Gene Details



PHEX and homologs in 7 species are found in 1109 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 II Human 8052 Genes GS244604: [MeSH] Neoplasms : D009369
Expand Tier II Human 706 Genes GS235946: [MeSH] Kidney Cortex : D007672
Expand Tier II Human 238 Genes GS244511: [MeSH] Metals, Light : D019565
Expand Tier II Human 350 Genes GS236887: [MeSH] Ear Diseases : D004427
Expand Tier II Human 6358 Genes GS238474: [MeSH] Hormones : D006728
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 196 Genes GS168129: MP:0010025 decreased total body fat amount
Expand Tier I Human 206 Genes GS231779: PC Geneset - "V$HNF3B_01" pathway genes
Expand Tier II Human 1241 Genes GS241538: [MeSH] Radiation, Ionizing : D011839
Expand Tier II Human 10505 Genes GS238504: [MeSH] Tissues : D014024
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier II Human 5416 Genes GS237717: [MeSH] Tissue Distribution : D014018
Expand Tier II Human 8606 Genes GS243926: [MeSH] Exons : D005091
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 171 Genes GS182225: GO:0008237 metallopeptidase activity
Expand Tier II Human 390 Genes GS245136: [MeSH] Frameshift Mutation : D016368
Expand Tier II Human 7112 Genes GS240775: [MeSH] Blood Proteins : D001798
Expand Tier II Human 671 Genes GS237844: [MeSH] Intestine, Small : D007421
Expand Tier II Human 111 Genes GS236770: [MeSH] X-Rays : D014965
Expand Tier II Human 962 Genes GS238428: [MeSH] Allelic Imbalance : D022981
Expand Tier I Human 152 Genes GS174979: HP:0011061 Abnormality of dental structure
Expand Tier II Human 11812 Genes GS236947: [MeSH] Brain : D001921
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 I Human 318 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier II Human 12069 Genes GS237417: [MeSH] Multigene Family : D005810
Expand Tier I Mouse MP 57 Genes GS165022: MP:0002857 cochlear ganglion degeneration
Expand Tier II Human 143 Genes GS240903: [MeSH] Intestinal Absorption : D007408
Expand Tier I Mouse MP 114 Genes GS169326: MP:0001664 abnormal digestion
Expand Tier II Human 70216 Genes GS235234: [MeSH] Biochemical Phenomena : D001669
Expand Tier II Human 31959 Genes GS237114: [MeSH] Regulatory Elements, Transcriptional : D050436
Expand Tier II Human 4634 Genes GS236717: [MeSH] Cell Survival : D002470
Expand Tier I Human 27 Genes GS171442: HP:0003155 Elevated alkaline phosphatase
Expand Tier II Human 96 Genes GS242923: [MeSH] Tooth Germ : D014083
Expand Tier II Human 11446 Genes GS236912: [MeSH] Biological Transport : D001692
Expand Tier II Human 4661 Genes GS238716: [MeSH] Genetic Linkage : D008040
Expand Tier II Human 10106 Genes GS234071: [MeSH] Protein Modification, Translational : D046188
Expand Tier I Human 31 Genes GS171877: HP:0002991 Abnormality of the fibula
Expand Tier II Human 15702 Genes GS245264: [MeSH] Nervous System : D009420
Expand Tier II Human 3240 Genes GS236066: [MeSH] Musculoskeletal Physiological Phenomena : D009142
Expand Tier I Human 375 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier II Human 745 Genes GS238514: [MeSH] Otorhinolaryngologic Diseases : D010038
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 II Human 15 Genes GS240884: [MeSH] Tooth Calcification : D014074
Expand Tier II Human 2216 Genes GS240927: [MeSH] Glucose : D005947
Expand Tier II Human 478 Genes GS244778: [MeSH] Skull : D012886
Expand Tier I Human 715 Genes GS227535: MSigDB Geneset - TGCCAAR_V$NF1_Q6
Expand Tier I Mouse MP 29 Genes GS163389: MP:0001850 increased susceptibility to otitis media
Expand Tier II Human 3073 Genes GS240942: [MeSH] Ion Pumps : D016623
Expand Tier I Mouse MP 24 Genes GS166737: MP:0004695 increased length of long bones
Expand Tier II Human 446 Genes GS245783: [MeSH] Genetic Diseases, X-Linked : D040181
