Gene Details



FKRP and homologs in 5 species are found in 582 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 Human 112 Genes GS174327: HP:0003198 Myopathy
Expand Tier I Mouse 973 Genes GS136900: ventral midbrain iron content 4 (Vmbic4, Published QTL Chr 7)
Expand Tier I Human 6 Genes GS176048: HP:0002359 Frequent falls
Expand Tier I Mouse MP 182 Genes GS163171: MP:0000854 abnormal cerebellum development
Expand Tier I Mouse MP 15 Genes GS166439: MP:0006221 optic nerve hypoplasia
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
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 I Human 269 Genes GS172261: HP:0000357 Abnormal location of ears
Expand Tier I Mouse 653 Genes GS135346: Avp transcript abundance QTL 1 (Avptaq1, Published QTL Chr 7)
Expand Tier I Mouse MP 30 Genes GS168741: MP:0009415 skeletal muscle degeneration
Expand Tier I Human 17 Genes GS172643: HP:0002365 Hypoplasia of the brainstem
Expand Tier I Human 178 Genes GS176151: HP:0000256 Macrocephaly
Expand Tier I Human 491 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Mouse MP 36 Genes GS168493: MP:0010090 increased circulating creatine kinase level
Expand Tier I Human 360 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human 135 Genes GS170969: HP:0000157 Abnormality of the tongue
Expand Tier I Human 168 Genes GS170916: HP:0008056 Aplasia/Hypoplasia affecting the eye
Expand Tier I Mouse GO 114 Genes GS186286: GO:0016485 protein processing
Expand Tier I Human 786 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Mouse MP 388 Genes GS165643: MP:0011088 partial neonatal lethality
Expand Tier I Mouse MP 781 Genes GS165992: MP:0008469 abnormal protein level
Expand Tier I Mouse MP 257 Genes GS165839: MP:0009701 abnormal birth body size
Expand Tier I Human 141 Genes GS174906: HP:0000545 Myopia
Expand Tier I Human 426 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Human GO 854 Genes GS203972: GO:0005615 extracellular space
Expand Tier III Fly 2671 Genes GS213271: Head and thorax heatmapping of Canton-S fruit flies with dietary restrictions
Expand Tier I Human 324 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Human 157 Genes GS171718: HP:0002808 Kyphosis
Expand Tier I Human 16 Genes GS173830: HP:0002913 Myoglobinuria
Expand Tier II Mouse 91 Genes GS35700: Whole Brain Gene expression correlates of Morphine distance (cm) travelled minutes 105-120 in Females BXD
Expand Tier I Mouse GO 8406 Genes GS177404: GO:0005737 cytoplasm
Expand Tier I Mouse MP 378 Genes GS167214: MP:0005319 abnormal enzyme/ coenzyme level
Expand Tier I Human GO 4169 Genes GS207925: GO:0034645 cellular macromolecule biosynthetic process
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 121 Genes GS203131: GO:0016485 protein processing
Expand Tier I Mouse MP 792 Genes GS170024: MP:0011086 partial postnatal lethality
Expand Tier I Human 19 Genes GS176247: HP:0002948 Vertebral fusion
Expand Tier I Mouse MP 1350 Genes GS165228: MP:0005382 craniofacial phenotype
Expand Tier I Mouse MP 38 Genes GS163906: MP:0009772 abnormal retinal development
Expand Tier I Human 9 Genes GS172223: HP:0001771 Achilles tendon contracture
Expand Tier I Mouse 973 Genes GS136531: prion resistance 2 (Prnr2, Published QTL Chr 7)
Expand Tier III Mouse 1048 Genes GS213200: Expression changes in the regulation of memory consolidation and synaptic function in FoxO6 vs. wild-type mice
Expand Tier I Human 392 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier III Fly 2674 Genes GS213272: Head and thorax heatmapping of reservatrol treated Canton-S fruit flies
Expand Tier I Human GO 4371 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Mouse GO 4114 Genes GS193414: GO:0044249 cellular biosynthetic process
Expand Tier I Mouse MP 115 Genes GS164129: MP:0001573 abnormal circulating alanine transaminase level
Expand Tier I Mouse GO 122 Genes GS193053: GO:0051604 protein maturation
Expand Tier I Mouse MP 2357 Genes GS163824: MP:0001259 abnormal body weight
Expand Tier I Mouse MP 507 Genes GS166591: MP:0004087 abnormal muscle fiber morphology
Expand Tier I Mouse MP 375 Genes GS163926: MP:0004097 abnormal cerebellar cortex morphology
Expand Tier I Mouse MP 331 Genes GS163432: MP:0006069 abnormal retinal neuronal layer morphology
Expand Tier I Human 741 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 69 Genes GS176437: HP:0002334 Abnormality of the cerebellar vermis
Expand Tier I Human 260 Genes GS170933: HP:0001288 Gait disturbance
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human 96 Genes GS172854: HP:0004302 Functional motor problems.
