Gene Details



KDM6A and homologs in 4 species are found in 392 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 10 Genes GS177033: HP:0000437 Depressed nasal tip
Expand Tier I Human 19 Genes GS171191: HP:0000412 Prominent ears
Expand Tier II Mouse 205 Genes GS35251: Striatum Gene expression correlates of Maximum startle response to 70 db in Females BXD
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Mouse MP 234 Genes GS167089: MP:0003232 abnormal forebrain development
Expand Tier I Human 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Mouse GO 919 Genes GS178388: GO:0055114 oxidation-reduction process
Expand Tier I Human 379 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier III Mouse 86 Genes GS34930: Whole Brain Gene expression correlates of Open Field - Total distance traveled 10-15 minutes [Basal Behavior] in Females BXD
Expand Tier I Human 146 Genes GS170968: HP:0000156 High-arched palate
Expand Tier I Human GO 2719 Genes GS199273: GO:0043233 organelle lumen
Expand Tier I Human 360 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human 157 Genes GS172363: HP:0004324 Increased body weight
Expand Tier I Human 150 Genes GS175411: HP:0100871 Abnormality of the palm
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 222 Genes GS173995: HP:0000508 Ptosis
Expand Tier I Human 426 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Human 324 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Human GO 60 Genes GS200520: GO:0035097 histone methyltransferase complex
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Mouse GO 3615 Genes GS178359: GO:0071840 cellular component organization or biogenesis
Expand Tier I Mouse GO 82 Genes GS185827: GO:0051213 dioxygenase activity
Expand Tier I Human 392 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Mouse GO 2762 Genes GS178357: GO:0071842 cellular component organization at cellular level
Expand Tier I Human GO 2098 Genes GS209551: GO:0031981 nuclear lumen
Expand Tier I Human GO 818 Genes GS197472: GO:0044451 nucleoplasm part
Expand Tier I Human 456 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Human GO 688 Genes GS193888: GO:0051276 chromosome organization
Expand Tier I Human 15 Genes GS172765: HP:0001680 Coarctation of aorta
Expand Tier I Human 741 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 47 Genes GS171564: HP:0000383 Abnormality of periauricular region
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Mouse 221 Genes GS127940: Cerebellum only - Allen Mouse Brain Atlas
Expand Tier I Human 492 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human GO 3885 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier I Human 157 Genes GS176639: HP:0011356 Regional abnormality of skin
Expand Tier I Human 384 Genes GS171708: HP:0000359 Abnormality of the inner ear
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier III Mouse 6105 Genes GS213074: Genes with suggestive difference in (B6PF1) vs (PB6F1 + B6 + PWD) comparison
Expand Tier III Mouse 8003 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampal tissue
Expand Tier I Human 105 Genes GS171199: HP:0001943 Hypoglycemia
Expand Tier I Human GO 60 Genes GS204655: GO:0016571 histone methylation
Expand Tier I Human GO 4097 Genes GS194307: GO:0016043 cellular component organization
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 164 Genes GS174994: HP:0002059 Cerebral atrophy
Expand Tier I Human GO 1477 Genes GS203369: GO:0005654 nucleoplasm
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 403 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Mouse GO 1777 Genes GS184445: GO:0044428 nuclear part
Expand Tier I Human GO 84 Genes GS202664: GO:0051213 dioxygenase activity
Expand Tier I Mouse GO 5103 Genes GS192512: GO:0003824 catalytic activity
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 2486 Genes GS201249: GO:0044428 nuclear part
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 709 Genes GS198755: GO:0016491 oxidoreductase activity
Expand Tier I Mouse MP 4173 Genes GS165527: MP:0005378 growth/size phenotype
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human 253 Genes GS171634: HP:0008050 Abnormality of the palpebral fissures
Expand Tier I Human GO 267 Genes GS200351: GO:0016569 covalent chromatin modification
Expand Tier I Human 384 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Human 201 Genes GS176660: HP:0000050 Hypoplastic genitalia
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier III Human 2430 Genes GS216491: Genes that are binding sites for CREB and zif268,transcription factors mediating nieuronal activity and plasticity, in Homo sapiens.
