Gene Details



DLL3 and homologs in 5 species are found in 936 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 Mouse MP 1246 Genes GS165707: MP:0000428 abnormal craniofacial morphology
Expand Tier I Mouse GO 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Human 98 Genes GS172242: HP:0004930 Abnormality of the pulmonary vasculature
Expand Tier I Human GO 48 Genes GS199084: GO:0045685 regulation of glial cell differentiation
Expand Tier II Human 1999 Genes GS242642: [MeSH] Endothelium : D004727
Expand Tier I Human 263 Genes GS227508: MSigDB Geneset - V$OCT1_01
Expand Tier II Human 644 Genes GS244888: [MeSH] Heart Defects, Congenital : D006330
Expand Tier I Human 145 Genes GS171320: HP:0100360 Contractures of the joints of the upper limbs
Expand Tier II Human 6985 Genes GS238182: [MeSH] Oncogene Proteins : D015513
Expand Tier I Mouse MP 124 Genes GS166501: MP:0003189 fused joints
Expand Tier I Mouse 969 Genes GS136900: ventral midbrain iron content 4 (Vmbic4, Published QTL Chr 7)
Expand Tier II Human 891 Genes GS239009: [MeSH] Paired Box Transcription Factors : D051761
Expand Tier II Human 40 Genes GS234487: [MeSH] Spinal Curvatures : D013121
Expand Tier I Mouse MP 38 Genes GS167812: MP:0000162 lordosis
Expand Tier I Human 190 Genes GS230388: MSigDB Geneset - GSE15659_RESTING_TREG_VS_NONSUPPRESSIVE_TCELL_UP
Expand Tier II Human 10505 Genes GS238504: [MeSH] Tissues : D014024
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier II Human 5416 Genes GS237717: [MeSH] Tissue Distribution : D014018
Expand Tier II Human 8606 Genes GS243926: [MeSH] Exons : D005091
Expand Tier I Mouse MP 24 Genes GS169514: MP:0002653 abnormal ependyma morphology
Expand Tier I Mouse MP 88 Genes GS170725: MP:0002566 abnormal sexual interaction
Expand Tier II Human 1479 Genes GS239473: [MeSH] High Mobility Group Proteins : D006609
Expand Tier I Human GO 93 Genes GS209892: GO:0050768 negative regulation of neurogenesis
Expand Tier II Human 14353 Genes GS244882: [MeSH] Epithelial Cells : D004847
Expand Tier I Mouse 1020 Genes GS136319: non-HDL QTL 6 (Nhdlq6, Published QTL Chr 7)
Expand Tier II Human 671 Genes GS237844: [MeSH] Intestine, Small : D007421
Expand Tier I Human 267 Genes GS172261: HP:0000357 Abnormal location of ears
Expand Tier II Human 11812 Genes GS236947: [MeSH] Brain : D001921
Expand Tier I Mouse 649 Genes GS135346: Avp transcript abundance QTL 1 (Avptaq1, Published QTL Chr 7)
Expand Tier I Human 641 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Rat 50 Genes GS233302: KEGG Geneset - "Notch signaling pathway" pathway genes
Expand Tier II Human 1599 Genes GS245714: [MeSH] Face : D005145
Expand Tier I Mouse 730 Genes GS136807: tuberculosis resistance 3 (Tbrs3, Published QTL Chr 7)
Expand Tier II Human 70216 Genes GS235234: [MeSH] Biochemical Phenomena : D001669
Expand Tier II Human 31959 Genes GS237114: [MeSH] Regulatory Elements, Transcriptional : D050436
Expand Tier II Human 4661 Genes GS238716: [MeSH] Genetic Linkage : D008040
Expand Tier I Human CTD 377 Genes GS124417: Propylthiouracil interacting genes (MeSH:D011441) in CTD
Expand Tier II Human 15702 Genes GS245264: [MeSH] Nervous System : D009420
Expand Tier II Human 3056 Genes GS245413: [MeSH] TGF-beta Superfamily Proteins : D055411
Expand Tier I Human 178 Genes GS176151: HP:0000256 Macrocephaly
Expand Tier I Mouse MP 216 Genes GS167156: MP:0000459 abnormal presacral vertebrae morphology
Expand Tier II Human 478 Genes GS244778: [MeSH] Skull : D012886
Expand Tier I Mouse MP 334 Genes GS166753: MP:0001935 decreased litter size
Expand Tier I Human 357 Genes GS172701: HP:0002650 Scoliosis
Expand Tier III Rat 680 Genes GS223247: Bone mineral density QTL 74 (Bmd74 Published QTL Chr 1)
Expand Tier I Human 8 Genes GS175688: HP:0000902 Rib fusion
Expand Tier II Human 149 Genes GS241478: [MeSH] Pericardium : D010496
Expand Tier I Human 187 Genes GS229082: MSigDB Geneset - GSE15659_NONSUPPRESSIVE_TCELL_VS_ACTIVATED_TREG_UP
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier II Human 7591 Genes GS239955: [MeSH] Amino Acid Motifs : D020816
Expand Tier I Human 174 Genes GS172293: HP:0001511 Intrauterine growth retardation
Expand Tier II Human 245 Genes GS244722: [MeSH] Wnt3 Protein : D060508
Expand Tier I Mouse MP 67 Genes GS169484: MP:0000729 abnormal myogenesis
Expand Tier I Mouse GO 179 Genes GS181529: GO:0010720 positive regulation of cell development
Expand Tier I Human 423 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier II Human 305 Genes GS235544: [MeSH] Amyloid Precursor Protein Secretases : D053829
Expand Tier I Human GO 441 Genes GS209602: GO:0051960 regulation of nervous system development
Expand Tier II Human 3419 Genes GS234275: [MeSH] Heterozygote : D006579
Expand Tier I Human 157 Genes GS171718: HP:0002808 Kyphosis
Expand Tier II Human 1807 Genes GS238780: [MeSH] Head : D006257