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 II Human 436 Genes GS240870: [MeSH] Bone Density : D015519
Expand Tier II Human 3455 Genes GS239907: [MeSH] Cell Surface Extensions : D022081
Expand Tier I Mouse MP 742 Genes GS165992: MP:0008469 abnormal protein level
Expand Tier II Human 14581 Genes GS241611: [MeSH] Organic Chemistry Processes : D055602
Expand Tier II Human 345 Genes GS236984: [MeSH] Acids, Noncarboxylic : D000148
Expand Tier II Human 158 Genes GS238624: [MeSH] Hydroxycholecalciferols : D006887
Expand Tier I Mouse MP 12 Genes GS165680: MP:0004380 short frontal bone
Expand Tier II Human 3920 Genes GS236691: [MeSH] Metals, Alkaline Earth : D008673
Expand Tier I Human 209 Genes GS229834: MSigDB Geneset - V$FOX_Q2
Expand Tier II Human 172 Genes GS243778: [MeSH] S100 Calcium Binding Protein G : D064030
Expand Tier I Human 234 Genes GS232076: PC Geneset - "V$HFH1_01" pathway genes
Expand Tier II Human 3419 Genes GS234275: [MeSH] Heterozygote : D006579
Expand Tier II Human 432 Genes GS236659: [MeSH] Codon, Terminator : D018388
Expand Tier II Human 7025 Genes GS239838: [MeSH] Luminescent Proteins : D008164
Expand Tier I Human GO 31 Genes GS205776: GO:0004177 aminopeptidase activity
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier II Human 2660 Genes GS244236: [MeSH] Homozygote : D006720
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 II Human 69 Genes GS243582: [MeSH] Phosphate Transport Proteins : D028061
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 II Human 8197 Genes GS239290: [MeSH] Cell Line, Transformed : D002461
Expand Tier I Human 247 Genes GS227429: MSigDB Geneset - V$TAL1ALPHAE47_01
Expand Tier I Mouse MP 619 Genes GS165194: MP:0001533 abnormal skeleton physiology
Expand Tier I Mouse MP 1246 Genes GS165228: MP:0005382 craniofacial phenotype
Expand Tier I Mouse MP 254 Genes GS170425: MP:0004508 abnormal pectoral girdle bone morphology
Expand Tier II Human 9719 Genes GS244871: [MeSH] Time Factors : D013997
Expand Tier II Human 14842 Genes GS237183: [MeSH] Growth and Development : D048788
Expand Tier II Human 9858 Genes GS242870: [MeSH] Polymorphism, Genetic : D011110
Expand Tier II Mouse 307 Genes GS35867: Striatum Gene expression correlates of Cocaine CPP - difference in percent test time spent relative to preconditioning in Males BXD
Expand Tier I Human 181 Genes GS175907: HP:0004349 Reduced bone mineral density
Expand Tier I Mouse MP 33 Genes GS166039: MP:0005352 small cranium
Expand Tier I Mouse MP 1015 Genes GS166660: MP:0001731 abnormal postnatal growth
Expand Tier II Human 178 Genes GS234375: [MeSH] Calcification, Physiologic : D002113
Expand Tier I Human 1 Genes GS172556: HP:0100686 Enthesitis
Expand Tier I Human GO 4338 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Human 194 Genes GS229147: MSigDB Geneset - GSE29618_MONOCYTE_VS_PDC_DN
Expand Tier I Human 208 Genes GS232566: PC Geneset - "V$FOX_Q2" pathway genes
Expand Tier II Human 284 Genes GS241040: [MeSH] Kidney Failure, Chronic : D007676
Expand Tier I Human 42 Genes GS171878: HP:0002992 Abnormality of the tibia
Expand Tier II Human 516 Genes GS237672: [MeSH] Core Binding Factor alpha Subunits : D050657
Expand Tier I Human CTD 20 Genes GS127274: beta-glycerophosphoric acid interacting genes (MeSH:C031463) in CTD
Expand Tier II Human 2956 Genes GS236925: [MeSH] Hematopoietic System : D006413
Expand Tier II Human 209 Genes GS244007: [MeSH] Secosteroids : D012632
Expand Tier II Human 1521 Genes GS241554: [MeSH] Biogenic Amines : D001679
Expand Tier II Human 12291 Genes GS238872: [MeSH] Central Nervous System : D002490
Expand Tier II Human 399 Genes GS241086: [MeSH] Renal Insufficiency : D051437
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 II Human 12 Genes GS241628: [MeSH] Phosphorus, Dietary : D016226
Expand Tier II Human 2454 Genes GS245143: [MeSH] Monosaccharides : D009005
