Gene Details



PEX1 and homologs in 4 species are found in 567 GeneSets:


- Entrez   - Ensembl   - GeneNetwork   - STRING   - Allen Brain Atlas   - Comparative Toxicogenomics Database  

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Human 387 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Human 19 Genes GS176512: HP:0004492 Widely patent fontanelles and sutures
Expand Tier I Human 72 Genes GS176436: HP:0000047 Hypospadias
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Mouse GO 641 Genes GS185985: GO:0016818 hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides
Expand Tier I Human 43 Genes GS176725: HP:0011425 Fetal ultrasound soft marker
Expand Tier I Human GO 1839 Genes GS205510: GO:0001883 purine nucleoside binding
Expand Tier I Human 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
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 282 Genes GS175900: HP:0009118 Aplasia/Hypoplasia of the mandible
Expand Tier I Mouse GO 2260 Genes GS189855: GO:0043168 anion binding
Expand Tier I Mouse GO 2 Genes GS189367: GO:0060151 peroxisome localization
Expand Tier I Human 99 Genes GS173687: HP:0001643 Patent ductus arteriosus
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
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 20 Genes GS175316: HP:0000565 Esotropia
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 Human 94 Genes GS173846: HP:0003355 Aminoaciduria
Expand Tier I Human 61 Genes GS175897: HP:0000939 Osteoporosis
Expand Tier I Human 125 Genes GS173384: HP:0002750 Delayed skeletal maturation
Expand Tier I Human 269 Genes GS172261: HP:0000357 Abnormal location of ears
Expand Tier I Human 156 Genes GS174002: HP:0000189 Narrow palate
Expand Tier I Human GO 2 Genes GS206231: GO:0060151 peroxisome localization
Expand Tier I Human 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 103 Genes GS174372: HP:0002024 Malabsorption
Expand Tier I Human 322 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier I Human 170 Genes GS174488: HP:0000525 Abnormality of the iris
Expand Tier I Human 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Mouse 237 Genes GS135965: HDL QTL 34 (Hdlq34, Published QTL Chr 5)
Expand Tier I Human 111 Genes GS171784: HP:0001399 Hepatic failure
Expand Tier I Human 84 Genes GS175531: HP:0000003 Multicystic kidney dysplasia
Expand Tier I Human 129 Genes GS173247: HP:0007957 Reduction of corneal clarity
Expand Tier I Mouse GO 1774 Genes GS184984: GO:0032553 ribonucleotide binding
Expand Tier I Human 150 Genes GS174586: HP:0005930 Abnormality of the epiphyses
Expand Tier I Mouse GO 404 Genes GS190247: GO:0032403 protein complex binding
Expand Tier I Mouse 363 Genes GS136917: vertebral morphology and mechanical traits 5 (Vmmt5, Published QTL Chr 5)
Expand Tier I Human 68 Genes GS173148: HP:0003712 Muscle hypertrophy
Expand Tier I Human GO 33 Genes GS205111: GO:0007031 peroxisome organization
Expand Tier II Mouse 358 Genes GS35852: Striatum Gene expression correlates of Cocaine CPP - difference in time spent relative to baseline drug exposure in Males BXD
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Human GO 5400 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Mouse GO 345 Genes GS185190: GO:0006605 protein targeting
Expand Tier I Mouse GO 1765 Genes GS183645: GO:0017076 purine nucleotide binding
Expand Tier I Human 47 Genes GS173284: HP:0000311 Round face
Expand Tier I Human 178 Genes GS176151: HP:0000256 Macrocephaly
Expand Tier I Human 374 Genes GS175815: HP:0011025 Abnormality of cardiovascular system physiology
Expand Tier I Human 104 Genes GS176638: HP:0011603 Congenital malformation of the great arteries
Expand Tier I Human 146 Genes GS170968: HP:0000156 High-arched palate
Expand Tier I Human 491 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Human 12 Genes GS174286: HP:0002570 Steatorrhea
Expand Tier I Human 30 Genes GS176144: HP:0001787 Abnormal delivery
Expand Tier I Human 135 Genes GS170969: HP:0000157 Abnormality of the tongue
Expand Tier I Human 602 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Human 150 Genes GS175411: HP:0100871 Abnormality of the palm
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Mouse GO 46 Genes GS191431: GO:0031903 microbody membrane
Expand Tier I Human 51 Genes GS172891: HP:0100538 Abnormality of the supraorbital ridges