Expand Tier I Human 46 Genes GS173882: HP:0001305 Dandy-Walker malformation
Expand Tier I Human 7 Genes GS176546: HP:0003724 Shoulder girdle muscle atrophy
Expand Tier I Mouse 984 Genes GS135458: bone mineral density 4 (Bomd4, Published QTL Chr 7)
Expand Tier I Mouse MP 63 Genes GS170695: MP:0002699 abnormal vitreous body morphology
Expand Tier I Human 492 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human 179 Genes GS176589: HP:0001273 Abnormality of the corpus callosum
Expand Tier I Human 319 Genes GS176591: HP:0001276 Hypertonia
Expand Tier I Human 4 Genes GS174255: HP:0007033 Cerebellar dysplasia
Expand Tier I Human 22 Genes GS172190: HP:0002187 Intellectual disability, profound
Expand Tier I Human 53 Genes GS173697: HP:0001319 Neonatal hypotonia
Expand Tier I Mouse MP 1183 Genes GS166409: MP:0002114 abnormal axial skeleton morphology
Expand Tier I Human GO 3885 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier I Human 10 Genes GS176947: HP:0006829 Severe muscular hypotonia
Expand Tier I Human 202 Genes GS175171: HP:0001315 Reduced tendon reflexes
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Human GO 1914 Genes GS198782: GO:0044459 plasma membrane part
Expand Tier I Mouse MP 86 Genes GS165143: MP:0003733 abnormal retinal inner nuclear layer morphology
Expand Tier I Mouse GO 17 Genes GS177768: GO:0016010 dystrophin-associated glycoprotein complex
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Human 170 Genes GS173988: HP:0000501 Glaucoma
Expand Tier I Human GO 553 Genes GS205302: GO:0000139 Golgi membrane
Expand Tier I Human 65 Genes GS174481: HP:0010576 Intracranial cystic lesion
Expand Tier I Human 17 Genes GS175676: HP:0007362 Aplasia/Hypoplasia of the brainstem
Expand Tier I Mouse GO 6473 Genes GS184448: GO:0044425 membrane part
Expand Tier I Human 38 Genes GS172993: HP:0001321 Cerebellar hypoplasia
Expand Tier I Human 5 Genes GS176928: HP:0003741 Congenital muscular dystrophy
Expand Tier I Human 446 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier I Human 123 Genes GS171946: HP:0002269 Abnormality of neuronal migration
Expand Tier I Human 358 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Mouse MP 482 Genes GS163429: MP:0000849 abnormal cerebellum morphology
Expand Tier I Mouse MP 1966 Genes GS166590: MP:0002873 normal phenotype
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Mouse GO 228 Genes GS185668: GO:0009100 glycoprotein metabolic process
Expand Tier I Human 88 Genes GS176588: HP:0001272 Cerebellar atrophy
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Mouse MP 20 Genes GS168736: MP:0009412 skeletal muscle fiber degeneration
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 266 Genes GS175823: HP:0002093 Respiratory insufficiency
Expand Tier I Mouse GO 5103 Genes GS192512: GO:0003824 catalytic activity
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 24 Genes GS176061: HP:0002355 Difficulty walking
Expand Tier I Mouse MP 1460 Genes GS164264: MP:0002082 postnatal lethality
Expand Tier I Mouse MP 3437 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Mouse MP 363 Genes GS167360: MP:0002200 abnormal brain ventricle/choroid plexus morphology
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human 84 Genes GS176462: HP:0100240 Synostosis of joints
Expand Tier II Mouse 85 Genes GS35535: Whole Brain Gene expression correlates of Morphine photocell counts minutes 105-120 in Females BXD
Expand Tier I Mouse MP 648 Genes GS164023: MP:0001961 abnormal reflex
Expand Tier I Mouse MP 36 Genes GS164038: MP:0003852 skeletal muscle necrosis
Expand Tier II Mouse 147 Genes GS36597: Whole Brain Gene expression correlates of Morphine vertical activity counts minutes 90-105 in Males BXD
Expand Tier I Mouse MP 239 Genes GS163662: MP:0005277 abnormal brainstem morphology
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 II Mouse 85 Genes GS36589: Striatum Gene expression correlates of Morphine vertical activity counts minutes 90-105 in Females BXD
Expand Tier I Human 20 Genes GS171252: HP:0003819 Death in childhood
Expand Tier I Mouse MP 491 Genes GS164448: MP:0005193 abnormal anterior eye segment morphology
Expand Tier I Mouse MP 239 Genes GS169262: MP:0003084 abnormal skeletal muscle fiber morphology
Expand Tier I Mouse 593 Genes GS136894: ventricular size 3 (Vent3, Published QTL Chr 7)
Expand Tier I Human 201 Genes GS176660: HP:0000050 Hypoplastic genitalia