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 Human 197 Genes GS229960: MSigDB Geneset - GSE29618_BCELL_VS_PDC_DAY7_FLU_VACCINE_DN
Expand Tier II Human 1752 Genes GS240560: [MeSH] Nucleotides, Cyclic : D009712
Expand Tier II Human 7543 Genes GS239550: [MeSH] Apoptosis : D017209
Expand Tier II Human 15855 Genes GS239444: [MeSH] Biological Evolution : D005075
Expand Tier I Mouse MP 3 Genes GS166733: MP:0004699 unilateral deafness
Expand Tier II Human 47 Genes GS235553: [MeSH] Osteocytes : D010011
Expand Tier II Human 1452 Genes GS244582: [MeSH] Cholestenes : D002782
Expand Tier I Mouse MP 63 Genes GS163407: MP:0004019 abnormal vitamin homeostasis
Expand Tier I Mouse MP 25 Genes GS165241: MP:0002966 decreased circulating alkaline phosphatase level
Expand Tier II Human 430 Genes GS240340: [MeSH] Nitroso Compounds : D009603
Expand Tier II Human 56846 Genes GS235305: [MeSH] DNA, Complementary : D018076
Expand Tier II Human 24839 Genes GS237194: [MeSH] Physiological Phenomena : D010829
Expand Tier II Human 8660 Genes GS239079: [MeSH] Cell Membrane : D002462
Expand Tier II Human 6533 Genes GS244610: [MeSH] Nervous System Diseases : D009422
Expand Tier II Human 233 Genes GS245599: [MeSH] Bone Diseases, Metabolic : D001851
Expand Tier II Human 8635 Genes GS239266: [MeSH] Morphogenesis : D009024
Expand Tier I Human 62 Genes GS176804: HP:0001850 Abnormality of the tarsal bones
Expand Tier II Human 67553 Genes GS240572: [MeSH] DNA : D004247
Expand Tier I Mouse MP 61 Genes GS163659: MP:0005272 abnormal temporal bone morphology
Expand Tier I Human 6 Genes GS176130: HP:0003017 Frayed, irregular metaphyses
Expand Tier I Human 401 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Mouse MP 1052 Genes GS166409: MP:0002114 abnormal axial skeleton morphology
Expand Tier II Human 170 Genes GS235132: [MeSH] Cholecalciferol : D002762
Expand Tier I Human GO 3863 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier II Human 65203 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier II Human 1950 Genes GS235382: [MeSH] Transgenes : D019076
Expand Tier I Mouse GO 2565 Genes GS192299: GO:0006793 phosphorus metabolic process
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 II Human 6568 Genes GS235980: [MeSH] Mechanical Phenomena : D055595
Expand Tier II Human 1533 Genes GS243717: [MeSH] Electromagnetic Radiation : D060733
Expand Tier II Human 15724 Genes GS239132: [MeSH] Gene Expression Regulation, Developmental : D018507
Expand Tier II Human 2894 Genes GS240460: [MeSH] Myocardium : D009206
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier II Human 18300 Genes GS238771: [MeSH] Transferases : D014166
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 II Human 100 Genes GS235025: [MeSH] Renal Tubular Transport, Inborn Errors : D015499
Expand Tier I Human 272 Genes GS227620: MSigDB Geneset - V$RFX1_02
Expand Tier I Human 2037 Genes GS228205: MSigDB Geneset - TTGTTT_V$FOXO4_01
Expand Tier II Human 31 Genes GS245978: [MeSH] Phosphorus Metabolism Disorders : D010760
Expand Tier II Human 67130 Genes GS241889: [MeSH] Molecular Structure : D015394
Expand Tier I Human 688 Genes GS232672: PC Geneset - "YTATTTTNR_V$MEF2_02" pathway genes
Expand Tier I Mouse MP 141 Genes GS167807: MP:0000165 abnormal long bone hypertrophic chondrocyte zone
Expand Tier II Human 4568 Genes GS239065: [MeSH] Urinary Tract : D014551
Expand Tier I Mouse MP 108 Genes GS163576: MP:0000202 abnormal circulating alkaline phosphatase level
Expand Tier I Mouse MP 73 Genes GS163848: MP:0001541 abnormal osteoclast physiology
Expand Tier II Human 8187 Genes GS234648: [MeSH] Alleles : D000483
Expand Tier I Mouse MP 21 Genes GS165921: MP:0000091 short premaxilla
Expand Tier II Human 2042 Genes GS235803: [MeSH] Biological Transport, Active : D001693
