Gene Details



DLL3 and homologs in 1 species are found in 256 GeneSets:


- Entrez   - GeneNetwork   - Allen Brain Atlas   - Comparative Toxicogenomics Database  

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Human 187 Genes GS171907: HP:0004299 Hernia of the abdominal wall
Expand Tier I Human 385 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Human 112 Genes GS171810: HP:0005651 Flexion contracture of finger
Expand Tier I Human 98 Genes GS172242: HP:0004930 Abnormality of the pulmonary vasculature
Expand Tier I Human GO 110 Genes GS203402: GO:0007498 mesoderm development
Expand Tier I Human GO 48 Genes GS199084: GO:0045685 regulation of glial cell differentiation
Expand Tier I Human 64 Genes GS175226: HP:0008713 Genitourinary tract malformation
Expand Tier I Human 270 Genes GS176826: HP:0000202 Oral cleft
Expand Tier I Human 145 Genes GS171320: HP:0100360 Contractures of the joints of the upper limbs
Expand Tier I Human GO 1454 Genes GS205144: GO:0048468 cell development
Expand Tier I Human GO 3108 Genes GS198685: GO:0048522 positive regulation of cellular process
Expand Tier I Human GO 1435 Genes GS205623: GO:0009888 tissue development
Expand Tier I Human GO 7609 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 260 Genes GS172033: HP:0000369 Low-set ears
Expand Tier I Human 541 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Human GO 25 Genes GS208457: GO:0045686 negative regulation of glial cell differentiation
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
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 36 Genes GS174317: HP:0010306 Short thorax
Expand Tier I Human 141 Genes GS174721: HP:0000772 Abnormality of the ribs
Expand Tier I Human GO 688 Genes GS210376: GO:0007417 central nervous system development
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 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 Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 2828 Genes GS198684: GO:0048523 negative regulation of cellular process
Expand Tier I Human GO 8094 Genes GS202316: GO:0050789 regulation of biological process
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human 280 Genes GS176231: HP:0010938 Abnormality of the external nose
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 2047 Genes GS203406: GO:0009653 anatomical structure morphogenesis
Expand Tier I Human GO 38 Genes GS207739: GO:0008593 regulation of Notch signaling pathway
Expand Tier I Human GO 535 Genes GS205331: GO:0051093 negative regulation of developmental process
Expand Tier I Human GO 1066 Genes GS196002: GO:0048699 generation of neurons
Expand Tier I Human 267 Genes GS172261: HP:0000357 Abnormal location of ears
Expand Tier I Human 322 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Human GO 118 Genes GS198320: GO:0010721 negative regulation of cell development
Expand Tier I Human 641 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human CTD 1069 Genes GS121343: Flavonoids interacting genes (MeSH:D005419) in CTD
Expand Tier I Human GO 5243 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human 189 Genes GS176745: HP:0010866 Abdominal wall defect
Expand Tier I Human GO 70 Genes GS204831: GO:0061053 somite development
Expand Tier I Human 288 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier I Human 1002 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier III Human 3028 Genes GS137407: Supplementary Table 2. Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Human 401 Genes GS174217: HP:0005105 Abnormal nasal morphology
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 Human 825 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 176 Genes GS175103: HP:0000288 Abnormality of the philtrum
Expand Tier III Human 287 Genes GS213273: GenAge compiled genes related to human aging
Expand Tier I Human 395 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human 189 Genes GS176004: HP:0100656 Thoracoabdominal wall defects
Expand Tier I Human 194 Genes GS172034: HP:0000368 Low-set, posteriorly rotated ears
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 116 Genes GS173868: HP:0002143 Abnormality of the spinal cord
Expand Tier I Human 375 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier I Human CTD 377 Genes GS124417: Propylthiouracil interacting genes (MeSH:D011441) in CTD
Expand Tier I Human GO 4 Genes GS210556: GO:0007386 compartment pattern specification
Expand Tier I Human GO 520 Genes GS201126: GO:0009792 embryo development ending in birth or egg hatching
Expand Tier I Human GO 635 Genes GS205146: GO:0009968 negative regulation of signal transduction
Expand Tier I Human GO 2308 Genes GS209215: GO:0007166 cell surface receptor signaling pathway
Expand Tier I Human GO 2653 Genes GS207797: GO:0030154 cell differentiation
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 444 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier I Human 178 Genes GS176151: HP:0000256 Macrocephaly
Expand Tier I Human GO 137 Genes GS208994: GO:0007219 Notch signaling pathway
Expand Tier I Human GO 4061 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human GO 18 Genes GS207816: GO:0048339 paraxial mesoderm development
Expand Tier I Human 357 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human 53 Genes GS176964: HP:0011217 Abnormal shape of the occiput
Expand Tier I Human 936 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human 8 Genes GS175688: HP:0000902 Rib fusion
