Gene Details



PHEX and homologs in 1 species are found in 190 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 601 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 174 Genes GS173901: HP:0002007 Frontal bossing
Expand Tier I Human GO 4567 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human 62 Genes GS176804: HP:0001850 Abnormality of the tarsal bones
Expand Tier I Human 281 Genes GS171204: HP:0011314 Abnormality of long bone morphology
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human 6 Genes GS176130: HP:0003017 Frayed, irregular metaphyses
Expand Tier I Human GO 386 Genes GS207498: GO:0001501 skeletal system development
Expand Tier I Human 403 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 34 Genes GS171863: HP:0008365 Abnormality of the talus
Expand Tier I Human GO 6769 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human CTD 429 Genes GS126896: Methylcholanthrene interacting genes (MeSH:D008748) in CTD
Expand Tier I Human CTD 74 Genes GS127132: Phosphorus interacting genes (MeSH:D010758) in CTD
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human GO 1439 Genes GS205623: GO:0009888 tissue development
Expand Tier I Human 34 Genes GS172194: HP:0002970 Genu varum
Expand Tier I Human GO 3885 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier I Human 558 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 6 Genes GS175503: HP:0010502 Fibular bowing
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 23 Genes GS170891: HP:0006480 Premature loss of teeth
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human CTD 57 Genes GS126599: Aluminum Oxide interacting genes (MeSH:D000537) in CTD
Expand Tier I Human GO 1914 Genes GS198782: GO:0044459 plasma membrane part
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human 26 Genes GS173861: HP:0002148 Hypophosphatemia
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
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 375 Genes GS209907: GO:0004175 endopeptidase activity
Expand Tier I Human GO 9213 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 Human 79 Genes GS173387: HP:0002757 Recurrent fractures
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 96 Genes GS174308: HP:0002979 Bowing of the legs
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 599 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human 166 Genes GS171901: HP:0010985 Gonosomal inheritance
Expand Tier I Human GO 5436 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human CTD 866 Genes GS126764: Calcitriol interacting genes (MeSH:D002117) in CTD
Expand Tier I Human 154 Genes GS174979: HP:0011061 Abnormality of dental structure
Expand Tier I Human 6 Genes GS171774: HP:0004912 Hypophosphatemic rickets
Expand Tier I Human 324 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Human CTD 91 Genes GS124279: alachlor interacting genes (MeSH:C000188) in CTD
Expand Tier I Human 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 15 Genes GS174575: HP:0100530 Abnormality of calcium-phosphate metabolism
Expand Tier I Human GO 5320 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human 322 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier I Human 1 Genes GS171798: HP:0008144 Flattening of the talar dome
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 126 Genes GS175665: HP:0006504 Abnormality involving the diaphyses of the limbs
Expand Tier I Human 232 Genes GS170999: HP:0000082 Abnormality of renal physiology
Expand Tier I Human GO 2464 Genes GS199032: GO:0036211 protein modification process
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 55 Genes GS171298: HP:0002829 Arthralgia
Expand Tier I Human 266 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 19 Genes GS172113: HP:0002980 Femoral bowing
Expand Tier I Human 27 Genes GS171442: HP:0003155 Elevated alkaline phosphatase
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 Human 117 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 GO 2558 Genes GS194336: GO:0043412 macromolecule modification
Expand Tier I Human 31 Genes GS171610: HP:0004379 Abnormality of alkaline phosphatase activity
Expand Tier I Human GO 1262 Genes GS199199: GO:0031226 intrinsic to plasma membrane
Expand Tier I Human 379 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human 246 Genes GS176806: HP:0003812 Phenotypic variability
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 5810 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human GO 1099 Genes GS195083: GO:0007267 cell-cell signaling
Expand Tier I Human GO 113 Genes GS203267: GO:0031214 biomineral tissue development
Expand Tier I Human GO 4070 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 108 Genes GS171228: HP:0002823 Abnormality of the femur
Expand Tier I Human 132 Genes GS173792: HP:0002815 Abnormality of the knees
Expand Tier I Human 941 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 27 Genes GS175974: HP:0004493 Craniofacial hyperostosis
Expand Tier I Human GO 101 Genes GS203109: GO:0008238 exopeptidase activity
Expand Tier I Human GO 4024 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human 551 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human 1 Genes GS173468: HP:0006432 Trapezoidal distal femoral condyles
Expand Tier I Human 8 Genes GS173609: HP:0002749 Osteomalacia
Expand Tier I Human 44 Genes GS174662: HP:0001423 X-linked dominant inheritance
Expand Tier I Human 786 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human GO 6151 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 518 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human GO 4034 Genes GS208978: GO:0043169 cation binding
Expand Tier I Human 391 Genes GS175537: HP:0011277 Abnormality of the urinary system physiology