Expand Tier I Human 86 Genes GS174858: HP:0200007 Abnormal size of the palpebral fissures
Expand Tier II Mouse 152 Genes GS35068: Striatum Gene expression correlates of Difference in time on rotarod between saline and ethanol in Females & Males BXD
Expand Tier I Human 384 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human 315 Genes GS176568: HP:0000486 Strabismus
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human 21 Genes GS176680: HP:0100276 Skin pits
Expand Tier III Mouse 1964 Genes GS865: Sey_Pax6_Age_Reduced_Linear_Incr
Expand Tier I Human 211 Genes GS175164: HP:0011927 Short digit
Expand Tier I Human 168 Genes GS170980: HP:0011362 Abnormal hair quantity
Expand Tier I Human GO 3409 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Human 9 Genes GS175324: HP:0001211 Abnormality of the fingertips
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 81 Genes GS171773: HP:0000532 Chorioretinal abnormality
Expand Tier I Human 220 Genes GS171791: HP:0000370 Abnormality of the middle ear
Expand Tier I Human 92 Genes GS171656: HP:0000610 Abnormality of the choroid
Expand Tier I Human 38 Genes GS171851: HP:0000592 Blue sclerae
Expand Tier I Mouse MP 1692 Genes GS169833: MP:0005380 embryogenesis phenotype
Expand Tier I Human 163 Genes GS176478: HP:0002119 Ventriculomegaly
Expand Tier I Human 553 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human 411 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human GO 3861 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Mouse GO 5247 Genes GS178448: GO:0005634 nucleus
Expand Tier I Human 291 Genes GS175335: HP:0000036 Abnormality of the penis
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 161 Genes GS171633: HP:0008373 Puberty and gonadal disorders
Expand Tier I Human 285 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 139 Genes GS171397: HP:0000177 Abnormality of upper lip
Expand Tier III Mouse 8107 Genes GS213076: Genes with suggestive difference in (B6) vs (B6PF1 + PB6F1 + PWD) comparison
Expand Tier I Mouse MP 574 Genes GS168379: MP:0002151 abnormal neural tube morphology/development
Expand Tier I Human 211 Genes GS173206: HP:0003241 Genital hypoplasia
Expand Tier I Human 157 Genes GS171968: HP:0000405 Conductive hearing impairment
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 93 Genes GS176289: HP:0002120 Cerebral cortical atrophy
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human 158 Genes GS171900: HP:0011452 Functional abnormality of the middle ear
Expand Tier I Mouse MP 14488 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Human 189 Genes GS176449: HP:0001671 Abnormality of the cardiac septa
Expand Tier II Mouse 13 Genes GS36070: Whole Brain Gene expression correlates of Light-Dark Box Transitions in Females BXD
Expand Tier I Human 49 Genes GS173398: HP:0000776 Congenital diaphragmatic hernia
Expand Tier I Human 50 Genes GS173561: HP:0000691 Microdontia
Expand Tier I Human 111 Genes GS176907: HP:0009804 Reduced number of teeth
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 Mouse MP 498 Genes GS162897: MP:0003984 embryonic growth retardation
Expand Tier I Human 122 Genes GS173563: HP:0000692 Misalignment of teeth
Expand Tier I Human 39 Genes GS172454: HP:0100335 Non-midline cleft lip
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 470 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Human 9 Genes GS172308: HP:0001998 Neonatal hypoglycemia
Expand Tier I Human 287 Genes GS175594: HP:0011014 Abnormal glucose homeostasis
Expand Tier I Mouse GO 610 Genes GS177169: GO:0051276 chromosome organization
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 409 Genes GS175670: HP:0007364 Aplasia/Hypoplasia of the cerebrum
Expand Tier I Human GO 124 Genes GS194338: GO:0043414 macromolecule methylation
Expand Tier II Mouse 204 Genes GS36472: Whole Brain Gene expression correlates of Morphine - Severity of ptosis in Females BXD
Expand Tier I Human 210 Genes GS175990: HP:0000463 Anteverted nares
Expand Tier I Human GO 3275 Genes GS199267: GO:0043234 protein complex
Expand Tier I Human GO 3307 Genes GS195110: GO:0071842 cellular component organization at cellular level
