Gene Details



PHEX and homologs in 7 species are found in 502 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 Mouse MP 1246 Genes GS165707: MP:0000428 abnormal craniofacial morphology
Expand Tier I Mouse GO 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Mouse MP 22 Genes GS169244: MP:0011228 abnormal vitamin D level
Expand Tier I Mouse MP 76 Genes GS170440: MP:0000062 increased bone mineral density
Expand Tier I Human CTD 75 Genes GS127132: Phosphorus interacting genes (MeSH:D010758) in CTD
Expand Tier I Mouse MP 279 Genes GS163596: MP:0000026 abnormal inner ear morphology
Expand Tier I Mouse MP 196 Genes GS168129: MP:0010025 decreased total body fat amount
Expand Tier I Human 33 Genes GS172194: HP:0002970 Genu varum
Expand Tier III Rat 177 Genes GS224554: Memory QTL 2 (Memor2 Published QTL Chr X)
Expand Tier I Mouse MP 411 Genes GS167813: MP:0000163 abnormal cartilage morphology
Expand Tier I Human GO 7609 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Mouse GO 289 Genes GS190608: GO:0001503 ossification
Expand Tier I Mouse MP 148 Genes GS163923: MP:0002896 abnormal bone mineralization
Expand Tier I Mouse MP 295 Genes GS167151: MP:0000454 abnormal jaw morphology
Expand Tier I Mouse MP 1485 Genes GS168559: MP:0002421 abnormal cell-mediated immunity
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Mouse GO 171 Genes GS182225: GO:0008237 metallopeptidase activity
Expand Tier I Mouse GO 5588 Genes GS193061: GO:0044444 cytoplasmic part
Expand Tier I Mouse GO 8630 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse GO 8650 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse GO 3537 Genes GS192041: GO:0043169 cation binding
Expand Tier I Human 166 Genes GS171901: HP:0010985 Gonosomal inheritance
Expand Tier I Human 152 Genes GS174979: HP:0011061 Abnormality of dental structure
Expand Tier I Human CTD 92 Genes GS124279: alachlor interacting genes (MeSH:C000188) in CTD
Expand Tier I Human 641 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 14 Genes GS174575: HP:0100530 Abnormality of calcium-phosphate metabolism
Expand Tier III Rat 985 Genes GS224236: Collagen induced arthritis QTL 18 (Cia18 Published QTL Chr X)
Expand Tier I Human 318 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier I Mouse MP 57 Genes GS165022: MP:0002857 cochlear ganglion degeneration
Expand Tier I Mouse MP 114 Genes GS169326: MP:0001664 abnormal digestion
Expand Tier I Mouse MP 114 Genes GS169666: MP:0003855 abnormal forelimb zeugopod morphology
Expand Tier I Human 27 Genes GS171442: HP:0003155 Elevated alkaline phosphatase
Expand Tier I Mouse GO 23778 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Human 116 Genes GS173868: HP:0002143 Abnormality of the spinal cord
Expand Tier I Human 31 Genes GS171877: HP:0002991 Abnormality of the fibula
Expand Tier I Human 375 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Mouse MP 65 Genes GS164014: MP:0001410 head bobbing
Expand Tier I Human GO 1098 Genes GS195083: GO:0007267 cell-cell signaling
Expand Tier I Human GO 4061 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human 120 Genes GS172358: HP:0003117 Abnormality of circulating hormone level
Expand Tier I Human GO 4014 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Mouse MP 29 Genes GS163389: MP:0001850 increased susceptibility to otitis media
Expand Tier I Mouse MP 24 Genes GS166737: MP:0004695 increased length of long bones
Expand Tier III Rat 178 Genes GS224840: Glucose level QTL 34 (Gluco34 Published QTL Chr X)
Expand Tier I Human 44 Genes GS174662: HP:0001423 X-linked dominant inheritance
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Mouse GO 5734 Genes GS190713: GO:0016021 integral to membrane
Expand Tier I Mouse MP 75 Genes GS168561: MP:0002427 disproportionate dwarf
Expand Tier I Mouse MP 742 Genes GS165992: MP:0008469 abnormal protein level
Expand Tier I Mouse MP 228 Genes GS163320: MP:0000031 abnormal cochlea morphology
Expand Tier I Mouse MP 2893 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier I Mouse MP 12 Genes GS165680: MP:0004380 short frontal bone
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Mouse MP 54 Genes GS169751: MP:0004359 short ulna
Expand Tier I Human GO 2455 Genes GS196595: GO:0006464 cellular protein modification process
Expand Tier I Mouse MP 68 Genes GS169209: MP:0003718 maternal effect
Expand Tier I Mouse GO 3548 Genes GS184566: GO:0019538 protein metabolic process
Expand Tier I Mouse MP 465 Genes GS169228: MP:0001406 abnormal gait
Expand Tier I Mouse MP 187 Genes GS169758: MP:0004765 decreased brainstem auditory evoked potential
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human GO 31 Genes GS205776: GO:0004177 aminopeptidase activity
