Gene Details



COL9A2 and homologs in 1 species are found in 182 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 GO 4567 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human GO 1244 Genes GS196080: GO:0040011 locomotion
Expand Tier I Human GO 1319 Genes GS208126: GO:0009605 response to external stimulus
Expand Tier I Human GO 2139 Genes GS210214: GO:0005576 extracellular region
Expand Tier I Human GO 3409 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
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 2 Genes GS175293: HP:0005086 Knee osteoarthritis
Expand Tier I Human GO 6 Genes GS195989: GO:0005593 FACIT collagen
Expand Tier I Human GO 386 Genes GS207498: GO:0001501 skeletal system development
Expand Tier I Human GO 675 Genes GS204996: GO:0048858 cell projection morphogenesis
Expand Tier I Human GO 1456 Genes GS205144: GO:0048468 cell development
Expand Tier I Human GO 6769 Genes GS210002: GO:0044444 cytoplasmic part
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 GO 522 Genes GS202795: GO:0007409 axonogenesis
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 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 37 Genes GS176719: HP:0000541 Retinal detachment
Expand Tier I Human 175 Genes GS174377: HP:0005927 Aplasia/Hypoplasia involving bones of the hand
Expand Tier I Human 129 Genes GS172916: HP:0003312 Abnormal form of the vertebral bodies
Expand Tier I Human GO 579 Genes GS204425: GO:0048812 neuron projection morphogenesis
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 384 Genes GS171708: HP:0000359 Abnormality of the inner ear
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 GO 571 Genes GS209569: GO:0048667 cell morphogenesis involved in neuron differentiation
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 8 Genes GS172618: HP:0000655 Vitreoretinal degeneration
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 700 Genes GS205439: GO:0031175 neuron projection development
Expand Tier I Human GO 593 Genes GS201060: GO:0042330 taxis
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
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 24 Genes GS174091: HP:0004327 Abnormality of the vitreous humor
Expand Tier I Human 9 Genes GS176223: HP:0003071 Flattened epiphyses
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 553 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human GO 2050 Genes GS203406: GO:0009653 anatomical structure morphogenesis
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 Human 1417 Genes GS219947: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier I Human GO 1067 Genes GS196002: GO:0048699 generation of neurons
Expand Tier I Human 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human GO 170 Genes GS196728: GO:0005788 endoplasmic reticulum lumen
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 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier III Human 3178 Genes GS137407: Supplementary Table 2. Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Human 55 Genes GS171298: HP:0002829 Arthralgia
Expand Tier I Human 150 Genes GS174586: HP:0005930 Abnormality of the epiphyses
Expand Tier I Human GO 78 Genes GS208009: GO:0005201 extracellular matrix structural constituent
Expand Tier I Human 202 Genes GS171631: HP:0008051 Abnormality of the retinal pigment epithelium
Expand Tier I Human GO 357 Genes GS208058: GO:0007411 axon guidance
Expand Tier I Human 41 Genes GS173378: HP:0002758 Osteoarthritis
Expand Tier I Human 34 Genes GS174909: HP:0000546 Retinal degeneration
Expand Human 1985 Genes GS219980: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human GO 212 Genes GS195507: GO:0043062 extracellular structure organization
Expand Tier I Human GO 4097 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human 46 Genes GS171463: HP:0004279 Short palm
Expand Tier I Human GO 593 Genes GS202940: GO:0006935 chemotaxis
Expand Tier I Human GO 2661 Genes GS207797: GO:0030154 cell differentiation
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 993 Genes GS209525: GO:0032989 cellular component morphogenesis
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 132 Genes GS173792: HP:0002815 Abnormality of the knees
Expand Tier I Human GO 211 Genes GS208505: GO:0030198 extracellular matrix organization
Expand Tier I Human GO 2719 Genes GS199273: GO:0043233 organelle lumen
Expand Human 134 Genes GS216536: Differentially expressed genes between suicide and non suicide mood disorder subjects in the Nucleus Accumbens.