Expand Tier I Human 15 Genes GS176629: HP:0000455 Broad nasal tip
Expand Tier I Mouse GO 4224 Genes GS193059: GO:0044446 intracellular organelle part
Expand Tier I Human 3 Genes GS175452: HP:0011398 Central hypotonia
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 180 Genes GS175902: HP:0003468 Abnormality of the vertebrae
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Mouse MP 953 Genes GS165160: MP:0006207 embryonic lethality during organogenesis
Expand Tier I Human 28 Genes GS172285: HP:0000826 Precocious puberty
Expand Tier I Mouse MP 344 Genes GS170107: MP:0003720 abnormal neural tube closure
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 237 Genes GS171395: HP:0000175 Cleft palate
Expand Tier I Human 545 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human GO 524 Genes GS194524: GO:0006325 chromatin organization
Expand Tier I Human 71 Genes GS171136: HP:0100840 Aplasia/Hypoplasia of the eyebrow
Expand Tier I Mouse MP 1692 Genes GS169603: MP:0001672 abnormal embryogenesis/ development
Expand Tier I Human 737 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Mouse GO 412 Genes GS183552: GO:0016568 chromatin modification
Expand Tier I Human 159 Genes GS176900: HP:0000218 High palate
Expand Tier I Human GO 427 Genes GS200350: GO:0016568 chromatin modification
Expand Tier I Human 10 Genes GS174585: HP:0009929 Abnormality of the columella
Expand Tier I Human 89 Genes GS176824: HP:0000204 Cleft upper lip
Expand Tier I Human 148 Genes GS171552: HP:0001382 Joint hypermobility
Expand Tier II Mouse 18 Genes GS36040: Whole Brain Gene expression correlates of Light-Dark Box Total distance traveled in light and dark compartments in Females BXD
Expand Tier I Human 6 Genes GS175322: HP:0001212 Prominent fingertip pads
Expand Tier I Human 212 Genes GS176185: HP:0100790 Hernia
Expand Tier I Human 56 Genes GS173337: HP:0000689 Dental malocclusion
Expand Tier I Human 90 Genes GS173087: HP:0000499 Abnormality of the eyelashes
Expand Tier I Human 578 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 601 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 438 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human 8 Genes GS176880: HP:0100267 Lip pit
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human 51 Genes GS177034: HP:0000436 Abnormality of the nasal tip
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 558 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Human 37 Genes GS175612: HP:0005346 Abnormal facial expression
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Mouse MP 1848 Genes GS167622: MP:0002152 abnormal brain morphology
Expand Tier I Human 67 Genes GS172844: HP:0000482 Microcornea
Expand Tier I Mouse 314 Genes GS136315: non-HDL QTL 2 (Nhdlq2, Published QTL Chr X)
Expand Tier I Human 168 Genes GS175668: HP:0007369 Atrophy/Degeneration affecting the cerebrum
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human 30 Genes GS174237: HP:0000535 Sparse eyebrow
Expand Tier II Mouse 321 Genes GS35261: Striatum Gene expression correlates of Maximum startle response to 80 db in Females BXD
Expand Tier I Human 142 Genes GS171178: HP:0000238 Hydrocephalus
Expand Tier I Human 114 Genes GS174643: HP:0005120 Abnormality of cardiac atrium
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
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 Mouse MP 815 Genes GS169062: MP:0000913 abnormal brain development
Expand Tier I Human 251 Genes GS171793: HP:0000377 Abnormality of the pinna
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 75 Genes GS174446: HP:0001120 Abnormality of corneal size
Expand Tier I Human GO 2464 Genes GS199032: GO:0036211 protein modification process
Expand Tier I Human 398 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Mouse GO 61 Genes GS183716: GO:0035097 histone methyltransferase complex
Expand Tier I Human 16 Genes GS172621: HP:0000656 Ectropion
Expand Tier I Human GO 2558 Genes GS194336: GO:0043412 macromolecule modification
Expand Tier I Mouse GO 9049 Genes GS180166: GO:0008152 metabolic process
Expand Tier I Mouse GO 62 Genes GS186444: GO:0034708 methyltransferase complex
Expand Tier I Human 46 Genes GS171463: HP:0004279 Short palm