Expand Tier II Mouse 262 Genes GS34191: Hippocampus Gene expression correlates of Number of entries into closed arms of plus maze in Males BXD
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier I Human CTD 6 Genes GS126372: Foscarnet interacting genes (MeSH:D017245) in CTD
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Mouse GO 8406 Genes GS177404: GO:0005737 cytoplasm
Expand Tier I Mouse GO 3080 Genes GS177265: GO:0048731 system development
Expand Tier I Mouse MP 361 Genes GS167214: MP:0005319 abnormal enzyme/ coenzyme level
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human 590 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Mouse MP 28 Genes GS166474: MP:0004993 decreased bone resorption
Expand Tier I Mouse GO 3597 Genes GS188142: GO:0048856 anatomical structure development
Expand Tier I Human 32 Genes GS176916: HP:0004437 Cranial hyperostosis
Expand Tier I Mouse GO 3442 Genes GS181533: GO:0046872 metal ion binding
Expand Tier I Mouse MP 89 Genes GS169795: MP:0004427 abnormal vestibular labyrinth morphology
Expand Tier I Mouse MP 619 Genes GS165194: MP:0001533 abnormal skeleton physiology
Expand Tier I Mouse MP 1246 Genes GS165228: MP:0005382 craniofacial phenotype
Expand Tier I Mouse MP 254 Genes GS170425: MP:0004508 abnormal pectoral girdle bone morphology
Expand Tier I Mouse MP 227 Genes GS169478: MP:0006395 abnormal epiphyseal plate morphology
Expand Tier II Mouse 307 Genes GS35867: Striatum Gene expression correlates of Cocaine CPP - difference in percent test time spent relative to preconditioning in Males BXD
Expand Tier I Mouse MP 19 Genes GS169725: MP:0005628 decreased circulating potassium level
Expand Tier I Human 181 Genes GS175907: HP:0004349 Reduced bone mineral density
Expand Tier I Mouse MP 33 Genes GS166039: MP:0005352 small cranium
Expand Tier I Mouse MP 1015 Genes GS166660: MP:0001731 abnormal postnatal growth
Expand Tier I Mouse MP 17 Genes GS170257: MP:0006021 abnormal Reissner membrane morphology
Expand Tier I Human CTD 44 Genes GS121416: Phosphorus, Dietary interacting genes (MeSH:D016226) in CTD
Expand Tier I Mouse MP 923 Genes GS167025: MP:0003953 abnormal hormone level
Expand Tier II Mouse 262 Genes GS36850: Hippocampus Gene expression correlates of Percentage of entries into closed arms of plus maze in Males BXD
Expand Tier I Human 1 Genes GS172556: HP:0100686 Enthesitis
Expand Tier I Mouse MP 799 Genes GS163226: MP:0003312 abnormal locomotor coordination
Expand Tier I Human GO 4338 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Mouse MP 282 Genes GS169534: MP:0005395 other phenotype
Expand Tier I Human 42 Genes GS171878: HP:0002992 Abnormality of the tibia
Expand Tier I Human CTD 20 Genes GS127274: beta-glycerophosphoric acid interacting genes (MeSH:C031463) in CTD
Expand Tier I Human GO 1974 Genes GS203688: GO:0008270 zinc ion binding
Expand Tier I Mouse MP 1446 Genes GS169133: MP:0002442 abnormal leukocyte physiology
Expand Tier I Mouse MP 2070 Genes GS163824: MP:0001259 abnormal body weight
Expand Tier I Mouse MP 254 Genes GS169241: MP:0000130 abnormal trabecular bone morphology
Expand Tier I Human 242 Genes GS175909: HP:0004348 Abnormality of bone mineral density
Expand Tier I Mouse GO 388 Genes GS192643: GO:0048471 perinuclear region of cytoplasm
Expand Tier I Mouse GO 8414 Genes GS185585: GO:0044710 single-organism metabolic process
Expand Tier I Mouse MP 204 Genes GS163107: MP:0000550 abnormal forelimb morphology
Expand Tier I Mouse MP 3 Genes GS166733: MP:0004699 unilateral deafness
Expand Tier I Mouse MP 63 Genes GS163407: MP:0004019 abnormal vitamin homeostasis
Expand Tier I Human GO 1276 Genes GS196726: GO:0005783 endoplasmic reticulum
Expand Tier I Mouse MP 25 Genes GS165241: MP:0002966 decreased circulating alkaline phosphatase level
Expand Tier I Human GO 4003 Genes GS208978: GO:0043169 cation binding
Expand Tier I Mouse MP 235 Genes GS168497: MP:0001256 abnormal body length
Expand Tier I Human 487 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Mouse MP 267 Genes GS167805: MP:0000150 abnormal rib morphology
Expand Tier I Mouse MP 255 Genes GS164126: MP:0001388 abnormal stationary movement
Expand Tier I Human 62 Genes GS176804: HP:0001850 Abnormality of the tarsal bones
Expand Tier I Mouse MP 61 Genes GS163659: MP:0005272 abnormal temporal bone morphology
Expand Tier I Mouse MP 175 Genes GS164059: MP:0006325 impaired hearing
Expand Tier I Human 6 Genes GS176130: HP:0003017 Frayed, irregular metaphyses
Expand Tier I Mouse MP 170 Genes GS164040: MP:0003856 abnormal hindlimb stylopod morphology
Expand Tier I Human 401 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human CTD 429 Genes GS126896: Methylcholanthrene interacting genes (MeSH:D008748) in CTD