Expand Tier I Human 598 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 4014 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human GO 62 Genes GS208396: GO:0014013 regulation of gliogenesis
Expand Tier I Human 550 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human GO 679 Genes GS204029: GO:0010648 negative regulation of cell communication
Expand Tier I Human 146 Genes GS172906: HP:0003319 Abnormality of the cervical spine
Expand Tier I Human 530 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human CTD 6287 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human 174 Genes GS172293: HP:0001511 Intrauterine growth retardation
Expand Tier I Human 263 Genes GS173014: HP:0010936 Abnormality of the lower urinary tract
Expand Tier I Human 636 Genes GS172032: HP:0000366 Abnormality of the nose
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 I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 487 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Human 423 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Human 401 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 4575 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Human 423 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Human 263 Genes GS175823: HP:0002093 Respiratory insufficiency
Expand Tier I Human GO 8578 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human 184 Genes GS171144: HP:0005280 Depressed nasal bridge
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human GO 441 Genes GS209602: GO:0051960 regulation of nervous system development
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 161 Genes GS175958: HP:0000795 Abnormality of the urethra
Expand Tier I Human 134 Genes GS171627: HP:0000470 Short neck
Expand Tier I Human 468 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Human 220 Genes GS171139: HP:0005288 Abnormality of the nares
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 I Human 776 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
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 I Human GO 2321 Genes GS206192: GO:0048583 regulation of response to stimulus
Expand Tier I Human 157 Genes GS171718: HP:0002808 Kyphosis
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human GO 1722 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Human GO 2026 Genes GS201132: GO:0010646 regulation of cell communication
Expand Tier I Human GO 2816 Genes GS209411: GO:0048869 cellular developmental process
Expand Tier I Human 64 Genes GS176161: HP:0100589 Urogenital fistula
Expand Tier I Human GO 4960 Genes GS199124: GO:0051716 cellular response to stimulus
Expand Tier I Human 121 Genes GS172789: HP:0001537 Umbilical hernia
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 123 Genes GS171384: HP:0001551 Abnormality of the umbilicus
Expand Tier I Human 19 Genes GS172915: HP:0003310 Abnormality of the odontoid process
Expand Tier I Human 886 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 407 Genes GS175670: HP:0007364 Aplasia/Hypoplasia of the cerebrum
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 3 Genes GS172686: HP:0003305 Block vertebrae
Expand Tier I Human 209 Genes GS175990: HP:0000463 Anteverted nares
Expand Tier I Human GO 3098 Genes GS203058: GO:0048519 negative regulation of biological process
Expand Tier I Human CTD 121 Genes GS124719: perchlorate interacting genes (MeSH:C494474) in CTD
Expand Tier I Human GO 166 Genes GS194334: GO:0042063 gliogenesis
Expand Tier I Human 15 Genes GS172211: HP:0003510 Severe short stature
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 CTD 276 Genes GS125409: Triiodothyronine interacting genes (MeSH:D014284) in CTD
Expand Tier I Human 164 Genes GS171654: HP:0003121 Limb joint contracture
Expand Tier I Human 418 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human GO 3506 Genes GS193991: GO:0048731 system development
Expand Tier I Human GO 208 Genes GS201404: GO:0009952 anterior/posterior pattern specification
Expand Tier I Human GO 85 Genes GS202909: GO:0035282 segmentation
Expand Tier I Human 60 Genes GS174720: HP:0000775 Abnormality of the diaphragm
Expand Tier I Human 19 Genes GS176247: HP:0002948 Vertebral fusion
Expand Tier I Human GO 23 Genes GS202166: GO:0048710 regulation of astrocyte differentiation
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human 344 Genes GS171309: HP:0000252 Microcephaly
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human GO 154 Genes GS198319: GO:0010720 positive regulation of cell development
Expand Tier I Human 484 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human GO 1006 Genes GS196988: GO:0045595 regulation of cell differentiation
Expand Tier I Human GO 4575 Genes GS206355: GO:0023052 signaling
Expand Tier I Human 296 Genes GS174145: HP:0005918 Abnormality of phalanx of finger
Expand Tier I Human 178 Genes GS175902: HP:0003468 Abnormality of the vertebrae
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 389 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Human 17 Genes GS173373: HP:0002937 Hemivertebrae
Expand Tier I Human 273 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 442 Genes GS175423: HP:0010461 Abnormality of the male genitalia
Expand Tier I Human GO 4065 Genes GS209199: GO:0007165 signal transduction
Expand Tier I Human GO 12 Genes GS204524: GO:0005112 Notch binding
Expand Tier I Human GO 60 Genes GS202820: GO:0001756 somitogenesis
Expand Tier I Human 525 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human GO 4701 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human 130 Genes GS173970: HP:0009473 Joint contracture of the hand
