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 601 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 387 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human GO 2139 Genes GS210214: GO:0005576 extracellular region
Expand Tier I Human GO 8 Genes GS209921: GO:0001527 microfibril
Expand Tier I Human 403 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 103 Genes GS173507: HP:0000520 Proptosis
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 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 414 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human 32 Genes GS171295: HP:0003508 Proportionate short stature
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 77 Genes GS172300: HP:0001991 Aplasia/Hypoplasia of the toes
Expand Tier I Human 143 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 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 124 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 170 Genes GS173988: HP:0000501 Glaucoma
Expand Tier I Human 17 Genes GS173461: HP:0001650 Aortic valve stenosis
Expand Tier I Human 579 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human 1495 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 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 GO 360 Genes GS210217: GO:0005578 proteinaceous extracellular matrix
Expand Tier I Human GO 185 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 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 67 Genes GS172588: HP:0001831 Short toe
Expand Tier I Human 322 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 489 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human 398 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human 397 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human GO 7311 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 1998 Genes GS203688: GO:0008270 zinc ion binding
Expand Tier I Human 12 Genes GS170954: HP:0000885 Broad ribs
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 263 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier I Human 62 Genes GS173692: HP:0001646 Abnormality of the aortic valve
Expand Tier I Human GO 2241 Genes GS209291: GO:0046914 transition metal ion binding
Expand Tier I Human 379 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 169 Genes GS171752: HP:0001713 Abnormality of cardiac ventricle
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 446 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier I Human GO 5810 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human 236 Genes GS174257: HP:0000309 Abnormality of the midface
Expand Tier I Human 358 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 94 Genes GS171105: HP:0006494 Aplasia/Hypoplasia involving bones of the feet
Expand Tier I Human 491 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Human 65 Genes GS171651: HP:0000618 Blindness
Expand Tier I Human 360 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 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 GO 8702 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 78 Genes GS172684: HP:0003307 Hyperlordosis
Expand Tier I Human 15 Genes GS173460: HP:0001653 Mitral regurgitation
Expand Tier I Human 150 Genes GS175411: HP:0100871 Abnormality of the palm
Expand Tier I Human 45 Genes GS176166: HP:0001256 Intellectual disability, mild
Expand Tier I Human 1213 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 150 Genes GS175074: HP:0001156 Brachydactyly syndrome
Expand Tier I Human 337 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 319 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Human 168 Genes GS170916: HP:0008056 Aplasia/Hypoplasia affecting the eye
Expand Tier I Human 397 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier I Human 11 Genes GS175392: HP:0011003 Severe Myopia
Expand Tier I Human 364 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human 533 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
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 8 Genes GS176246: HP:0001783 Broad metatarsal
Expand Tier I Human 189 Genes GS176449: HP:0001671 Abnormality of the cardiac septa
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 27 Genes GS173688: HP:0001642 Pulmonic stenosis
Expand Tier I Human 263 Genes GS176692: HP:0009815 Aplasia/Hypoplasia of the extremities
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 489 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 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 544 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier III Human 2178 Genes GS222813: The Drugable Gene Interaction Database
Expand Tier I Human 54 Genes GS175935: HP:0000248 Brachycephaly
Expand Tier I Human GO 5321 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 141 Genes GS174906: HP:0000545 Myopia
Expand Tier I Human CTD 1551 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 948 Genes GS199468: GO:0006508 proteolysis
Expand Tier I Human 186 Genes GS171144: HP:0005280 Depressed nasal bridge
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 211 Genes GS175164: HP:0011927 Short digit
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 215 Genes GS176973: HP:0001072 Thickened skin
Expand Tier I Human 588 Genes GS175098: HP:0000284 Abnormality of the ocular region
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 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 CTD 738 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 180 Genes GS199022: GO:0008237 metallopeptidase activity
Expand Tier I Human 1223 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 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 39 Genes GS172678: HP:0009117 Aplasia/Hypoplasia of the maxilla
Expand Tier I Human 739 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human 35 Genes GS173309: HP:0002938 Lumbar hyperlordosis
Expand Tier I Human 2 Genes GS173409: HP:0002682 Broad skull
Expand Tier I Human GO 558 Genes GS205544: GO:0070011 peptidase activity, acting on L-amino acid peptides
Expand Tier I Human 421 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human 302 Genes GS176029: HP:0009116 Aplasia/Hypoplasia involving bones of the skull
Expand Tier I Human GO 580 Genes GS199006: GO:0008233 peptidase activity
Expand Tier I Human 121 Genes GS175023: HP:0001629 Ventricular septal defect
Expand Tier I Human 311 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 189 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier I Human GO 11955 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 1097 Genes GS201255: GO:0044421 extracellular region part
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 189 Genes GS172253: HP:0001376 Limitation of joint mobility
Expand Tier I Human 12 Genes GS172101: HP:0000586 Shallow orbits
Expand Tier I Human 298 Genes GS174145: HP:0005918 Abnormality of phalanx of finger
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 5 Genes GS175743: HP:0001230 Broad metacarpals
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human 4 Genes GS171856: HP:0000594 Shallow anterior chamber
Expand Tier I Human 118 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 2353 Genes GS208037: GO:0016787 hydrolase activity
Expand Tier I Human GO 3934 Genes GS198323: GO:0046872 metal ion binding
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human 358 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Human 545 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human 344 Genes GS174378: HP:0000518 Cataract