Expand Tier I Human 214 Genes GS229145: MSigDB Geneset - V$HNF3B_01
Expand Tier II Human 3036 Genes GS241690: [MeSH] Female Urogenital Diseases : D052776
Expand Tier II Human 78 Genes GS244616: [MeSH] Cathepsin B : D002401
Expand Tier I Mouse MP 855 Genes GS169075: MP:0002078 abnormal glucose homeostasis
Expand Tier I Human 134 Genes GS231854: PC Geneset - "V$EVI1_02" pathway genes
Expand Tier II Human 59585 Genes GS234621: [MeSH] Chemical Actions and Uses : D020164
Expand Tier II Human 62071 Genes GS235061: [MeSH] Amino Acids, Peptides, and Proteins : D000602
Expand Tier I Mouse MP 443 Genes GS165877: MP:0002136 abnormal kidney physiology
Expand Tier I Human 719 Genes GS232230: PC Geneset - "TGTTTGY_V$HNF3_Q6" pathway genes
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 II Human 7284 Genes GS236354: [MeSH] Gene Deletion : D017353
Expand Tier I Mouse GO 2190 Genes GS191129: GO:0016787 hydrolase activity
Expand Tier II Human 9312 Genes GS236231: [MeSH] Antigens : D000941
Expand Tier II Human 10296 Genes GS240252: [MeSH] Intercellular Signaling Peptides and Proteins : D036341
Expand Tier I Mouse GO 6473 Genes GS184448: GO:0044425 membrane part
Expand Tier II Human 8099 Genes GS236751: [MeSH] Polymorphism, Single Nucleotide : D020641
Expand Tier II Human 23706 Genes GS235056: [MeSH] Peptides : D010455
Expand Tier II Human 47536 Genes GS236298: [MeSH] Gene Expression : D015870
Expand Tier II Human 15 Genes GS245720: [MeSH] Hydroxyapatites : D006882
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 II Human 3287 Genes GS237404: [MeSH] Chromosomes, Human, 6-12 and X : D002906
Expand Tier III Rat 411 Genes GS224329: Insulin dependent diabetes mellitus QTL 5 (Iddm5 Published QTL Chr X)
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 II Human 36279 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier I Mouse MP 262 Genes GS164346: MP:0006335 abnormal hearing electrophysiology
Expand Tier II Human 397 Genes GS240006: [MeSH] Potassium : D011188
Expand Tier II Human 155 Genes GS237022: [MeSH] Dihydroxycholecalciferols : D004100
Expand Tier II Human 1652 Genes GS237456: [MeSH] Kidney Diseases : D007674
Expand Tier II Human 38809 Genes GS236076: [MeSH] Protein Conformation : D011487
Expand Tier II Human 4298 Genes GS241873: [MeSH] Glycoconjugates : D006001
Expand Tier II Human 3099 Genes GS238210: [MeSH] Steroids : D013256
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Mouse GO 5892 Genes GS180036: GO:0032501 multicellular organismal process
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 II Human 3826 Genes GS236535: [MeSH] Calcium : D002118
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 185 Genes GS227318: MSigDB Geneset - V$HNF3_Q6
Expand Tier I Human 780 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 138 Genes GS174847: HP:0000940 Abnormal diaphysis morphology
Expand Tier I Mouse MP 65 Genes GS168471: MP:0002187 abnormal fibula morphology
Expand Tier II Human 524 Genes GS234076: [MeSH] Core Binding Factors : D050660
Expand Tier II Human 50108 Genes GS239769: [MeSH] Gene Library : D015723
Expand Tier I Mouse MP 2432 Genes GS167542: MP:0001790 abnormal immune system physiology
Expand Tier II Human 14459 Genes GS239072: [MeSH] Recombinant Proteins : D011994
Expand Tier I Mouse MP 3051 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier II Human 29996 Genes GS237597: [MeSH] Cell Physiological Processes : D055648
Expand Tier I Mouse MP 391 Genes GS168851: MP:0002451 abnormal macrophage physiology
Expand Tier II Human 2962 Genes GS245304: [MeSH] Bone Marrow Cells : D001854
Expand Tier II Human 218 Genes GS234558: [MeSH] Creatinine : D003404
Expand Tier I Mouse MP 76 Genes GS169236: MP:0000135 decreased compact bone thickness
Expand Tier II Human 5853 Genes GS241597: [MeSH] Disease Models, Animal : D004195
