Gene Details



PEX1 and homologs in 1 species are found in 458 GeneSets:


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

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Human 385 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 34 Genes GS171863: HP:0008365 Abnormality of the talus
Expand Tier I Human 877 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human GO 1496 Genes GS201792: GO:0032559 adenyl ribonucleotide binding
Expand Tier I Human 53 Genes GS170905: HP:0004400 Abnormality of the pylorus
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 42 Genes GS176725: HP:0011425 Fetal ultrasound soft marker
Expand Tier I Human 260 Genes GS172033: HP:0000369 Low-set ears
Expand Tier I Human GO 1821 Genes GS205510: GO:0001883 purine nucleoside binding
Expand Tier I Human 829 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human CTD 4424 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 411 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human 82 Genes GS172098: HP:0000582 Upslanted palpebral fissure
Expand Tier I Human 92 Genes GS171656: HP:0000610 Abnormality of the choroid
Expand Tier I Human 541 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 31 Genes GS173968: HP:0008207 Primary adrenal insufficiency
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 535 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Human GO 354 Genes GS208384: GO:0016887 ATPase activity
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human 280 Genes GS175900: HP:0009118 Aplasia/Hypoplasia of the mandible
Expand Tier I Human 99 Genes GS173687: HP:0001643 Patent ductus arteriosus
Expand Tier I Human 20 Genes GS175316: HP:0000565 Esotropia
Expand Tier I Human 107 Genes GS176899: HP:0002353 EEG abnormality
Expand Tier I Human 70 Genes GS177025: HP:0010628 Facial palsy
Expand Tier I Human 132 Genes GS171835: HP:0011329 Abnormality of cranial sutures
Expand Tier I Human 94 Genes GS173846: HP:0003355 Aminoaciduria
Expand Tier I Human 60 Genes GS175897: HP:0000939 Osteoporosis
Expand Tier I Human 550 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human 407 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human 122 Genes GS173384: HP:0002750 Delayed skeletal maturation
Expand Tier I Human 16 Genes GS175019: HP:0001623 Breech presentation
Expand Tier I Human GO 1832 Genes GS205511: GO:0001882 nucleoside binding
Expand Tier I Human 267 Genes GS172261: HP:0000357 Abnormal location of ears
Expand Tier I Human 156 Genes GS174002: HP:0000189 Narrow palate
Expand Tier I Human GO 158 Genes GS200264: GO:0008022 protein C-terminus binding
Expand Tier I Human GO 2 Genes GS206231: GO:0060151 peroxisome localization
Expand Tier I Human 641 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 100 Genes GS174372: HP:0002024 Malabsorption
Expand Tier I Human 318 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier I Human 170 Genes GS174488: HP:0000525 Abnormality of the iris
Expand Tier I Human 840 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 110 Genes GS171784: HP:0001399 Hepatic failure
Expand Tier I Human 288 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier I Human 84 Genes GS175531: HP:0000003 Multicystic kidney dysplasia
Expand Tier I Human 11 Genes GS171425: HP:0002416 Subependymal cysts
Expand Tier I Human 129 Genes GS173247: HP:0007957 Reduction of corneal clarity
Expand Tier I Human 1002 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human 28 Genes GS176794: HP:0002967 Cubitus valgus
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 148 Genes GS174586: HP:0005930 Abnormality of the epiphyses
Expand Tier I Human 486 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human 68 Genes GS173148: HP:0003712 Muscle hypertrophy
Expand Tier I Human 56 Genes GS175070: HP:0000973 Cutis laxa
Expand Tier I Human GO 33 Genes GS205111: GO:0007031 peroxisome organization
Expand Tier I Human GO 2364 Genes GS207365: GO:0005829 cytosol
Expand Tier I Human GO 5348 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Human 283 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier I Human 158 Genes GS174814: HP:0001639 Hypertrophic cardiomyopathy
Expand Tier I Human 375 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier I Human 105 Genes GS175571: HP:0011492 Abnormality of corneal stroma
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 GO 1123 Genes GS196794: GO:0046907 intracellular transport
Expand Tier I Human 372 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 489 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 936 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human 598 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 99 Genes GS171649: HP:0011849 Abnormal bone ossification