Expand Tier I Mouse MP 1052 Genes GS166409: MP:0002114 abnormal axial skeleton morphology
Expand Tier I Human GO 3863 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier I Mouse MP 48 Genes GS169137: MP:0003408 increased width of hypertrophic chondrocyte zone
Expand Tier I Mouse GO 2565 Genes GS192299: GO:0006793 phosphorus metabolic process
Expand Tier I Human 22 Genes GS170891: HP:0006480 Premature loss of teeth
Expand Tier I Human GO 5623 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Mouse GO 1079 Genes GS178401: GO:0019637 organophosphate metabolic process
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Human GO 1905 Genes GS198782: GO:0044459 plasma membrane part
Expand Tier I Mouse MP 12 Genes GS168555: MP:0003116 rickets
Expand Tier I Mouse MP 3159 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Mouse MP 88 Genes GS164071: MP:0005108 abnormal ulna morphology
Expand Tier I Human 6 Genes GS171819: HP:0000117 Decreased renal tubular phosphate reabsorption
Expand Tier I Human 21 Genes GS172603: HP:0000127 Renal salt wasting
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human CTD 29 Genes GS121286: Phosphates interacting genes (MeSH:D010710) in CTD
Expand Tier I Mouse MP 1317 Genes GS169832: MP:0005381 digestive/alimentary phenotype
Expand Tier I Mouse MP 141 Genes GS167807: MP:0000165 abnormal long bone hypertrophic chondrocyte zone
Expand Tier I Mouse MP 108 Genes GS163576: MP:0000202 abnormal circulating alkaline phosphatase level
Expand Tier I Mouse MP 73 Genes GS163848: MP:0001541 abnormal osteoclast physiology
Expand Tier I Mouse MP 959 Genes GS166244: MP:0002752 abnormal somatic nervous system morphology
Expand Tier I Human 78 Genes GS173387: HP:0002757 Recurrent fractures
Expand Tier I Mouse MP 21 Genes GS165921: MP:0000091 short premaxilla
Expand Tier I Human 93 Genes GS174308: HP:0002979 Bowing of the legs
Expand Tier I Human GO 9088 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Mouse MP 67 Genes GS166533: MP:0004509 abnormal pelvic girdle bone morphology
Expand Tier I Mouse MP 855 Genes GS169075: MP:0002078 abnormal glucose homeostasis
Expand Tier I Mouse GO 5225 Genes GS189860: GO:0043167 ion binding
Expand Tier I Mouse MP 443 Genes GS165877: MP:0002136 abnormal kidney physiology
Expand Tier I Human 232 Genes GS170999: HP:0000082 Abnormality of renal physiology
Expand Tier I Human 262 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier I Mouse GO 2190 Genes GS191129: GO:0016787 hydrolase activity
Expand Tier I Human 825 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Mouse MP 27 Genes GS164560: MP:0004870 small premaxilla
Expand Tier I Human 18 Genes GS172113: HP:0002980 Femoral bowing
Expand Tier I Mouse GO 6473 Genes GS184448: GO:0044425 membrane part
Expand Tier I Mouse MP 779 Genes GS166118: MP:0002109 abnormal limb morphology
Expand Tier I Human 31 Genes GS171610: HP:0004379 Abnormality of alkaline phosphatase activity
Expand Tier I Human GO 1254 Genes GS199199: GO:0031226 intrinsic to plasma membrane
Expand Tier III Rat 411 Genes GS224329: Insulin dependent diabetes mellitus QTL 5 (Iddm5 Published QTL Chr X)
Expand Tier I Mouse MP 3522 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Human GO 5764 Genes GS206742: GO:0043167 ion binding
Expand Tier I Mouse MP 11 Genes GS163533: MP:0004652 small caudal vertebrae
Expand Tier I Human GO 113 Genes GS203267: GO:0031214 biomineral tissue development
Expand Tier I Mouse MP 1764 Genes GS165386: MP:0001262 decreased body weight
Expand Tier I Mouse MP 262 Genes GS164346: MP:0006335 abnormal hearing electrophysiology
Expand Tier I Mouse MP 378 Genes GS165361: MP:0004624 abnormal thoracic cage morphology
Expand Tier I Mouse MP 1112 Genes GS169774: MP:0001846 increased inflammatory response
Expand Tier I Mouse MP 87 Genes GS164962: MP:0002855 abnormal cochlear ganglion morphology
Expand Tier I Mouse MP 2283 Genes GS169391: MP:0002066 abnormal motor capabilities/coordination/movement
Expand Tier I Human 115 Genes GS172364: HP:0003111 Abnormality of ion homeostasis
Expand Tier I Human 39 Genes GS174178: HP:0100774 Hyperostosis
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier I Human 25 Genes GS172554: HP:0100685 Abnormality of Sharpey fibers
Expand Tier I Human 96 Genes GS174851: HP:0000944 Abnormality of the metaphyses
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Mouse MP 462 Genes GS168996: MP:0009643 abnormal urine homeostasis
Expand Tier I Mouse GO 5892 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier I Mouse MP 81 Genes GS168361: MP:0000102 abnormal nasal bone morphology
Expand Tier I Mouse MP 137 Genes GS163075: MP:0000558 abnormal tibia morphology