Expand Tier I Human GO 1840 Genes GS197443: GO:0032549 ribonucleoside binding
Expand Tier I Human 29 Genes GS172938: HP:0010655 Epiphyseal stippling
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 Human 786 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 264 Genes GS173014: HP:0010936 Abnormality of the lower urinary tract
Expand Tier I Human GO 1559 Genes GS201869: GO:0008104 protein localization
Expand Tier I Mouse 171 Genes GS136452: postnatal body weight growth 14 (Pbwg14, Published QTL Chr 5)
Expand Tier I Human 639 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human 222 Genes GS173995: HP:0000508 Ptosis
Expand Tier I Human 81 Genes GS172726: HP:0000268 Dolichocephaly
Expand Tier II Mouse 354 Genes GS84167: METH responses for home cage activity (Published QTL, Chr 5)
Expand Tier I Mouse GO 1870 Genes GS192986: GO:0006996 organelle organization
Expand Tier I Human 20 Genes GS171497: HP:0002282 Heterotopia
Expand Tier I Human 426 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Human 37 Genes GS173707: HP:0000846 Adrenal insufficiency
Expand Tier I Human 324 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Human 125 Genes GS174854: HP:0001410 Decreased liver function
Expand Tier I Human 149 Genes GS176098: HP:0000927 Abnormality of skeletal maturation
Expand Tier I Human 114 Genes GS174412: HP:0007477 Abnormal dermatoglyphics
Expand Tier I Human 66 Genes GS176033: HP:0011039 Abnormality of the helix
Expand Tier I Human 473 Genes GS171893: HP:0011458 Abdominal symptom
Expand Tier I Human GO 2625 Genes GS196343: GO:0036094 small molecule binding
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 739 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Mouse GO 385 Genes GS180235: GO:0007017 microtubule-based process
Expand Tier I Human GO 54 Genes GS209150: GO:0005778 peroxisomal membrane
Expand Tier I Human GO 790 Genes GS210137: GO:0016462 pyrophosphatase activity
Expand Tier I Mouse GO 8406 Genes GS177404: GO:0005737 cytoplasm
Expand Tier I Mouse GO 3493 Genes GS177570: GO:0016043 cellular component organization
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human CTD 2047 Genes GS127205: Tamoxifen interacting genes (MeSH:D013629) in CTD
Expand Tier I Human 283 Genes GS172060: HP:0001508 Failure to thrive
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Mouse GO 3615 Genes GS178359: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human 84 Genes GS174760: HP:0002376 Developmental regression
Expand Tier I Human 303 Genes GS172416: HP:0002242 Abnormality of the intestine
Expand Tier I Human 117 Genes GS172063: HP:0000107 Renal cysts
Expand Tier I Human 48 Genes GS176364: HP:0008034 Abnormal iris pigmentation
Expand Tier I Mouse GO 1380 Genes GS185054: GO:0008104 protein localization
Expand Tier I Mouse GO 209 Genes GS190368: GO:0042623 ATPase activity, coupled
Expand Tier I Human 486 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Mouse GO 4001 Genes GS183543: GO:0051179 localization
Expand Tier I Mouse GO 602 Genes GS178909: GO:0017111 nucleoside-triphosphatase activity
Expand Tier II Mouse 311 Genes GS35867: Striatum Gene expression correlates of Cocaine CPP - difference in percent test time spent relative to preconditioning in Males BXD
Expand Tier I Human GO 423 Genes GS197015: GO:0007017 microtubule-based process
Expand Tier I Human 392 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Mouse GO 12 Genes GS193189: GO:0016558 protein import into peroxisome matrix
Expand Tier I Mouse GO 2762 Genes GS178357: GO:0071842 cellular component organization at cellular level
Expand Tier I Human 184 Genes GS175907: HP:0004349 Reduced bone mineral density
Expand Tier I Mouse 363 Genes GS136259: muscle Gapd decay rate 2 (Mgdr2, Published QTL Chr 5)
Expand Tier I Human 174 Genes GS171806: HP:0005656 Positional foot deformities
Expand Tier I Human 70 Genes GS172568: HP:0000348 High forehead
Expand Tier I Human 18 Genes GS172543: HP:0000835 Adrenal hypoplasia
Expand Tier I Human 104 Genes GS175835: HP:0007759 Opacification of the corneal stroma
Expand Tier I Human CTD 1453 Genes GS121893: Vitamin E interacting genes (MeSH:D014810) in CTD
Expand Tier I Human 344 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human 16 Genes GS175977: HP:0006579 Prolonged neonatal jaundice