Expand Tier I Human 147 Genes GS175411: HP:0100871 Abnormality of the palm
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human 51 Genes GS172891: HP:0100538 Abnormality of the supraorbital ridges
Expand Tier I Human GO 1822 Genes GS197443: GO:0032549 ribonucleoside binding
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
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 10 Genes GS171161: HP:0004734 Renal cortical microcysts
Expand Tier I Human 530 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 263 Genes GS173014: HP:0010936 Abnormality of the lower urinary tract
Expand Tier I Human GO 1555 Genes GS201869: GO:0008104 protein localization
Expand Tier I Human 636 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human 187 Genes GS176449: HP:0001671 Abnormality of the cardiac septa
Expand Tier I Human 222 Genes GS173995: HP:0000508 Ptosis
Expand Tier I Human 243 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 496 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Human 80 Genes GS172726: HP:0000268 Dolichocephaly
Expand Tier I Human GO 6347 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human 19 Genes GS171497: HP:0002282 Heterotopia
Expand Tier I Human 521 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Human 423 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Human 36 Genes GS173707: HP:0000846 Adrenal insufficiency
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 323 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Human 113 Genes GS173647: HP:0012072 Aciduria
Expand Tier I Human 404 Genes GS173743: HP:0001999 Abnormal facial shape
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 66 Genes GS173753: HP:0000510 Retinitis pigmentosa
Expand Tier I Human 124 Genes GS174854: HP:0001410 Decreased liver function
Expand Tier I Human 11 Genes GS174890: HP:0001341 Olfactory lobe agenesis
Expand Tier I Human 468 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Human 213 Genes GS176973: HP:0001072 Thickened skin
Expand Tier I Human 146 Genes GS176098: HP:0000927 Abnormality of skeletal maturation
Expand Tier I Human GO 1500 Genes GS203649: GO:0030554 adenyl nucleotide binding
Expand Tier I Human 112 Genes GS174412: HP:0007477 Abnormal dermatoglyphics
Expand Tier I Human 66 Genes GS176033: HP:0011039 Abnormality of the helix
Expand Tier I Human CTD 5081 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Human 472 Genes GS171893: HP:0011458 Abdominal symptom
Expand Tier I Human 27 Genes GS171913: HP:0010458 Female pseudohermaphroditism
Expand Tier I Human GO 2603 Genes GS196343: GO:0036094 small molecule binding
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
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 88 Genes GS174101: HP:0001018 Abnormal palmar dermatoglyphics
Expand Tier I Human GO 1266 Genes GS197769: GO:0045184 establishment of protein localization
Expand Tier I Human GO 931 Genes GS195273: GO:0070727 cellular macromolecule localization
Expand Tier I Human 886 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 407 Genes GS175670: HP:0007364 Aplasia/Hypoplasia of the cerebrum
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 736 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human 209 Genes GS175990: HP:0000463 Anteverted nares
Expand Tier I Human GO 54 Genes GS209150: GO:0005778 peroxisomal membrane
Expand Tier I Human GO 786 Genes GS210137: GO:0016462 pyrophosphatase activity
Expand Tier I Human 18 Genes GS171886: HP:0000627 Posterior embryotoxon
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human CTD 2048 Genes GS127205: Tamoxifen interacting genes (MeSH:D013629) in CTD
Expand Tier I Human 282 Genes GS172060: HP:0001508 Failure to thrive
Expand Tier I Human 173 Genes GS175117: HP:0001883 Talipes
Expand Tier I Human GO 3300 Genes GS195110: GO:0071842 cellular component organization at cellular level
Expand Tier I Human 590 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human 84 Genes GS174760: HP:0002376 Developmental regression
Expand Tier I Human 95 Genes GS176616: HP:0000662 Night blindness
Expand Tier I Human 300 Genes GS172416: HP:0002242 Abnormality of the intestine
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 128 Genes GS174657: HP:0001425 Heterogeneous
Expand Tier I Human 46 Genes GS170961: HP:0000158 Macroglossia
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 116 Genes GS172063: HP:0000107 Renal cysts
Expand Tier I Human 48 Genes GS176364: HP:0008034 Abnormal iris pigmentation
Expand Tier I Human 123 Genes GS176799: HP:0001265 Hyporeflexia
Expand Tier I Human 484 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human 307 Genes GS175805: HP:0003271 Visceromegaly