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Human 384 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human 221 Genes GS172288: HP:0000358 Posteriorly rotated ears
Expand Tier I Human 315 Genes GS176568: HP:0000486 Strabismus
Expand Tier I Mouse GO 3978 Genes GS188506: GO:0010467 gene expression
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Mouse MP 37 Genes GS166561: MP:0003648 abnormal radial glial cell morphology
Expand Tier I Mouse GO 785 Genes GS187113: GO:0005615 extracellular space
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 Human GO 6151 Genes GS201252: GO:0044425 membrane part
Expand Tier I Mouse 585 Genes GS136238: mandible size 5 (Manz5, Published QTL Chr 7)
Expand Tier I Human GO 91 Genes GS198475: GO:0042383 sarcolemma
Expand Tier I Mouse GO 4218 Genes GS192073: GO:1901576 organic substance biosynthetic process
Expand Tier I Mouse GO 7644 Genes GS188399: GO:0044238 primary metabolic process
Expand Tier I Mouse GO 186 Genes GS185669: GO:0009101 glycoprotein biosynthetic process
Expand Tier I Human 64 Genes GS174379: HP:0002084 Encephalocele
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human CTD 4423 Genes GS123718: Ethinyl Estradiol interacting genes (MeSH:D004997) in CTD
Expand Tier I Human 81 Genes GS171773: HP:0000532 Chorioretinal abnormality
Expand Tier I Mouse 901 Genes GS135415: bronchial hyperresponsiveness 6 (Bhr6, Published QTL Chr 7)
Expand Tier I Human 92 Genes GS171656: HP:0000610 Abnormality of the choroid
Expand Tier I Human 545 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Mouse MP 3110 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Mouse MP 48 Genes GS170191: MP:0008511 thin retinal inner nuclear layer
Expand Tier I Mouse MP 1615 Genes GS165789: MP:0005369 muscle phenotype
Expand Tier I Human GO 323 Genes GS202501: GO:0009101 glycoprotein biosynthetic process
Expand Tier I Mouse MP 115 Genes GS163174: MP:0000857 abnormal cerebellar foliation
Expand Tier I Human 163 Genes GS176478: HP:0002119 Ventriculomegaly
Expand Tier I Human GO 3861 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Mouse MP 1989 Genes GS169530: MP:0005390 skeleton phenotype
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 285 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier I Human 8 Genes GS174113: HP:0008981 Calf muscle hypertrophy
Expand Tier I Human 105 Genes GS175571: HP:0011492 Abnormality of corneal stroma
Expand Tier I Human 139 Genes GS171397: HP:0000177 Abnormality of upper lip
Expand Tier I Mouse MP 484 Genes GS163292: MP:0003091 abnormal cell migration
Expand Tier I Mouse MP 380 Genes GS167917: MP:0000952 abnormal CNS glial cell morphology
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 MP 190 Genes GS167518: MP:0001312 abnormal cornea morphology
Expand Tier I Mouse GO 57 Genes GS186812: GO:0005791 rough endoplasmic reticulum
Expand Tier I Human GO 4283 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Human 498 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Mouse MP 289 Genes GS170158: MP:0000074 abnormal neurocranium morphology
Expand Tier I Mouse MP 93 Genes GS166794: MP:0002941 increased circulating alanine transaminase level
Expand Tier I Human 416 Genes GS173147: HP:0011283 Abnormality of the metencephalon
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 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 98 Genes GS171910: HP:0003828 Variable expressivity
Expand Tier I Human GO 3275 Genes GS199267: GO:0043234 protein complex
Expand Tier I Mouse 975 Genes GS136602: sperm beat cross frequency (Sbcf, Published QTL Chr 7)
Expand Tier I Human 173 Genes GS175117: HP:0001883 Talipes
Expand Tier I Human 32 Genes GS171753: HP:0001712 Left ventricular hypertrophy
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 189 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier I Human 46 Genes GS170961: HP:0000158 Macroglossia
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 132 Genes GS174606: HP:0001608 Abnormality of the voice
Expand Tier I Human 545 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Mouse MP 865 Genes GS167759: MP:0000787 abnormal telencephalon morphology
Expand Tier I Human 737 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human 8 Genes GS171731: HP:0003547 Shoulder girdle muscle weakness
Expand Tier I Human CTD 5725 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Mouse 973 Genes GS136264: modifier of mammary tumor progression 1 (Mmtp1, Published QTL Chr 7)
Expand Tier I Mouse MP 108 Genes GS169489: MP:0000747 muscle weakness