Expand Tier I Human GO 2432 Genes GS209108: GO:0000166 nucleotide binding
Expand Tier I Mouse GO 361 Genes GS187220: GO:0033365 protein localization to organelle
Expand Tier I Human 237 Genes GS174292: HP:0011968 Feeding difficulties
Expand Tier I Mouse 357 Genes GS135231: activity-distance traveled 2 (Actd2, Published QTL Chr 5)
Expand Tier I Human 35 Genes GS176655: HP:0000056 Abnormality of the clitoris
Expand Tier I Human GO 2 Genes GS206228: GO:0060152 microtubule-based peroxisome localization
Expand Tier I Human 456 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human 157 Genes GS176612: HP:0000272 Malar flattening
Expand Tier I Human 101 Genes GS171997: HP:0001762 Talipes equinovarus
Expand Tier I Mouse 360 Genes GS136365: obesity QTL 11 (Obq11, Published QTL Chr 5)
Expand Tier I Mouse GO 175 Genes GS183468: GO:0008022 protein C-terminus binding
Expand Tier I Mouse GO 650 Genes GS191728: GO:0008289 lipid binding
Expand Tier I Human 246 Genes GS175909: HP:0004348 Abnormality of bone mineral density
Expand Tier I Human GO 77 Genes GS205614: GO:0044438 microbody part
Expand Tier I Human 210 Genes GS174857: HP:0200006 Slanting of the palpebral fissure
Expand Tier I Mouse GO 1745 Genes GS188652: GO:0001882 nucleoside binding
Expand Tier I Human 12 Genes GS175932: HP:0000244 Brachyturricephaly
Expand Tier I Human 348 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier I Human 177 Genes GS173048: HP:0005557 Abnormality of the zygomatic arch
Expand Tier I Human 397 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier I Mouse GO 1366 Genes GS193632: GO:0051649 establishment of localization in cell
Expand Tier I Human 398 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Human 741 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Mouse GO 78 Genes GS189791: GO:0072594 establishment of protein localization to organelle
Expand Tier I Human 489 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Mouse GO 1209 Genes GS178284: GO:0031090 organelle membrane
Expand Tier I Human GO 1836 Genes GS201799: GO:0032550 purine ribonucleoside binding
Expand Tier I Human GO 1877 Genes GS201800: GO:0032553 ribonucleotide binding
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 117 Genes GS170989: HP:0010766 Ectopic calcification
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human 18 Genes GS174615: HP:0004359 Abnormality of fatty-acid metabolism
Expand Tier II Mouse 105 Genes GS35904: Neocortex Gene expression correlates of Handling induced convulsions 4 hrs after ethanol in Females & Males BXD
Expand Tier I Human 78 Genes GS174649: HP:0000954 Single transverse palmar crease
Expand Tier I Human 11 Genes GS175604: HP:0005989 Redundant neck skin
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 Mouse GO 1736 Genes GS188651: GO:0001883 purine nucleoside binding
Expand Tier I Human 124 Genes GS175492: HP:0000512 Abnormal electroretinogram
Expand Tier I Human 62 Genes GS176804: HP:0001850 Abnormality of the tarsal bones
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 36 Genes GS174701: HP:0000556 Retinal dystrophy
Expand Tier I Human GO 19 Genes GS207128: GO:0072662 protein localization to peroxisome
Expand Tier I Mouse GO 46 Genes GS192217: GO:0005778 peroxisomal membrane
Expand Tier I Human 202 Genes GS175171: HP:0001315 Reduced tendon reflexes
Expand Tier I Human 102 Genes GS177035: HP:0001928 Abnormality of coagulation
Expand Tier I Human GO 2108 Genes GS209928: GO:0006996 organelle organization
Expand Tier I Human 157 Genes GS176639: HP:0011356 Regional abnormality of skin
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human 384 Genes GS171708: HP:0000359 Abnormality of the inner ear
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Human 154 Genes GS175880: HP:0007370 Aplasia/Hypoplasia of the corpus callosum
Expand Tier I Human GO 167 Genes GS210585: GO:0051640 organelle localization
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Mouse GO 17 Genes GS177096: GO:0006625 protein targeting to peroxisome
Expand Tier I Human 170 Genes GS173988: HP:0000501 Glaucoma
Expand Tier I Human 249 Genes GS176844: HP:0000429 Abnormality of the nasal alae
Expand Tier I Human 579 Genes GS171253: HP:0002817 Abnormality of the upper limb