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human GO 421 Genes GS197015: GO:0007017 microtubule-based process
Expand Tier I Human 389 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human 181 Genes GS175907: HP:0004349 Reduced bone mineral density
Expand Tier I Human 99 Genes GS176774: HP:0001005 Dermatological manifestations of systemic disorders
Expand Tier I Human GO 278 Genes GS207263: GO:0042623 ATPase activity, coupled
Expand Tier I Human GO 3310 Genes GS209452: GO:0006810 transport
Expand Tier I Human 174 Genes GS171806: HP:0005656 Positional foot deformities
Expand Tier I Human 59 Genes GS172412: HP:0002244 Abnormality of the small intestine
Expand Tier I Human 70 Genes GS172568: HP:0000348 High forehead
Expand Tier I Human 837 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 34 Genes GS176212: HP:0000474 Thickened nuchal skin fold
Expand Tier I Human 273 Genes GS172516: HP:0001347 Hyperreflexia
Expand Tier I Human 18 Genes GS172543: HP:0000835 Adrenal hypoplasia
Expand Tier I Human 542 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human 104 Genes GS175835: HP:0007759 Opacification of the corneal stroma
Expand Tier I Human CTD 1454 Genes GS121893: Vitamin E interacting genes (MeSH:D014810) in CTD
Expand Tier I Human 342 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human 15 Genes GS175977: HP:0006579 Prolonged neonatal jaundice
Expand Tier I Human 159 Genes GS175096: HP:0000286 Epicanthus
Expand Tier I Human GO 2410 Genes GS209108: GO:0000166 nucleotide binding
Expand Tier I Human 214 Genes GS172139: HP:0010993 Abnormality of the cerebral subcortex
Expand Tier I Human 236 Genes GS174292: HP:0011968 Feeding difficulties
Expand Tier I Human 86 Genes GS172871: HP:0010490 Abnormality of the palmar creases
Expand Tier I Human 733 Genes GS176186: HP:0000079 Abnormality of the urinary system
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 454 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Human 607 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human 86 Genes GS172544: HP:0000834 Abnormality of the adrenal glands
Expand Tier I Human 156 Genes GS176612: HP:0000272 Malar flattening
Expand Tier I Human 101 Genes GS171997: HP:0001762 Talipes equinovarus
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 5732 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 242 Genes GS175909: HP:0004348 Abnormality of bone mineral density
Expand Tier I Human GO 3364 Genes GS194459: GO:0051234 establishment of localization
Expand Tier I Human GO 77 Genes GS205614: GO:0044438 microbody part
Expand Tier I Human 207 Genes GS174857: HP:0200006 Slanting of the palpebral fissure
Expand Tier I Human 12 Genes GS175932: HP:0000244 Brachyturricephaly
Expand Tier I Human 346 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier I Human 72 Genes GS176656: HP:0000055 Abnormality of female external genitalia
Expand Tier I Human 175 Genes GS173048: HP:0005557 Abnormality of the zygomatic arch
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 317 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Human 395 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier I Human 397 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Human 68 Genes GS174450: HP:0006703 Aplasia/Hypoplasia of the lungs
Expand Tier I Human 483 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Human 737 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 487 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human GO 1818 Genes GS201799: GO:0032550 purine ribonucleoside binding
Expand Tier I Human GO 1859 Genes GS201800: GO:0032553 ribonucleotide binding
Expand Tier I Human 53 Genes GS172660: HP:0002021 Pyloric stenosis
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 116 Genes GS170989: HP:0010766 Ectopic calcification
Expand Tier I Human 576 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 532 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human GO 1820 Genes GS205820: GO:0033036 macromolecule localization
Expand Tier I Human GO 1809 Genes GS202716: GO:0035639 purine ribonucleoside triphosphate binding
Expand Tier I Human 18 Genes GS174615: HP:0004359 Abnormality of fatty-acid metabolism
Expand Tier I Human 19 Genes GS176673: HP:0008048 Abnormality of the line of Schwalbe
Expand Tier I Human 76 Genes GS174649: HP:0000954 Single transverse palmar crease
Expand Tier I Human 11 Genes GS175604: HP:0005989 Redundant neck skin
Expand Tier I Human 489 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human 598 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 435 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier I Human 173 Genes GS173901: HP:0002007 Frontal bossing