Expand Tier I Human 257 Genes GS227162: MSigDB Geneset - V$E12_Q6
Expand Tier I Human 121 Genes GS172789: HP:0001537 Umbilical hernia
Expand Tier I Mouse GO 1833 Genes GS184324: GO:0010646 regulation of cell communication
Expand Tier II Human 2133 Genes GS239689: [MeSH] Wnt Proteins : D051153
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Mouse GO 2994 Genes GS186215: GO:0048519 negative regulation of biological process
Expand Tier II Human 2660 Genes GS244236: [MeSH] Homozygote : D006720
Expand Tier I Mouse GO 3080 Genes GS177265: GO:0048731 system development
Expand Tier I Human 15 Genes GS172211: HP:0003510 Severe short stature
Expand Tier I Human GO 208 Genes GS201404: GO:0009952 anterior/posterior pattern specification
Expand Tier I Mouse GO 2955 Genes GS181893: GO:0048522 positive regulation of cellular process
Expand Tier I Mouse GO 3597 Genes GS188142: GO:0048856 anatomical structure development
Expand Tier III Rat 1482 Genes GS224475: Bone structure and strength QTL 54 (Bss54 Published QTL Chr 1)
Expand Tier I Mouse MP 781 Genes GS170024: MP:0011086 partial postnatal lethality
Expand Tier I Human 19 Genes GS176247: HP:0002948 Vertebral fusion
Expand Tier I Mouse MP 619 Genes GS165194: MP:0001533 abnormal skeleton physiology
Expand Tier I Mouse MP 1246 Genes GS165228: MP:0005382 craniofacial phenotype
Expand Tier I Mouse MP 254 Genes GS170425: MP:0004508 abnormal pectoral girdle bone morphology
Expand Tier I Mouse GO 64 Genes GS187973: GO:0061053 somite development
Expand Tier II Human 9980 Genes GS243345: [MeSH] Alternative Splicing : D017398
Expand Tier II Human 9719 Genes GS244871: [MeSH] Time Factors : D013997
Expand Tier I Mouse 969 Genes GS136531: prion resistance 2 (Prnr2, Published QTL Chr 7)
Expand Tier I Human GO 1006 Genes GS196988: GO:0045595 regulation of cell differentiation
Expand Tier II Human 14842 Genes GS237183: [MeSH] Growth and Development : D048788
Expand Tier II Human 9858 Genes GS242870: [MeSH] Polymorphism, Genetic : D011110
Expand Tier I Human 389 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Human 273 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier II Human 1419 Genes GS242436: [MeSH] Arteries : D001158
Expand Tier I Human GO 12 Genes GS204524: GO:0005112 Notch binding
Expand Tier I Mouse 169 Genes GS228573: MSigDB Geneset - ESC_V6.5_UP_EARLY.V1_UP
Expand Tier I Mouse MP 530 Genes GS164258: MP:0002084 abnormal developmental patterning
Expand Tier II Human 635 Genes GS237772: [MeSH] Feedback, Physiological : D025461
Expand Tier I Mouse GO 548 Genes GS188289: GO:0009968 negative regulation of signal transduction
Expand Tier I Mouse GO 46 Genes GS185745: GO:0048708 astrocyte differentiation
Expand Tier II Human 160 Genes GS239298: [MeSH] Presenilin-1 : D053764
Expand Tier I Mouse MP 55 Genes GS166588: MP:0005222 abnormal somite size
Expand Tier I Human 198 Genes GS230122: MSigDB Geneset - GSE22886_IGG_IGA_MEMORY_BCELL_VS_BLOOD_PLASMA_CELL_UP
Expand Tier II Human 4022 Genes GS234926: [MeSH] Epithelium : D004848
Expand Tier I Mouse GO 1828 Genes GS189485: GO:0023051 regulation of signaling
Expand Tier II Human 6705 Genes GS234738: [MeSH] Proto-Oncogene Proteins : D011518
Expand Tier II Human 2956 Genes GS236925: [MeSH] Hematopoietic System : D006413
Expand Tier II Human 12291 Genes GS238872: [MeSH] Central Nervous System : D002490
Expand Tier I Mouse MP 254 Genes GS169241: MP:0000130 abnormal trabecular bone morphology
Expand Tier III Rat 767 Genes GS223930: Blood pressure QTL 267 (Bp267 Published QTL Chr 1)
Expand Tier I Mouse GO 912 Genes GS179236: GO:0048699 generation of neurons
Expand Tier I Human GO 777 Genes GS206190: GO:0048585 negative regulation of response to stimulus
Expand Tier I Human 186 Genes GS173355: HP:0002205 Recurrent respiratory infections
Expand Tier I Mouse MP 29 Genes GS162820: MP:0002907 abnormal parturition
Expand Tier II Human 7543 Genes GS239550: [MeSH] Apoptosis : D017209
Expand Tier I Human GO 898 Genes GS201125: GO:0009790 embryo development
Expand Tier II Human 46864 Genes GS243659: [MeSH] RNA, Messenger : D012333
Expand Tier II Human 3165 Genes GS235939: [MeSH] Cerebral Cortex : D002540
Expand Tier I Human 192 Genes GS232124: PC Geneset - "V$HEN1_02" pathway genes
Expand Tier I Mouse MP 235 Genes GS168497: MP:0001256 abnormal body length
Expand Tier I Human 737 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human CTD 99 Genes GS123208: Methimazole interacting genes (MeSH:D008713) in CTD
Expand Tier II Human 56846 Genes GS235305: [MeSH] DNA, Complementary : D018076
Expand Tier II Human 12802 Genes GS237481: [MeSH] Recombination, Genetic : D011995
Expand Tier II Human 24839 Genes GS237194: [MeSH] Physiological Phenomena : D010829
Expand Tier I Human GO 1766 Genes GS194455: GO:0051239 regulation of multicellular organismal process