Expand Tier I Mouse MP 724 Genes GS168155: MP:0005502 abnormal renal/urinary system physiology
Expand Tier I Human 14 Genes GS173610: HP:0002748 Rickets
Expand Tier I Mouse GO 5103 Genes GS192512: GO:0003824 catalytic activity
Expand Tier I Mouse 301 Genes GS136883: testis weight (Tswt, Published QTL Chr X)
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier III Mouse 5790 Genes GS213077: Genes with suggestive difference in (PWD) vs (PB6F1 + B6PF1 + B6) comparison
Expand Tier I Human 780 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 138 Genes GS174847: HP:0000940 Abnormal diaphysis morphology
Expand Tier I Human 101 Genes GS172692: HP:0002659 Increased susceptibility to fractures
Expand Tier I Mouse MP 65 Genes GS168471: MP:0002187 abnormal fibula morphology
Expand Tier I Mouse MP 165 Genes GS168687: MP:0000592 short tail
Expand Tier I Mouse MP 293 Genes GS164127: MP:0001570 abnormal circulating enzyme level
Expand Tier I Mouse MP 2432 Genes GS167542: MP:0001790 abnormal immune system physiology
Expand Tier I Mouse MP 314 Genes GS163933: MP:0001765 abnormal ion homeostasis
Expand Tier I Mouse MP 3051 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Mouse MP 50 Genes GS166930: MP:0002820 abnormal premaxilla morphology
Expand Tier I Mouse MP 391 Genes GS168851: MP:0002451 abnormal macrophage physiology
Expand Tier I Human GO 3506 Genes GS193991: GO:0048731 system development
Expand Tier III Rat 336 Genes GS223965: Non-insulin dependent diabetes mellitus QTL 16 (Niddm16 Published QTL Chr X)
Expand Tier III Mouse 51 Genes GS820: UCSD_CEREBELLUM_Int_Age_Geno
Expand Tier III Rat 3415 Genes GS135132: bHR vs bLR genes different in Nucleus Acumbens
Expand Tier I Mouse MP 2 Genes GS165130: MP:0011447 abnormal renal glucose reabsorption
Expand Tier I Mouse 627 Genes GS128586: Rotarod Baseline Chr# X
Expand Tier I Human 238 Genes GS172433: HP:0002644 Abnormality of pelvic girdle bone morphology
Expand Tier I Mouse MP 76 Genes GS169236: MP:0000135 decreased compact bone thickness
Expand Tier I Mouse MP 487 Genes GS166123: MP:0002102 abnormal ear morphology
Expand Tier I Mouse MP 3761 Genes GS165527: MP:0005378 growth/size phenotype
Expand Tier I Mouse MP 68 Genes GS169328: MP:0001666 abnormal intestinal absorption
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier III Rat 3415 Genes GS135133: bHR vs bLR genes different in Hippocampus
Expand Tier I Human GO 3902 Genes GS198323: GO:0046872 metal ion binding
Expand Tier I Mouse GO 84 Genes GS190545: GO:0030282 bone mineralization
Expand Tier I Mouse MP 297 Genes GS166649: MP:0011504 abnormal limb long bone morphology
Expand Tier I Mouse MP 29 Genes GS164332: MP:0005298 abnormal clavicle morphology
Expand Tier I Mouse MP 108 Genes GS163412: MP:0004016 decreased bone mass
Expand Tier III Mouse 8331 Genes GS128199: Alcohol Preference union of 86 Gene Sets
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Mouse MP 44 Genes GS169136: MP:0005401 abnormal fat-soluble vitamin level
Expand Tier III Rat 426 Genes GS224012: Urinary albumin excretion QTL 27 (Uae27 Published QTL Chr X)
Expand Tier I Mouse MP 280 Genes GS162933: MP:0005636 abnormal mineral homeostasis
Expand Tier I Mouse 310 Genes GS136739: small testis weight 2 (Smtw2, Published QTL Chr X)
Expand Tier I Human GO 105 Genes GS199822: GO:0004222 metalloendopeptidase activity
Expand Tier I Mouse MP 9 Genes GS168175: MP:0004338 small clavicle
Expand Tier I Human CTD 105 Genes GS124172: Arsenates interacting genes (MeSH:D001149) in CTD
Expand Tier I Human GO 2539 Genes GS203335: GO:0048513 organ development
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Human 88 Genes GS173329: HP:0000682 Abnormality of dental enamel
Expand Tier I Human 160 Genes GS175806: HP:0001417 X-linked inheritance
Expand Tier I Mouse MP 23 Genes GS163091: MP:0000195 hypocalcemia
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Mouse MP 247 Genes GS166029: MP:0000960 abnormal sensory ganglion morphology
Expand Tier I Human GO 6073 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 514 Genes GS174081: HP:0004322 Short stature
Expand Tier I Mouse MP 48 Genes GS169144: MP:0004355 short radius
Expand Tier I Mouse GO 1204 Genes GS188763: GO:0009888 tissue development
Expand Tier I Mouse GO 7644 Genes GS188399: GO:0044238 primary metabolic process
Expand Tier I Mouse MP 256 Genes GS167056: MP:0004686 decreased length of long bones
Expand Tier I Human 511 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Mouse MP 83 Genes GS170510: MP:0002764 short tibia
Expand Tier I Human 123 Genes GS170894: HP:0006487 Bowing of the long bones
Expand Tier I Mouse MP 50 Genes GS164273: MP:0000043 organ of Corti degeneration
