellum Gene expression correlates of Suppression of activity in altered context in Females BXD
Expand Tier I Mouse MP 257 Genes GS165839: MP:0009701 abnormal birth body size
Expand Tier I Mouse MP 124 Genes GS163468: MP:0010499 abnormal ventricle myocardium morphology
Expand Tier I Mouse MP 3019 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier I Mouse MP 471 Genes GS169228: MP:0001406 abnormal gait
Expand Tier II Mouse 72 Genes GS34871: Cerebellum Gene expression correlates of Open Field - Percentage center time in Females BXD
Expand Tier II Mouse 256 Genes GS34191: Hippocampus Gene expression correlates of Number of entries into closed arms of plus maze in Males BXD
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
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 Human GO 204 Genes GS210485: GO:0007601 visual perception
Expand Tier I Mouse MP 189 Genes GS168193: MP:0000966 decreased sensory neuron number
Expand Tier I Mouse MP 1350 Genes GS165228: MP:0005382 craniofacial phenotype
Expand Tier I Mouse 973 Genes GS136531: prion resistance 2 (Prnr2, Published QTL Chr 7)
Expand Tier I Mouse MP 116 Genes GS167462: MP:0002795 dilated cardiomyopathy
Expand Tier I Human 140 Genes GS174860: HP:0010549 Paralysis due to lesions of the principle motor tracts
Expand Tier I Mouse MP 1082 Genes GS166660: MP:0001731 abnormal postnatal growth
Expand Tier I Mouse 831 Genes GS136728: susceptibility to lung cancer 30 (Sluc30, Published QTL Chr 7)
Expand Tier II Mouse 256 Genes GS36850: Hippocampus Gene expression correlates of Percentage of entries into closed arms of plus maze in Males BXD
Expand Tier I Mouse MP 336 Genes GS169191: MP:0000281 abnormal interventricular septum morphology
Expand Tier I Mouse MP 814 Genes GS163226: MP:0003312 abnormal locomotor coordination
Expand Tier I Human 344 Genes GS174378: HP:0000518 Cataract
Expand Tier I Mouse MP 749 Genes GS167833: MP:0001784 abnormal fluid regulation
Expand Tier I Human GO 495 Genes GS209225: GO:0007600 sensory perception
Expand Tier I Mouse MP 520 Genes GS165595: MP:0010545 abnormal heart layer morphology
Expand Tier II Mouse 47 Genes GS36443: Cerebellum Gene expression correlates of Open Field -Total distance in the perimeter in Females BXD
Expand Tier I Mouse MP 2357 Genes GS163824: MP:0001259 abnormal body weight
Expand Tier I Human 416 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Mouse MP 511 Genes GS164555: MP:0005329 abnormal myocardium layer morphology
Expand Tier I Mouse MP 216 Genes GS167439: MP:0000443 abnormal snout morphology
Expand Tier I Mouse MP 298 Genes GS164949: MP:0001504 abnormal posture
Expand Tier I Mouse MP 331 Genes GS163432: MP:0006069 abnormal retinal neuronal layer morphology
Expand Tier I Human 97 Genes GS173091: HP:0004374 Hemiplegia/hemiparesis
Expand Tier I Mouse 585 Genes GS136233: mandible length 7 (Manln7, Published QTL Chr 7)
Expand Tier I Mouse MP 574 Genes GS166743: MP:0002229 neurodegeneration
Expand Tier I Human 398 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Mouse MP 2606 Genes GS165397: MP:0001265 decreased body size
Expand Tier I Mouse MP 3494 Genes GS170601: MP:0005621 abnormal cell physiology
Expand Tier I Human 260 Genes GS170933: HP:0001288 Gait disturbance
Expand Tier II Mouse 362 Genes GS35286: Striatum Gene expression correlates of Prepulse inhibition at 80db in Females & Males BXD
Expand Tier I Mouse MP 3543 Genes GS169095: MP:0004924 abnormal behavior
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 1236 Genes GS202899: GO:0050877 neurological system process
Expand Tier I Mouse 984 Genes GS135458: bone mineral density 4 (Bomd4, Published QTL Chr 7)
Expand Tier I Human 319 Genes GS176591: HP:0001276 Hypertonia
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Mouse MP 19 Genes GS167310: MP:0008513 thin retinal inner plexiform layer
Expand Tier I Mouse MP 120 Genes GS162866: MP:0005241 abnormal retinal ganglion layer morphology
Expand Tier I Human GO 6769 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Mouse MP 162 Genes GS167355: MP:0000445 short snout
Expand Tier I Mouse 2121 Genes GS128593: Average rotarod training latency Chr# 7
Expand Tier I Mouse MP 738 Genes GS168826: MP:0005294 abnormal heart ventricle morphology
Expand Tier I Mouse MP 4592 Genes GS165537: MP:0005376 homeostasis/metabolism phenotype
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 MP 574 Genes GS167217: MP:0001325 abnormal retina morphology