Expand Tier II Human 562 Genes GS237837: [MeSH] Pituitary Gland : D010902
Expand Tier III Rat 1656 Genes GS223864: Stress Responsive Adrenal Weight QTL 1 (Sradr1 Published QTL Chr 1)
Expand Tier I Mouse MP 267 Genes GS167805: MP:0000150 abnormal rib morphology
Expand Tier I Human 532 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Mouse MP 104 Genes GS164406: MP:0004609 vertebral fusion
Expand Tier I Human GO 676 Genes GS206354: GO:0023057 negative regulation of signaling
Expand Tier I Human 34 Genes GS170804: HP:0003298 Spina bifida occulta
Expand Tier I Mouse 980 Genes GS135458: bone mineral density 4 (Bomd4, Published QTL Chr 7)
Expand Tier I Human GO 680 Genes GS205338: GO:0051094 positive regulation of developmental process
Expand Tier III Rat 1704 Genes GS223785: Anxiety related response QTL 24 (Anxrr24 Published QTL Chr 1)
Expand Tier I Human 489 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Mouse GO 1172 Genes GS178426: GO:0005102 receptor binding
Expand Tier II Human 8635 Genes GS239266: [MeSH] Morphogenesis : D009024
Expand Tier II Human 621 Genes GS235650: [MeSH] Hypothalamo-Hypophyseal System : D007030
Expand Tier II Human 6240 Genes GS236309: [MeSH] Viral Regulatory and Accessory Proteins : D054334
Expand Tier II Human 39830 Genes GS245976: [MeSH] Cellular Structures : D022082
Expand Tier II Human 67553 Genes GS240572: [MeSH] DNA : D004247
Expand Tier II Human 31495 Genes GS241930: [MeSH] Mutation : D009154
Expand Tier II Human 9281 Genes GS241137: [MeSH] Cell Growth Processes : D048708
Expand Tier I Mouse GO 712 Genes GS188482: GO:0051094 positive regulation of developmental process
Expand Tier II Human 2552 Genes GS243025: [MeSH] Neuroglia : D009457
Expand Tier I Human 401 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 196 Genes GS174756: HP:0011947 Respiratory tract infection
Expand Tier II Human 20510 Genes GS237794: [MeSH] Oligodeoxyribonucleotides : D009838
Expand Tier I Human 7 Genes GS175186: HP:0010772 Anomalous pulmonary venous return
Expand Tier I Mouse GO 5111 Genes GS189484: GO:0023052 signaling
Expand Tier I Mouse MP 1052 Genes GS166409: MP:0002114 abnormal axial skeleton morphology
Expand Tier II Human 43280 Genes GS236911: [MeSH] Transcription, Genetic : D014158
Expand Tier II Human 5908 Genes GS234387: [MeSH] Movement : D009068
Expand Tier II Human 65203 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier II Human 1950 Genes GS235382: [MeSH] Transgenes : D019076
Expand Tier II Human 1155 Genes GS238243: [MeSH] Bone Diseases : D001847
Expand Tier I Human 234 Genes GS175523: HP:0000008 Abnormality of female internal genitalia
Expand Tier I Human GO 1095 Genes GS208716: GO:2000026 regulation of multicellular organismal development
Expand Tier I Mouse GO 903 Genes GS184317: GO:0009790 embryo development
Expand Tier I Mouse 730 Genes GS136966: weight loss response 4 (Wtlr4, Published QTL Chr 7)
Expand Tier I Human 127 Genes GS172916: HP:0003312 Abnormal form of the vertebral bodies
Expand Tier I Human GO 306 Genes GS209956: GO:0003002 regionalization
Expand Tier I Human GO 5623 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Mouse MP 214 Genes GS168408: MP:0000585 kinked tail
Expand Tier II Human 640 Genes GS237443: [MeSH] Ear, Inner : D007758
Expand Tier I Mouse GO 71 Genes GS191469: GO:0014013 regulation of gliogenesis
Expand Tier I Mouse MP 3159 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier II Human 15724 Genes GS239132: [MeSH] Gene Expression Regulation, Developmental : D018507
Expand Tier II Human 2894 Genes GS240460: [MeSH] Myocardium : D009206
Expand Tier II Human 18300 Genes GS238771: [MeSH] Transferases : D014166
Expand Tier III Rat 2534 Genes GS223810: Cardiac mass QTL 52 (Cm52 Published QTL Chr 1)
Expand Tier II Human 38 Genes GS240249: [MeSH] Scoliosis : D012600
Expand Tier II Human 79329 Genes GS243722: [MeSH] Genetic Structures : D040342
Expand Tier II Human 67130 Genes GS241889: [MeSH] Molecular Structure : D015394
Expand Tier II Human 63 Genes GS244008: [MeSH] Ribs : D012272
Expand Tier I Mouse GO 441 Genes GS180207: GO:0045596 negative regulation of cell differentiation
Expand Tier I Human 248 Genes GS176844: HP:0000429 Abnormality of the nasal alae
Expand Tier II Human 4568 Genes GS239065: [MeSH] Urinary Tract : D014551
Expand Tier I Human 576 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human 31 Genes GS176375: HP:0000269 Prominent occiput
Expand Tier I Mouse MP 959 Genes GS166244: MP:0002752 abnormal somatic nervous system morphology
Expand Tier I Human GO 2828 Genes GS198684: GO:0048523 negative regulation of cellular process
Expand Tier II Human 8187 Genes GS234648: [MeSH] Alleles : D000483
Expand Tier I Human 280 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human GO 2047 Genes GS203406: GO:0009653 anatomical structure morphogenesis