Expand Tier II Human 1266 Genes GS238927: [MeSH] Noxae : D009676
Expand Tier I Mouse MP 3761 Genes GS165527: MP:0005378 growth/size phenotype
Expand Tier I Mouse MP 68 Genes GS169328: MP:0001666 abnormal intestinal absorption
Expand Tier I Human 190 Genes GS227643: MSigDB Geneset - PIGF_UP.V1_UP
Expand Tier II Human 14819 Genes GS244426: [MeSH] Tumor Cells, Cultured : D014407
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier II Human 7823 Genes GS235095: [MeSH] Digestive System : D004064
Expand Tier I Human 226 Genes GS232592: PC Geneset - "V$GATA1_01" pathway genes
Expand Tier II Human 327 Genes GS239682: [MeSH] Nitrosourea Compounds : D009607
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 II Human 13237 Genes GS241118: [MeSH] Binding Sites : D001665
Expand Tier I Mouse MP 108 Genes GS163412: MP:0004016 decreased bone mass
Expand Tier II Human 18 Genes GS244753: [MeSH] Apatites : D001031
Expand Tier III Mouse 8331 Genes GS128199: Alcohol Preference union of 86 Gene Sets
Expand Tier II Human 12343 Genes GS236576: [MeSH] Promoter Regions, Genetic : D011401
Expand Tier II Human 3054 Genes GS245998: [MeSH] Musculoskeletal Physiological Processes : D043702
Expand Tier II Human 1603 Genes GS236279: [MeSH] Radiation : D011827
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 II Human 792 Genes GS237157: [MeSH] Digestive System and Oral Physiological Phenomena : D055688
Expand Tier II Human 179 Genes GS245999: [MeSH] Evoked Potentials : D005071
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 266 Genes GS232204: PC Geneset - "V$RFX1_02" pathway genes
Expand Tier II Human 555 Genes GS236462: [MeSH] Caspases, Initiator : D053471
Expand Tier II Human 73996 Genes GS244482: [MeSH] Nucleic Acids, Nucleotides, and Nucleosides : D009706
Expand Tier II Human 615 Genes GS234720: [MeSH] Glycopeptides : D006020
Expand Tier I Mouse MP 23 Genes GS163091: MP:0000195 hypocalcemia
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier II Human 9876 Genes GS239522: [MeSH] Growth : D006128
Expand Tier I Human GO 6073 Genes GS201252: GO:0044425 membrane part
Expand Tier II Human 5171 Genes GS245493: [MeSH] Purines : D011687
Expand Tier I Mouse MP 48 Genes GS169144: MP:0004355 short radius
Expand Tier II Human 58105 Genes GS235797: [MeSH] DNA Probes : D015342
Expand Tier II Human 29719 Genes GS237296: [MeSH] RNA, Antisense : D016372
Expand Tier II Human 674 Genes GS237541: [MeSH] Neoplasms, Connective and Soft Tissue : D018204
Expand Tier I Mouse GO 1204 Genes GS188763: GO:0009888 tissue development
Expand Tier I Mouse GO 7644 Genes GS188399: GO:0044238 primary metabolic process
Expand Tier I Mouse MP 256 Genes GS167056: MP:0004686 decreased length of long bones
Expand Tier II Human 2540 Genes GS235825: [MeSH] Oxygenases : D010105
Expand Tier I Human 280 Genes GS228445: MSigDB Geneset - V$TATA_C
Expand Tier II Human 373 Genes GS245482: [MeSH] Acids : D000143
Expand Tier I Mouse MP 14 Genes GS169442: MP:0008158 increased diameter of femur
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 II Human 19354 Genes GS242551: [MeSH] Physiological Processes : D055705
Expand Tier III Mouse 169 Genes GS246692: Age-dependent gene expression changes in lungs of D2 at 18 and 2 months
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier II Human 290 Genes GS245266: [MeSH] Renal Insufficiency, Chronic : D051436
Expand Tier II Human 9473 Genes GS241940: [MeSH] Urogenital System : D014566
Expand Tier I Mouse MP 245 Genes GS165425: MP:0010119 abnormal bone mineral density
Expand Tier II Human 198 Genes GS242503: [MeSH] Osteopontin : D053495
Expand Tier II Human 28877 Genes GS238592: [MeSH] Cells, Cultured : D002478
Expand Tier II Human 749 Genes GS235521: [MeSH] Gastroenteritis : D005759
Expand Tier II Human 3354 Genes GS243507: [MeSH] Heart : D006321
