Gene Details



ADAMTS10 and homologs in 1 species are found in 165 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 598 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 123 Genes GS175583: HP:0010438 Abnormality of the ventricular septum
Expand Tier I Human 385 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human GO 2112 Genes GS210214: GO:0005576 extracellular region
Expand Tier I Human GO 8 Genes GS209921: GO:0001527 microfibril
Expand Tier I Human 401 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 877 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 102 Genes GS173507: HP:0000520 Proptosis
Expand Tier I Human GO 3863 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier I Human 554 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 411 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human 31 Genes GS171295: HP:0003508 Proportionate short stature
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 76 Genes GS172300: HP:0001991 Aplasia/Hypoplasia of the toes
Expand Tier I Human 141 Genes GS174721: HP:0000772 Abnormality of the ribs
Expand Tier I Human 68 Genes GS176574: HP:0008062 Aplasia/Hypoplasia affecting the anterior segment of the eye
Expand Tier I Human GO 370 Genes GS209907: GO:0004175 endopeptidase activity
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human 123 Genes GS171102: HP:0006493 Aplasia/Hypoplasia involving bones of the lower limbs
Expand Tier I Human 99 Genes GS173687: HP:0001643 Patent ductus arteriosus
Expand Tier I Human 169 Genes GS173988: HP:0000501 Glaucoma
Expand Tier I Human 17 Genes GS173461: HP:0001650 Aortic valve stenosis
Expand Tier I Human 576 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 112 Genes GS173465: HP:0001654 Abnormality of the heart valves
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 550 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human GO 361 Genes GS210217: GO:0005578 proteinaceous extracellular matrix
Expand Tier I Human GO 186 Genes GS201254: GO:0044420 extracellular matrix part
Expand Tier I Human 90 Genes GS170889: HP:0006482 Abnormality of dental morphology
Expand Tier I Human 156 Genes GS174002: HP:0000189 Narrow palate
Expand Tier I Human 641 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 66 Genes GS172588: HP:0001831 Short toe
Expand Tier I Human 318 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier I Human 17 Genes GS174141: HP:0005916 Abnormal metacarpal morphology
Expand Tier I Human 18 Genes GS171852: HP:0000593 Abnormality of the anterior chamber
Expand Tier I Human 486 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human 395 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human 12 Genes GS170954: HP:0000885 Broad ribs
Expand Tier I Human 262 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier I Human 375 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 169 Genes GS171752: HP:0001713 Abnormality of cardiac ventricle
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 444 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier I Human GO 5764 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human 356 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human 104 Genes GS176638: HP:0011603 Congenital malformation of the great arteries
Expand Tier I Human 31 Genes GS170915: HP:0006009 Broad phalanx
Expand Tier I Human 93 Genes GS171105: HP:0006494 Aplasia/Hypoplasia involving bones of the feet
Expand Tier I Human 489 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Human 65 Genes GS171651: HP:0000618 Blindness
Expand Tier I Human 357 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human 52 Genes GS174808: HP:0001633 Abnormality of the mitral valve
Expand Tier I Human 7 Genes GS173383: HP:0002753 Thin bony cortex
Expand Tier I Human 55 Genes GS173685: HP:0001641 Abnormality of the pulmonary valve
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 8645 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 77 Genes GS172684: HP:0003307 Hyperlordosis
Expand Tier I Human 15 Genes GS173460: HP:0001653 Mitral regurgitation
Expand Tier I Human 147 Genes GS175411: HP:0100871 Abnormality of the palm
Expand Tier I Human 45 Genes GS176166: HP:0001256 Intellectual disability, mild
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 12 Genes GS194800: GO:0043205 fibril
Expand Tier I Human 31 Genes GS172056: HP:0001500 Broad finger
Expand Tier I Human 147 Genes GS175074: HP:0001156 Brachydactyly syndrome
Expand Tier I Human 335 Genes GS174076: HP:0009122 Aplasia/Hypoplasia affecting bones of the axial skeleton
Expand Tier I Human 53 Genes GS174451: HP:0006705 Abnormality of the atrioventricular valves
Expand Tier I Human 317 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Human 167 Genes GS170916: HP:0008056 Aplasia/Hypoplasia affecting the eye
Expand Tier I Human 395 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier I Human 11 Genes GS175392: HP:0011003 Severe Myopia
Expand Tier I Human 361 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human 530 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 636 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human 8 Genes GS176246: HP:0001783 Broad metatarsal