Expand Tier I Human GO 535 Genes GS205331: GO:0051093 negative regulation of developmental process
Expand Tier I Mouse GO 19 Genes GS190909: GO:0048339 paraxial mesoderm development
Expand Tier II Human 59585 Genes GS234621: [MeSH] Chemical Actions and Uses : D020164
Expand Tier II Human 62071 Genes GS235061: [MeSH] Amino Acids, Peptides, and Proteins : D000602
Expand Tier I Human 401 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier II Human 7284 Genes GS236354: [MeSH] Gene Deletion : D017353
Expand Tier I Human 825 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier II Human 9312 Genes GS236231: [MeSH] Antigens : D000941
Expand Tier II Human 3405 Genes GS235775: [MeSH] Basic Helix-Loop-Helix Transcription Factors : D051792
Expand Tier III Human 287 Genes GS213273: GenAge compiled genes related to human aging
Expand Tier I Mouse MP 12 Genes GS162830: MP:0008530 abnormal rostral-caudal patterning of the somites
Expand Tier I Mouse GO 588 Genes GS184318: GO:0009792 embryo development ending in birth or egg hatching
Expand Tier II Human 10296 Genes GS240252: [MeSH] Intercellular Signaling Peptides and Proteins : D036341
Expand Tier I Mouse GO 6473 Genes GS184448: GO:0044425 membrane part
Expand Tier II Human 8099 Genes GS236751: [MeSH] Polymorphism, Single Nucleotide : D020641
Expand Tier II Human 23706 Genes GS235056: [MeSH] Peptides : D010455
Expand Tier II Human 47536 Genes GS236298: [MeSH] Gene Expression : D015870
Expand Tier II Human 3773 Genes GS234965: [MeSH] Cell Adhesion Molecules : D015815
Expand Tier II Human 13815 Genes GS240409: [MeSH] Drosophila Proteins : D029721
Expand Tier II Human 4947 Genes GS239154: [MeSH] Lymphocytes : D008214
Expand Tier I Human GO 520 Genes GS201126: GO:0009792 embryo development ending in birth or egg hatching
Expand Tier I Mouse MP 3522 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Human 444 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier II Human 2221 Genes GS240993: [MeSH] Intestines : D007422
Expand Tier II Human 9754 Genes GS243806: [MeSH] Time : D013995
Expand Tier I Mouse MP 101 Genes GS166581: MP:0004599 abnormal vertebral arch morphology
Expand Tier II Human 36279 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier I Mouse MP 378 Genes GS165361: MP:0004624 abnormal thoracic cage morphology
Expand Tier I Mouse MP 80 Genes GS164488: MP:0005225 abnormal vertebrae development
Expand Tier I Human 196 Genes GS230632: MSigDB Geneset - GSE3982_BCELL_VS_EFF_MEMORY_CD4_TCELL_UP
Expand Tier I Mouse GO 8386 Genes GS189751: GO:0050794 regulation of cellular process
Expand Tier I Mouse 1026 Genes GS128580: BECs at LORR Recovery Chr# 7
Expand Tier I Mouse GO 92 Genes GS192057: GO:0007219 Notch signaling pathway
Expand Tier I Mouse GO 5654 Genes GS182325: GO:0051716 cellular response to stimulus
Expand Tier I Mouse MP 134 Genes GS163872: MP:0000961 abnormal dorsal root ganglion morphology
Expand Tier I Human GO 62 Genes GS208396: GO:0014013 regulation of gliogenesis
Expand Tier II Human 38809 Genes GS236076: [MeSH] Protein Conformation : D011487
Expand Tier II Human 19302 Genes GS236470: [MeSH] DNA-Binding Proteins : D004268
Expand Tier II Human 3004 Genes GS240265: [MeSH] Neurons, Afferent : D009475
Expand Tier II Human 21260 Genes GS238232: [MeSH] Nucleoproteins : D009698
Expand Tier II Human 5702 Genes GS236303: [MeSH] Ligases : D008025
Expand Tier II Human 15356 Genes GS234761: [MeSH] Reproductive Physiological Processes : D055704
Expand Tier II Human 1052 Genes GS245634: [MeSH] Aorta : D001011
Expand Tier I Mouse 969 Genes GS135988: Hfe modifier 1 (Hfem1, Published QTL Chr 7)
Expand Tier I Human 146 Genes GS172906: HP:0003319 Abnormality of the cervical spine
Expand Tier II Human 809 Genes GS237105: [MeSH] Veins : D014680
Expand Tier I Human CTD 6287 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Mouse MP 2283 Genes GS169391: MP:0002066 abnormal motor capabilities/coordination/movement
Expand Tier I Human 193 Genes GS228425: MSigDB Geneset - GSE22886_IGA_VS_IGM_MEMORY_BCELL_UP
Expand Tier I Human 57 Genes GS232586: PC Geneset - "Notch signaling pathway" pathway genes
Expand Tier II Human 3077 Genes GS241268: [MeSH] Blood Vessels : D001808
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Mouse GO 25 Genes GS191526: GO:0045686 negative regulation of glial cell differentiation
Expand Tier I Mouse GO 8942 Genes GS185492: GO:0050789 regulation of biological process
Expand Tier I Human 401 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Mouse MP 57 Genes GS163813: MP:0004645 decreased vertebrae number
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier I Mouse MP 12 Genes GS167741: MP:0004206 abnormal dermomyotome development
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 263 Genes GS175823: HP:0002093 Respiratory insufficiency