Expand Tier I Mouse MP 94 Genes GS166248: MP:0000088 short mandible
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 II Human 11221 Genes GS237257: [MeSH] Pathologic Processes : D010335
Expand Tier I Human 241 Genes GS231951: PC Geneset - "V$TAL1ALPHAE47_01" pathway genes
Expand Tier I Mouse MP 345 Genes GS166408: MP:0002115 abnormal limb bone morphology
Expand Tier II Human 406 Genes GS239087: [MeSH] S100 Proteins : D009418
Expand Tier I Human 961 Genes GS227285: MSigDB Geneset - CTTTAAR_UNKNOWN
Expand Tier I Mouse GO 571 Genes GS188685: GO:0070011 peptidase activity, acting on L-amino acid peptides
Expand Tier II Human 1465 Genes GS238205: [MeSH] Toxic Actions : D004786
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier II Human 28 Genes GS237548: [MeSH] Hypophosphatemia : D017674
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 II Human 230 Genes GS243948: [MeSH] Phosphoric Acids : D010756
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 II Human 20775 Genes GS245804: [MeSH] Transcription Factors : D014157
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 II Human 23211 Genes GS235538: [MeSH] Protein Binding : D011485
Expand Tier II Human 413 Genes GS243410: [MeSH] Mutagens : D009153
Expand Tier II Human 4360 Genes GS243856: [MeSH] Muscle, Striated : D054792
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier II Human 10133 Genes GS235960: [MeSH] Connective Tissue Cells : D003239
Expand Tier II Human 5399 Genes GS243780: [MeSH] COS Cells : D019556
Expand Tier I Human 143 Genes GS228389: MSigDB Geneset - RAAGNYNNCTTY_UNKNOWN
Expand Tier I Mouse GO 360 Genes GS192965: GO:0004175 endopeptidase activity
Expand Tier II Human 10298 Genes GS238960: [MeSH] Membrane Glycoproteins : D008562
Expand Tier II Human 61 Genes GS239760: [MeSH] Biogenic Polyamines : D015317
Expand Tier I Human 691 Genes GS232110: PC Geneset - "TGCCAAR_V$NF1_Q6" pathway genes
Expand Tier II Human 1763 Genes GS236913: [MeSH] Colonic Diseases : D003108
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 II Human 2555 Genes GS242366: [MeSH] Inheritance Patterns : D040582
Expand Tier I Human 9 Genes GS171002: HP:0003165 Elevated circulating parathyroid hormone (PTH) level
Expand Tier II Human 45 Genes GS237407: [MeSH] Spermidine : D013095
Expand Tier I Mouse MP 83 Genes GS163408: MP:0002968 increased circulating alkaline phosphatase level
Expand Tier II Human 18 Genes GS244275: [MeSH] Hypophosphatemia, Familial : D007015
Expand Tier II Human 3577 Genes GS234895: [MeSH] Zebrafish Proteins : D029961
Expand Tier II Human 87 Genes GS238862: [MeSH] Evoked Potentials, Auditory : D005072
Expand Tier II Human 650 Genes GS243363: [MeSH] Polymorphism, Single-Stranded Conformational : D018807
Expand Tier I Human 138 Genes GS227140: MSigDB Geneset - chrxp22
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier II Human 13218 Genes GS245439: [MeSH] Protein Kinases : D011494
Expand Tier III Mouse 8151 Genes GS213076: Genes with suggestive difference in (B6) vs (B6PF1 + PB6F1 + PWD) comparison
Expand Tier II Human 3143 Genes GS234697: [MeSH] Tumor Markers, Biological : D014408
Expand Tier II Human 58766 Genes GS243866: [MeSH] Laboratory Chemicals : D019995
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 II Human 2758 Genes GS242618: [MeSH] Apoptosis Regulatory Proteins : D051017
Expand Tier I Human 12202 Genes GS232685: PC Geneset - "Homo sapiens" pathway genes
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 III Mouse 169 Genes GS246690: Age-dependent gene expression changes in lungs of B6 at 18 and 2 months,
Expand Tier I Human GO 100 Genes GS203109: GO:0008238 exopeptidase activity
Expand Tier II Human 2460 Genes GS245677: [MeSH] X Chromosome : D014960
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 II Human 425 Genes GS237688: [MeSH] Cathepsins : D002403
