Gene Details



DLL3 and homologs in 3 species are found in 503 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 Mouse MP 1350 Genes GS165707: MP:0000428 abnormal craniofacial morphology
Expand Tier I Human 187 Genes GS171907: HP:0004299 Hernia of the abdominal wall
Expand Tier I Mouse GO 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Human 387 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Mouse MP 969 Genes GS164257: MP:0002085 abnormal embryonic tissue morphology
Expand Tier I Human 99 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 I Human 271 Genes GS176826: HP:0000202 Oral cleft
Expand Tier I Human 146 Genes GS171320: HP:0100360 Contractures of the joints of the upper limbs
Expand Tier I Mouse MP 127 Genes GS166501: MP:0003189 fused joints
Expand Tier I Human GO 3121 Genes GS198685: GO:0048522 positive regulation of cellular process
Expand Tier I Mouse 973 Genes GS136900: ventral midbrain iron content 4 (Vmbic4, Published QTL Chr 7)
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Mouse MP 223 Genes GS167526: MP:0000157 abnormal sternum morphology
Expand Tier I Mouse MP 38 Genes GS167812: MP:0000162 lordosis
Expand Tier I Mouse MP 36 Genes GS166697: MP:0001539 decreased caudal vertebrae number
Expand Tier I Human GO 25 Genes GS208457: GO:0045686 negative regulation of glial cell differentiation
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Mouse MP 24 Genes GS169514: MP:0002653 abnormal ependyma morphology
Expand Tier I Mouse MP 90 Genes GS170725: MP:0002566 abnormal sexual interaction
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 Human GO 429 Genes GS210555: GO:0007389 pattern specification process
Expand Tier I Human GO 93 Genes GS209892: GO:0050768 negative regulation of neurogenesis
Expand Tier I Mouse 1024 Genes GS136319: non-HDL QTL 6 (Nhdlq6, Published QTL Chr 7)
Expand Tier I Human 269 Genes GS172261: HP:0000357 Abnormal location of ears
Expand Tier I Mouse 653 Genes GS135346: Avp transcript abundance QTL 1 (Avptaq1, Published QTL Chr 7)
Expand Tier I Human 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Mouse 730 Genes GS136807: tuberculosis resistance 3 (Tbrs3, Published QTL Chr 7)
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 176 Genes GS175103: HP:0000288 Abnormality of the philtrum
Expand Tier I Human 189 Genes GS176004: HP:0100656 Thoracoabdominal wall defects
Expand Tier I Mouse GO 2678 Genes GS181892: GO:0048523 negative regulation of cellular process
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Human 117 Genes GS173868: HP:0002143 Abnormality of the spinal cord
Expand Tier I Human CTD 374 Genes GS124417: Propylthiouracil interacting genes (MeSH:D011441) in CTD
Expand Tier I Human GO 2317 Genes GS209215: GO:0007166 cell surface receptor signaling pathway
Expand Tier I Human GO 2661 Genes GS207797: GO:0030154 cell differentiation
Expand Tier I Human 178 Genes GS176151: HP:0000256 Macrocephaly
Expand Tier I Human GO 4070 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Mouse MP 242 Genes GS167156: MP:0000459 abnormal presacral vertebrae morphology
Expand Tier I Mouse MP 343 Genes GS166753: MP:0001935 decreased litter size
Expand Tier I Human 360 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human 8 Genes GS175688: HP:0000902 Rib fusion
Expand Tier I Human 602 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Mouse 958 Genes GS136745: spermatogenesis defect 3 (Spmd3, Published QTL Chr 7)
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 4024 Genes GS205002: GO:0048856 anatomical structure development
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 177 Genes GS172293: HP:0001511 Intrauterine growth retardation
Expand Tier I Human 264 Genes GS173014: HP:0010936 Abnormality of the lower urinary tract
Expand Tier I Mouse GO 5734 Genes GS190713: GO:0016021 integral to membrane
Expand Tier I Mouse MP 3 Genes GS168403: MP:0000589 thin tail
Expand Tier I Human 639 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Mouse MP 67 Genes GS169484: MP:0000729 abnormal myogenesis
Expand Tier I Human 490 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Mouse GO 179 Genes GS181529: GO:0010720 positive regulation of cell development