Expand Tier I Mouse GO 5892 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier I Human GO 8578 Genes GS196930: GO:0065007 biological regulation
Expand Tier II Human 732 Genes GS238120: [MeSH] T-Box Domain Proteins : D020825
Expand Tier I Human 54 Genes GS176473: HP:0003498 Disproportionate short stature
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier III Mouse 5790 Genes GS213077: Genes with suggestive difference in (PWD) vs (PB6F1 + B6PF1 + B6) comparison
Expand Tier I Mouse GO 134 Genes GS187579: GO:0010001 glial cell differentiation
Expand Tier I Human 112 Genes GS171616: HP:0100490 Camptodactyly of finger
Expand Tier I Human 780 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier II Human 8754 Genes GS241960: [MeSH] Protein Structure, Secondary : D017433
Expand Tier I Human GO 1722 Genes GS198004: GO:0007399 nervous system development
Expand Tier III Rat 828 Genes GS224872: Sensitivity to stroke QTL 4 (Strs4 Published QTL Chr 1)
Expand Tier I Mouse MP 165 Genes GS168687: MP:0000592 short tail
Expand Tier I Mouse GO 1166 Genes GS191779: GO:2000026 regulation of multicellular organismal development
Expand Tier II Human 50108 Genes GS239769: [MeSH] Gene Library : D015723
Expand Tier I Mouse MP 1430 Genes GS164264: MP:0002082 postnatal lethality
Expand Tier II Human 58105 Genes GS242107: [MeSH] Chemical Processes : D055599
Expand Tier I Human GO 3098 Genes GS203058: GO:0048519 negative regulation of biological process
Expand Tier II Human 32929 Genes GS243578: [MeSH] Reading Frames : D016364
Expand Tier II Human 855 Genes GS238444: [MeSH] Nose : D009666
Expand Tier II Human 14459 Genes GS239072: [MeSH] Recombinant Proteins : D011994
Expand Tier I Mouse MP 3051 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Mouse MP 352 Genes GS167360: MP:0002200 abnormal brain ventricle/choroid plexus morphology
Expand Tier I Human 53 Genes GS173835: HP:0003422 Vertebral segmentation defect
Expand Tier I Human 84 Genes GS176462: HP:0100240 Synostosis of joints
Expand Tier II Human 29996 Genes GS237597: [MeSH] Cell Physiological Processes : D055648
Expand Tier II Human 4413 Genes GS239859: [MeSH] Prosencephalon : D016548
Expand Tier I Human GO 3506 Genes GS193991: GO:0048731 system development
Expand Tier I Mouse MP 246 Genes GS163546: MP:0001688 abnormal somite development
Expand Tier II Human 3755 Genes GS240256: [MeSH] Chromosomal Proteins, Non-Histone : D002868
Expand Tier II Human 12085 Genes GS240544: [MeSH] Pregnancy : D011247
Expand Tier II Human 805 Genes GS245608: [MeSH] Ectoderm : D004475
Expand Tier II Human 2962 Genes GS245304: [MeSH] Bone Marrow Cells : D001854
Expand Tier I Human GO 23 Genes GS202166: GO:0048710 regulation of astrocyte differentiation
Expand Tier III Rat 3415 Genes GS135132: bHR vs bLR genes different in Nucleus Acumbens
Expand Tier I Mouse GO 37 Genes GS190836: GO:0008593 regulation of Notch signaling pathway
Expand Tier I Mouse MP 44 Genes GS166109: MP:0008317 abnormal paravertebral ganglion morphology
Expand Tier I Mouse GO 583 Genes GS190900: GO:0043009 chordate embryonic development
Expand Tier I Mouse MP 76 Genes GS169236: MP:0000135 decreased compact bone thickness
Expand Tier II Human 20421 Genes GS237820: [MeSH] DNA Primers : D017931
Expand Tier I Human 246 Genes GS231646: PC Geneset - "V$E12_Q6" pathway genes
Expand Tier II Human 5853 Genes GS241597: [MeSH] Disease Models, Animal : D004195
Expand Tier III Rat 1129 Genes GS224484: Heart rate QTL 1 (Hrtrt1 Published QTL Chr 1)
Expand Tier I Human 296 Genes GS174145: HP:0005918 Abnormality of phalanx of finger
Expand Tier I Mouse GO 290 Genes GS193014: GO:0003002 regionalization
Expand Tier I Mouse MP 3761 Genes GS165527: MP:0005378 growth/size phenotype
Expand Tier II Human 23569 Genes GS235276: [MeSH] Signal Transduction : D015398
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Mouse GO 13 Genes GS179679: GO:0048712 negative regulation of astrocyte differentiation
Expand Tier I Human GO 4065 Genes GS209199: GO:0007165 signal transduction
Expand Tier III Rat 3415 Genes GS135133: bHR vs bLR genes different in Hippocampus
Expand Tier II Human 839 Genes GS238687: [MeSH] Disease : D004194
Expand Tier II Human 2517 Genes GS246018: [MeSH] Heart Diseases : D006331
Expand Tier II Human 7823 Genes GS235095: [MeSH] Digestive System : D004064
Expand Tier II Human 821 Genes GS235519: [MeSH] Syndrome : D013577
Expand Tier I Human 130 Genes GS173970: HP:0009473 Joint contracture of the hand
Expand Tier II Human 318 Genes GS241890: [MeSH] SOXB1 Transcription Factors : D055748
Expand Tier I Human GO 494 Genes GS200286: GO:0060284 regulation of cell development
Expand Tier II Human 3675 Genes GS235207: [MeSH] Telencephalon : D013687
Expand Mouse 122 Genes GS213213: Collaborative Cross Cecum Microflora Parabiclique2 CC03.9t.8g.8g
Expand Tier II Human 12343 Genes GS236576: [MeSH] Promoter Regions, Genetic : D011401