Expand Tier I Human 89 Genes GS176824: HP:0000204 Cleft upper lip
Expand Tier I Mouse MP 7 Genes GS169879: MP:0010235 abnormal retina inner limiting membrane morphology
Expand Tier I Mouse MP 639 Genes GS164032: MP:0004811 abnormal neuron physiology
Expand Tier I Mouse MP 3494 Genes GS170601: MP:0005621 abnormal cell physiology
Expand Tier II Mouse 83 Genes GS34349: Striatum Gene expression correlates of Morphine Open Field TOTAL distance (cm) travelled in Females & Males BXD
Expand Tier I Mouse MP 3543 Genes GS169095: MP:0004924 abnormal behavior
Expand Tier I Mouse MP 34 Genes GS168743: MP:0009419 skeletal muscle fibrosis
Expand Tier I Mouse MP 1963 Genes GS166718: MP:0002169 no abnormal phenotype detected
Expand Tier I Human 258 Genes GS175602: HP:0002087 Abnormality of the upper respiratory tract
Expand Tier I Human 35 Genes GS173690: HP:0001644 Dilated cardiomyopathy
Expand Tier I Human GO 1178 Genes GS201075: GO:0005794 Golgi apparatus
Expand Tier I Mouse MP 238 Genes GS170688: MP:0002697 abnormal eye size
Expand Tier I Mouse MP 633 Genes GS163101: MP:0008540 abnormal cerebrum morphology
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human 530 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human GO 1736 Genes GS208734: GO:0016740 transferase activity
Expand Tier I Human GO 20 Genes GS194508: GO:0016010 dystrophin-associated glycoprotein complex
Expand Tier I Human 47 Genes GS172604: HP:0005445 Widened posterior fossa
Expand Tier I Human GO 5152 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier I Mouse MP 110 Genes GS167442: MP:0000440 domed cranium
Expand Tier I Mouse GO 1440 Genes GS181988: GO:0044459 plasma membrane part
Expand Tier I Mouse MP 176 Genes GS165640: MP:0002269 muscular atrophy
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 Human 17 Genes GS173239: HP:0001339 Lissencephaly
Expand Tier I Human 274 Genes GS172372: HP:0000648 Optic atrophy
Expand Tier I Human GO 1205 Genes GS194505: GO:1901135 carbohydrate derivative metabolic process
Expand Tier I Mouse MP 379 Genes GS164530: MP:0000801 abnormal temporal lobe morphology
Expand Tier I Mouse MP 140 Genes GS169804: MP:0003731 abnormal retinal outer nuclear layer morphology
Expand Tier I Human 24 Genes GS174091: HP:0004327 Abnormality of the vitreous humor
Expand Tier I Mouse MP 815 Genes GS169062: MP:0000913 abnormal brain development
Expand Tier I Mouse 1023 Genes GS136742: Streptococcus pneumoniae infection resistance 1 (Spir1, Published QTL Chr 7)
Expand Tier I Mouse MP 682 Genes GS166407: MP:0002116 abnormal craniofacial bone morphology
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human GO 5320 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 75 Genes GS174446: HP:0001120 Abnormality of corneal size
Expand Tier I Human 41 Genes GS172019: HP:0001360 Holoprosencephaly
Expand Tier I Mouse MP 342 Genes GS166450: MP:0011089 complete perinatal lethality
Expand Tier I Human 9 Genes GS174227: HP:0001445 Abnormality of the hip-girdle musculature
Expand Tier I Mouse MP 21 Genes GS166991: MP:0009414 skeletal muscle fiber necrosis
Expand Tier I Human 344 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Human 398 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier II Mouse 91 Genes GS36602: Whole Brain Gene expression correlates of Morphine vertical activity counts minutes 105-120 in Females & Males BXD
Expand Tier I Human 38 Genes GS173880: HP:0005750 Contractures of the joints of the lower limbs
Expand Tier I Human 196 Genes GS172034: HP:0000368 Low-set, posteriorly rotated ears
Expand Tier I Human 197 Genes GS175785: HP:0002500 Abnormality of the cerebral white matter
Expand Tier I Human 195 Genes GS174813: HP:0001638 Cardiomyopathy
Expand Tier I Mouse MP 92 Genes GS170195: MP:0008515 thin retinal outer nuclear layer
Expand Tier I Mouse GO 9049 Genes GS180166: GO:0008152 metabolic process
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 Human 246 Genes GS176806: HP:0003812 Phenotypic variability
Expand Tier I Mouse DRG 1187 Genes provisional GS87137: Table S2: List of probe-sets of genes differentially expressed among the four inbred strains of mice. Gene Ranks [DRG]
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 26 Genes GS170797: HP:0003560 Muscular dystrophy
Expand Tier I Mouse MP 51 Genes GS169180: MP:0000752 dystrophic muscle
Expand Tier I Mouse GO 1006 Genes GS184267: GO:0005794 Golgi apparatus