Expand Tier I Human 178 Genes GS176589: HP:0001273 Abnormality of the corpus callosum
Expand Tier I Human 317 Genes GS176591: HP:0001276 Hypertonia
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
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 278 Genes GS171204: HP:0011314 Abnormality of long bone morphology
Expand Tier I Human GO 10576 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 754 Genes GS195665: GO:0017111 nucleoside-triphosphatase activity
Expand Tier I Human GO 120 Genes GS198371: GO:0042579 microbody
Expand Tier I Human 529 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human 532 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human 401 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 36 Genes GS174701: HP:0000556 Retinal dystrophy
Expand Tier I Human GO 1851 Genes GS200446: GO:0017076 purine nucleotide binding
Expand Tier I Human GO 19 Genes GS207128: GO:0072662 protein localization to peroxisome
Expand Tier I Human GO 6743 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 554 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Human 201 Genes GS175171: HP:0001315 Reduced tendon reflexes
Expand Tier I Human 101 Genes GS177035: HP:0001928 Abnormality of coagulation
Expand Tier I Human GO 2104 Genes GS209928: GO:0006996 organelle organization
Expand Tier I Human 155 Genes GS176639: HP:0011356 Regional abnormality of skin
Expand Tier I Human 20 Genes GS173102: HP:0010808 Protruding tongue
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human GO 1745 Genes GS210579: GO:0051649 establishment of localization in cell
Expand Tier I Human 384 Genes GS171708: HP:0000359 Abnormality of the inner ear
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 Human 153 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 Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human 169 Genes GS173988: HP:0000501 Glaucoma
Expand Tier I Human 248 Genes GS176844: HP:0000429 Abnormality of the nasal alae
Expand Tier I Human GO 6256 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human 576 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human 13 Genes GS174191: HP:0001591 Bell-shaped chest
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 121 Genes GS175588: HP:0001311 Neurophysiological abnormality
Expand Tier I Human 27 Genes GS176587: HP:0001271 Polyneuropathy
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 9088 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 596 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human 280 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human 15 Genes GS175060: HP:0001088 Brushfield spots
Expand Tier I Human 248 Genes GS171793: HP:0000377 Abnormality of the pinna
Expand Tier I Human 322 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Human GO 20 Genes GS200896: GO:0043574 peroxisomal transport
Expand Tier I Human GO 1965 Genes GS210586: GO:0051641 cellular localization
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 65 Genes GS174481: HP:0010576 Intracranial cystic lesion
Expand Tier I Human GO 5400 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human GO 295 Genes GS207143: GO:0032403 protein complex binding
Expand Tier I Human 262 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier I Human 401 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Human 825 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 201 Genes GS171631: HP:0008051 Abnormality of the retinal pigment epithelium
Expand Tier I Human 341 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Human 79 Genes GS171836: HP:0011328 Abnormality of fontanelles
Expand Tier I Human 194 Genes GS172034: HP:0000368 Low-set, posteriorly rotated ears
Expand Tier I Human 10 Genes GS175077: HP:0001401 Intrahepatic biliary dysgenesis
Expand Tier I Human 196 Genes GS175785: HP:0002500 Abnormality of the cerebral white matter
Expand Tier I Human 257 Genes GS172272: HP:0001197 Abnormality of prenatal development or birth
Expand Tier I Human 193 Genes GS174813: HP:0001638 Cardiomyopathy
Expand Tier I Human 64 Genes GS175020: HP:0001622 Premature birth
Expand Tier I Human 55 Genes GS175055: HP:0001080 Biliary tract abnormality
Expand Tier I Human GO 13 Genes GS210133: GO:0016558 protein import into peroxisome matrix
Expand Tier I Human GO 5908 Genes GS195199: GO:0005634 nucleus
Expand Tier I Human GO 4085 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human CTD 86 Genes GS125740: Lithium interacting genes (MeSH:D008094) in CTD
Expand Tier I Human GO 498 Genes GS202005: GO:0006605 protein targeting
Expand Tier I Human 169 Genes GS171752: HP:0001713 Abnormality of cardiac ventricle