Expand Tier I Mouse MP 320 Genes GS169927: MP:0004174 abnormal spine curvature
Expand Tier I Mouse GO 3311 Genes GS192279: GO:0007166 cell surface receptor signaling pathway
Expand Tier I Human 426 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Mouse MP 3019 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier I Human GO 440 Genes GS209602: GO:0051960 regulation of nervous system development
Expand Tier I Mouse MP 2057 Genes GS169835: MP:0005389 reproductive system phenotype
Expand Tier I Mouse GO 588 Genes GS189483: GO:0023057 negative regulation of signaling
Expand Tier I Human 157 Genes GS171718: HP:0002808 Kyphosis
Expand Tier I Human GO 2033 Genes GS201132: GO:0010646 regulation of cell communication
Expand Tier I Human 121 Genes GS172789: HP:0001537 Umbilical hernia
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Mouse GO 1833 Genes GS184324: GO:0010646 regulation of cell communication
Expand Tier I Human 19 Genes GS172915: HP:0003310 Abnormality of the odontoid process
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Mouse GO 2994 Genes GS186215: GO:0048519 negative regulation of biological process
Expand Tier I Mouse GO 3080 Genes GS177265: GO:0048731 system development
Expand Tier I Human 16 Genes GS172211: HP:0003510 Severe short stature
Expand Tier I Human 165 Genes GS171654: HP:0003121 Limb joint contracture
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 I Mouse MP 792 Genes GS170024: MP:0011086 partial postnatal lethality
Expand Tier I Human 19 Genes GS176247: HP:0002948 Vertebral fusion
Expand Tier I Mouse MP 700 Genes GS165194: MP:0001533 abnormal skeleton physiology
Expand Tier I Mouse MP 1350 Genes GS165228: MP:0005382 craniofacial phenotype
Expand Tier I Mouse MP 257 Genes GS170425: MP:0004508 abnormal pectoral girdle bone morphology
Expand Tier I Mouse GO 64 Genes GS187973: GO:0061053 somite development
Expand Tier I Mouse 973 Genes GS136531: prion resistance 2 (Prnr2, Published QTL Chr 7)
Expand Tier I Human 486 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human GO 1010 Genes GS196988: GO:0045595 regulation of cell differentiation
Expand Tier I Human 392 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Human 275 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier I Human GO 12 Genes GS204524: GO:0005112 Notch binding
Expand Tier I Mouse 831 Genes GS136728: susceptibility to lung cancer 30 (Sluc30, Published QTL Chr 7)
Expand Tier I Mouse MP 533 Genes GS164258: MP:0002084 abnormal developmental patterning
Expand Tier I Mouse GO 446 Genes GS192944: GO:0050767 regulation of neurogenesis
Expand Tier I Mouse GO 548 Genes GS188289: GO:0009968 negative regulation of signal transduction
Expand Tier I Human GO 31 Genes GS208390: GO:0014014 negative regulation of gliogenesis
Expand Tier I Mouse GO 46 Genes GS185745: GO:0048708 astrocyte differentiation
Expand Tier I Mouse MP 55 Genes GS166588: MP:0005222 abnormal somite size
Expand Tier I Mouse MP 223 Genes GS167810: MP:0000160 kyphosis
Expand Tier I Mouse GO 1828 Genes GS189485: GO:0023051 regulation of signaling
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 Mouse MP 255 Genes GS169241: MP:0000130 abnormal trabecular bone morphology
Expand Tier I Mouse MP 25 Genes GS169781: MP:0000737 abnormal myotome development
Expand Tier I Mouse GO 912 Genes GS179236: GO:0048699 generation of neurons
Expand Tier I Human GO 781 Genes GS206190: GO:0048585 negative regulation of response to stimulus
Expand Tier I Human 187 Genes GS173355: HP:0002205 Recurrent respiratory infections
Expand Tier I Mouse MP 30 Genes GS162820: MP:0002907 abnormal parturition
Expand Tier I Human GO 899 Genes GS201125: GO:0009790 embryo development
Expand Tier I Mouse MP 261 Genes GS168497: MP:0001256 abnormal body length
Expand Tier I Human 741 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 I Human GO 1770 Genes GS194455: GO:0051239 regulation of multicellular organismal process
Expand Tier I Mouse MP 272 Genes GS167805: MP:0000150 abnormal rib morphology
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Mouse MP 105 Genes GS164406: MP:0004609 vertebral fusion
Expand Tier I Human GO 678 Genes GS206354: GO:0023057 negative regulation of signaling