Expand Tier I Human GO 4283 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Human 489 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human 36 Genes GS172652: HP:0100529 Abnormality of phosphate homeostasis
Expand Tier I Human 117 Genes GS172364: HP:0003111 Abnormality of ion homeostasis
Expand Tier III Human 2178 Genes GS222813: The Drugable Gene Interaction Database
Expand Tier I Human 39 Genes GS174178: HP:0100774 Hyperostosis
Expand Tier I Human 514 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human GO 5321 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human 25 Genes GS172554: HP:0100685 Abnormality of Sharpey fibers
Expand Tier I Human 289 Genes GS173167: HP:0100491 Abnormality of the joints of the lower limbs
Expand Tier I Human 98 Genes GS174851: HP:0000944 Abnormality of the metaphyses
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 1218 Genes GS197008: GO:0005887 integral to plasma membrane
Expand Tier I Human GO 4593 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Human 578 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human GO 3254 Genes GS200602: GO:0044267 cellular protein metabolic process
Expand Tier I Human GO 948 Genes GS199468: GO:0006508 proteolysis
Expand Tier I Human GO 1178 Genes GS201075: GO:0005794 Golgi apparatus
Expand Tier I Human 126 Genes GS170894: HP:0006487 Bowing of the long bones
Expand Tier I Human 14 Genes GS173610: HP:0002748 Rickets
Expand Tier I Human 18 Genes GS175565: HP:0003025 Irregular metaphyses
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 32 Genes GS172698: HP:0002653 Bone pain
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human GO 2464 Genes GS196595: GO:0006464 cellular protein modification process
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human 141 Genes GS174847: HP:0000940 Abnormal diaphysis morphology
Expand Tier I Human 102 Genes GS172692: HP:0002659 Increased susceptibility to fractures
Expand Tier I Human 1 Genes GS172531: HP:0008117 Shortening of the talar neck
Expand Tier I Human GO 180 Genes GS199022: GO:0008237 metallopeptidase activity
Expand Tier I Human GO 6651 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 11 Genes GS176908: HP:0002176 Spinal cord compression
Expand Tier I Human GO 32 Genes GS205776: GO:0004177 aminopeptidase activity
Expand Tier I Human CTD 217 Genes GS123274: 2,4-diaminotoluene interacting genes (MeSH:C010914) in CTD
Expand Tier I Human CTD 6 Genes GS126372: Foscarnet interacting genes (MeSH:D017245) in CTD
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human CTD 209 Genes GS124951: Atrazine interacting genes (MeSH:D001280) in CTD
Expand Tier I Human GO 558 Genes GS205544: GO:0070011 peptidase activity, acting on L-amino acid peptides
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human 174 Genes GS171148: HP:0011218 Abnormal shape of the frontal region
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human 19 Genes GS172642: HP:0002982 Tibial bowing
Expand Tier I Human GO 3513 Genes GS193991: GO:0048731 system development
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human GO 580 Genes GS199006: GO:0008233 peptidase activity
Expand Tier I Human GO 468 Genes GS209583: GO:0048471 perinuclear region of cytoplasm
Expand Tier I Human 32 Genes GS176916: HP:0004437 Cranial hyperostosis
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human 240 Genes GS172433: HP:0002644 Abnormality of pelvic girdle bone morphology
Expand Tier I Human 21 Genes GS172605: HP:0000124 Renal tubular dysfunction
Expand Tier I Human CTD 6 Genes GS125438: Levamisole interacting genes (MeSH:D007978) in CTD
Expand Tier I Human GO 4593 Genes GS206355: GO:0023052 signaling
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human 2 Genes GS175049: HP:0006285 Hypomineralization of enamel
Expand Tier I Human 184 Genes GS175907: HP:0004349 Reduced bone mineral density
Expand Tier I Human GO 2353 Genes GS208037: GO:0016787 hydrolase activity
Expand Tier I Human GO 3934 Genes GS198323: GO:0046872 metal ion binding
Expand Tier I Human CTD 44 Genes GS121416: Phosphorus, Dietary interacting genes (MeSH:D016226) in CTD
Expand Tier I Human 268 Genes GS172365: HP:0003110 Abnormality of urine homeostasis
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human GO 4719 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 1 Genes GS172556: HP:0100686 Enthesitis
Expand Tier I Human GO 4371 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human 43 Genes GS171878: HP:0002992 Abnormality of the tibia
Expand Tier I Human GO 7311 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human CTD 20 Genes GS127274: beta-glycerophosphoric acid interacting genes (MeSH:C031463) in CTD
Expand Tier I Human GO 1998 Genes GS203688: GO:0008270 zinc ion binding
Expand Tier I Human 737 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human 14 Genes GS171557: HP:0003416 Spinal canal stenosis
Expand Tier I Human GO 105 Genes GS199822: GO:0004222 metalloendopeptidase activity
Expand Tier I Human CTD 105 Genes GS124172: Arsenates interacting genes (MeSH:D001149) in CTD
Expand Tier I Human GO 2241 Genes GS209291: GO:0046914 transition metal ion binding
Expand Tier I Human GO 2545 Genes GS203335: GO:0048513 organ development
Expand Tier I Human 53 Genes GS172644: HP:0002981 Abnormality of the calf
Expand Tier I Human 83 Genes GS172024: HP:0001369 Arthritis
Expand Tier I Human 246 Genes GS175909: HP:0004348 Abnormality of bone mineral density
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 89 Genes GS173329: HP:0000682 Abnormality of dental enamel
Expand Tier I Human GO 8702 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 990 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human 160 Genes GS175806: HP:0001417 X-linked inheritance
Expand Tier I Human GO 1281 Genes GS196726: GO:0005783 endoplasmic reticulum
Expand Tier I Human 319 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part