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 Mouse MP 3543 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier I Human 274 Genes GS172372: HP:0000648 Optic atrophy
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 Mouse GO 123 Genes GS193540: GO:0007601 visual perception
Expand Tier I Mouse MP 1007 Genes GS164742: MP:0001732 postnatal growth retardation
Expand Tier I Mouse MP 135 Genes GS165074: MP:0010563 increased heart right ventricle size
Expand Tier I Mouse MP 140 Genes GS169804: MP:0003731 abnormal retinal outer nuclear layer morphology
Expand Tier I Mouse MP 17 Genes GS169901: MP:0008507 thin retinal ganglion layer
Expand Tier II Mouse 78 Genes GS36047: Striatum Gene expression correlates of Light- Dark Box Total seconds spent in light compartment in Females & Males BXD
Expand Tier I Mouse MP 983 Genes GS166244: MP:0002752 abnormal somatic nervous system morphology
Expand Tier I Mouse MP 40 Genes GS169801: MP:0003734 abnormal retinal inner plexiform layer morphology
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Mouse 1023 Genes GS136742: Streptococcus pneumoniae infection resistance 1 (Spir1, Published QTL Chr 7)
Expand Tier I Mouse MP 86 Genes GS170015: MP:0005608 cardiac interstitial fibrosis
Expand Tier I Mouse MP 990 Genes GS169075: MP:0002078 abnormal glucose homeostasis
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Mouse MP 1130 Genes GS163227: MP:0003313 abnormal locomotor activation
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Mouse MP 243 Genes GS167797: MP:0008772 increased heart ventricle size
Expand Tier I Mouse MP 1041 Genes GS168683: MP:0000598 abnormal liver morphology
Expand Tier I Human 344 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Mouse MP 756 Genes GS170683: MP:0003743 abnormal facial morphology
Expand Tier I Mouse MP 92 Genes GS170195: MP:0008515 thin retinal outer nuclear layer
Expand Tier I Mouse MP 585 Genes GS165985: MP:0000965 abnormal sensory neuron morphology
Expand Tier I Mouse 910 Genes GS135938: HDL level 38 (Hdl38, Published QTL Chr 7)
Expand Tier I Mouse MP 647 Genes GS164446: MP:0005195 abnormal posterior eye segment morphology
Expand Tier I Mouse 910 Genes GS135746: experimental allergic encephalomyelitis susceptibility 12 (Eae12, Published QTL Chr 7)
Expand Tier I Mouse MP 487 Genes GS167105: MP:0008948 decreased neuron number
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 Mouse MP 90 Genes GS164236: MP:0008056 abnormal retinal ganglion cell morphology
Expand Tier I Human 358 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Mouse MP 343 Genes GS167907: MP:0003921 abnormal heart left ventricle morphology
Expand Tier I Human 472 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Mouse MP 1856 Genes GS165386: MP:0001262 decreased body weight
Expand Tier I Mouse MP 39 Genes GS163522: MP:0006309 decreased retinal ganglion cell number
Expand Tier I Mouse 1027 Genes GS128580: BECs at LORR Recovery Chr# 7
Expand Tier I Mouse MP 1222 Genes GS165535: MP:0005370 liver/biliary system phenotype
Expand Tier I Mouse MP 1420 Genes GS163052: MP:0000266 abnormal heart morphology
Expand Tier I Human 135 Genes GS172857: HP:0004305 Involuntary movements
Expand Tier I Mouse 973 Genes GS135988: Hfe modifier 1 (Hfem1, Published QTL Chr 7)
Expand Tier I Human 364 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Mouse MP 2406 Genes GS169391: MP:0002066 abnormal motor capabilities/coordination/movement
Expand Tier I Mouse MP 1476 Genes GS169531: MP:0005391 vision/eye phenotype
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Mouse MP 833 Genes GS163103: MP:0000003 abnormal adipose tissue morphology
Expand Tier I Mouse MP 898 Genes GS169390: MP:0002067 abnormal sensory capabilities/reflexes/nociception
Expand Tier I Mouse MP 140 Genes GS169625: MP:0005437 abnormal glycogen level
Expand Tier I Human 699 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human 544 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Mouse MP 116 Genes GS166899: MP:0001330 abnormal optic nerve morphology
Expand Tier I Human 512 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Mouse GO 5892 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier I Mouse MP 1825 Genes GS168956: MP:0003491 abnormal voluntary movement
Expand Tier I Mouse MP 159 Genes GS169054: MP:0005438 abnormal glycogen homeostasis
Expand Tier I Mouse MP 592 Genes GS165809: MP:0002864 abnormal ocular fundus morphology
Expand Tier I Mouse MP 17 Genes GS163514: MP:0006303 abnormal retinal nerve fiber layer morphology