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 281 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human 15 Genes GS175060: HP:0001088 Brushfield spots
Expand Tier I Mouse 357 Genes GS136236: mandible asymmetry 3 (Many3, Published QTL Chr 5)
Expand Tier I Human GO 20 Genes GS200896: GO:0043574 peroxisomal transport
Expand Tier I Human GO 1972 Genes GS210586: GO:0051641 cellular localization
Expand Tier I Human 65 Genes GS174481: HP:0010576 Intracranial cystic lesion
Expand Tier I Human GO 5452 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Mouse GO 5225 Genes GS189860: GO:0043167 ion binding
Expand Tier I Human 266 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
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 Mouse GO 2190 Genes GS191129: GO:0016787 hydrolase activity
Expand Tier I Mouse GO 57 Genes GS188755: GO:0044438 microbody part
Expand Tier I Human 10 Genes GS175077: HP:0001401 Intrahepatic biliary dysgenesis
Expand Tier I Human 56 Genes GS175055: HP:0001080 Biliary tract abnormality
Expand Tier I Human GO 5948 Genes GS195199: GO:0005634 nucleus
Expand Tier I Human GO 4097 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human 169 Genes GS171752: HP:0001713 Abnormality of cardiac ventricle
Expand Tier I Human 282 Genes GS172572: HP:0000347 Micrognathia
Expand Tier I Human GO 4144 Genes GS200341: GO:0051179 localization
Expand Tier I Human GO 5810 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human 123 Genes GS171946: HP:0002269 Abnormality of neuronal migration
Expand Tier I Human 25 Genes GS176654: HP:0000057 Clitoromegaly
Expand Tier I Human 358 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human 472 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human 68 Genes GS176572: HP:0008064 Ichthyosiform abnormality of the skin
Expand Tier I Human GO 798 Genes GS202828: GO:0016817 hydrolase activity, acting on acid anhydrides
Expand Tier I Mouse GO 17 Genes GS190231: GO:0072662 protein localization to peroxisome
Expand Tier I Human 364 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier III Mouse 167 Genes GS35878: Hippocampus Gene expression correlates of Number of entries into closed arms of plus maze [Ethanol] in Females BXD
Expand Tier I Mouse GO 30 Genes GS188256: GO:0007031 peroxisome organization
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
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 54 Genes GS175935: HP:0000248 Brachycephaly
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 Human 512 Genes GS174836: HP:0001098 Abnormality of the fundus
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 15 Genes GS176370: HP:0000262 Turricephaly
Expand Tier I Human 10 Genes GS172004: HP:0003455 Elevated long chain fatty acids
Expand Tier I Mouse GO 1736 Genes GS180644: GO:0032549 ribonucleoside binding
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 435 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
Expand Tier I Mouse 1565 Genes GS128591: Average rotarod training latency Chr# 5
Expand Tier I Human GO 19 Genes GS207127: GO:0072663 establishment of protein localization to peroxisome
Expand Tier I Human 232 Genes GS173288: HP:0000316 Hypertelorism
Expand Tier I Mouse GO 2 Genes GS189364: GO:0060152 microtubule-based peroxisome localization
Expand Tier I Human 56 Genes GS171030: HP:0010946 Dilatation of the renal pelvis
Expand Tier I Human GO 120 Genes GS209169: GO:0005777 peroxisome
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 121 Genes GS172672: HP:0004337 Abnormality of amino acid metabolism
Expand Tier I Human 266 Genes GS172415: HP:0002240 Hepatomegaly
Expand Tier I Human 46 Genes GS174388: HP:0002089 Pulmonary hypoplasia
Expand Tier I Human 302 Genes GS176029: HP:0009116 Aplasia/Hypoplasia involving bones of the skull
Expand Tier I Human 73 Genes GS176571: HP:0008067 Abnormally lax or hyperextensible skin
Expand Tier I Human 8 Genes GS172978: HP:0006894 Hypoplastic olfactory lobes
Expand Tier I Human 121 Genes GS175023: HP:0001629 Ventricular septal defect
Expand Tier I Human 62 Genes GS175742: HP:0011733 Abnormality of adrenal physiology
Expand Tier I Human 311 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier I Human 57 Genes GS171029: HP:0010944 Abnormality of the renal pelvis