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 280 Genes GS172572: HP:0000347 Micrognathia
Expand Tier I Human GO 4134 Genes GS200341: GO:0051179 localization
Expand Tier I Human GO 2411 Genes GS203886: GO:1901265 nucleoside phosphate binding
Expand Tier I Human GO 5764 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human 122 Genes GS171946: HP:0002269 Abnormality of neuronal migration
Expand Tier I Human 25 Genes GS176654: HP:0000057 Clitoromegaly
Expand Tier I Human 356 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human 471 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 58 Genes GS174923: HP:0008572 External ear malformation
Expand Tier I Human GO 794 Genes GS202828: GO:0016817 hydrolase activity, acting on acid anhydrides
Expand Tier I Human 66 Genes GS174788: HP:0000239 Large fontanelles
Expand Tier I Human 53 Genes GS176964: HP:0011217 Abnormal shape of the occiput
Expand Tier I Human 396 Genes GS171100: HP:0000759 Abnormality of the peripheral nervous system
Expand Tier I Human 335 Genes GS174076: HP:0009122 Aplasia/Hypoplasia affecting bones of the axial skeleton
Expand Tier I Human 361 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human CTD 6287 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human 390 Genes GS175537: HP:0011277 Abnormality of the urinary system physiology
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 1068 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 69 Genes GS172585: HP:0001832 Abnormality of the metatarsal bones
Expand Tier I Human 157 Genes GS174877: HP:0001892 Abnormal bleeding
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human 541 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 344 Genes GS172989: HP:0001324 Muscle weakness
Expand Tier I Human 469 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human 53 Genes GS175935: HP:0000248 Brachycephaly
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 510 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Human 35 Genes GS175029: HP:0009891 Hypoplasia of the supraorbital ridges
Expand Tier I Human 263 Genes GS175823: HP:0002093 Respiratory insufficiency
Expand Tier I Human 184 Genes GS171144: HP:0005280 Depressed nasal bridge
Expand Tier I Human 128 Genes GS171905: HP:0004297 Abnormality of the biliary system
Expand Tier I Human 15 Genes GS176370: HP:0000262 Turricephaly
Expand Tier I Human 263 Genes GS176477: HP:0002118 Abnormality of the cerebral ventricles
Expand Tier I Human 10 Genes GS172004: HP:0003455 Elevated long chain fatty acids
Expand Tier I Human 138 Genes GS174289: HP:0002577 Abnormality of the stomach
Expand Tier I Human 161 Genes GS175958: HP:0000795 Abnormality of the urethra
Expand Tier I Human 220 Genes GS171139: HP:0005288 Abnormality of the nares
Expand Tier I Human 583 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 776 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human GO 1228 Genes GS199113: GO:0015031 protein transport
Expand Tier I Human 780 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 433 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
Expand Tier I Human 614 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human GO 19 Genes GS207127: GO:0072663 establishment of protein localization to peroxisome
Expand Tier I Human 231 Genes GS173288: HP:0000316 Hypertelorism
Expand Tier I Human GO 4201 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human 56 Genes GS171030: HP:0010946 Dilatation of the renal pelvis
Expand Tier I Human 39 Genes GS175738: HP:0011732 Abnormality of adrenal morphology
Expand Tier I Human 542 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human 64 Genes GS176627: HP:0000457 Flat nose
Expand Tier I Human GO 120 Genes GS209169: GO:0005777 peroxisome
Expand Tier I Human 66 Genes GS175160: HP:0002538 Abnormality of the cerebral cortex
Expand Tier I Human 532 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Human GO 1844 Genes GS201794: GO:0032555 purine ribonucleotide binding
Expand Tier I Human 121 Genes GS172672: HP:0004337 Abnormality of amino acid metabolism
Expand Tier I Human 263 Genes GS172415: HP:0002240 Hepatomegaly
Expand Tier I Human 173 Genes GS171148: HP:0011218 Abnormal shape of the frontal region
Expand Tier I Human 77 Genes GS172699: HP:0002652 Skeletal dysplasia
Expand Tier I Human GO 1925 Genes GS201025: GO:0071702 organic substance transport
Expand Tier I Human 418 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human 621 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human 46 Genes GS174388: HP:0002089 Pulmonary hypoplasia
Expand Tier I Human 381 Genes GS175714: HP:0011389 Functional abnormality of the inner ear
Expand Tier I Human 300 Genes GS176029: HP:0009116 Aplasia/Hypoplasia involving bones of the skull