Expand Tier II Mouse 124 Genes GS34361: Whole Brain Gene expression correlates of Morphine TOTAL vertical activity counts in Females & Males BXD
Expand Tier I Mouse GO 1149 Genes GS179957: GO:0005783 endoplasmic reticulum
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 111 Genes GS177023: HP:0010876 Abnormality of circulating protein level
Expand Tier I Human 399 Genes GS171100: HP:0000759 Abnormality of the peripheral nervous system
Expand Tier I Human 39 Genes GS175557: HP:0002515 Waddling gait
Expand Tier I Human 551 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 16 Genes GS176886: HP:0100261 Abnormal tendon morphology
Expand Tier I Human 18 Genes GS176941: HP:0002791 Hypoventilation
Expand Tier I Mouse MP 1476 Genes GS169531: MP:0005391 vision/eye phenotype
Expand Tier I Human 391 Genes GS175537: HP:0011277 Abnormality of the urinary system physiology
Expand Tier I Human 346 Genes GS172989: HP:0001324 Muscle weakness
Expand Tier I Mouse MP 64 Genes GS168366: MP:0000109 abnormal parietal bone morphology
Expand Tier I Mouse MP 592 Genes GS165809: MP:0002864 abnormal ocular fundus morphology
Expand Tier I Mouse GO 987 Genes GS177766: GO:1901135 carbohydrate derivative metabolic process
Expand Tier I Mouse GO 8145 Genes GS190714: GO:0016020 membrane
Expand Tier I Human 263 Genes GS176477: HP:0002118 Abnormality of the cerebral ventricles
Expand Tier I Human 588 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
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 Mouse MP 3924 Genes GS163934: MP:0001764 abnormal homeostasis
Expand Tier I Human GO 6651 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 143 Genes GS176586: HP:0001270 Motor delay
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 GO 362 Genes GS177764: GO:1901137 carbohydrate derivative biosynthetic process
Expand Tier I Human 107 Genes GS172094: HP:0000589 Coloboma
Expand Tier I Human 14 Genes GS171865: HP:0008366 Contractures involving the joints of the feet
Expand Tier I Human 120 Genes GS177000: HP:0001291 Abnormality of the cranial nerves
Expand Tier I Human 7 Genes GS172976: HP:0003749 Pelvic girdle muscle weakness
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 641 Genes GS136214: lupus BXSB x NZW 6 (Lxw6, Published QTL Chr 7)
Expand Tier I Human 79 Genes GS173516: HP:0000301 Abnormality of facial musculature
Expand Tier I Human 346 Genes GS171309: HP:0000252 Microcephaly
Expand Tier I Human 416 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Mouse MP 124 Genes GS164473: MP:0006009 abnormal neuronal migration
Expand Tier I Mouse MP 4772 Genes GS165524: MP:0010769 abnormal survival
Expand Tier I Human 445 Genes GS175423: HP:0010461 Abnormality of the male genitalia
Expand Tier II Mouse 47 Genes GS35501: Cerebellum Gene expression correlates of Neurogenesis- BrdU labeled new neurons in Adult Rostral Migratory Stream 1 hr post BrdU in Females & Males BXD
Expand Tier I Human 268 Genes GS172365: HP:0003110 Abnormality of urine homeostasis
Expand Tier I Human 98 Genes GS176867: HP:0003577 Congenital onset
Expand Tier I Mouse MP 3815 Genes GS165243: MP:0010770 preweaning lethality
Expand Tier I Human 358 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Human 64 Genes GS172899: HP:0011815 Cephalocele
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 7311 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human GO 5047 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Tier I Mouse GO 7552 Genes GS180452: GO:0044237 cellular metabolic process
Expand Tier I Human 203 Genes GS174706: HP:0000553 Abnormality of the uvea
Expand Tier I Human 515 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human 38 Genes GS171754: HP:0001711 Abnormality of the left ventricle
Expand Tier I Human 27 Genes GS173870: HP:0001302 Pachygyria
Expand Tier I Human 199 Genes GS171637: HP:0008872 Feeding difficulties in infancy
Expand Tier I Mouse GO 2991 Genes GS182469: GO:0043234 protein complex
Expand Tier I Mouse 940 Genes GS136189: lipoprotein QTL 5 (Lprq5, Published QTL Chr 7)
Expand Tier I Mouse MP 562 Genes GS163436: MP:0000841 abnormal hindbrain morphology
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Human 83 Genes GS175811: HP:0011021 Abnormality of circulating enzyme level
Expand Tier I Human 200 Genes GS174812: HP:0001637 Abnormality of the myocardium
Expand Tier I Mouse MP 2663 Genes GS168995: MP:0009642 abnormal blood homeostasis
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Mouse GO 6435 Genes GS177531: GO:0043170 macromolecule metabolic process