Expand Tier I Human 34 Genes GS170804: HP:0003298 Spina bifida occulta
Expand Tier I Mouse 984 Genes GS135458: bone mineral density 4 (Bomd4, Published QTL Chr 7)
Expand Tier I Human GO 682 Genes GS205338: GO:0051094 positive regulation of developmental process
Expand Tier I Human 492 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Mouse GO 1172 Genes GS178426: GO:0005102 receptor binding
Expand Tier I Mouse GO 712 Genes GS188482: GO:0051094 positive regulation of developmental process
Expand Tier I Human 403 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 197 Genes GS174756: HP:0011947 Respiratory tract infection
Expand Tier I Human 7 Genes GS175186: HP:0010772 Anomalous pulmonary venous return
Expand Tier I Mouse MP 1183 Genes GS166409: MP:0002114 abnormal axial skeleton morphology
Expand Tier I Mouse GO 5111 Genes GS189484: GO:0023052 signaling
Expand Tier I Human 235 Genes GS175523: HP:0000008 Abnormality of female internal genitalia
Expand Tier I Human GO 1096 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 129 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 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Mouse MP 221 Genes GS168408: MP:0000585 kinked tail
Expand Tier I Mouse MP 3543 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier I Mouse GO 71 Genes GS191469: GO:0014013 regulation of gliogenesis
Expand Tier I Mouse GO 441 Genes GS180207: GO:0045596 negative regulation of cell differentiation
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 Human 32 Genes GS176375: HP:0000269 Prominent occiput
Expand Tier I Mouse MP 983 Genes GS166244: MP:0002752 abnormal somatic nervous system morphology
Expand Tier I Human GO 2833 Genes GS198684: GO:0048523 negative regulation of cellular process
Expand Tier I Human 281 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human GO 2050 Genes GS203406: GO:0009653 anatomical structure morphogenesis
Expand Tier I Human GO 537 Genes GS205331: GO:0051093 negative regulation of developmental process
Expand Tier I Mouse GO 19 Genes GS190909: GO:0048339 paraxial mesoderm development
Expand Tier I Human 403 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier III Human 288 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 I Mouse GO 6473 Genes GS184448: GO:0044425 membrane part
Expand Tier I Human GO 520 Genes GS201126: GO:0009792 embryo development ending in birth or egg hatching
Expand Tier I Mouse MP 3716 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Human 446 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier I Mouse MP 101 Genes GS166581: MP:0004599 abnormal vertebral arch morphology
Expand Tier I Mouse MP 384 Genes GS165361: MP:0004624 abnormal thoracic cage morphology
Expand Tier I Mouse MP 80 Genes GS164488: MP:0005225 abnormal vertebrae development
Expand Tier I Mouse 1027 Genes GS128580: BECs at LORR Recovery Chr# 7
Expand Tier I Mouse GO 8386 Genes GS189751: GO:0050794 regulation of cellular process
Expand Tier I Mouse GO 5654 Genes GS182325: GO:0051716 cellular response to stimulus
Expand Tier I Mouse GO 92 Genes GS192057: GO:0007219 Notch signaling pathway
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 I Mouse 973 Genes GS135988: Hfe modifier 1 (Hfem1, Published QTL Chr 7)
Expand Tier I Human 148 Genes GS172906: HP:0003319 Abnormality of the cervical spine
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Mouse MP 2406 Genes GS169391: MP:0002066 abnormal motor capabilities/coordination/movement
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Mouse GO 8942 Genes GS185492: GO:0050789 regulation of biological process
Expand Tier I Mouse GO 25 Genes GS191526: GO:0045686 negative regulation of glial cell differentiation
Expand Tier I Human 403 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Mouse MP 59 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 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 266 Genes GS175823: HP:0002093 Respiratory insufficiency
Expand Tier I Mouse GO 5892 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier I Human GO 8622 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human 56 Genes GS176473: HP:0003498 Disproportionate short stature