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Mouse GO 690 Genes GS180673: GO:0044451 nucleoplasm part
Expand Tier I Human GO 79 Genes GS194897: GO:0008213 protein alkylation
Expand Tier I Human 11 Genes GS172129: HP:0000637 Long palpebral fissure
Expand Tier I Human 551 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 150 Genes GS175074: HP:0001156 Brachydactyly syndrome
Expand Tier I Human 263 Genes GS176692: HP:0009815 Aplasia/Hypoplasia of the extremities
Expand Tier I Human 426 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Human 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human GO 2673 Genes GS205543: GO:0070013 intracellular organelle lumen
Expand Tier I Human GO 83 Genes GS209319: GO:0016701 oxidoreductase activity, acting on single donors with incorporation of molecular oxygen
Expand Tier I Human 263 Genes GS176477: HP:0002118 Abnormality of the cerebral ventricles
Expand Tier I Human 162 Genes GS175958: HP:0000795 Abnormality of the urethra
Expand Tier I Human 221 Genes GS171139: HP:0005288 Abnormality of the nares
Expand Tier I Human 588 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier II Mouse 86 Genes GS36459: Striatum Gene expression correlates of Morphine - Postural Effects in Males BXD
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 616 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse GO 4333 Genes GS184452: GO:0044422 organelle part
Expand Tier I Human 149 Genes GS172295: HP:0001513 Obesity
Expand Tier I Human GO 4213 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human GO 6651 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 29 Genes GS171563: HP:0000384 Preauricular skin tag
Expand Tier I Mouse MP 5057 Genes GS165525: MP:0010768 mortality/aging
Expand Tier II Mouse 54 Genes GS34940: Whole Brain Gene expression correlates of Open Field - Total distance traveled 15-20 minutes in Females BXD
Expand Tier I Human GO 135 Genes GS209139: GO:0032259 methylation
Expand Tier I Human 107 Genes GS172094: HP:0000589 Coloboma
Expand Tier I Human 60 Genes GS174720: HP:0000775 Abnormality of the diaphragm
Expand Tier I Human 381 Genes GS175714: HP:0011389 Functional abnormality of the inner ear
Expand Tier I Human 111 Genes GS174806: HP:0001631 Defect in the atrial septum
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human 346 Genes GS171309: HP:0000252 Microcephaly
Expand Tier I Human 23 Genes GS175308: HP:0000298 Mask-like facies
Expand Tier II Mouse 427 Genes GS35271: Striatum Gene expression correlates of Maximum startle response to 85 db in Females BXD
Expand Tier I Human 198 Genes GS174236: HP:0000534 Abnormality of the eyebrow
Expand Tier I Mouse MP 4772 Genes GS165524: MP:0010769 abnormal survival
Expand Tier I Human 368 Genes GS170971: HP:0000407 Sensorineural hearing impairment
Expand Tier I Human 445 Genes GS175423: HP:0010461 Abnormality of the male genitalia
Expand Tier I Human 88 Genes GS173938: HP:0001679 Abnormality of the aorta
Expand Tier I Human 129 Genes GS174925: HP:0000769 Abnormality of the breast
Expand Tier I Mouse MP 3815 Genes GS165243: MP:0010770 preweaning lethality
Expand Tier I Mouse MP 568 Genes GS166535: MP:0010865 prenatal growth retardation
Expand Tier I Mouse GO 471 Genes GS177784: GO:0006325 chromatin organization
Expand Tier I Human GO 7311 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human 394 Genes GS172362: HP:0004325 Decreased body weight
Expand Tier I Human 320 Genes GS175597: HP:0011013 Abnormality of carbohydrate metabolism/homeostasis
Expand Tier I Human 203 Genes GS174706: HP:0000553 Abnormality of the uvea
Expand Tier I Human 515 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human 199 Genes GS171637: HP:0008872 Feeding difficulties in infancy
Expand Tier I Human 3 Genes GS173899: HP:0002000 Short columella
Expand Tier I Mouse GO 2991 Genes GS182469: GO:0043234 protein complex
Expand Tier I Mouse MP 61 Genes GS169149: MP:0003400 kinked neural tube
Expand Tier I Human GO 79 Genes GS200922: GO:0006479 protein methylation
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier III Mouse 659 Genes GS874: Differential expression in Meander-tail (mea) vs. BLKS controls.