Expand Tier I Mouse MP 123 Genes GS164266: MP:0000812 abnormal dentate gyrus morphology
Expand Tier I Mouse MP 23 Genes GS163045: MP:0003083 abnormal tibialis anterior morphology
Expand Tier I Mouse MP 663 Genes GS165437: MP:0000438 abnormal cranium morphology
Expand Tier I Mouse MP 1628 Genes GS167505: MP:0008762 embryonic lethality
Expand Tier I Human GO 8702 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 990 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human 63 Genes GS174833: HP:0006817 Aplasia/Hypoplasia of the cerebellar vermis
Expand Tier I Mouse GO 3583 Genes GS180236: GO:0032991 macromolecular complex
Expand Tier I Human 98 Genes GS176756: HP:0011420 Death
Expand Tier I Mouse MP 255 Genes GS166583: MP:0001513 limb grasping
Expand Tier I Human GO 133 Genes GS209994: GO:0051604 protein maturation
Expand Tier I Mouse MP 363 Genes GS167748: MP:0000788 abnormal cerebral cortex morphology
Expand Tier I Human GO 4276 Genes GS207858: GO:0009059 macromolecule biosynthetic process
Expand Tier I Human 250 Genes GS172246: HP:0001371 Flexion contracture
Expand Tier I Human 433 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Human 172 Genes GS173476: HP:0002311 Incoordination
Expand Tier I Mouse MP 2263 Genes GS164262: MP:0002080 prenatal lethality
Expand Tier I Human GO 551 Genes GS194503: GO:1901137 carbohydrate derivative biosynthetic process
Expand Tier I Human 74 Genes GS171850: HP:0002414 Spina bifida
Expand Tier I Mouse MP 226 Genes GS162928: MP:0006108 abnormal hindbrain development
Expand Tier I Mouse MP 2200 Genes GS165465: MP:0003633 abnormal nervous system physiology
Expand Tier I Human GO 5321 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Mouse GO 8072 Genes GS184218: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 3254 Genes GS200602: GO:0044267 cellular protein metabolic process
Expand Tier I Human 56 Genes GS176885: HP:0002693 Abnormality of the skull base
Expand Tier I Human 1 Genes GS173745: HP:0005162 Impaired left ventricular function
Expand Tier I Mouse GO 5650 Genes GS183848: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 63 Genes GS175327: HP:0000568 Microphthalmos
Expand Tier I Human 271 Genes GS176826: HP:0000202 Oral cleft
Expand Tier I Mouse MP 1724 Genes GS164220: MP:0002882 abnormal neuron morphology
Expand Tier I Mouse MP 1055 Genes GS166120: MP:0002106 abnormal muscle physiology
Expand Tier I Mouse MP 246 Genes GS170738: MP:0001056 abnormal cranial nerve morphology
Expand Tier I Mouse MP 86 Genes GS168450: MP:0009404 centrally nucleated skeletal muscle fibers
Expand Tier I Human 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 275 Genes GS170962: HP:0000159 Abnormality of the lip
Expand Tier I Mouse GO 3706 Genes GS188641: GO:0071944 cell periphery
Expand Tier I Human 537 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Mouse GO 3473 Genes GS190950: GO:0009059 macromolecule biosynthetic process
Expand Tier I Mouse MP 1274 Genes GS164320: MP:0003861 abnormal nervous system development
Expand Tier I Mouse MP 762 Genes GS166154: MP:0011098 complete embryonic lethality during organogenesis
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Human 85 Genes GS173946: HP:0002438 Cerebellar malformation
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 Human 109 Genes GS176899: HP:0002353 EEG abnormality
Expand Tier I Mouse GO 8650 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse MP 396 Genes GS170108: MP:0003727 abnormal retinal layer morphology
Expand Tier I Human 182 Genes GS174612: HP:0001600 Abnormality of the larynx
Expand Tier I Human 170 Genes GS174488: HP:0000525 Abnormality of the iris
Expand Tier I Mouse MP 124 Genes GS167703: MP:0009964 abnormal cerebellum lobule morphology
Expand Tier I Human 129 Genes GS173247: HP:0007957 Reduction of corneal clarity
Expand Tier I Human 68 Genes GS173148: HP:0003712 Muscle hypertrophy
Expand Tier II Mouse 104 Genes GS36737: Whole Brain Gene expression correlates of Morphine vertical activity counts minutes 75-90 in Females & Males BXD
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Human 107 Genes GS173786: HP:0003457 EMG abnormality
Expand Tier I Human 14 Genes GS172228: HP:0002194 Delayed gross motor development
Expand Tier I Human 117 Genes GS173868: HP:0002143 Abnormality of the spinal cord
Expand Tier I Human 24 Genes GS171839: HP:0003458 EMG: myopathic abnormalities