Expand Tier III Rat 466 Genes GS223763: Collagen induced arthritis QTL 2 (Cia2 Published QTL Chr 1)
Expand Tier II Human 614 Genes GS235458: [MeSH] Nasal Mucosa : D009297
Expand Tier II Human 11815 Genes GS238961: [MeSH] Nerve Tissue Proteins : D009419
Expand Tier I Human 394 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier II Human 1240 Genes GS238245: [MeSH] Cerebellum : D002531
Expand Tier I Human GO 44 Genes GS202578: GO:0048708 astrocyte differentiation
Expand Tier I Mouse 200 Genes GS227915: MSigDB Geneset - GSE32423_CTRL_VS_IL7_IL4_MEMORY_CD8_TCELL_DN
Expand Tier I Human 382 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Mouse GO 105 Genes GS181530: GO:0010721 negative regulation of cell development
Expand Tier I Human GO 6548 Genes GS209863: GO:0050896 response to stimulus
Expand Tier II Human 18755 Genes GS242691: [MeSH] Embryonic Structures : D004628
Expand Tier I Human GO 2020 Genes GS206356: GO:0023051 regulation of signaling
Expand Tier II Human 3299 Genes GS239484: [MeSH] Gastrointestinal Tract : D041981
Expand Tier II Mouse 899 Genes GS84191: alcohol preference 7 QTL (Ap7q, Published QTL, Chr 7)
Expand Tier II Human 2796 Genes GS239355: [MeSH] Body Patterning : D019521
Expand Tier II Human 58261 Genes GS239502: [MeSH] Nucleic Acid Probes : D015341
Expand Tier III Rat 1532 Genes GS224632: Blood pressure QTL 96 (Bp96 Published QTL Chr 1)
Expand Tier I Human 16 Genes GS171717: HP:0005108 Abnormality of the intervertebral disk
Expand Tier I Human 12 Genes GS171740: HP:0003521 Disproportionate short-trunk short stature
Expand Tier II Human 30111 Genes GS244835: [MeSH] Chromosomes : D002875
Expand Tier I Human 381 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier II Human 3385 Genes GS237069: [MeSH] Congenital Abnormalities : D000013
Expand Tier I Mouse MP 1436 Genes GS166712: MP:0002161 abnormal fertility/fecundity
Expand Tier II Human 3394 Genes GS244643: [MeSH] Receptor Protein-Tyrosine Kinases : D020794
Expand Tier I Human 136 Genes GS171202: HP:0100627 Displacement of the external urethral meatus
Expand Tier I Human 604 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier II Human 173 Genes GS241281: [MeSH] Immunoglobulin J Recombination Signal Sequence-Binding Protein : D051819
Expand Tier II Human 812 Genes GS233959: [MeSH] SOX Transcription Factors : D055747
Expand Tier I Human 219 Genes GS172288: HP:0000358 Posteriorly rotated ears
Expand Tier I Human GO 144 Genes GS204441: GO:0010001 glial cell differentiation
Expand Tier II Human 5769 Genes GS235447: [MeSH] Blood Cells : D001773
Expand Tier II Human 2272 Genes GS239652: [MeSH] Genes, Recessive : D005808
Expand Tier I Mouse MP 106 Genes GS166241: MP:0002751 abnormal autonomic nervous system morphology
Expand Tier I Human 39 Genes GS172815: HP:0000337 Broad forehead
Expand Tier II Human 73996 Genes GS244482: [MeSH] Nucleic Acids, Nucleotides, and Nucleosides : D009706
Expand Tier I Mouse MP 178 Genes GS169017: MP:0002932 abnormal joint morphology
Expand Tier II Human 9240 Genes GS237965: [MeSH] Peptide Hydrolases : D010447
Expand Tier I Mouse MP 247 Genes GS166029: MP:0000960 abnormal sensory ganglion morphology
Expand Tier II Human 9876 Genes GS239522: [MeSH] Growth : D006128
Expand Tier I Mouse GO 710 Genes GS189324: GO:0048585 negative regulation of response to stimulus
Expand Tier I Human GO 6073 Genes GS201252: GO:0044425 membrane part
Expand Tier II Human 3286 Genes GS243170: [MeSH] Respiratory System : D012137
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 514 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human 28 Genes GS173311: HP:0010651 Abnormality of the meninges
Expand Tier II Human 58105 Genes GS235797: [MeSH] DNA Probes : D015342
Expand Tier II Human 29719 Genes GS237296: [MeSH] RNA, Antisense : D016372
Expand Tier II Human 4977 Genes GS239472: [MeSH] Homeodomain Proteins : D018398
Expand Tier I Human GO 121 Genes GS209893: GO:0050769 positive regulation of neurogenesis
Expand Tier I Mouse GO 1204 Genes GS188763: GO:0009888 tissue development
Expand Tier II Human 41481 Genes GS234192: [MeSH] Gene Expression Regulation : D005786
Expand Tier I Human GO 7650 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier II Human 52588 Genes GS245685: [MeSH] RNA : D012313
Expand Tier I Human 75 Genes GS172219: HP:0010301 Spinal dysraphism
Expand Tier I Human 117 Genes GS170853: HP:0006261 Abnormality of phalangeal joints of the hand
Expand Tier I Human 2227 Genes GS232290: PC Geneset - "GGGAGGRR_V$MAZ_Q6" pathway genes
Expand Tier I Human GO 17 Genes GS204939: GO:0045746 negative regulation of Notch signaling pathway
Expand Tier I Human 1913 Genes GS232025: PC Geneset - "CTTTGT_V$LEF1_Q2" pathway genes
Expand Tier I Mouse GO 369 Genes GS181032: GO:0001701 in utero embryonic development