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Mouse MP 1628 Genes GS167505: MP:0008762 embryonic lethality
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 Mouse GO 3583 Genes GS180236: GO:0032991 macromolecular complex
Expand Tier I Human 2 Genes GS171611: HP:0007655 Eversion of lateral third of lower eyelids
Expand Tier I Human 6 Genes GS173312: HP:0011298 Prominent digit pad
Expand Tier I Human 64 Genes GS171273: HP:0100542 Abnormal localization of kidneys
Expand Tier I Human 433 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Human 34 Genes GS172418: HP:0000567 Chorioretinal coloboma
Expand Tier I Mouse MP 2263 Genes GS164262: MP:0002080 prenatal lethality
Expand Tier I Human 44 Genes GS171854: HP:0000591 Abnormality of the sclera
Expand Tier I Human 567 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human GO 5321 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human 289 Genes GS173167: HP:0100491 Abnormality of the joints of the lower limbs
Expand Tier I Mouse GO 1628 Genes GS177813: GO:0031974 membrane-enclosed lumen
Expand Tier I Mouse GO 1381 Genes GS192610: GO:0031981 nuclear lumen
Expand Tier I Human GO 3254 Genes GS200602: GO:0044267 cellular protein metabolic process
Expand Tier I Human 53 Genes GS176772: HP:0001007 Hirsutism
Expand Tier II Mouse 28 Genes GS36503: Cerebellum Gene expression correlates of Morphine - wet dog shakes in Females BXD
Expand Tier I Mouse MP 969 Genes GS164257: MP:0002085 abnormal embryonic tissue morphology
Expand Tier I Mouse MP 254 Genes GS169371: MP:0000929 open neural tube
Expand Tier I Human 271 Genes GS176826: HP:0000202 Oral cleft
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 275 Genes GS170962: HP:0000159 Abnormality of the lip
Expand Tier I Mouse GO 778 Genes GS186526: GO:0005654 nucleoplasm
Expand Tier I Human 537 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Mouse MP 1274 Genes GS164320: MP:0003861 abnormal nervous system development
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Mouse GO 8630 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 203 Genes GS175802: HP:0003272 Abnormality of the hip bone
Expand Tier I Human 109 Genes GS176899: HP:0002353 EEG abnormality
Expand Tier I Mouse GO 8650 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse GO 3537 Genes GS192041: GO:0043169 cation binding
Expand Tier I Human 166 Genes GS171901: HP:0010985 Gonosomal inheritance
Expand Tier I Human 181 Genes GS175391: HP:0011004 Abnormality of the systemic arterial tree
Expand Tier I Human 156 Genes GS174002: HP:0000189 Narrow palate
Expand Tier I Mouse MP 318 Genes GS166291: MP:0011108 partial embryonic lethality during organogenesis
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Mouse 3109 Genes GS127923: Cerebellum - Allen Mouse Brain Atlas
Expand Tier I Human 19 Genes GS171795: HP:0000378 Cupped ear
Expand Tier I Human 602 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Mouse GO 735 Genes GS181962: GO:0016491 oxidoreductase activity
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human 533 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Human 264 Genes GS173014: HP:0010936 Abnormality of the lower urinary tract
Expand Tier I Human 639 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human 490 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Mouse GO 1870 Genes GS192986: GO:0006996 organelle organization
Expand Tier I Human GO 62 Genes GS203291: GO:0034708 methyltransferase complex
Expand Tier I Mouse MP 3019 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 2464 Genes GS196595: GO:0006464 cellular protein modification process
Expand Tier I Human 114 Genes GS174412: HP:0007477 Abnormal dermatoglyphics
Expand Tier I Human 473 Genes GS171893: HP:0011458 Abdominal symptom
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier I Mouse GO 3493 Genes GS177570: GO:0016043 cellular component organization
Expand Tier I Mouse MP 870 Genes GS168593: MP:0002088 abnormal embryonic growth/weight/body size
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Mouse GO 3442 Genes GS181533: GO:0046872 metal ion binding
Expand Tier I Human 486 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human GO 2764 Genes GS194555: GO:0031974 membrane-enclosed lumen
Expand Tier I Human 79 Genes GS171959: HP:0000400 Macrotia
Expand Tier II Mouse 31 Genes GS34910: Whole Brain Gene expression correlates of Open Field - Total distance traveled 0-5 minutes in Females BXD
Expand Tier I Human 453 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human 237 Genes GS174292: HP:0011968 Feeding difficulties
Expand Tier I Human 239 Genes GS174066: HP:0100737 Abnormality of the hard palate
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human 111 Genes GS173580: HP:0011994 Abnormality of the atrial septum