Expand Tier I Human 187 Genes GS176449: HP:0001671 Abnormality of the cardiac septa
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 27 Genes GS173688: HP:0001642 Pulmonic stenosis
Expand Tier I Human 261 Genes GS176692: HP:0009815 Aplasia/Hypoplasia of the extremities
Expand Tier I Human 514 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human GO 4003 Genes GS208978: GO:0043169 cation binding
Expand Tier I Human 487 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human 30 Genes GS172669: HP:0003103 Abnormal cortical bone morphology
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 1068 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 69 Genes GS172585: HP:0001832 Abnormality of the metatarsal bones
Expand Tier I Human 487 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Human 423 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Human 541 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier III Human 2216 Genes GS222813: The Druggable Gene Interaction Database
Expand Tier I Human 53 Genes GS175935: HP:0000248 Brachycephaly
Expand Tier I Human GO 5280 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 140 Genes GS174906: HP:0000545 Myopia
Expand Tier I Human CTD 1556 Genes GS125506: Valproic Acid interacting genes (MeSH:D014635) in CTD
Expand Tier I Human 122 Genes GS173563: HP:0000692 Misalignment of teeth
Expand Tier I Human GO 940 Genes GS199468: GO:0006508 proteolysis
Expand Tier I Human 184 Genes GS171144: HP:0005280 Depressed nasal bridge
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 208 Genes GS175164: HP:0011927 Short digit
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 213 Genes GS176973: HP:0001072 Thickened skin
Expand Tier I Human 583 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human 776 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 780 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 433 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
Expand Tier I Human CTD 739 Genes GS126989: Hydralazine interacting genes (MeSH:D006830) in CTD
Expand Tier I Human 20 Genes GS171556: HP:0001387 Joint stiffness
Expand Tier I Human GO 178 Genes GS199022: GO:0008237 metallopeptidase activity
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human GO 425 Genes GS196302: GO:0031012 extracellular matrix
Expand Tier I Human 886 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 39 Genes GS172678: HP:0009117 Aplasia/Hypoplasia of the maxilla
Expand Tier I Human 736 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human 34 Genes GS173309: HP:0002938 Lumbar hyperlordosis
Expand Tier I Human 2 Genes GS173409: HP:0002682 Broad skull
Expand Tier I Human GO 550 Genes GS205544: GO:0070011 peptidase activity, acting on L-amino acid peptides
Expand Tier I Human 418 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human 300 Genes GS176029: HP:0009116 Aplasia/Hypoplasia involving bones of the skull
Expand Tier I Human GO 572 Genes GS199006: GO:0008233 peptidase activity
Expand Tier I Human 121 Genes GS175023: HP:0001629 Ventricular septal defect
Expand Tier I Human 309 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier I Human 25 Genes GS174125: HP:0008063 Aplasia/Hypoplasia of the lens
Expand Tier I Human 187 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human 39 Genes GS173054: HP:0000327 Hypoplasia of the maxilla
Expand Tier I Human 30 Genes GS175042: HP:0009768 Broad phalanges of the hand
Expand Tier I Human GO 1094 Genes GS201255: GO:0044421 extracellular region part
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 187 Genes GS172253: HP:0001376 Limitation of joint mobility
Expand Tier I Human 12 Genes GS172101: HP:0000586 Shallow orbits
Expand Tier I Human 296 Genes GS174145: HP:0005918 Abnormality of phalanx of finger
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 5 Genes GS175743: HP:0001230 Broad metacarpals
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 4 Genes GS171856: HP:0000594 Shallow anterior chamber
Expand Tier I Human 116 Genes GS172076: HP:0001163 Abnormality of the metacarpal bones
Expand Tier I Human 16 Genes GS175270: HP:0001169 Broad palm
Expand Tier I Human GO 2331 Genes GS208037: GO:0016787 hydrolase activity
Expand Tier I Human GO 3902 Genes GS198323: GO:0046872 metal ion binding
Expand Tier I Human 525 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human 356 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Human 542 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human 342 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human 394 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human GO 7259 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human 43 Genes GS173055: HP:0000326 Abnormality of the maxilla
Expand Tier I Human 28 Genes GS175052: HP:0001083 Ectopia lentis
Expand Tier I Human GO 1974 Genes GS203688: GO:0008270 zinc ion binding
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 62 Genes GS173692: HP:0001646 Abnormality of the aortic valve
Expand Tier I Human GO 2216 Genes GS209291: GO:0046914 transition metal ion binding
Expand Tier I Human 233 Genes GS174257: HP:0000309 Abnormality of the midface