Expand Tier I Mouse MP 55 Genes GS163980: MP:0006089 abnormal vestibular saccule morphology
Expand Tier I Mouse MP 137 Genes GS166173: MP:0004986 abnormal osteoblast morphology
Expand Tier I Mouse MP 14 Genes GS169442: MP:0008158 increased diameter of femur
Expand Tier I Mouse MP 627 Genes GS169708: MP:0005416 abnormal circulating protein level
Expand Tier III Rat 413 Genes GS224776: Estrogen-dependent pituitary mass QTL 12 (Edpm12 Published QTL Chr X)
Expand Tier I Mouse MP 4 Genes GS169249: MP:0011221 decreased intestinal calcium absorption
Expand Tier I Human 34 Genes GS171863: HP:0008365 Abnormality of the talus
Expand Tier I Human GO 1435 Genes GS205623: GO:0009888 tissue development
Expand Tier I Mouse MP 4 Genes GS167138: MP:0003167 abnormal scala tympani morphology
Expand Tier I Mouse MP 95 Genes GS168396: MP:0010031 abnormal cranium size
Expand Tier I Human 6 Genes GS175503: HP:0010502 Fibular bowing
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Mouse MP 245 Genes GS165425: MP:0010119 abnormal bone mineral density
Expand Tier I Mouse MP 42 Genes GS168282: MP:0004471 short nasal bone
Expand Tier I Mouse MP 111 Genes GS167685: MP:0003109 short femur
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Mouse MP 1562 Genes GS168149: MP:0005508 abnormal skeleton morphology
Expand Tier I Mouse MP 94 Genes GS166248: MP:0000088 short mandible
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human 26 Genes GS173861: HP:0002148 Hypophosphatemia
Expand Tier II Mouse 40 Genes GS36364: Striatum Gene expression correlates of Open Field - Total rears 0-5 minutes in Females BXD
Expand Tier I Mouse MP 2788 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Mouse MP 1743 Genes GS164263: MP:0002083 premature death
Expand Tier I Mouse MP 632 Genes GS169331: MP:0001663 abnormal digestive system physiology
Expand Tier I Human GO 370 Genes GS209907: GO:0004175 endopeptidase activity
Expand Tier I Mouse MP 106 Genes GS169237: MP:0000134 abnormal compact bone thickness
Expand Tier I Mouse MP 345 Genes GS166408: MP:0002115 abnormal limb bone morphology
Expand Tier I Mouse GO 571 Genes GS188685: GO:0070011 peptidase activity, acting on L-amino acid peptides
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Mouse MP 165 Genes GS163071: MP:0000559 abnormal femur morphology
Expand Tier I Human GO 5359 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human CTD 870 Genes GS126764: Calcitriol interacting genes (MeSH:D002117) in CTD
Expand Tier I Human 6 Genes GS171774: HP:0004912 Hypophosphatemic rickets
Expand Tier I Mouse 288 Genes GS136623: Stem cell proliferation 11 (Scpro11, Published QTL Chr X)
Expand Tier I Mouse MP 1296 Genes GS169773: MP:0001845 abnormal inflammatory response
Expand Tier I Mouse MP 1674 Genes GS169530: MP:0005390 skeleton phenotype
Expand Tier I Human 123 Genes GS175665: HP:0006504 Abnormality involving the diaphyses of the limbs
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier I Mouse GO 360 Genes GS192965: GO:0004175 endopeptidase activity
Expand Tier I Mouse MP 702 Genes GS167922: MP:0000959 abnormal somatic sensory system morphology
Expand Tier I Human 41 Genes GS173378: HP:0002758 Osteoarthritis
Expand Tier I Human 9 Genes GS171002: HP:0003165 Elevated circulating parathyroid hormone (PTH) level
Expand Tier I Mouse MP 83 Genes GS163408: MP:0002968 increased circulating alkaline phosphatase level
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier III Mouse 8151 Genes GS213076: Genes with suggestive difference in (B6) vs (B6PF1 + PB6F1 + PWD) comparison
Expand Tier I Mouse MP 144 Genes GS169301: MP:0000547 short limbs
Expand Tier I Human 107 Genes GS171228: HP:0002823 Abnormality of the femur
Expand Tier I Human 129 Genes GS173792: HP:0002815 Abnormality of the knees
Expand Tier I Human 936 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 100 Genes GS203109: GO:0008238 exopeptidase activity
Expand Tier I Mouse MP 161 Genes GS169277: MP:0001081 abnormal cranial ganglia morphology
Expand Tier I Mouse MP 173 Genes GS168718: MP:0002998 abnormal bone remodeling
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human 1 Genes GS173468: HP:0006432 Trapezoidal distal femoral condyles
Expand Tier I Mouse MP 394 Genes GS165567: MP:0008271 abnormal bone ossification
Expand Tier I Mouse MP 11449 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Mouse MP 263 Genes GS163094: MP:0000192 abnormal mineral level
Expand Tier I Mouse MP 366 Genes GS163664: MP:0005274 abnormal viscerocranium morphology
Expand Tier I Human GO 4250 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Mouse MP 8 Genes GS167432: MP:0004348 long femur
Expand Tier III Human 2217 Genes GS222813: The Druggable Gene Interaction Database