Expand Tier II Human 5311 Genes GS237981: [MeSH] Leukocytes, Mononuclear : D007963
Expand Tier I Human 112 Genes GS171810: HP:0005651 Flexion contracture of finger
Expand Tier II Human 20860 Genes GS239302: [MeSH] Oligonucleotides : D009841
Expand Tier I Human 1139 Genes GS232656: PC Geneset - "RYTTCCTG_V$ETS2_B" pathway genes
Expand Tier I Mouse MP 26 Genes GS170265: MP:0006029 abnormal sclerotome morphology
Expand Tier III Rat 1482 Genes GS224478: Bone structure and strength QTL 53 (Bss53 Published QTL Chr 1)
Expand Tier III Rat 1027 Genes GS224721: Serum cholesterol QTL 36 (Scl36 Published QTL Chr 1)
Expand Tier I Human GO 110 Genes GS203402: GO:0007498 mesoderm development
Expand Tier I Human 64 Genes GS175226: HP:0008713 Genitourinary tract malformation
Expand Tier II Human 1485 Genes GS242199: [MeSH] Diencephalon : D004027
Expand Tier I Mouse GO 3293 Genes GS186214: GO:0048518 positive regulation of biological process
Expand Tier II Human 771 Genes GS241594: [MeSH] Neurosecretory Systems : D009490
Expand Tier II Human 394 Genes GS242515: [MeSH] Spine : D013131
Expand Tier I Mouse 198 Genes GS228641: MSigDB Geneset - GSE39820_TGFBETA3_IL6_VS_TGFBETA3_IL6_IL23A_TREATED_CD4_TCELL_UP
Expand Tier I Human GO 1454 Genes GS205144: GO:0048468 cell development
Expand Tier II Human 3263 Genes GS237180: [MeSH] Genetic Markers : D005819
Expand Tier I Human GO 1435 Genes GS205623: GO:0009888 tissue development
Expand Tier II Mouse 417 Genes GS35351: Cerebellum Gene expression correlates of Mechanical Nociception - Tail Clip Test in Males BXD
Expand Tier I Rat DRG 3886 Genes provisional GS86769: Table S2: HIPPOCAMPUS MGC MICROARRAY [DRG]
Expand Tier II Human 19354 Genes GS242551: [MeSH] Physiological Processes : D055705
Expand Tier II Human 10034 Genes GS243396: [MeSH] Neoplasm Proteins : D009363
Expand Tier I Mouse GO 86 Genes GS192949: GO:0050768 negative regulation of neurogenesis
Expand Tier II Human 1437 Genes GS243751: [MeSH] Hematopoietic Stem Cells : D006412
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Mouse MP 98 Genes GS167525: MP:0000154 rib fusion
Expand Tier II Human 9473 Genes GS241940: [MeSH] Urogenital System : D014566
Expand Tier I Human 260 Genes GS172033: HP:0000369 Low-set ears
Expand Tier II Human 213 Genes GS241743: [MeSH] Thorax : D013909
Expand Tier II Human 28877 Genes GS238592: [MeSH] Cells, Cultured : D002478
Expand Tier II Human 5846 Genes GS235187: [MeSH] Blood : D001769
Expand Tier I Mouse 897 Genes GS135415: bronchial hyperresponsiveness 6 (Bhr6, Published QTL Chr 7)
Expand Tier I Human 541 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier II Human 3354 Genes GS243507: [MeSH] Heart : D006321
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human GO 514 Genes GS207807: GO:0043009 chordate embryonic development
Expand Tier I Human 219 Genes GS228840: MSigDB Geneset - V$MAZR_01
Expand Tier I Mouse MP 1562 Genes GS168149: MP:0005508 abnormal skeleton morphology
Expand Tier I Mouse 200 Genes GS228535: MSigDB Geneset - GSE15324_NAIVE_VS_ACTIVATED_CD8_TCELL_UP
Expand Tier I Mouse MP 55 Genes GS168441: MP:0001008 abnormal sympathetic ganglion morphology
Expand Tier I Human 36 Genes GS174317: HP:0010306 Short thorax
Expand Tier I Human 141 Genes GS174721: HP:0000772 Abnormality of the ribs
Expand Tier I Mouse GO 592 Genes GS187168: GO:0010648 negative regulation of cell communication
Expand Tier I Mouse MP 2788 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Mouse MP 721 Genes GS168294: MP:0003699 abnormal female reproductive system physiology
Expand Tier I Mouse MP 106 Genes GS169237: MP:0000134 abnormal compact bone thickness
Expand Tier I Human GO 688 Genes GS210376: GO:0007417 central nervous system development
Expand Tier II Human 11221 Genes GS237257: [MeSH] Pathologic Processes : D010335
Expand Tier I Mouse MP 1548 Genes GS165789: MP:0005369 muscle phenotype
Expand Tier II Human 181 Genes GS245064: [MeSH] Presenilins : D053763
Expand Tier I Human 2919 Genes GS229203: MSigDB Geneset - GGGCGGR_V$SP1_Q6
Expand Tier I Mouse MP 1669 Genes GS169833: MP:0005380 embryogenesis phenotype
Expand Tier II Human 2533 Genes GS234080: [MeSH] Lung : D008168
Expand Tier III Rat 734 Genes GS224623: Serum cholesterol level QTL 6 (Scl6 Published QTL Chr 1)
Expand Tier II Human 4400 Genes GS240538: [MeSH] Embryonic Development : D047108
Expand Tier I Mouse GO 553 Genes GS188475: GO:0051093 negative regulation of developmental process
Expand Tier I Human 550 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human GO 5359 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human GO 1066 Genes GS196002: GO:0048699 generation of neurons
Expand Tier I Human GO 118 Genes GS198320: GO:0010721 negative regulation of cell development
Expand Tier I Mouse MP 108 Genes GS169785: MP:0000733 abnormal muscle development