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier III Mouse 5726 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 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human GO 1724 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Mouse MP 176 Genes GS168687: MP:0000592 short tail
Expand Tier I Mouse GO 1166 Genes GS191779: GO:2000026 regulation of multicellular organismal development
Expand Tier I Mouse MP 1460 Genes GS164264: MP:0002082 postnatal lethality
Expand Tier I Human GO 3104 Genes GS203058: GO:0048519 negative regulation of biological process
Expand Tier I Mouse MP 3437 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Mouse MP 363 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 I Human GO 3513 Genes GS193991: GO:0048731 system development
Expand Tier I Mouse MP 247 Genes GS163546: MP:0001688 abnormal somite development
Expand Tier I Human GO 23 Genes GS202166: GO:0048710 regulation of astrocyte differentiation
Expand Tier III Rat 3441 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 82 Genes GS169236: MP:0000135 decreased compact bone thickness
Expand Tier I Human 298 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 4173 Genes GS165527: MP:0005378 growth/size phenotype
Expand Tier I Human 17 Genes GS173373: HP:0002937 Hemivertebrae
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Mouse GO 13 Genes GS179679: GO:0048712 negative regulation of astrocyte differentiation
Expand Tier I Mouse MP 4772 Genes GS165524: MP:0010769 abnormal survival
Expand Tier I Human 445 Genes GS175423: HP:0010461 Abnormality of the male genitalia
Expand Tier I Human GO 4084 Genes GS209199: GO:0007165 signal transduction
Expand Tier I Mouse MP 251 Genes GS169609: MP:0001674 abnormal triploblastic development
Expand Tier I Human GO 60 Genes GS202820: GO:0001756 somitogenesis
Expand Tier I Mouse MP 30 Genes GS167522: MP:0000153 rib bifurcation
Expand Tier I Human GO 4719 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human 130 Genes GS173970: HP:0009473 Joint contracture of the hand
Expand Tier I Mouse MP 438 Genes GS169234: MP:0000137 abnormal vertebrae morphology
Expand Tier I Mouse MP 3815 Genes GS165243: MP:0010770 preweaning lethality
Expand Tier I Human GO 493 Genes GS200286: GO:0060284 regulation of cell development
Expand Mouse 122 Genes GS213213: Collaborative Cross Cecum Microflora Parabiclique2 CC03.9t.8g.8g
Expand Tier I Mouse MP 35 Genes GS164513: MP:0001691 abnormal somite shape
Expand Tier I Mouse GO 55 Genes GS185983: GO:0001756 somitogenesis
Expand Tier I Mouse 1024 Genes GS136253: modifier of Dlk1 (mdlk1, Published QTL Chr 7)
Expand Tier I Human GO 1136 Genes GS205691: GO:0022008 neurogenesis
Expand Tier I Human 397 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Mouse MP 160 Genes GS164247: MP:0001680 abnormal mesoderm development
Expand Tier I Human GO 44 Genes GS202578: GO:0048708 astrocyte differentiation
Expand Tier I Human 384 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 6585 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human GO 2027 Genes GS206356: GO:0023051 regulation of signaling
Expand Tier I Human 271 Genes GS172637: HP:0010460 Abnormality of the female genitalia
Expand Tier I Mouse 940 Genes GS136189: lipoprotein QTL 5 (Lprq5, Published QTL Chr 7)
Expand Tier I Mouse MP 61 Genes GS169149: MP:0003400 kinked neural tube
Expand Tier I Human GO 3446 Genes GS203057: GO:0048518 positive regulation of biological process
Expand Tier II Mouse 929 Genes GS84191: alcohol preference 7 QTL (Ap7q, Published QTL, Chr 7)
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human 17 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 I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Human 384 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Mouse MP 1485 Genes GS166712: MP:0002161 abnormal fertility/fecundity
Expand Tier I Human 34 Genes GS172548: HP:0001522 Death in infancy
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Mouse GO 1378 Genes GS188287: GO:0048468 cell development
Expand Tier I Mouse 730 Genes GS136592: reactive oxygen species QTL 1 (Rosq1, Published QTL Chr 7)
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 Mouse MP 663 Genes GS165437: MP:0000438 abnormal cranium morphology