Expand Tier I Mouse MP 286 Genes GS170158: MP:0000074 abnormal neurocranium morphology
Expand Tier I Human GO 4575 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Mouse MP 112 Genes GS163333: MP:0004231 abnormal calcium ion homeostasis
Expand Tier I Human 1 Genes GS172531: HP:0008117 Shortening of the talar neck
Expand Tier I Human GO 178 Genes GS199022: GO:0008237 metallopeptidase activity
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Mouse GO 600 Genes GS182209: GO:0008233 peptidase activity
Expand Tier I Human CTD 218 Genes GS123274: 2,4-diaminotoluene interacting genes (MeSH:C010914) in CTD
Expand Tier I Mouse GO 98 Genes GS183020: GO:0004222 metalloendopeptidase activity
Expand Tier I Mouse GO 3605 Genes GS190682: GO:0007275 multicellular organismal development
Expand Tier I Human CTD 210 Genes GS124951: Atrazine interacting genes (MeSH:D001280) in CTD
Expand Tier I Human 19 Genes GS172642: HP:0002982 Tibial bowing
Expand Tier I Mouse MP 112 Genes GS167808: MP:0000166 abnormal chondrocyte morphology
Expand Tier I Mouse MP 28 Genes GS162824: MP:0002903 abnormal circulating parathyroid hormone level
Expand Tier I Human GO 572 Genes GS199006: GO:0008233 peptidase activity
Expand Tier I Mouse MP 23 Genes GS164470: MP:0001566 hyperphosphatemia
Expand Tier I Human GO 467 Genes GS209583: GO:0048471 perinuclear region of cytoplasm
Expand Tier I Mouse MP 1502 Genes GS168560: MP:0002420 abnormal adaptive immunity
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse MP 85 Genes GS167643: MP:0000034 abnormal vestibule morphology
Expand Tier I Mouse MP 72 Genes GS163751: MP:0004540 small maxilla
Expand Tier I Human 21 Genes GS172605: HP:0000124 Renal tubular dysfunction
Expand Tier I Mouse MP 3168 Genes GS169827: MP:0005387 immune system phenotype
Expand Tier I Human CTD 6 Genes GS125438: Levamisole interacting genes (MeSH:D007978) in CTD
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 2 Genes GS175049: HP:0006285 Hypomineralization of enamel
Expand Tier I Mouse GO 108 Genes GS186422: GO:0031214 biomineral tissue development
Expand Tier I Mouse MP 60 Genes GS169698: MP:0004945 abnormal bone resorption
Expand Tier I Human 525 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human 837 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Mouse MP 201 Genes GS163825: MP:0001258 decreased body length
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier III Mouse 3218 Genes GS213073: Genes with suggestive difference in (PB6F1) vs (B6PF1 + B6 + PWD) comparison
Expand Tier I Mouse MP 226 Genes GS167806: MP:0000164 abnormal cartilage development
Expand Tier I Mouse MP 1589 Genes GS165260: MP:0001392 abnormal locomotor behavior
Expand Tier I Mouse MP 47 Genes GS169238: MP:0000133 abnormal long bone metaphysis morphology
Expand Tier I Mouse MP 6 Genes GS163108: MP:0010110 abnormal renal phosphate reabsorbtion
Expand Tier I Human 733 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Mouse MP 510 Genes GS166404: MP:0002113 abnormal skeleton development
Expand Tier I Mouse MP 4 Genes GS163738: MP:0011219 abnormal intestinal calcium absorption
Expand Tier I Mouse MP 149 Genes GS167152: MP:0000455 abnormal maxilla morphology
Expand Tier I Human GO 2216 Genes GS209291: GO:0046914 transition metal ion binding
Expand Tier I Mouse MP 551 Genes GS170236: MP:0005452 abnormal adipose tissue amount
Expand Tier I Human 52 Genes GS172644: HP:0002981 Abnormality of the calf
Expand Tier I Human 83 Genes GS172024: HP:0001369 Arthritis
Expand Tier I Mouse MP 282 Genes GS169967: MP:0001408 stereotypic behavior
Expand Tier I Mouse MP 1093 Genes GS165536: MP:0005371 limbs/digits/tail phenotype
Expand Tier I Human 317 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Mouse MP 656 Genes GS165538: MP:0005377 hearing/vestibular/ear phenotype
Expand Tier I Mouse GO 2279 Genes GS186488: GO:0048513 organ development
Expand Tier I Mouse MP 56 Genes GS167172: MP:0004351 short humerus
Expand Tier I Mouse MP 2489 Genes GS165397: MP:0001265 decreased body size
Expand Tier I Mouse MP 66 Genes GS164466: MP:0001562 abnormal circulating calcium level
Expand Tier I Mouse MP 328 Genes GS168218: MP:0001963 abnormal hearing physiology
Expand Tier I Mouse MP 29 Genes GS170511: MP:0002765 short fibula
Expand Tier I Mouse MP 52 Genes GS167354: MP:0008525 decreased cranium height
Expand Tier I Mouse MP 3159 Genes GS169095: MP:0004924 abnormal behavior
Expand Tier I Mouse MP 384 Genes GS164570: MP:0003878 abnormal ear physiology
Expand Tier I Mouse MP 176 Genes GS165255: MP:0001394 circling
Expand Tier I Human 576 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human GO 1166 Genes GS201075: GO:0005794 Golgi apparatus
