Gene Details



SHOX and homologs in 2 species are found in 232 GeneSets:


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

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Human 387 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Human 1 Genes GS173472: HP:0006436 Shortening of the tibia
Expand Tier I Human 131 Genes GS175744: HP:0001231 Abnormality of the fingernails
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 30 Genes GS173982: HP:0001454 Abnormality of the upper arm
Expand Tier I Human 60 Genes GS174088: HP:0003366 Abnormality of the femoral neck and head region
Expand Tier I Human 179 Genes GS174214: HP:0009466 Radial deviation of finger
Expand Tier I Human GO 3737 Genes GS194038: GO:1901362 organic cyclic compound biosynthetic process
Expand Tier I Human 15 Genes GS171103: HP:0006492 Aplasia/Hypoplasia of the fibula
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 34 Genes GS172194: HP:0002970 Genu varum
Expand Tier I Human 16 Genes GS175109: HP:0003956 Bowed forearm bones
Expand Tier I Human GO 2332 Genes GS195643: GO:0003677 DNA binding
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 GO 5152 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human GO 5216 Genes GS208954: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human 175 Genes GS174377: HP:0005927 Aplasia/Hypoplasia involving bones of the hand
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 22 Genes GS171098: HP:0006498 Aplasia/Hypoplasia of the patella
Expand Tier I Human GO 336 Genes GS196532: GO:0000975 regulatory region DNA binding
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 23 Genes GS174211: HP:0009465 Ulnar deviation of finger
Expand Tier I Human 56 Genes GS175733: HP:0010049 Short metacarpal
Expand Tier I Human 21 Genes GS172117: HP:0002984 Hypoplasia of the radius
Expand Tier I Human 77 Genes GS172300: HP:0001991 Aplasia/Hypoplasia of the toes
Expand Tier I Human 282 Genes GS175900: HP:0009118 Aplasia/Hypoplasia of the mandible
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human 212 Genes GS174189: HP:0001597 Abnormality of the nail
Expand Tier I Human 5 Genes GS174277: HP:0010042 Aplasia/Hypoplasia of the 4th metacarpal
Expand Tier I Human 2 Genes GS171294: HP:0006248 Limited wrist movement
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human 186 Genes GS173740: HP:0009485 Radial deviation of the hand or of fingers of the hand
Expand Tier I Human 124 Genes GS171102: HP:0006493 Aplasia/Hypoplasia involving bones of the lower limbs
Expand Tier I Human 579 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human 203 Genes GS175802: HP:0003272 Abnormality of the hip bone
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 599 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human 553 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human 156 Genes GS174002: HP:0000189 Narrow palate
Expand Tier I Human 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 67 Genes GS172588: HP:0001831 Short toe
Expand Tier I Human 1 Genes GS176448: HP:0006459 Dorsal subluxation of ulna
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 GO 5452 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
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 150 Genes GS174586: HP:0005930 Abnormality of the epiphyses
Expand Tier I Human 68 Genes GS173148: HP:0003712 Muscle hypertrophy
Expand Tier I Human 398 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human 1 Genes GS176520: HP:0008845 Mesomelic short stature
Expand Tier I Human 41 Genes GS173378: HP:0002758 Osteoarthritis
Expand Tier I Human 2 Genes GS174079: HP:0002762 Multiple exostoses
Expand Tier I Human 11 Genes GS172115: HP:0002986 Radial bowing
Expand Tier I Human 21 Genes GS175859: HP:0006443 Patellar aplasia
Expand Tier I Human GO 5400 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Human 31 Genes GS171877: HP:0002991 Abnormality of the fibula
Expand Tier I Human 46 Genes GS175084: HP:0008384 Aplastic/hypoplastic fingernail
Expand Tier I Human 5 Genes GS172291: HP:0003067 Madelung deformity
Expand Tier I Human 263 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier I Human GO 5948 Genes GS195199: GO:0005634 nucleus
Expand Tier I Human 43 Genes GS176332: HP:0008873 Disproportionate short-limb short stature
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 282 Genes GS172572: HP:0000347 Micrognathia
Expand Tier I Human 446 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier I Human GO 4070 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human GO 4446 Genes GS203072: GO:0090304 nucleic acid metabolic process
Expand Tier I Human 146 Genes GS170968: HP:0000156 High-arched palate
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 80 Genes GS175083: HP:0008386 Aplasia/Hypoplasia of the nails
Expand Tier I Human 360 Genes GS172701: HP:0002650 Scoliosis
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 58 Genes GS171822: HP:0000112 Nephropathy