Expand Tier I Human 837 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human GO 31 Genes GS208390: GO:0014014 negative regulation of gliogenesis
Expand Tier I Human GO 494 Genes GS200286: GO:0060284 regulation of cell development
Expand Tier I Human 236 Genes GS171395: HP:0000175 Cleft palate
Expand Tier I Human 542 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 1135 Genes GS205691: GO:0022008 neurogenesis
Expand Tier I Human 394 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human 238 Genes GS174066: HP:0100737 Abnormality of the hard palate
Expand Tier I Human GO 44 Genes GS202578: GO:0048708 astrocyte differentiation
Expand Tier I Human 382 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Human GO 6548 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 733 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human 8 Genes GS172183: HP:0011718 Abnormality of the pulmonary veins
Expand Tier I Human GO 2020 Genes GS206356: GO:0023051 regulation of signaling
Expand Tier I Human 607 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human 270 Genes GS172637: HP:0010460 Abnormality of the female genitalia
Expand Tier I Human GO 3432 Genes GS203057: GO:0048518 positive regulation of biological process
Expand Tier I Human 1046 Genes GS174453: HP:0001438 Abnormality of the abdomen
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 I Human 381 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human 34 Genes GS172548: HP:0001522 Death in infancy
Expand Tier I Human 917 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human GO 777 Genes GS206190: GO:0048585 negative regulation of response to stimulus
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 I Human GO 496 Genes GS196986: GO:0045597 positive regulation of cell differentiation
Expand Tier I Human GO 431 Genes GS196987: GO:0045596 negative regulation of cell differentiation
Expand Tier I Human 219 Genes GS172288: HP:0000358 Posteriorly rotated ears
Expand Tier I Human 186 Genes GS173355: HP:0002205 Recurrent respiratory infections
Expand Tier I Human GO 144 Genes GS204441: GO:0010001 glial cell differentiation
Expand Tier I Human GO 1770 Genes GS205147: GO:0009966 regulation of signal transduction
Expand Tier I Human 985 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human GO 1587 Genes GS196772: GO:0048646 anatomical structure formation involved in morphogenesis
Expand Tier I Human 97 Genes GS176756: HP:0011420 Death
Expand Tier I Human 39 Genes GS172815: HP:0000337 Broad forehead
Expand Tier I Human GO 898 Genes GS201125: GO:0009790 embryo development
Expand Tier I Human 317 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Human 249 Genes GS172246: HP:0001371 Flexion contracture
Expand Tier I Human GO 6073 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human 430 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 212 Genes GS176185: HP:0100790 Hernia
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 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 I Human 74 Genes GS171850: HP:0002414 Spina bifida
Expand Tier I Human 218 Genes GS175994: HP:0000464 Abnormality of the neck
Expand Tier I Human GO 1202 Genes GS195176: GO:0005102 receptor binding
Expand Tier I Human GO 121 Genes GS209893: GO:0050769 positive regulation of neurogenesis
Expand Tier I Human GO 1766 Genes GS194455: GO:0051239 regulation of multicellular organismal process
Expand Tier I Human GO 7650 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier I Human 532 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human 75 Genes GS172219: HP:0010301 Spinal dysraphism
Expand Tier I Human GO 676 Genes GS206354: GO:0023057 negative regulation of signaling
Expand Tier I Human 78 Genes GS175969: HP:0000069 Abnormality of the ureter
Expand Tier I Human 117 Genes GS170853: HP:0006261 Abnormality of phalangeal joints of the hand
Expand Tier I Human 22 Genes GS173165: HP:0002435 Meningocele
Expand Tier I Human 34 Genes GS170804: HP:0003298 Spina bifida occulta
Expand Tier I Human GO 17 Genes GS204939: GO:0045746 negative regulation of Notch signaling pathway
Expand Tier I Human GO 680 Genes GS205338: GO:0051094 positive regulation of developmental process
Expand Tier I Human 489 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human 598 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 435 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier I Human GO 4554 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human GO 1430 Genes GS206618: GO:0050793 regulation of developmental process
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human 529 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 401 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 196 Genes GS174756: HP:0011947 Respiratory tract infection
Expand Tier I Human 153 Genes GS175067: HP:0001159 Syndactyly
Expand Tier I Human 7 Genes GS175186: HP:0010772 Anomalous pulmonary venous return
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 228 Genes GS171908: HP:0004298 Abnormality of the abdominal wall
Expand Tier I Human 554 Genes GS175530: HP:0000002 Abnormality of body height
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 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 Human 676 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human 31 Genes GS171295: HP:0003508 Proportionate short stature
Expand Tier I Human GO 398 Genes GS209887: GO:0050767 regulation of neurogenesis
Expand Tier I Human 248 Genes GS176844: HP:0000429 Abnormality of the nasal alae