Expand Tier I Human 17 Genes GS175565: HP:0003025 Irregular metaphyses
Expand Tier I Human 598 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 173 Genes GS173901: HP:0002007 Frontal bossing
Expand Tier I Human GO 4554 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Mouse MP 131 Genes GS164723: MP:0004592 small mandible
Expand Tier I Mouse MP 566 Genes GS166891: MP:0003795 abnormal bone structure
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 Mouse MP 246 Genes GS168871: MP:0004738 abnormal brainstem auditory evoked potential
Expand Tier I Mouse MP 37 Genes GS163473: MP:0006397 disorganized long bone epiphyseal plate
Expand Tier I Human GO 386 Genes GS207498: GO:0001501 skeletal system development
Expand Tier I Mouse MP 38 Genes GS163089: MP:0000198 hypophosphatemia
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 Mouse MP 38 Genes GS169223: MP:0002668 abnormal circulating potassium level
Expand Tier I Mouse MP 162 Genes GS169704: MP:0003857 abnormal hindlimb zeugopod morphology
Expand Tier I Human 554 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Mouse MP 62 Genes GS169793: MP:0004425 abnormal otolith organ morphology
Expand Tier I Mouse MP 4019 Genes GS165537: MP:0005376 homeostasis/metabolism phenotype
Expand Tier I Mouse MP 88 Genes GS166246: MP:0002759 abnormal caudal vertebrae morphology
Expand Tier I Mouse MP 105 Genes GS167442: MP:0000440 domed cranium
Expand Tier I Mouse 288 Genes GS135733: dietary obesity 7 (Dob7, Published QTL Chr X)
Expand Tier I Mouse MP 54 Genes GS169125: MP:0005400 abnormal vitamin level
Expand Tier I Human CTD 57 Genes GS126599: Aluminum Oxide interacting genes (MeSH:D000537) in CTD
Expand Tier I Mouse MP 497 Genes GS170104: MP:0003723 abnormal long bone morphology
Expand Tier I Mouse MP 91 Genes GS168835: MP:0005296 abnormal humerus morphology
Expand Tier I Mouse MP 180 Genes GS163063: MP:0000042 abnormal organ of Corti morphology
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse GO 862 Genes GS182673: GO:0006508 proteolysis
Expand Tier I Mouse MP 983 Genes GS164742: MP:0001732 postnatal growth retardation
Expand Tier I Mouse MP 500 Genes GS166405: MP:0002111 abnormal tail morphology
Expand Tier I Mouse MP 95 Genes GS168358: MP:0000107 abnormal frontal bone morphology
Expand Tier I Mouse GO 5859 Genes GS182404: GO:0031224 intrinsic to membrane
Expand Tier I Mouse 223 Genes GS135779: exercise endurance QTL 1 (Eeq1, Published QTL Chr X)
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human 596 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human 322 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Mouse MP 602 Genes GS166407: MP:0002116 abnormal craniofacial bone morphology
Expand Tier I Mouse MP 1473 Genes GS167098: MP:0001819 abnormal immune cell physiology
Expand Tier I Mouse GO 23359 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human GO 5243 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human 1 Genes GS171798: HP:0008144 Flattening of the talar dome
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Mouse MP 7 Genes GS167131: MP:0009877 exostosis
Expand Tier I Human GO 2455 Genes GS199032: GO:0036211 protein modification process
Expand Tier I Human 54 Genes GS171298: HP:0002829 Arthralgia
Expand Tier I Mouse MP 3 Genes GS164823: MP:0011476 abnormal urine nucleotide level
Expand Tier I Mouse MP 190 Genes GS167155: MP:0000458 abnormal mandible morphology
Expand Tier I Human GO 2549 Genes GS194336: GO:0043412 macromolecule modification
Expand Tier I Mouse GO 9049 Genes GS180166: GO:0008152 metabolic process
Expand Tier I Mouse MP 4 Genes GS167762: MP:0006025 distended Reissner membrane
Expand Tier I Mouse MP 38 Genes GS163361: MP:0010107 abnormal renal reabsorbtion
Expand Tier I Mouse MP 209 Genes GS165114: MP:0004426 abnormal cochlear labyrinth morphology
Expand Tier I Human 245 Genes GS176806: HP:0003812 Phenotypic variability
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Mouse MP 202 Genes GS164841: MP:0006357 abnormal circulating mineral level
Expand Tier I Mouse GO 1006 Genes GS184267: GO:0005794 Golgi apparatus
Expand Tier I Mouse MP 209 Genes GS164394: MP:0003055 abnormal long bone epiphyseal plate morphology
Expand Tier I Mouse GO 1149 Genes GS179957: GO:0005783 endoplasmic reticulum
Expand Tier I Mouse MP 23 Genes GS165879: MP:0000039 abnormal otic capsule morphology
Expand Tier I Mouse MP 98 Genes GS170337: MP:0003854 abnormal forelimb stylopod morphology
Expand Tier I Human 27 Genes GS175974: HP:0004493 Craniofacial hyperostosis
Expand Tier I Human 550 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Human 191 Genes GS225611: http://www.broadinstitute.org/gsea/msigdb/cards/HALLMARK_COMPLEMENT