Expand Tier I Human 38 Genes GS172268: HP:0001193 Ulnar deviation of the hand or of fingers of the hand
Expand Tier I Human 55 Genes GS172097: HP:0000580 Pigmentary retinopathy
Expand Tier I Human 123 Genes GS176695: HP:0009811 Abnormality of the elbow
Expand Tier I Human 79 Genes GS173516: HP:0000301 Abnormality of facial musculature
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 Human 346 Genes GS171309: HP:0000252 Microcephaly
Expand Tier I Human 188 Genes GS171512: HP:0007703 Abnormal retinal pigmentation
Expand Tier I Human 48 Genes GS173434: HP:0100625 Enlarged thorax
Expand Tier I Human 92 Genes GS172356: HP:0003119 Abnormality of lipid metabolism
Expand Tier I Human GO 499 Genes GS204077: GO:0033365 protein localization to organelle
Expand Tier I Human 56 Genes GS171290: HP:0000126 Hydronephrosis
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human 183 Genes GS176955: HP:0000431 Wide nasal bridge
Expand Tier I Mouse GO 1449 Genes GS186798: GO:0030554 adenyl nucleotide binding
Expand Tier I Human 368 Genes GS170971: HP:0000407 Sensorineural hearing impairment
Expand Tier I Human 445 Genes GS175423: HP:0010461 Abnormality of the male genitalia
Expand Tier I Human GO 2353 Genes GS208037: GO:0016787 hydrolase activity
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 82 Genes GS171786: HP:0001396 Cholestasis
Expand Tier I Human 268 Genes GS172365: HP:0003110 Abnormality of urine homeostasis
Expand Tier I Human 253 Genes GS171634: HP:0008050 Abnormality of the palpebral fissures
Expand Tier I Mouse GO 939 Genes GS190471: GO:0005829 cytosol
Expand Tier I Human 98 Genes GS176867: HP:0003577 Congenital onset
Expand Tier I Human 33 Genes GS174910: HP:0000543 Optic disc pallor
Expand Tier I Human 224 Genes GS175459: HP:0009484 Deviation of the hand or of fingers of the hand
Expand Tier I Human 11 Genes GS174568: HP:0011040 Abnormality of the intrahepatic bile duct
Expand Tier I Human 188 Genes GS171167: HP:0000235 Abnormality of the fontanelles and cranial sutures
Expand Tier I Human 16 Genes GS171264: HP:0002630 Fat malabsorption
Expand Tier I Mouse GO 134 Genes GS192236: GO:0005777 peroxisome
Expand Tier I Human 358 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Human GO 688 Genes GS203895: GO:0006886 intracellular protein transport
Expand Tier I Human GO 2392 Genes GS206737: GO:0043168 anion binding
Expand Tier I Human 308 Genes GS172100: HP:0000587 Abnormality of the optic nerve
Expand Tier I Human 397 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human 394 Genes GS172362: HP:0004325 Decreased body weight
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 30 Genes GS176293: HP:0002126 Polymicrogyria
Expand Tier I Human 199 Genes GS171637: HP:0008872 Feeding difficulties in infancy
Expand Tier I Human CTD 1522 Genes GS124579: Selenium interacting genes (MeSH:D012643) in CTD
Expand Tier I Human 271 Genes GS172637: HP:0010460 Abnormality of the female genitalia
Expand Tier I Human 61 Genes GS175162: HP:0002536 Abnormal cortical gyration
Expand Tier I Mouse GO 2872 Genes GS178360: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Human 70 Genes GS173601: HP:0010827 Abnormality of the seventh cranial nerve
Expand Tier I Human 196 Genes GS173872: HP:0011368 Epidermal thickening
Expand Tier I Human GO 928 Genes GS208787: GO:0034613 cellular protein localization
Expand Tier II Mouse 36 Genes GS34915: Whole Brain Gene expression correlates of Open Field - Total distance traveled 0-5 minutes in Males BXD
Expand Tier I Human 51 Genes GS172610: HP:0010864 Intellectual disability, severe
Expand Tier I Human 102 Genes GS173545: HP:0010647 Abnormal elasticity of skin
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Human 236 Genes GS174257: HP:0000309 Abnormality of the midface
Expand Tier I Human 384 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human 200 Genes GS174812: HP:0001637 Abnormality of the myocardium
Expand Tier I Human 20 Genes GS173959: HP:0001582 Redundant skin
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 137 Genes GS171202: HP:0100627 Displacement of the external urethral meatus
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human GO 77 Genes GS205613: GO:0044439 peroxisomal part
Expand Tier I Human GO 2373 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human 221 Genes GS172288: HP:0000358 Posteriorly rotated ears