Expand Tier I Mouse GO 34 Genes GS181039: GO:0001709 cell fate determination
Expand Tier I Human GO 498 Genes GS196986: GO:0045597 positive regulation of cell differentiation
Expand Tier I Human GO 433 Genes GS196987: GO:0045596 negative regulation of cell differentiation
Expand Tier I Human 221 Genes GS172288: HP:0000358 Posteriorly rotated ears
Expand Tier I Human GO 144 Genes GS204441: GO:0010001 glial cell differentiation
Expand Tier I Mouse GO 1463 Genes GS189746: GO:0050793 regulation of developmental process
Expand Tier I Human 990 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Mouse GO 499 Genes GS192660: GO:0051960 regulation of nervous system development
Expand Tier I Human GO 1588 Genes GS196772: GO:0048646 anatomical structure formation involved in morphogenesis
Expand Tier I Human 98 Genes GS176756: HP:0011420 Death
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 I Mouse MP 181 Genes GS169017: MP:0002932 abnormal joint morphology
Expand Tier I Mouse GO 1850 Genes GS186562: GO:0009653 anatomical structure morphogenesis
Expand Tier I Mouse GO 95 Genes GS186558: GO:0007498 mesoderm development
Expand Tier I Human 250 Genes GS172246: HP:0001371 Flexion contracture
Expand Tier I Mouse MP 248 Genes GS166029: MP:0000960 abnormal sensory ganglion morphology
Expand Tier I Mouse GO 710 Genes GS189324: GO:0048585 negative regulation of response to stimulus
Expand Tier I Human GO 6151 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human 433 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 518 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human 28 Genes GS173311: HP:0010651 Abnormality of the meninges
Expand Tier I Human 74 Genes GS171850: HP:0002414 Spina bifida
Expand Tier I Human 220 Genes GS175994: HP:0000464 Abnormality of the neck
Expand Tier I Human GO 1211 Genes GS195176: GO:0005102 receptor binding
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 I Human GO 7689 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier I Mouse MP 360 Genes GS163635: MP:0001933 abnormal litter size
Expand Tier I Mouse GO 370 Genes GS193610: GO:0007389 pattern specification process
Expand Tier I Mouse MP 36 Genes GS163830: MP:0008029 abnormal paraxial mesoderm morphology
Expand Tier I Human 76 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 GO 17 Genes GS204939: GO:0045746 negative regulation of Notch signaling pathway
Expand Tier I Mouse GO 369 Genes GS181032: GO:0001701 in utero embryonic development
Expand Tier I Human 112 Genes GS171810: HP:0005651 Flexion contracture of finger
Expand Tier I Mouse MP 26 Genes GS170265: MP:0006029 abnormal sclerotome morphology
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 I Mouse GO 3293 Genes GS186214: GO:0048518 positive regulation of biological process
Expand Tier I Human GO 1456 Genes GS205144: GO:0048468 cell development
Expand Tier II Mouse 415 Genes GS35351: Cerebellum Gene expression correlates of Mechanical Nociception - Tail Clip Test in Males BXD
Expand Tier I Human GO 1439 Genes GS205623: GO:0009888 tissue development
Expand Tier I Mouse GO 86 Genes GS192949: GO:0050768 negative regulation of neurogenesis
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Mouse MP 99 Genes GS167525: MP:0000154 rib fusion
Expand Tier I Human 262 Genes GS172033: HP:0000369 Low-set ears
Expand Tier I Mouse 901 Genes GS135415: bronchial hyperresponsiveness 6 (Bhr6, Published QTL Chr 7)
Expand Tier I Human 545 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Human 1569 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 Mouse MP 1817 Genes GS168149: MP:0005508 abnormal skeleton morphology
Expand Tier I Mouse MP 55 Genes GS168441: MP:0001008 abnormal sympathetic ganglion morphology
Expand Tier I Human 37 Genes GS174317: HP:0010306 Short thorax
Expand Tier I Human 143 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 3110 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Mouse MP 743 Genes GS168294: MP:0003699 abnormal female reproductive system physiology
Expand Tier I Mouse MP 117 Genes GS169237: MP:0000134 abnormal compact bone thickness
Expand Tier I Human GO 688 Genes GS210376: GO:0007417 central nervous system development