Expand Tier I Mouse MP 1038 Genes GS169114: MP:0004196 abnormal prenatal growth/weight/body size
Expand Tier I Mouse GO 8414 Genes GS185585: GO:0044710 single-organism metabolic process
Expand Tier I Human 398 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Human GO 4034 Genes GS208978: GO:0043169 cation binding
Expand Tier I Human 36 Genes GS172842: HP:0000480 Retinal coloboma
Expand Tier I Human 6 Genes GS175290: HP:0005338 Sparse lateral eyebrow
Expand Tier I Mouse GO 79 Genes GS192384: GO:0016701 oxidoreductase activity, acting on single donors with incorporation of molecular oxygen
Expand Tier I Human 534 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human GO 2108 Genes GS209928: GO:0006996 organelle organization
Expand Tier I Human 129 Genes GS172916: HP:0003312 Abnormal form of the vertebral bodies
Expand Tier II Mouse 86 Genes GS34920: Whole Brain Gene expression correlates of Open Field - Total distance traveled 10-15 minutes in Females BXD
Expand Tier I Human 179 Genes GS171047: HP:0008736 Hypoplasia of penis
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human 249 Genes GS176844: HP:0000429 Abnormality of the nasal alae
Expand Tier I Human 579 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Mouse MP 1083 Genes GS167755: MP:0000783 abnormal forebrain morphology
Expand Tier I Human 123 Genes GS175588: HP:0001311 Neurophysiological abnormality
Expand Tier I Human 281 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Mouse GO 5225 Genes GS189860: GO:0043167 ion binding
Expand Tier I Human 403 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Human 313 Genes GS176642: HP:0011355 Localized skin lesion
Expand Tier I Human GO 29 Genes GS197254: GO:0051568 histone H3-K4 methylation
Expand Tier I Human GO 5948 Genes GS195199: GO:0005634 nucleus
Expand Tier I Human 202 Genes GS174764: HP:0007367 Atrophy/Degeneration affecting the central nervous system
Expand Tier I Mouse MP 3716 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Human 472 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human 16 Genes GS174486: HP:0000527 Long eyelashes
Expand Tier I Mouse GO 78 Genes GS192382: GO:0016702 oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen
Expand Tier I Human 121 Genes GS170890: HP:0006483 Abnormal number of teeth
Expand Tier I Human 699 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human 544 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 512 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Human 32 Genes GS172593: HP:0010609 Skin tags
Expand Tier I Human 534 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Human 30 Genes GS171054: HP:0004673 Decreased facial expression
Expand Tier II Mouse 53 Genes GS36498: Cerebellum Gene expression correlates of Morphine - wet dog shakes in Females & Males BXD
Expand Tier I Human 114 Genes GS175593: HP:0011015 Abnormality of blood glucose concentration
Expand Tier I Human 240 Genes GS172433: HP:0002644 Abnormality of pelvic girdle bone morphology
Expand Tier I Human 35 Genes GS171655: HP:0000611 Choroid coloboma
Expand Tier I Human GO 3934 Genes GS198323: GO:0046872 metal ion binding
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Human 397 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Mouse GO 2872 Genes GS178360: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Mouse GO 1582 Genes GS188684: GO:0070013 intracellular organelle lumen
Expand Tier I Human 137 Genes GS171202: HP:0100627 Displacement of the external urethral meatus
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human 47 Genes GS174712: HP:0002553 Highly arched eyebrow
Expand Tier I Human 160 Genes GS175806: HP:0001417 X-linked inheritance
Expand Tier I Mouse GO 1587 Genes GS182475: GO:0043233 organelle lumen
Expand Tier I Human 474 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Human 3 Genes GS174080: HP:0002761 Generalized joint laxity
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Mouse 272 Genes GS135241: activity 2 (Actvty2, Published QTL Chr X)
Expand Tier I Human 518 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human GO 261 Genes GS204656: GO:0016570 histone modification
Expand Tier I Human 388 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Human 514 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human GO 46 Genes GS210534: GO:0034968 histone lysine methylation
Expand Tier I Human 101 Genes GS176684: HP:0008678 Renal hypoplasia/aplasia
Expand Tier I Human 175 Genes GS174377: HP:0005927 Aplasia/Hypoplasia involving bones of the hand
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
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 GO 82 Genes GS209317: GO:0016702 oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Human 90 Genes GS170889: HP:0006482 Abnormality of dental morphology