Expand Tier III Mouse 5726 Genes GS213077: Genes with suggestive difference in (PWD) vs (PB6F1 + B6PF1 + B6) comparison
Expand Tier II Mouse 48 Genes GS34247: Hippocampus Gene expression correlates of Activity in altered context during presentation of cue in Females BXD
Expand Tier I Mouse MP 461 Genes GS169957: MP:0001402 hypoactivity
Expand Tier I Mouse MP 3924 Genes GS163934: MP:0001764 abnormal homeostasis
Expand Tier I Mouse MP 5057 Genes GS165525: MP:0010768 mortality/aging
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 Mouse MP 3437 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Mouse MP 1086 Genes GS165869: MP:0002138 abnormal hepatobiliary system morphology
Expand Tier I Mouse MP 407 Genes GS163197: MP:0006113 abnormal heart septum morphology
Expand Tier I Mouse MP 440 Genes GS169225: MP:0000358 abnormal cell morphology
Expand Tier I Mouse DRG 2537 Genes provisional GS86906: Table S1: Additional data file 1 is a table listing the results of two-way ANOVA (FDR < 1%). Lists of probe sets and gene names altered by strain (3457). [DRG]
Expand Tier I Mouse MP 648 Genes GS164023: MP:0001961 abnormal reflex
Expand Tier I Mouse MP 845 Genes GS165539: MP:0005375 adipose tissue phenotype
Expand Tier I Mouse MP 73 Genes GS168793: MP:0005439 decreased glycogen level
Expand Tier I Mouse 641 Genes GS136214: lupus BXSB x NZW 6 (Lxw6, Published QTL Chr 7)
Expand Tier I Mouse GO 1603 Genes GS177409: GO:0005739 mitochondrion
Expand Tier I Mouse MP 18 Genes GS166008: MP:0001492 abnormal pilomotor reflex
Expand Tier II Mouse 91 Genes GS35291: Striatum Gene expression correlates of Prepulse inhibition at 85db in Females BXD
Expand Tier I Mouse MP 111 Genes GS169367: MP:0005405 axon degeneration
Expand Tier I Human 416 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Mouse MP 4173 Genes GS165527: MP:0005378 growth/size phenotype
Expand Tier I Mouse GO 2138 Genes GS186067: GO:0050877 neurological system process
Expand Tier I Mouse MP 156 Genes GS166015: MP:0006036 abnormal mitochondrial physiology
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Mouse MP 4772 Genes GS165524: MP:0010769 abnormal survival
Expand Tier I Mouse MP 466 Genes GS163138: MP:0005253 abnormal eye physiology
Expand Tier I Human 161 Genes GS176803: HP:0001260 Dysarthria
Expand Tier I Mouse MP 329 Genes GS166596: MP:0005334 abnormal fat pad morphology
Expand Tier I Mouse GO 2498 Genes GS193018: GO:0003008 system process
Expand Tier I Human GO 1518 Genes GS194138: GO:0005739 mitochondrion
Expand Tier I Human 913 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Mouse MP 3815 Genes GS165243: MP:0010770 preweaning lethality
Expand Tier I Mouse 593 Genes GS136894: ventricular size 3 (Vent3, Published QTL Chr 7)
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 308 Genes GS172100: HP:0000587 Abnormality of the optic nerve
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 Mouse 585 Genes GS136096: long bones 6 (Lbn6, Published QTL Chr 7)
Expand Tier II Mouse 44 Genes GS26259: Cerebellum Gene expression correlates of Thermal Nociception Tail Withdrawal Test in Females BXD
Expand Tier I Mouse 940 Genes GS136189: lipoprotein QTL 5 (Lprq5, Published QTL Chr 7)
Expand Tier I Human CTD 1191 Genes GS125069: Sodium Selenite interacting genes (MeSH:D018038) in CTD
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 I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Mouse MP 123 Genes GS168775: MP:0002753 dilated heart left ventricle
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Mouse MP 2644 Genes GS169829: MP:0005385 cardiovascular system phenotype
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Mouse DRG 2693 Genes GS87380: Table S1: Additional data file 1 is a table listing the results of two-way ANOVA (FDR < 1%). (Whole Table) [DRG]
Expand Tier I Mouse 585 Genes GS136238: mandible size 5 (Manz5, Published QTL Chr 7)
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 172 Genes GS173476: HP:0002311 Incoordination
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 Mouse MP 2200 Genes GS165465: MP:0003633 abnormal nervous system physiology
Expand Tier I Human GO 205 Genes GS209987: GO:0050953 sensory perception of light stimulus
Expand Tier I Mouse MP 154 Genes GS164826: MP:0010577 abnormal heart right ventricle size
Expand Tier I Mouse MP 259 Genes GS163855: MP:0000010 abnormal abdominal fat pad morphology
Expand Tier III Mouse 2289 Genes GS216489: Genes that are binding sites of CREB and zif268, transcription factors mediating neuronal activity and plasticity, in Mus musculus.