Expand Tier I Mouse MP 1615 Genes GS165789: MP:0005369 muscle phenotype
Expand Tier I Mouse MP 1692 Genes GS169833: MP:0005380 embryogenesis phenotype
Expand Tier I Human 553 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Mouse GO 553 Genes GS188475: GO:0051093 negative regulation of developmental process
Expand Tier I Human GO 5436 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human GO 1067 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 I Mouse MP 1989 Genes GS169530: MP:0005390 skeleton phenotype
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 Mouse MP 7 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 I Mouse MP 2485 Genes GS168012: MP:0010832 lethality during fetal growth through weaning
Expand Tier I Mouse MP 710 Genes GS167922: MP:0000959 abnormal somatic sensory system morphology
Expand Tier I Human 112 Genes GS172569: HP:0000343 Long philtrum
Expand Tier I Human 285 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier I Human 378 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier I Human GO 4 Genes GS210556: GO:0007386 compartment pattern specification
Expand Tier III Mouse 8107 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 I Mouse MP 574 Genes GS168379: MP:0002151 abnormal neural tube morphology/development
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 Mouse 653 Genes GS135679: Crhr1 transcript abundance QTL 1 (Crhr1taq1, Published QTL Chr 7)
Expand Tier I Mouse MP 399 Genes GS165567: MP:0008271 abnormal bone ossification
Expand Tier I Mouse MP 14488 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 681 Genes GS204029: GO:0010648 negative regulation of cell communication
Expand Tier I Mouse MP 1108 Genes GS166117: MP:0002108 abnormal muscle morphology
Expand Tier I Mouse MP 122 Genes GS164105: MP:0003047 abnormal thoracic vertebrae morphology
Expand Tier I Mouse GO 2538 Genes GS190893: GO:0030154 cell differentiation
Expand Tier I Human 49 Genes GS173398: HP:0000776 Congenital diaphragmatic hernia
Expand Tier I Human 245 Genes GS176694: HP:0009810 Abnormality of the joints of the upper limbs
Expand Tier I Mouse GO 72 Genes GS186079: GO:0035282 segmentation
Expand Tier I Human GO 4593 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
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 GO 2335 Genes GS206192: GO:0048583 regulation of response to stimulus
Expand Tier I Mouse 728 Genes GS135381: bone density traits 4 (Bdt4, Published QTL Chr 7)
Expand Tier I Mouse GO 510 Genes GS180206: GO:0045597 positive regulation of cell differentiation
Expand Tier I Human GO 2824 Genes GS209411: GO:0048869 cellular developmental process
Expand Tier I Human 64 Genes GS176161: HP:0100589 Urogenital fistula
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Mouse 2087 Genes GS128573: Ethanol Induced Hypothermia Chr# 7
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 Mouse GO 3605 Genes GS190682: GO:0007275 multicellular organismal development
Expand Tier I Mouse MP 120 Genes GS169185: MP:0000755 hindlimb paralysis
Expand Tier I Human 3 Genes GS172686: HP:0003305 Block vertebrae
Expand Tier I Human 210 Genes GS175990: HP:0000463 Anteverted nares
Expand Tier I Human GO 166 Genes GS194334: GO:0042063 gliogenesis
Expand Tier I Mouse 975 Genes GS136602: sperm beat cross frequency (Sbcf, Published QTL Chr 7)
Expand Tier I Mouse GO 12 Genes GS187662: GO:0005112 Notch binding
Expand Tier I Mouse GO 534 Genes GS193432: GO:0007417 central nervous system development
Expand Tier I Mouse MP 4 Genes GS165359: MP:0004626 vertebral compression
Expand Tier I Mouse GO 4 Genes GS193611: GO:0007386 compartment pattern specification
Expand Tier I Mouse MP 141 Genes GS166579: MP:0005221 abnormal rostral-caudal axis patterning
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Mouse GO 1038 Genes GS180208: GO:0045595 regulation of cell differentiation
Expand Tier I Human GO 154 Genes GS198319: GO:0010720 positive regulation of cell development
Expand Tier I Mouse GO 980 Genes GS188826: GO:0022008 neurogenesis
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 51 Genes GS170334: MP:0003345 decreased rib number