Expand Tier I Human GO 1480 Genes GS205179: GO:0005524 ATP binding
Expand Tier I Mouse GO 1598 Genes GS188957: GO:0033036 macromolecule localization
Expand Tier I Human 990 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human 63 Genes GS174527: HP:0000952 Jaundice
Expand Tier I Human 162 Genes GS175556: HP:0011675 Arrhythmia
Expand Tier I Human 315 Genes GS176568: HP:0000486 Strabismus
Expand Tier I Human 474 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Mouse GO 1034 Genes GS182314: GO:0015031 protein transport
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human 17 Genes GS172788: HP:0000803 Renal cortical cysts
Expand Tier I Human 433 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Human 39 Genes GS173314: HP:0010656 Abnormal epiphyseal ossification
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 518 Genes GS174081: HP:0004322 Short stature
Expand Tier I Mouse GO 3268 Genes GS177721: GO:0051234 establishment of localization
Expand Tier I Mouse 361 Genes GS136628: small effect CIA locus 1 (Secia1, Published QTL Chr 5)
Expand Tier I Human GO 54 Genes GS208357: GO:0031903 microbody membrane
Expand Tier I Human 220 Genes GS175994: HP:0000464 Abnormality of the neck
Expand Tier I Mouse GO 134 Genes GS181579: GO:0042579 microbody
Expand Tier I Human 388 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Human 22 Genes GS172329: HP:0005469 Flat occiput
Expand Tier I Human 514 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human GO 5321 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human GO 280 Genes GS202739: GO:0017038 protein import
Expand Tier I Mouse GO 57 Genes GS188754: GO:0044439 peroxisomal part
Expand Tier I Human 11 Genes GS176861: HP:0010964 Abnormality of long-chain fatty-acid metabolism
Expand Tier I Human 229 Genes GS175577: HP:0003202 Amyotrophy
Expand Tier I Human 76 Genes GS171176: HP:0001547 Abnormality of the morphology of the rib cage
Expand Tier I Human GO 793 Genes GS202822: GO:0016818 hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides
Expand Tier I Human 95 Genes GS170930: HP:0001284 Areflexia
Expand Tier I Human 123 Genes GS175583: HP:0010438 Abnormality of the ventricular septum
Expand Tier I Human GO 3409 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Mouse GO 133 Genes GS193638: GO:0051640 organelle localization
Expand Tier I Mouse GO 2439 Genes GS179580: GO:0036094 small molecule binding
Expand Tier I Human 34 Genes GS171863: HP:0008365 Abnormality of the talus
Expand Tier I Human GO 1510 Genes GS201792: GO:0032559 adenyl ribonucleotide binding
Expand Tier I Mouse GO 827 Genes GS180025: GO:0046907 intracellular transport
Expand Tier I Human 53 Genes GS170905: HP:0004400 Abnormality of the pylorus
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Mouse GO 1686 Genes GS184220: GO:0071702 organic substance transport
Expand Tier I Human 262 Genes GS172033: HP:0000369 Low-set ears
Expand Tier I Human CTD 4423 Genes GS123718: Ethinyl Estradiol interacting genes (MeSH:D004997) in CTD
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
Expand Tier I Human 81 Genes GS171773: HP:0000532 Chorioretinal abnormality
Expand Tier I Human 414 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human 83 Genes GS172098: HP:0000582 Upslanted palpebral fissure
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 Human 32 Genes GS173968: HP:0008207 Primary adrenal insufficiency
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human GO 354 Genes GS208384: GO:0016887 ATPase activity
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Mouse GO 263 Genes GS191457: GO:0016887 ATPase activity
Expand Tier I Human 70 Genes GS177025: HP:0010628 Facial palsy
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Human 132 Genes GS171835: HP:0011329 Abnormality of cranial sutures
Expand Tier I Human 553 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human 411 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human 16 Genes GS175019: HP:0001623 Breech presentation
Expand Tier I Human GO 1850 Genes GS205511: GO:0001882 nucleoside binding
Expand Tier I Human GO 158 Genes GS200264: GO:0008022 protein C-terminus binding
Expand Tier I Mouse GO 5247 Genes GS178448: GO:0005634 nucleus