Expand Tier I Mouse MP 11449 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier II Human 23476 Genes GS237836: [MeSH] Carrier Proteins : D002352
Expand Tier II Human 37 Genes GS239300: [MeSH] Spermine : D013096
Expand Tier II Human 959 Genes GS239375: [MeSH] Osteoblasts : D010006
Expand Tier II Human 5168 Genes GS244578: [MeSH] Liver : D008099
Expand Tier II Human 5087 Genes GS234776: [MeSH] Endocrine System : D004703
Expand Tier II Human 2037 Genes GS237303: [MeSH] Mutation, Missense : D020125
Expand Tier II Human 235 Genes GS240932: [MeSH] Chromosomes, Human, X : D041321
Expand Tier II Human 16221 Genes GS239275: [MeSH] Intracellular Signaling Peptides and Proteins : D047908
Expand Tier II Human 58901 Genes GS243233: [MeSH] Specialty Uses of Chemicals : D020313
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 II Human 47 Genes GS240950: [MeSH] Sodium-Phosphate Cotransporter Proteins : D050608
Expand Tier II Human 26 Genes GS245174: [MeSH] Dental Physiological Processes : D055690
Expand Tier II Human 289 Genes GS243183: [MeSH] Hearing Loss : D034381
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 II Human 118 Genes GS245753: [MeSH] Gluconeogenesis : D005943
Expand Tier I Human GO 4575 Genes GS204007: GO:0044700 single organism signaling
Expand Tier II Human 3712 Genes GS235130: [MeSH] Gene Expression Regulation, Enzymologic : D015971
Expand Tier II Human 2584 Genes GS235299: [MeSH] Physical Processes : D055586
Expand Tier II Human 8204 Genes GS235729: [MeSH] Membrane Transport Proteins : D026901
Expand Tier II Human 1429 Genes GS236780: [MeSH] Musculoskeletal Development : D041641
Expand Tier II Human 66 Genes GS237154: [MeSH] Odontoblasts : D009804
Expand Tier II Human 4573 Genes GS243554: [MeSH] Nervous System Physiological Phenomena : D009424
Expand Tier II Human 294 Genes GS234810: [MeSH] Polyamines : D011073
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 1073 Genes GS228914: MSigDB Geneset - RYTTCCTG_V$ETS2_B
Expand Tier II Human 2569 Genes GS235802: [MeSH] Homeostasis : D006706
Expand Tier II Human 13 Genes GS243213: [MeSH] Rickets, Hypophosphatemic : D063730
Expand Tier II Human 2584 Genes GS241649: [MeSH] Tumor Necrosis Factor-alpha : D014409
Expand Tier I Mouse MP 112 Genes GS163333: MP:0004231 abnormal calcium ion homeostasis
Expand Tier II Human 2732 Genes GS239261: [MeSH] Calcium-Binding Proteins : D002135
Expand Tier II Human 65 Genes GS239586: [MeSH] Neprilysin : D015260
Expand Tier II Human 36882 Genes GS236241: [MeSH] Protein Structure, Tertiary : D017434
Expand Tier II Human 6413 Genes GS235807: [MeSH] Cytokines : D016207
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 II Human 535 Genes GS234717: [MeSH] Neoplasms, Connective Tissue : D009372
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 II Human 238 Genes GS234045: [MeSH] Phosphorus Acids : D017976
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 II Human 172 Genes GS239403: [MeSH] Calbindins : D064026
Expand Tier II Human 1185 Genes GS241590: [MeSH] Extracellular Matrix : D005109
Expand Tier I Human 19 Genes GS172642: HP:0002982 Tibial bowing
Expand Tier II Human 20 Genes GS236080: [MeSH] Sodium-Phosphate Cotransporter Proteins, Type III : D050611
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 II Human 1935 Genes GS237129: [MeSH] Glycoside Hydrolases : D006026
Expand Tier II Human 438 Genes GS242426: [MeSH] Dentition : D003817
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 II Human 21049 Genes GS244735: [MeSH] Mutagenesis : D016296
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 II Human 45 Genes GS234309: [MeSH] Dentin : D003804
Expand Tier II Human 186 Genes GS238066: [MeSH] Femur : D005269
Expand Tier I Mouse MP 85 Genes GS167643: MP:0000034 abnormal vestibule morphology