Expand Tier I Mouse GO 53 Genes GS182284: GO:0045685 regulation of glial cell differentiation
Expand Tier I Mouse MP 26 Genes GS169156: MP:0004704 short vertebral column
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 Mouse MP 210 Genes GS163825: MP:0001258 decreased body length
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 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Mouse GO 6204 Genes GS184629: GO:0005515 protein binding
Expand Tier II Mouse 70 Genes GS34978: Hippocampus Gene expression correlates of Open Field - Habituation ratio (First:Last intervals) in Females & Males BXD
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 MP 513 Genes GS166404: MP:0002113 abnormal skeleton development
Expand Tier I Human 8 Genes GS172183: HP:0011718 Abnormality of the pulmonary veins
Expand Tier I Mouse GO 203 Genes GS188441: GO:0045165 cell fate commitment
Expand Tier I Mouse 973 Genes GS136264: modifier of mammary tumor progression 1 (Mmtp1, Published QTL Chr 7)
Expand Tier I Mouse GO 5221 Genes GS179211: GO:0007154 cell communication
Expand Tier I Mouse GO 160 Genes GS177596: GO:0042063 gliogenesis
Expand Tier I Mouse GO 4725 Genes GS192265: GO:0007165 signal transduction
Expand Tier I Human GO 1776 Genes GS205147: GO:0009966 regulation of signal transduction
Expand Tier I Mouse GO 9323 Genes GS180152: GO:0065007 biological regulation
Expand Tier I Mouse GO 193 Genes GS184601: GO:0009952 anterior/posterior pattern specification
Expand Tier I Mouse MP 1211 Genes GS165536: MP:0005371 limbs/digits/tail phenotype
Expand Tier I Human 319 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Mouse MP 2606 Genes GS165397: MP:0001265 decreased body size
Expand Tier I Mouse MP 380 Genes GS163569: MP:0002557 abnormal social/conspecific interaction
Expand Tier I Human 212 Genes GS176185: HP:0100790 Hernia
Expand Tier I Mouse MP 3543 Genes GS169095: MP:0004924 abnormal behavior
Expand Tier I Human 78 Genes GS175969: HP:0000069 Abnormality of the ureter
Expand Tier I Human 22 Genes GS173165: HP:0002435 Meningocele
Expand Tier I Mouse GO 2030 Genes GS189326: GO:0048583 regulation of response to stimulus
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 GO 4567 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human GO 1434 Genes GS206618: GO:0050793 regulation of developmental process
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Mouse GO 1398 Genes GS181215: GO:0007399 nervous system development
Expand Tier I Mouse MP 631 Genes GS166891: MP:0003795 abnormal bone structure
Expand Tier I Human 530 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human GO 386 Genes GS207498: GO:0001501 skeletal system development
Expand Tier I Human 153 Genes GS175067: HP:0001159 Syndactyly
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Mouse MP 12 Genes GS168198: MP:0000963 fused dorsal root ganglion
Expand Tier I Mouse MP 65 Genes GS169373: MP:0004322 abnormal sternebra morphology
Expand Tier I Human 229 Genes GS171908: HP:0004298 Abnormality of the abdominal wall
Expand Tier I Human 558 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Mouse 2121 Genes GS128593: Average rotarod training latency Chr# 7
Expand Tier I Mouse MP 90 Genes GS166246: MP:0002759 abnormal caudal vertebrae morphology
Expand Tier I Mouse 831 Genes GS136263: modifier of mammary tumor growth 3 (Mmtg3, Published QTL Chr 7)
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 32 Genes GS171295: HP:0003508 Proportionate short stature
Expand Tier I Mouse GO 14 Genes GS188080: GO:0045746 negative regulation of Notch signaling pathway
Expand Tier I Human GO 397 Genes GS209887: GO:0050767 regulation of neurogenesis
Expand Tier I Mouse MP 67 Genes GS163584: MP:0001007 abnormal sympathetic system morphology
Expand Tier I Mouse MP 544 Genes GS166405: MP:0002111 abnormal tail morphology
Expand Tier I Mouse GO 5859 Genes GS182404: GO:0031224 intrinsic to membrane
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 8137 Genes GS202316: GO:0050789 regulation of biological process
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 38 Genes GS207739: GO:0008593 regulation of Notch signaling pathway
Expand Tier I Mouse 1023 Genes GS136742: Streptococcus pneumoniae infection resistance 1 (Spir1, Published QTL Chr 7)