Expand Tier I Mouse MP 159 Genes GS168088: MP:0011110 partial preweaning lethality
Expand Tier I Human 414 Genes GS172195: HP:0000504 Abnormality of vision
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 Mouse MP 177 Genes GS166600: MP:0005330 cardiomyopathy
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Mouse MP 3110 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Mouse MP 1777 Genes GS164263: MP:0002083 premature death
Expand Tier I Mouse MP 2099 Genes GS165616: MP:0002127 abnormal cardiovascular system morphology
Expand Tier I Mouse MP 181 Genes GS163841: MP:0008022 dilated heart ventricle
Expand Tier I Mouse MP 1615 Genes GS165789: MP:0005369 muscle phenotype
Expand Tier I Mouse MP 308 Genes GS169416: MP:0004937 dilated heart
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Mouse MP 376 Genes GS168021: MP:0000745 tremors
Expand Tier I Human 215 Genes GS176167: HP:0001257 Spasticity
Expand Tier I Mouse MP 22 Genes GS167727: MP:0010398 decreased liver glycogen level
Expand Tier I Mouse MP 104 Genes GS168646: MP:0001429 dehydration
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 Mouse MP 710 Genes GS167922: MP:0000959 abnormal somatic sensory system morphology
Expand Tier I Human 95 Genes GS171217: HP:0003487 Babinski sign
Expand Tier III Mouse 8107 Genes GS213076: Genes with suggestive difference in (B6) vs (B6PF1 + PB6F1 + PWD) comparison
Expand Tier II Mouse 23 Genes GS36142: Striatum Gene expression correlates of Activity during 2ndtone shock pairing in Females BXD
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Mouse 653 Genes GS135679: Crhr1 transcript abundance QTL 1 (Crhr1taq1, Published QTL Chr 7)
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Mouse MP 14488 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Human 498 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Mouse MP 130 Genes GS164948: MP:0001505 hunched posture
Expand Tier I Mouse MP 29 Genes GS165239: MP:0010725 thin interventricular septum
Expand Tier I Human 416 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Mouse 2087 Genes GS128573: Ethanol Induced Hypothermia Chr# 7
Expand Tier I Mouse 585 Genes GS136298: maternal performance (Mprf, Published QTL Chr 7)
Expand Tier I Human 316 Genes GS170825: HP:0002167 Neurological speech impairment
Expand Tier II Mouse 72 Genes GS35011: Cerebellum Gene expression correlates of Open Field-Total time in perimeter in Females BXD
Expand Tier I Mouse 975 Genes GS136602: sperm beat cross frequency (Sbcf, Published QTL Chr 7)
Expand Tier I Mouse MP 75 Genes GS166238: MP:0002754 dilated heart right ventricle
Expand Tier I Human 261 Genes GS176172: HP:0001251 Ataxia
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse MP 256 Genes GS165811: MP:0009703 decreased birth body size
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Mouse MP 951 Genes GS165427: MP:0000432 abnormal head morphology
Expand Tier I Human 273 Genes GS172516: HP:0001347 Hyperreflexia
Expand Tier I Mouse GO 1550 Genes GS192290: GO:0007600 sensory perception
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 MP 213 Genes GS167908: MP:0003920 abnormal heart right ventricle morphology
Expand Tier I Mouse MP 1385 Genes GS163971: MP:0002092 abnormal eye morphology
Expand Tier I Mouse MP 642 Genes GS170236: MP:0005452 abnormal adipose tissue amount
Expand Tier I Mouse MP 553 Genes GS165385: MP:0008946 abnormal neuron number
Expand Tier I Mouse 973 Genes GS136264: modifier of mammary tumor progression 1 (Mmtp1, Published QTL Chr 7)