Expand Tier I Human 48 Genes GS172742: HP:0006887 Intellectual disability, progressive
Expand Tier I Human 73 Genes GS176571: HP:0008067 Abnormally lax or hyperextensible skin
Expand Tier I Human 120 Genes GS177000: HP:0001291 Abnormality of the cranial nerves
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 61 Genes GS175742: HP:0011733 Abnormality of adrenal physiology
Expand Tier I Human 309 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 121 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 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human 344 Genes GS171309: HP:0000252 Microcephaly
Expand Tier I Human 187 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 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 182 Genes GS176955: HP:0000431 Wide nasal bridge
Expand Tier I Human 368 Genes GS170971: HP:0000407 Sensorineural hearing impairment
Expand Tier I Human 442 Genes GS175423: HP:0010461 Abnormality of the male genitalia
Expand Tier I Human GO 2331 Genes GS208037: GO:0016787 hydrolase activity
Expand Tier I Human 205 Genes GS176283: HP:0009830 Peripheral neuropathy
Expand Tier I Human 81 Genes GS171786: HP:0001396 Cholestasis
Expand Tier I Human 267 Genes GS172365: HP:0003110 Abnormality of urine homeostasis
Expand Tier I Human 250 Genes GS171634: HP:0008050 Abnormality of the palpebral fissures
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 222 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 187 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 Human 356 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Human GO 687 Genes GS203895: GO:0006886 intracellular protein transport
Expand Tier I Human GO 2374 Genes GS206737: GO:0043168 anion binding
Expand Tier I Human 308 Genes GS172100: HP:0000587 Abnormality of the optic nerve
Expand Tier I Human 394 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human 393 Genes GS172362: HP:0004325 Decreased body weight
Expand Tier I Human 203 Genes GS174706: HP:0000553 Abnormality of the uvea
Expand Tier I Human 513 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 198 Genes GS171637: HP:0008872 Feeding difficulties in infancy
Expand Tier I Human CTD 1523 Genes GS124579: Selenium interacting genes (MeSH:D012643) in CTD
Expand Tier I Human 270 Genes GS172637: HP:0010460 Abnormality of the female genitalia
Expand Tier I Human 60 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 Human 194 Genes GS173872: HP:0011368 Epidermal thickening
Expand Tier I Human GO 927 Genes GS208787: GO:0034613 cellular protein localization
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 1046 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human 233 Genes GS174257: HP:0000309 Abnormality of the midface
Expand Tier I Human 381 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human 198 Genes GS174812: HP:0001637 Abnormality of the myocardium
Expand Tier I Human 20 Genes GS173959: HP:0001582 Redundant skin
Expand Tier I Human 917 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 136 Genes GS171202: HP:0100627 Displacement of the external urethral meatus
Expand Tier I Human 604 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 2361 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human 219 Genes GS172288: HP:0000358 Posteriorly rotated ears
Expand Tier I Human GO 1466 Genes GS205179: GO:0005524 ATP binding
Expand Tier I Human 985 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Human 282 Genes GS222704: test
Expand Tier I Human 62 Genes GS174527: HP:0000952 Jaundice
Expand Tier I Human 160 Genes GS175556: HP:0011675 Arrhythmia
Expand Tier I Human 313 Genes GS176568: HP:0000486 Strabismus
Expand Tier I Human 469 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human 17 Genes GS172788: HP:0000803 Renal cortical cysts
Expand Tier I Human 430 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 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 170 Genes GS173476: HP:0002311 Incoordination
Expand Tier I Human 514 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human GO 54 Genes GS208357: GO:0031903 microbody membrane
Expand Tier I Human 218 Genes GS175994: HP:0000464 Abnormality of the neck
Expand Tier I Human 386 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Human 22 Genes GS172329: HP:0005469 Flat occiput
Expand Tier I Human 511 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human GO 5280 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human GO 280 Genes GS202739: GO:0017038 protein import
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 789 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 3402 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level