Expand Tier I Human 324 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Mouse MP 682 Genes GS166407: MP:0002116 abnormal craniofacial bone morphology
Expand Tier I Human CTD 1068 Genes GS121343: Flavonoids interacting genes (MeSH:D005419) in CTD
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human GO 5320 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human GO 70 Genes GS204831: GO:0061053 somite development
Expand Tier I Mouse GO 1466 Genes GS180001: GO:0048646 anatomical structure formation involved in morphogenesis
Expand Tier I Mouse GO 1860 Genes GS177717: GO:0051239 regulation of multicellular organismal process
Expand Tier I Human 398 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human 196 Genes GS172034: HP:0000368 Low-set, posteriorly rotated ears
Expand Tier I Mouse GO 2710 Genes GS192471: GO:0048869 cellular developmental process
Expand Tier II Mouse 45 Genes GS34982: Hippocampus Gene expression correlates of Open Field - Habituation ratio (First:Last intervals) in Males BXD
Expand Tier I Mouse 910 Genes GS135938: HDL level 38 (Hdl38, Published QTL Chr 7)
Expand Tier I Mouse 910 Genes GS135746: experimental allergic encephalomyelitis susceptibility 12 (Eae12, Published QTL Chr 7)
Expand Tier I Human GO 638 Genes GS205146: GO:0009968 negative regulation of signal transduction
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 137 Genes GS208994: GO:0007219 Notch signaling pathway
Expand Tier I Human GO 18 Genes GS207816: GO:0048339 paraxial mesoderm development
Expand Tier I Mouse GO 144 Genes GS192950: GO:0050769 positive regulation of neurogenesis
Expand Tier I Human 54 Genes GS176964: HP:0011217 Abnormal shape of the occiput
Expand Tier I Human 551 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Mouse GO 338 Genes GS190605: GO:0001501 skeletal system development
Expand Tier I Mouse MP 14 Genes GS165662: MP:0010152 abnormal brain ependyma morphology
Expand Tier I Mouse MP 134 Genes GS164109: MP:0003048 abnormal cervical vertebrae morphology
Expand Tier I Mouse MP 70 Genes GS163811: MP:0004643 abnormal vertebrae number
Expand Tier I Mouse MP 187 Genes GS169179: MP:0000753 paralysis
Expand Tier I Human 426 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Mouse MP 162 Genes GS166889: MP:0003797 abnormal compact bone morphology
Expand Tier I Mouse GO 32 Genes GS191463: GO:0014014 negative regulation of gliogenesis
Expand Tier I Mouse MP 1825 Genes GS168956: MP:0003491 abnormal voluntary movement
Expand Tier I Human 186 Genes GS171144: HP:0005280 Depressed nasal bridge
Expand Tier I Mouse GO 8145 Genes GS190714: GO:0016020 membrane
Expand Tier I Mouse MP 136 Genes GS164110: MP:0003049 abnormal lumbar vertebrae morphology
Expand Tier I Mouse GO 549 Genes GS183491: GO:0060284 regulation of cell development
Expand Tier I Mouse MP 684 Genes GS169663: MP:0004703 abnormal vertebral column morphology
Expand Tier I Human 162 Genes GS175958: HP:0000795 Abnormality of the urethra
Expand Tier I Human 136 Genes GS171627: HP:0000470 Short neck
Expand Tier I Human 221 Genes GS171139: HP:0005288 Abnormality of the nares
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse GO 4073 Genes GS180034: GO:0032502 developmental process
Expand Tier I Human GO 4983 Genes GS199124: GO:0051716 cellular response to stimulus
Expand Tier I Human 123 Genes GS171384: HP:0001551 Abnormality of the umbilicus
Expand Tier I Mouse MP 5057 Genes GS165525: MP:0010768 mortality/aging
Expand Tier I Mouse 940 Genes GS135417: beta-carboline induced seizures 4 (Bis4, Published QTL Chr 7)
Expand Tier I Human CTD 121 Genes GS124719: perchlorate interacting genes (MeSH:C494474) in CTD
Expand Tier I Mouse MP 712 Genes GS164770: MP:0009250 abnormal appendicular skeleton morphology
Expand Tier I Human CTD 277 Genes GS125409: Triiodothyronine interacting genes (MeSH:D014284) in CTD
Expand Tier I Human 421 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human GO 85 Genes GS202909: GO:0035282 segmentation
Expand Tier I Mouse MP 8 Genes GS166890: MP:0003794 delayed somite formation
Expand Tier I Mouse MP 1688 Genes GS168174: MP:0001919 abnormal reproductive system physiology