Expand Tier II Mouse 85 Genes GS35520: Whole Brain Gene expression correlates of Morphine photocell counts minutes 90-105 in Females BXD
Expand Tier I Mouse MP 85 Genes GS169664: MP:0001314 corneal opacity
Expand Tier I Human 602 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Mouse 958 Genes GS136745: spermatogenesis defect 3 (Spmd3, Published QTL Chr 7)
Expand Tier I Human 51 Genes GS175893: HP:0000932 Abnormality of the posterior cranial fossa
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human 106 Genes GS175048: HP:0006824 Cranial nerve paralysis
Expand Tier I Human 533 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Mouse GO 5734 Genes GS190713: GO:0016021 integral to membrane
Expand Tier I Human GO 5223 Genes GS207857: GO:0009058 biosynthetic process
Expand Tier I Mouse MP 3019 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human 15 Genes GS175202: HP:0007126 Proximal amyotrophy
Expand Tier I Human 473 Genes GS171893: HP:0011458 Abdominal symptom
Expand Tier I Mouse GO 3548 Genes GS184566: GO:0019538 protein metabolic process
Expand Tier II Mouse 81 Genes GS36617: Whole Brain Gene expression correlates of Morphine vertical activity counts minutes 120-135 in Females & Males BXD
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 26 Genes GS174445: HP:0001435 Abnormality of the shoulder girdle musculature
Expand Tier I Human 137 Genes GS175674: HP:0007360 Aplasia/Hypoplasia of the cerebellum
Expand Tier II Mouse 63 Genes GS36647: Whole Brain Gene expression correlates of Morphine vertical activity counts minutes 150-165 in Females & Males BXD
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier I Human GO 384 Genes GS202500: GO:0009100 glycoprotein metabolic process
Expand Tier I Human 165 Genes GS171654: HP:0003121 Limb joint contracture
Expand Tier I Human 18 Genes GS173156: HP:0003325 Limb-girdle muscle weakness
Expand Tier I Human 42 Genes GS174226: HP:0001446 Abnormality of the musculature of the upper limbs
Expand Tier I Human 486 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human 16 Genes GS174448: HP:0001430 Abnormality of the calf musculature
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human 140 Genes GS174860: HP:0010549 Paralysis due to lesions of the principle motor tracts
Expand Tier I Mouse 831 Genes GS136728: susceptibility to lung cancer 30 (Sluc30, Published QTL Chr 7)
Expand Tier I Human 174 Genes GS171806: HP:0005656 Positional foot deformities
Expand Tier I Mouse MP 1571 Genes GS164133: MP:0005076 abnormal cell differentiation
Expand Tier I Mouse MP 474 Genes GS169176: MP:0000759 abnormal skeletal muscle morphology
Expand Tier I Human 104 Genes GS175835: HP:0007759 Opacification of the corneal stroma
Expand Tier I Human 344 Genes GS174378: HP:0000518 Cataract
Expand Tier I Mouse MP 306 Genes GS169962: MP:0001286 abnormal eye development
Expand Tier I Human 237 Genes GS174292: HP:0011968 Feeding difficulties
Expand Tier I Mouse MP 749 Genes GS167833: MP:0001784 abnormal fluid regulation
Expand Tier I Human 239 Genes GS174066: HP:0100737 Abnormality of the hard palate
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human 35 Genes GS174741: HP:0003394 Muscle cramps
Expand Tier I Human 416 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Mouse GO 8414 Genes GS185585: GO:0044710 single-organism metabolic process
Expand Tier I Human 71 Genes GS174073: HP:0009127 Abnormality of the musculature of the limbs
Expand Tier I Mouse 585 Genes GS136233: mandible length 7 (Manln7, Published QTL Chr 7)
Expand Tier I Human GO 1281 Genes GS196726: GO:0005783 endoplasmic reticulum
Expand Tier I Mouse MP 66 Genes GS169946: MP:0000825 dilated lateral ventricles
Expand Tier I Mouse MP 994 Genes GS168502: MP:0002058 neonatal lethality
Expand Tier I Human 489 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human 72 Genes GS171643: HP:0003701 Proximal muscle weakness
Expand Tier I Human 34 Genes GS171944: HP:0003324 Generalized muscle weakness
Expand Tier I Mouse MP 486 Genes GS169630: MP:0001785 edema
Expand Tier I Human GO 1771 Genes GS196284: GO:0012505 endomembrane system
Expand Tier I Mouse MP 153 Genes GS169046: MP:0009398 abnormal skeletal muscle fiber size
Expand Tier I Human 11 Genes GS176402: HP:0003797 Limb-girdle muscle atrophy
Expand Tier I Human 10 Genes GS171720: HP:0005109 Abnormality of the Achilles tendon
Expand Tier I Mouse MP 77 Genes GS168900: MP:0000749 muscle degeneration