Expand Tier I Human 291 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier I Human 11 Genes GS171425: HP:0002416 Subependymal cysts
Expand Tier I Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human 28 Genes GS176794: HP:0002967 Cubitus valgus
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 489 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human 56 Genes GS175070: HP:0000973 Cutis laxa
Expand Tier I Human GO 2368 Genes GS207365: GO:0005829 cytosol
Expand Tier I Human 285 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier I Human 160 Genes GS174814: HP:0001639 Hypertrophic cardiomyopathy
Expand Tier I Human 378 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier I Human 105 Genes GS175571: HP:0011492 Abnormality of corneal stroma
Expand Tier III Mouse 8107 Genes GS213076: Genes with suggestive difference in (B6) vs (B6PF1 + PB6F1 + PWD) comparison
Expand Tier I Human GO 1127 Genes GS196794: GO:0046907 intracellular transport
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 Human 101 Genes GS171649: HP:0011849 Abnormal bone ossification
Expand Tier I Mouse GO 17 Genes GS184095: GO:0043574 peroxisomal transport
Expand Tier I Mouse 361 Genes GS136070: immune response to Factor IX QTL 1 (Imrfq1, Published QTL Chr 5)
Expand Tier I Mouse 253 Genes GS136042: insulin dependent diabetes susceptibility 15 (Idd15, Published QTL Chr 5)
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human 10 Genes GS171161: HP:0004734 Renal cortical microcysts
Expand Tier I Human 189 Genes GS176449: HP:0001671 Abnormality of the cardiac septa
Expand Tier I Human 245 Genes GS176694: HP:0009810 Abnormality of the joints of the upper limbs
Expand Tier I Human 21 Genes GS175210: HP:0010537 Wide cranial sutures
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 Human 525 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 113 Genes GS173647: HP:0012072 Aciduria
Expand Tier I Human 405 Genes GS173743: HP:0001999 Abnormal facial shape
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 66 Genes GS173753: HP:0000510 Retinitis pigmentosa
Expand Tier I Human 11 Genes GS174890: HP:0001341 Olfactory lobe agenesis
Expand Tier I Human 470 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Human 215 Genes GS176973: HP:0001072 Thickened skin
Expand Tier I Human GO 1514 Genes GS203649: GO:0030554 adenyl nucleotide binding
Expand Tier I Human CTD 5075 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Human 27 Genes GS171913: HP:0010458 Female pseudohermaphroditism
Expand Tier I Human 26 Genes GS174249: HP:0001840 Metatarsus adductus
Expand Tier I Human GO 19 Genes GS193813: GO:0006625 protein targeting to peroxisome
Expand Tier I Human 90 Genes GS174101: HP:0001018 Abnormal palmar dermatoglyphics
Expand Tier I Human GO 1269 Genes GS197769: GO:0045184 establishment of protein localization
Expand Tier I Human GO 932 Genes GS195273: GO:0070727 cellular macromolecule localization
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 409 Genes GS175670: HP:0007364 Aplasia/Hypoplasia of the cerebrum
Expand Tier I Human 210 Genes GS175990: HP:0000463 Anteverted nares
Expand Tier I Human 18 Genes GS171886: HP:0000627 Posterior embryotoxon
Expand Tier I Human 173 Genes GS175117: HP:0001883 Talipes
Expand Tier I Human GO 3307 Genes GS195110: GO:0071842 cellular component organization at cellular level
Expand Tier I Mouse GO 4224 Genes GS193059: GO:0044446 intracellular organelle part
Expand Tier I Human 96 Genes GS176616: HP:0000662 Night blindness
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 46 Genes GS170961: HP:0000158 Macroglossia
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 123 Genes GS176799: HP:0001265 Hyporeflexia
Expand Tier I Human 310 Genes GS175805: HP:0003271 Visceromegaly
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Mouse GO 1444 Genes GS184976: GO:0032559 adenyl ribonucleotide binding
Expand Tier I Human 100 Genes GS176774: HP:0001005 Dermatological manifestations of systemic disorders
Expand Tier I Mouse GO 1081 Genes GS180977: GO:0045184 establishment of protein localization
Expand Tier I Mouse GO 521 Genes GS187032: GO:0006886 intracellular protein transport
Expand Tier I Human GO 278 Genes GS207263: GO:0042623 ATPase activity, coupled