Expand Tier I Human GO 328 Genes GS202371: GO:0044212 transcription regulatory region DNA binding
Expand Tier I Human GO 4024 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human GO 1006 Genes GS195678: GO:0003700 sequence-specific DNA binding transcription factor activity
Expand Tier I Human 150 Genes GS175074: HP:0001156 Brachydactyly syndrome
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human 337 Genes GS174076: HP:0009122 Aplasia/Hypoplasia affecting bones of the axial skeleton
Expand Tier I Human GO 336 Genes GS208604: GO:0001067 regulatory region nucleic acid binding
Expand Tier I Human 786 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 639 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human 30 Genes GS176474: HP:0009821 Hypoplasia involving forearm bones
Expand Tier I Human 263 Genes GS176692: HP:0009815 Aplasia/Hypoplasia of the extremities
Expand Tier I Human 245 Genes GS176694: HP:0009810 Abnormality of the joints of the upper limbs
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 69 Genes GS172585: HP:0001832 Abnormality of the metatarsal bones
Expand Tier I Human 490 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Human 426 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Human 212 Genes GS171106: HP:0006496 Aplasia/Hypoplasia involving bones of the upper limbs
Expand Tier I Human GO 5223 Genes GS207857: GO:0009058 biosynthetic process
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 8 Genes GS175564: HP:0003027 Mesomelia
Expand Tier I Human 186 Genes GS171144: HP:0005280 Depressed nasal bridge
Expand Tier I Human 150 Genes GS176233: HP:0004209 Clinodactyly of the 5th finger
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
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 56 Genes GS176473: HP:0003498 Disproportionate short stature
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human CTD 228 Genes GS127198: Carmustine interacting genes (MeSH:D002330) in CTD
Expand Tier I Human 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 435 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
Expand Tier I 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 68 Genes GS172110: HP:0002983 Micromelia
Expand Tier I Human GO 3201 Genes GS204204: GO:0006351 transcription, DNA-dependent
Expand Tier I Human 118 Genes GS174314: HP:0002973 Abnormality of the forearm
Expand Tier I Human 53 Genes GS171286: HP:0002996 Limited elbow movement
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 84 Genes GS172316: HP:0003026 Short long bones
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 35 Genes GS173309: HP:0002938 Lumbar hyperlordosis
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 4169 Genes GS207925: GO:0034645 cellular macromolecule biosynthetic process
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 5379 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Human 19 Genes GS172642: HP:0002982 Tibial bowing
Expand Tier I Human 17 Genes GS170886: HP:0006488 Bowing of the arm
Expand Tier I Human GO 3513 Genes GS193991: GO:0048731 system development
Expand Tier I Human 20 Genes GS172151: HP:0002673 Coxa valga
Expand Tier I Human 302 Genes GS176029: HP:0009116 Aplasia/Hypoplasia involving bones of the skull
Expand Tier I Human GO 3626 Genes GS198456: GO:0019438 aromatic compound biosynthetic process
Expand Tier I Human GO 3917 Genes GS203908: GO:0016070 RNA metabolic process
Expand Tier I Human GO 5601 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Human 50 Genes GS174380: HP:0010624 Aplastic/hypoplastic toenails
Expand Tier I Human 14 Genes GS176201: HP:0100777 Exostoses
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 360 Genes GS174099: HP:0011793 Neoplasm by anatomical site
Expand Tier I Human 62 Genes GS174139: HP:0005914 Aplasia/Hypoplasia involving the metacarpal bones
Expand Tier I Human 38 Genes GS172268: HP:0001193 Ulnar deviation of the hand or of fingers of the hand
Expand Tier I Human 7 Genes GS173432: HP:0010012 Abnormality of the 4th metacarpal
Expand Tier I Human 123 Genes GS176695: HP:0009811 Abnormality of the elbow
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 GO 5558 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human 486 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human 189 Genes GS172253: HP:0001376 Limitation of joint mobility
Expand Tier I Human GO 3310 Genes GS194088: GO:0003676 nucleic acid binding
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 GS173924: HP:0004986 Rudimentary to absent fibulae
Expand Tier I Human 118 Genes GS172076: HP:0001163 Abnormality of the metacarpal bones
Expand Tier I Human 1 Genes GS175145: HP:0100745 Abnormality of the humeroulnar joint
Expand Tier I Human 10 Genes GS173531: HP:0005772 Aplasia/Hypoplasia of the tibia
Expand Tier I Human 20 Genes GS175698: HP:0003022 Hypoplasia of the ulna