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 150 Genes GS175411: HP:0100871 Abnormality of the palm
Expand Tier I Human 39 Genes GS175557: HP:0002515 Waddling gait
Expand Tier I Human GO 4024 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human GO 2741 Genes GS195668: GO:0042221 response to chemical stimulus
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human GO 1281 Genes GS196726: GO:0005783 endoplasmic reticulum
Expand Tier I Human CTD 1760 Genes GS123048: Tretinoin interacting genes (MeSH:D014212) in CTD
Expand Human 1417 Genes GS219983: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier I Human 11 Genes GS175392: HP:0011003 Severe Myopia
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human 364 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
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 260 Genes GS170933: HP:0001288 Gait disturbance
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human 212 Genes GS171106: HP:0006496 Aplasia/Hypoplasia involving bones of the upper limbs
Expand Tier I Human 544 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 388 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 89 Genes GS198230: GO:0005581 collagen
Expand Human 1985 Genes GS219986: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human 52 Genes GS176559: HP:0000483 Astigmatism
Expand Tier I Human GO 794 Genes GS209568: GO:0048666 neuron development
Expand Tier I Human 2 Genes GS176394: HP:0004982 Flat, irregular epiphyses
Expand Tier I Human GO 2673 Genes GS205543: GO:0070013 intracellular organelle lumen
Expand Tier I Human 289 Genes GS173167: HP:0100491 Abnormality of the joints of the lower limbs
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 3 Genes GS202614: GO:0005594 collagen type IX
Expand Tier I Human 578 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 512 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Human 141 Genes GS174906: HP:0000545 Myopia
Expand Tier I Human 126 Genes GS170894: HP:0006487 Bowing of the long bones
Expand Tier I Human 11 Genes GS175773: HP:0010582 Irregular epiphyses
Expand Tier I Human 324 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Human 405 Genes GS173743: HP:0001999 Abnormal facial shape
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Human 1985 Genes GS219964: http://www.broadinstitute.org/gsea/msigdb/cards/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 35 Genes GS172848: HP:0000488 Retinopathy
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 GO 938 Genes GS210237: GO:0000902 cell morphogenesis
Expand Tier I Human 68 Genes GS172110: HP:0002983 Micromelia
Expand Tier I Human GO 1724 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Human GO 2824 Genes GS209411: GO:0048869 cellular developmental process
Expand Tier I Human GO 4213 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 543 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human GO 425 Genes GS196302: GO:0031012 extracellular matrix
Expand Human 1985 Genes GS219747: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Human 1417 Genes GS219730: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier I Human 79 Genes GS172699: HP:0002652 Skeletal dysplasia
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Human 1417 Genes GS219977: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier I Human GO 3307 Genes GS195110: GO:0071842 cellular component organization at cellular level
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 381 Genes GS175714: HP:0011389 Functional abnormality of the inner ear
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 189 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier I Human GO 621 Genes GS199651: GO:0005198 structural molecule activity
Expand Tier I Human GO 930 Genes GS200809: GO:0030030 cell projection organization
Expand Tier I Human 240 Genes GS172433: HP:0002644 Abnormality of pelvic girdle bone morphology
Expand Tier I Human 56 Genes GS176099: HP:0000926 Platyspondyly
Expand Tier I Human GO 6 Genes GS194227: GO:0030020 extracellular matrix structural constituent conferring tensile strength
Expand Tier I Human GO 1097 Genes GS201255: GO:0044421 extracellular region part
Expand Tier I Human 188 Genes GS171512: HP:0007703 Abnormal retinal pigmentation
Expand Tier I Human 189 Genes GS172253: HP:0001376 Limitation of joint mobility
Expand Tier I Human GO 986 Genes GS204095: GO:0030182 neuron differentiation
Expand Tier I Human 180 Genes GS175902: HP:0003468 Abnormality of the vertebrae
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 919 Genes GS197025: GO:0044432 endoplasmic reticulum part
Expand Tier I Human 368 Genes GS170971: HP:0000407 Sensorineural hearing impairment
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human GO 2764 Genes GS194555: GO:0031974 membrane-enclosed lumen
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
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 GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human 55 Genes GS172140: HP:0002857 Genu valgum
Expand Tier I Human GO 1136 Genes GS205691: GO:0022008 neurogenesis
Expand Tier I Human GO 6585 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 515 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human GO 699 Genes GS210236: GO:0000904 cell morphogenesis involved in differentiation
Expand Tier I Human 60 Genes GS172311: HP:0100691 Abnormality of the curvature of the cornea
Expand Tier I Human 157 Genes GS176612: HP:0000272 Malar flattening
Expand Tier I Human CTD 4389 Genes GS123768: Cyclosporine interacting genes (MeSH:D016572) in CTD
Expand Tier I Human 236 Genes GS174257: HP:0000309 Abnormality of the midface
Expand Tier I Human 83 Genes GS172024: HP:0001369 Arthritis
Expand Tier I Human 12 Genes GS172695: HP:0002656 Epiphyseal dysplasia
Expand Tier I Human GO 687 Genes GS197017: GO:0032990 cell part morphogenesis
Expand Tier I Human 148 Genes GS171552: HP:0001382 Joint hypermobility
Expand Tier I Human 177 Genes GS173048: HP:0005557 Abnormality of the zygomatic arch
Expand Tier I Human GO 1588 Genes GS196772: GO:0048646 anatomical structure formation involved in morphogenesis
Expand Tier I Human GO 10 Genes GS209361: GO:0030934 anchoring collagen
Expand Tier I Human 9 Genes GS171392: HP:0003502 Mild short stature
Expand Tier III Human 2403 Genes GS137413: Supplementary Table 2. CNA Overall results of WGCNA combined with differential expression between alcoholics and controls