Expand Tier I Human GO 3318 Genes GS209452: GO:0006810 transport
Expand Tier I Human 59 Genes GS172412: HP:0002244 Abnormality of the small intestine
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 35 Genes GS176212: HP:0000474 Thickened nuchal skin fold
Expand Tier I Human 273 Genes GS172516: HP:0001347 Hyperreflexia
Expand Tier I Human 545 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human 160 Genes GS175096: HP:0000286 Epicanthus
Expand Tier I Human 215 Genes GS172139: HP:0010993 Abnormality of the cerebral subcortex
Expand Tier I Mouse GO 6204 Genes GS184629: GO:0005515 protein binding
Expand Tier I Human 88 Genes GS172871: HP:0010490 Abnormality of the palmar creases
Expand Tier I Human 737 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human 87 Genes GS172544: HP:0000834 Abnormality of the adrenal glands
Expand Tier I Human 8 Genes GS171244: HP:0003146 Hypocholesterolemia
Expand Tier I Human 3 Genes GS172270: HP:0008167 Very long chain fatty acid accumulation
Expand Tier I Human 134 Genes GS175172: HP:0004354 Abnormality of carboxylic acid metabolism
Expand Tier I Human 159 Genes GS176900: HP:0000218 High palate
Expand Tier I Human CTD 5725 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Human 40 Genes GS172125: HP:0003107 Abnormality of cholesterol metabolism
Expand Tier I Human GO 3372 Genes GS194459: GO:0051234 establishment of localization
Expand Tier I Mouse GO 1724 Genes GS185881: GO:0035639 purine ribonucleoside triphosphate binding
Expand Tier I Human 72 Genes GS176656: HP:0000055 Abnormality of female external genitalia
Expand Tier I Human GO 208 Genes GS206667: GO:0072594 establishment of protein localization to organelle
Expand Tier I Human 117 Genes GS174102: HP:0011799 Abnormality of facial soft tissue
Expand Tier I Human 319 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Mouse GO 643 Genes GS185991: GO:0016817 hydrolase activity, acting on acid anhydrides
Expand Tier I Human 68 Genes GS174450: HP:0006703 Aplasia/Hypoplasia of the lungs
Expand Tier I Human 487 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Human 53 Genes GS172660: HP:0002021 Pyloric stenosis
Expand Tier I Mouse GO 777 Genes GS178522: GO:0070727 cellular macromolecule localization
Expand Tier I Human 578 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human GO 1825 Genes GS205820: GO:0033036 macromolecule localization
Expand Tier I Human GO 1827 Genes GS202716: GO:0035639 purine ribonucleoside triphosphate binding
Expand Tier I Human 19 Genes GS176673: HP:0008048 Abnormality of the line of Schwalbe
Expand Tier I Human 601 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 438 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier I Human 174 Genes GS173901: HP:0002007 Frontal bossing
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human 281 Genes GS171204: HP:0011314 Abnormality of long bone morphology
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 758 Genes GS195665: GO:0017111 nucleoside-triphosphatase activity
Expand Tier I Human GO 120 Genes GS198371: GO:0042579 microbody
Expand Tier I Human 530 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human GO 1869 Genes GS200446: GO:0017076 purine nucleotide binding
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 558 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Mouse GO 1733 Genes GS184983: GO:0032550 purine ribonucleoside binding
Expand Tier I Human 20 Genes GS173102: HP:0010808 Protruding tongue
Expand Tier I Human GO 1751 Genes GS210579: GO:0051649 establishment of localization in cell
Expand Tier I Human 33 Genes GS172582: HP:0001838 Vertical talus
Expand Tier I Human 274 Genes GS172372: HP:0000648 Optic atrophy
Expand Tier I Mouse GO 2263 Genes GS192174: GO:0000166 nucleotide binding
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human 13 Genes GS174191: HP:0001591 Bell-shaped chest
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 27 Genes GS176587: HP:0001271 Polyneuropathy
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human 599 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Mouse GO 241 Genes GS185901: GO:0017038 protein import
Expand Tier I Human 251 Genes GS171793: HP:0000377 Abnormality of the pinna
Expand Tier I Human 324 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function