Expand Tier I Human 8 Genes GS173609: HP:0002749 Osteomalacia
Expand Tier I Human 390 Genes GS175537: HP:0011277 Abnormality of the urinary system physiology
Expand Tier I Mouse MP 85 Genes GS164137: MP:0000552 abnormal radius morphology
Expand Tier I Mouse MP 675 Genes GS163103: MP:0000003 abnormal adipose tissue morphology
Expand Tier I Mouse MP 151 Genes GS166889: MP:0003797 abnormal compact bone morphology
Expand Tier I Mouse MP 14 Genes GS164833: MP:0008753 abnormal osteocyte morphology
Expand Tier I Mouse MP 957 Genes GS168848: MP:0002452 abnormal antigen presenting cell physiology
Expand Tier I Human GO 1210 Genes GS197008: GO:0005887 integral to plasma membrane
Expand Tier I Human GO 940 Genes GS199468: GO:0006508 proteolysis
Expand Tier I Mouse MP 1731 Genes GS168956: MP:0003491 abnormal voluntary movement
Expand Tier I Mouse MP 47 Genes GS167771: MP:0008151 increased diameter of long bones
Expand Tier I Mouse GO 8145 Genes GS190714: GO:0016020 membrane
Expand Tier I Mouse MP 636 Genes GS169663: MP:0004703 abnormal vertebral column morphology
Expand Tier I Human 32 Genes GS172698: HP:0002653 Bone pain
Expand Tier I Mouse MP 9 Genes GS162818: MP:0002905 decreased circulating parathyroid hormone level
Expand Tier I Human 776 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Mouse MP 58 Genes GS165996: MP:0000097 short maxilla
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse MP 3424 Genes GS163934: MP:0001764 abnormal homeostasis
Expand Tier I Mouse GO 4073 Genes GS180034: GO:0032502 developmental process
Expand Tier I Human GO 6605 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Mouse MP 4902 Genes GS165525: MP:0010768 mortality/aging
Expand Tier I Human 10 Genes GS176908: HP:0002176 Spinal cord compression
Expand Tier I Human GO 550 Genes GS205544: GO:0070011 peptidase activity, acting on L-amino acid peptides
Expand Tier I Human 173 Genes GS171148: HP:0011218 Abnormal shape of the frontal region
Expand Tier I Mouse MP 642 Genes GS164770: MP:0009250 abnormal appendicular skeleton morphology
Expand Tier I Mouse MP 247 Genes GS163316: MP:0000035 abnormal membranous labyrinth morphology
Expand Tier I Mouse MP 57 Genes GS168319: MP:0004470 small nasal bone
Expand Tier I Mouse MP 687 Genes GS165539: MP:0005375 adipose tissue phenotype
Expand Tier I Mouse MP 60 Genes GS166611: MP:0002835 abnormal cranial suture morphology
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 4575 Genes GS206355: GO:0023052 signaling
Expand Tier I Mouse MP 19 Genes GS162821: MP:0002900 abnormal urine phosphate level
Expand Tier I Mouse MP 4624 Genes GS165524: MP:0010769 abnormal survival
Expand Tier I Human GO 2331 Genes GS208037: GO:0016787 hydrolase activity
Expand Tier I Mouse MP 207 Genes GS167140: MP:0003169 abnormal scala media morphology
Expand Tier I Human 267 Genes GS172365: HP:0003110 Abnormality of urine homeostasis
Expand Tier I Human GO 4701 Genes GS195977: GO:0007154 cell communication
Expand Tier I Mouse MP 10 Genes GS164834: MP:0009445 osteomalacia
Expand Tier I Mouse MP 391 Genes GS169234: MP:0000137 abnormal vertebrae morphology
Expand Tier I Mouse MP 11 Genes GS169605: MP:0001670 abnormal intestinal mineral absorption
Expand Tier I Human GO 7259 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Mouse MP 16 Genes GS169426: MP:0008152 decreased diameter of femur
Expand Tier I Mouse GO 7552 Genes GS180452: GO:0044237 cellular metabolic process
Expand Tier I Human 14 Genes GS171557: HP:0003416 Spinal canal stenosis
Expand Tier I Mouse MP 814 Genes GS164301: MP:0005418 abnormal circulating hormone level
Expand Tier I Mouse MP 597 Genes GS167717: MP:0002419 abnormal innate immunity
Expand Tier I Mouse MP 159 Genes GS163724: MP:0000436 abnormal head movements
Expand Tier I Mouse MP 1173 Genes GS165798: MP:0005367 renal/urinary system phenotype
Expand Tier I Mouse MP 23 Genes GS167772: MP:0008150 decreased diameter of long bones
Expand Tier I Mouse GO 23849 Genes GS180164: GO:0008150 biological_process
Expand Tier I Mouse MP 14 Genes GS162822: MP:0002901 increased urine phosphate level
Expand Tier I Mouse MP 2337 Genes GS168995: MP:0009642 abnormal blood homeostasis
Expand Tier I Human 917 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 316 Genes GS163098: MP:0000556 abnormal hindlimb morphology
Expand Tier I Mouse MP 583 Genes GS165437: MP:0000438 abnormal cranium morphology
Expand Tier I Human GO 8645 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 985 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Mouse MP 59 Genes GS164471: MP:0001565 abnormal circulating phosphate level
Expand Tier I Mouse MP 22 Genes GS166040: MP:0005353 abnormal patella morphology