Expand Tier I Mouse MP 3543 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier I Human 179 Genes GS171047: HP:0008736 Hypoplasia of penis
Expand Tier I Human 154 Genes GS175880: HP:0007370 Aplasia/Hypoplasia of the corpus callosum
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Mouse MP 983 Genes GS166244: MP:0002752 abnormal somatic nervous system morphology
Expand Tier I Mouse MP 1083 Genes GS167755: MP:0000783 abnormal forebrain morphology
Expand Tier I Human 123 Genes GS175588: HP:0001311 Neurophysiological abnormality
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 4 Genes GS172917: HP:0008305 Exercise-induced myoglobinuria
Expand Tier I Mouse MP 425 Genes GS169631: MP:0004166 abnormal limbic system morphology
Expand Tier I Mouse DRG 321 Genes provisional GS86920: Table S3: Detailed description of Gene Ontology analysis presented in Table 1 and Table 2. Inter strain GO [DRG]
Expand Tier I Mouse MP 158 Genes GS170033: MP:0003358 abnormal hypaxial muscle morphology
Expand Tier I Mouse MP 3716 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Human 169 Genes GS171752: HP:0001713 Abnormality of cardiac ventricle
Expand Tier I Mouse GO 1686 Genes GS191796: GO:0016740 transferase activity
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 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 II Mouse 90 Genes GS35826: Cerebellum Gene expression correlates of Cocaine CPP - Time (s) in saline paired compartment a in Males BXD
Expand Tier I Mouse MP 37 Genes GS168947: MP:0010089 abnormal circulating creatine kinase level
Expand Tier I Mouse MP 2406 Genes GS169391: MP:0002066 abnormal motor capabilities/coordination/movement
Expand Tier I Mouse MP 898 Genes GS169390: MP:0002067 abnormal sensory capabilities/reflexes/nociception
Expand Tier I Mouse MP 15 Genes GS164146: MP:0004246 abnormal extensor digitorum longus morphology
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 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 MP 16 Genes GS170272: MP:0008259 abnormal optic disc morphology
Expand Tier I Mouse GO 3614 Genes GS180229: GO:0005886 plasma membrane
Expand Tier I Human GO 47 Genes GS203663: GO:0005791 rough endoplasmic reticulum
Expand Tier I Mouse MP 297 Genes GS164127: MP:0001570 abnormal circulating enzyme level
Expand Tier I Human 67 Genes GS175160: HP:0002538 Abnormality of the cerebral cortex
Expand Tier I Human 534 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Human 72 Genes GS171658: HP:0000612 Iris coloboma
Expand Tier I Mouse GO 1041 Genes GS184451: GO:0044421 extracellular region part
Expand Tier I Mouse GO 1825 Genes GS193270: GO:0005576 extracellular region
Expand Tier I Human 7 Genes GS171319: HP:0007260 Type II lissencephaly
Expand Tier I Human 9 Genes GS176816: HP:0008968 Muscle hypertrophy of the lower extremities
Expand Tier I Mouse GO 101 Genes GS181685: GO:0042383 sarcolemma
Expand Tier I Human GO 672 Genes GS205609: GO:0044431 Golgi apparatus part
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Human 397 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Mouse 585 Genes GS136096: long bones 6 (Lbn6, Published QTL Chr 7)
Expand Tier I Human 61 Genes GS175162: HP:0002536 Abnormal cortical gyration
Expand Tier I Human 70 Genes GS173601: HP:0010827 Abnormality of the seventh cranial nerve
Expand Tier I Mouse GO 3382 Genes GS191021: GO:0034645 cellular macromolecule biosynthetic process
Expand Tier II Mouse 929 Genes GS84191: alcohol preference 7 QTL (Ap7q, Published QTL, Chr 7)
Expand Tier II Mouse 68 Genes GS36739: Striatum Gene expression correlates of Morphine vertical activity counts minutes 75-90 in Females BXD
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human GO 2373 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human 42 Genes GS172670: HP:0002363 Abnormality of the brainstem
Expand Tier II Mouse 47 Genes GS33990: Striatum Gene expression correlates of Morphine distance (cm) travelled minutes 75-90 in Females & Males BXD
Expand Tier I Human 41 Genes GS171758: HP:0001714 Ventricular hypertrophy
Expand Tier I Mouse MP 373 Genes GS164526: MP:0000807 abnormal hippocampus morphology
Expand Tier I Human GO 835 Genes GS210330: GO:0006412 translation
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 28 Genes GS173311: HP:0010651 Abnormality of the meninges
Expand Tier I Human 388 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Human 76 Genes GS172219: HP:0010301 Spinal dysraphism
Expand Tier I Human 229 Genes GS175577: HP:0003202 Amyotrophy