Expand Tier I Human GO 3287 Genes GS205266: GO:0032774 RNA biosynthetic process
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human 47 Genes GS174089: HP:0003367 Abnormality of the femoral neck
Expand Tier I Human 86 Genes GS175086: HP:0008388 Abnormality of the toenails
Expand Tier I Human 202 Genes GS176242: HP:0004207 Abnormality of the 5th finger
Expand Tier I Human 1 Genes GS173236: HP:0003102 Increased carrying angle
Expand Tier I Human 224 Genes GS175459: HP:0009484 Deviation of the hand or of fingers of the hand
Expand Tier I Human 913 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human 112 Genes GS176480: HP:0009826 Hypoplasia involving bones of the extremities
Expand Tier I Human 1 Genes GS171181: HP:0006381 Rudimentary fibula
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 55 Genes GS172140: HP:0002857 Genu valgum
Expand Tier I Human 50 Genes GS172266: HP:0001191 Abnormality of the carpal bones
Expand Tier I Human GO 5962 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human 397 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human 15 Genes GS172482: HP:0003032 Short femoral neck
Expand Tier I Human GO 7311 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human GO 5047 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Tier I Human 83 Genes GS171875: HP:0002997 Abnormality of the ulna
Expand Tier I Human 26 Genes GS176818: HP:0010622 Neoplasm of the skeletal system
Expand Tier I Human 202 Genes GS171413: HP:0004097 Deviation of finger
Expand Tier I Human 737 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human 150 Genes GS175149: HP:0009179 Deviation of the 5th finger
Expand Tier I Human 456 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Human GO 3573 Genes GS203607: GO:0034654 nucleobase-containing compound biosynthetic process
Expand Tier I Human GO 3640 Genes GS206953: GO:0018130 heterocycle biosynthetic process
Expand Tier I Human 103 Genes GS171478: HP:0002818 Abnormality of the radius
Expand Tier I Human 63 Genes GS175660: HP:0006501 Aplasia/Hypoplasia of the radius
Expand Tier I Human 5 Genes GS175975: HP:0010044 Short 4th metacarpal
Expand Tier I Human 159 Genes GS176900: HP:0000218 High palate
Expand Tier I Human 53 Genes GS172644: HP:0002981 Abnormality of the calf
Expand Tier I Human 76 Genes GS176150: HP:0003019 Abnormality of the wrist
Expand Tier I Human 49 Genes GS176729: HP:0003042 Elbow dislocation
Expand Tier I Human GO 3721 Genes GS194499: GO:0044271 cellular nitrogen compound biosynthetic process
Expand Tier I Human GO 143 Genes GS196530: GO:0000976 transcription regulatory region sequence-specific DNA binding
Expand Tier I Human 83 Genes GS172024: HP:0001369 Arthritis
Expand Tier I Human 9 Genes GS172493: HP:0003038 Fibular hypoplasia
Expand Tier I Human 10 Genes GS173229: HP:0005736 Hypoplastic tibia
Expand Tier I Human 94 Genes GS171105: HP:0006494 Aplasia/Hypoplasia involving bones of the feet
Expand Tier I Human 397 Genes GS171067: HP:0002664 Neoplasm
Expand Tier I Human 71 Genes GS175658: HP:0006503 Aplasia/Hypoplasia involving forearm bones
Expand Tier I Human GO 680 Genes GS196540: GO:0043565 sequence-specific DNA binding
Expand Tier I Human 348 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier I Human 9 Genes GS171876: HP:0002990 Fibular aplasia
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 78 Genes GS172684: HP:0003307 Hyperlordosis
Expand Tier I Human 24 Genes GS171104: HP:0006495 Aplasia/Hypoplasia of the ulna
Expand Tier I Human 319 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Human GO 1008 Genes GS204232: GO:0001071 nucleic acid binding transcription factor activity
Expand Tier I Human GO 4276 Genes GS207858: GO:0009059 macromolecule biosynthetic process
Expand Tier I Human 397 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 41 Genes GS174482: HP:0010579 Cone-shaped epiphysis
Expand Tier I Human 30 Genes GS176012: HP:0003045 Abnormality of the patella
Expand Tier I Human 518 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human GO 5369 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier I Human 489 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human 567 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human 289 Genes GS173167: HP:0100491 Abnormality of the joints of the lower limbs
Expand Tier I Human 126 Genes GS170894: HP:0006487 Bowing of the long bones
Expand Tier I Human 211 Genes GS175164: HP:0011927 Short digit
Expand Tier I Human 601 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human GO 4567 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human 29 Genes GS176426: HP:0003063 Abnormality of the humerus
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human GO 1393 Genes GS193937: GO:0006366 transcription from RNA polymerase II promoter
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 530 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human GO 4713 Genes GS205364: GO:0010467 gene expression