Expand Tier II Human 7492 Genes GS234348: [MeSH] Inorganic Chemicals : D007287
Expand Tier I Mouse MP 72 Genes GS163751: MP:0004540 small maxilla
Expand Tier II Human 7137 Genes GS234179: [MeSH] DNA, Intergenic : D021901
Expand Tier I Human 21 Genes GS172605: HP:0000124 Renal tubular dysfunction
Expand Tier II Human 5015 Genes GS240747: [MeSH] Endocrine Glands : D004702
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 II Human 8998 Genes GS240602: [MeSH] Biological Markers : D015415
Expand Tier II Human 521 Genes GS234903: [MeSH] Adaptation, Biological : D000220
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier II Human 4779 Genes GS245543: [MeSH] Receptors, Peptide : D018000
Expand Tier II Human 2342 Genes GS241507: [MeSH] Mixed Function Oxygenases : D006899
Expand Tier I Human 2 Genes GS175049: HP:0006285 Hypomineralization of enamel
Expand Tier II Human 153 Genes GS235166: [MeSH] Duodenum : D004386
Expand Tier II Human 9229 Genes GS243125: [MeSH] Organic Chemicals : D009930
Expand Tier II Human 7595 Genes GS245839: [MeSH] Cell Division : D002455
Expand Tier I Mouse GO 108 Genes GS186422: GO:0031214 biomineral tissue development
Expand Tier II Human 5871 Genes GS237484: [MeSH] Congenital, Hereditary, and Neonatal Diseases and Abnormalities : D009358
Expand Tier II Human 1545 Genes GS242097: [MeSH] Fibroblast Growth Factors : D005346
Expand Tier II Human 694 Genes GS239867: [MeSH] Symporters : D027981
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 II Human 73356 Genes GS238415: [MeSH] Genome Components : D040481
Expand Tier II Human 6285 Genes GS244045: [MeSH] Molecular Mechanisms of Pharmacological Action : D045504
Expand Tier I Human 837 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier II Human 2449 Genes GS244720: [MeSH] Cysteine Proteases : D057056
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 II Human 39556 Genes GS238930: [MeSH] Molecular Conformation : D008968
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 II Human 58262 Genes GS240750: [MeSH] Molecular Probes : D015335
Expand Tier I Mouse MP 510 Genes GS166404: MP:0002113 abnormal skeleton development
Expand Tier II Human 528 Genes GS240062: [MeSH] Nutrition Processes : D052796
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 687 Genes GS227437: MSigDB Geneset - YTATTTTNR_V$MEF2_02
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 II Human 846 Genes GS238360: [MeSH] Lower Gastrointestinal Tract : D041741
Expand Tier II Human 4244 Genes GS234130: [MeSH] Genetic Diseases, Inborn : D030342
Expand Tier II Human 9423 Genes GS239448: [MeSH] Heterocyclic Compounds : D006571
Expand Tier II Human 3824 Genes GS236425: [MeSH] Signs and Symptoms : D012816
Expand Tier I Human 83 Genes GS172024: HP:0001369 Arthritis
Expand Tier II Human 301 Genes GS244354: [MeSH] Tooth : D014070
Expand Tier II Human 5901 Genes GS239964: [MeSH] Lipids : D008055
Expand Tier II Human 4107 Genes GS234842: [MeSH] Peptide Fragments : D010446
Expand Tier I Mouse MP 282 Genes GS169967: MP:0001408 stereotypic behavior
Expand Tier II Human 1030 Genes GS242703: [MeSH] Ploidies : D011003
Expand Tier II Human 1273 Genes GS241348: [MeSH] Cytochrome P-450 Enzyme System : D003577
Expand Tier II Human 288 Genes GS235191: [MeSH] Y Chromosome : D014998
Expand Tier II Human 2795 Genes GS245892: [MeSH] Musculoskeletal Diseases : D009140
Expand Tier II Human 55514 Genes GS238409: [MeSH] Gene Components : D040461
Expand Tier I Mouse MP 1093 Genes GS165536: MP:0005371 limbs/digits/tail phenotype
Expand Tier II Human 2871 Genes GS236551: [MeSH] Aging : D000375
Expand Tier II Human 774 Genes GS239224: [MeSH] Metals, Alkali : D008672
Expand Tier II Human 8626 Genes GS243166: [MeSH] Pharmacologic Actions : D020228
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