Expand Tier I Human 189 Genes GS176745: HP:0010866 Abdominal wall defect
Expand Tier II Human 7014 Genes GS240404: [MeSH] Immune System : D007107
Expand Tier II Human 20775 Genes GS245804: [MeSH] Transcription Factors : D014157
Expand Tier I Mouse MP 1674 Genes GS169530: MP:0005390 skeleton phenotype
Expand Tier II Human 23211 Genes GS235538: [MeSH] Protein Binding : D011485
Expand Tier I Human 288 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier II Human 4360 Genes GS243856: [MeSH] Muscle, Striated : D054792
Expand Tier I Human 1002 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Mouse MP 6 Genes GS164083: MP:0004673 splayed ribs
Expand Tier I Human GO 13 Genes GS196439: GO:0048712 negative regulation of astrocyte differentiation
Expand Tier I Human 110 Genes GS173939: HP:0006101 Finger syndactyly
Expand Tier II Human 10298 Genes GS238960: [MeSH] Membrane Glycoproteins : D008562
Expand Tier I Mouse MP 2423 Genes GS168012: MP:0010832 lethality during fetal growth through weaning
Expand Tier I Mouse MP 702 Genes GS167922: MP:0000959 abnormal somatic sensory system morphology
Expand Tier II Human 2555 Genes GS242366: [MeSH] Inheritance Patterns : D040582
Expand Tier III Rat 1482 Genes GS224476: Bone structure and strength QTL 55 (Bss55 Published QTL Chr 1)
Expand Tier I Human 112 Genes GS172569: HP:0000343 Long philtrum
Expand Tier I Human 283 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier I Human 375 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier II Human 103 Genes GS239774: [MeSH] Receptor, Notch2 : D051883
Expand Tier II Human 9707 Genes GS235744: [MeSH] Neurons : D009474
Expand Tier I Human GO 4 Genes GS210556: GO:0007386 compartment pattern specification
Expand Tier II Human 13218 Genes GS245439: [MeSH] Protein Kinases : D011494
Expand Tier III Mouse 8151 Genes GS213076: Genes with suggestive difference in (B6) vs (B6PF1 + PB6F1 + PWD) comparison
Expand Tier I Mouse GO 5111 Genes GS187146: GO:0044700 single organism signaling
Expand Tier III Rat 1641 Genes GS223264: Neuroinflammation QTL 8 (Neuinf8 Published QTL Chr 1)
Expand Tier I Mouse MP 568 Genes GS168379: MP:0002151 abnormal neural tube morphology/development
Expand Tier II Human 5285 Genes GS238828: [MeSH] Locomotion : D008124
Expand Tier II Human 3143 Genes GS234697: [MeSH] Tumor Markers, Biological : D014408
Expand Tier II Human 58766 Genes GS243866: [MeSH] Laboratory Chemicals : D019995
Expand Tier II Human 705 Genes GS245663: [MeSH] Endoderm : D004707
Expand Tier II Human 2194 Genes GS235041: [MeSH] Glycosyltransferases : D016695
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 Mouse 649 Genes GS135679: Crhr1 transcript abundance QTL 1 (Crhr1taq1, Published QTL Chr 7)
Expand Tier I Mouse MP 394 Genes GS165567: MP:0008271 abnormal bone ossification
Expand Tier I Mouse MP 11449 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Mouse GO 1575 Genes GS188290: GO:0009966 regulation of signal transduction
Expand Tier I Human GO 679 Genes GS204029: GO:0010648 negative regulation of cell communication
Expand Tier I Mouse MP 1057 Genes GS166117: MP:0002108 abnormal muscle morphology
Expand Tier II Human 23476 Genes GS237836: [MeSH] Carrier Proteins : D002352
Expand Tier II Human 5087 Genes GS234776: [MeSH] Endocrine System : D004703
Expand Tier III Rat 1758 Genes GS223048: Hepatocarcinoma susceptibility QTL 2 (Hcas2 Published QTL Chr 1)
Expand Tier I Mouse GO 2538 Genes GS190893: GO:0030154 cell differentiation
Expand Tier I Mouse MP 120 Genes GS164105: MP:0003047 abnormal thoracic vertebrae morphology
Expand Tier II Human 6867 Genes GS243608: [MeSH] Viral Proteins : D014764
Expand Tier I Human 49 Genes GS173398: HP:0000776 Congenital diaphragmatic hernia
Expand Tier I Human 243 Genes GS176694: HP:0009810 Abnormality of the joints of the upper limbs
Expand Tier II Human 16221 Genes GS239275: [MeSH] Intracellular Signaling Peptides and Proteins : D047908
Expand Tier II Human 58901 Genes GS243233: [MeSH] Specialty Uses of Chemicals : D020313
Expand Tier I Mouse GO 72 Genes GS186079: GO:0035282 segmentation
Expand Tier I Human 189 Genes GS228974: MSigDB Geneset - GSE36476_YOUNG_VS_OLD_DONOR_MEMORY_CD4_TCELL_DN
Expand Tier I Human GO 4575 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Tier I Mouse 200 Genes GS228938: MSigDB Geneset - GSE17721_CTRL_VS_CPG_24H_BMDM_UP
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 1073 Genes GS228914: MSigDB Geneset - RYTTCCTG_V$ETS2_B
Expand Tier II Human 2569 Genes GS235802: [MeSH] Homeostasis : D006706
Expand Tier I Human 468 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier II Human 15607 Genes GS241444: [MeSH] Reproductive Physiological Phenomena : D055703
Expand Tier II Human 499 Genes GS235763: [MeSH] Chromosomes, Human, Pair 19 : D002888
Expand Tier I Human GO 2321 Genes GS206192: GO:0048583 regulation of response to stimulus