Gene Details



HES7 and homologs in 4 species are found in 491 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 GO 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Human 99 Genes GS172242: HP:0004930 Abnormality of the pulmonary vasculature
Expand Tier I Mouse GO 894 Genes GS182704: GO:0051172 negative regulation of nitrogen compound metabolic process
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 Mouse 1047 Genes GS135864: femur length in high growth mice 4 (Feml4, Published QTL Chr 11)
Expand Tier I Mouse 1061 Genes GS136647: serum IGFBP-5 level QTL 6 (Si5lq6, Published QTL Chr 11)
Expand Tier I Mouse GO 1392 Genes GS184458: GO:0009892 negative regulation of metabolic process
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier II Mouse 86 Genes GS26119: Positional candidate genes for Thermal Nociception Hot Plate Avg of 2Trials [Pain] in Females for Significant BXD QTL on Chr11 from 68 to 70 Mb
Expand Tier I Mouse 996 Genes GS136853: Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 5 (Tmevd5, Published QTL Chr 11)
Expand Tier I Human 269 Genes GS172261: HP:0000357 Abnormal location of ears
Expand Tier I Human 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Mouse 595 Genes GS129171: pregnancy QTL 1 (Pregq1 Published QTL Chr 11)
Expand Tier I Human 178 Genes GS176151: HP:0000256 Macrocephaly
Expand Tier I Mouse 870 Genes GS136432: pulmonary adenoma susceptibility 5 (Pas5, Published QTL Chr 11)
Expand Tier I Human 360 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Mouse GO 4619 Genes GS191019: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier II Mouse 835 Genes GS84252: alcohol preference locus (Published QTL, Chr 11)
Expand Tier I Mouse MP 679 Genes GS170021: MP:0011087 complete neonatal lethality
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 Mouse GO 3776 Genes GS187887: GO:0080090 regulation of primary metabolic process
Expand Tier I Human 426 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Mouse GO 2763 Genes GS189669: GO:2000112 regulation of cellular macromolecule biosynthetic process
Expand Tier I Human GO 2896 Genes GS206108: GO:2001141 regulation of RNA biosynthetic process
Expand Tier I Human 157 Genes GS171718: HP:0002808 Kyphosis
Expand Tier I Mouse GO 4353 Genes GS192017: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human 121 Genes GS172789: HP:0001537 Umbilical hernia
Expand Tier I Mouse GO 779 Genes GS178588: GO:0045892 negative regulation of transcription, DNA-dependent
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 GO 4169 Genes GS207925: GO:0034645 cellular macromolecule biosynthetic process
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Mouse GO 3865 Genes GS193238: GO:0031323 regulation of cellular metabolic process
Expand Tier I Human GO 3917 Genes GS203908: GO:0016070 RNA metabolic process
Expand Tier I Mouse 1008 Genes GS136767: streptozotocin induced diabetes susceptibility (Stzid, Published QTL Chr 11)
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 GO 64 Genes GS187973: GO:0061053 somite development
Expand Tier I Mouse MP 680 Genes GS170243: MP:0011085 complete postnatal lethality
Expand Tier I Human 392 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Mouse 988 Genes GS136696: systematic lupus erythematosus susceptibility 13 (Sle13, Published QTL Chr 11)
Expand Tier I Mouse MP 533 Genes GS164258: MP:0002084 abnormal developmental patterning
Expand Tier I Mouse 885 Genes GS136294: modifier of Trp53 1 (Motp1, Published QTL Chr 11)
Expand Tier I Mouse 988 Genes GS136481: plasmacytoma susceptibility 3 (Pcyts3, Published QTL Chr 11)
Expand Tier I Mouse GO 4114 Genes GS193414: GO:0044249 cellular biosynthetic process
Expand Tier I Mouse 869 Genes GS136581: red blood cell QTL 3 (Rbcq3, Published QTL Chr 11)
Expand Tier I Mouse MP 55 Genes GS166588: MP:0005222 abnormal somite size
Expand Tier I Mouse MP 50 Genes GS169928: MP:0004173 abnormal intervertebral disk morphology
Expand Tier I Mouse GO 378 Genes GS188784: GO:0008134 transcription factor binding
Expand Tier I Human 741 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Mouse 3319 Genes GS127931: Olfactory bulb - Allen Mouse Brain Atlas
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 Mouse GO 176 Genes GS186208: GO:0048511 rhythmic process
Expand Tier I Human 492 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human 403 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Mouse MP 1183 Genes GS166409: MP:0002114 abnormal axial skeleton morphology
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 GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier III Mouse 6105 Genes GS213074: Genes with suggestive difference in (B6PF1) vs (PB6F1 + B6 + PWD) comparison
Expand Tier I Mouse GO 3021 Genes GS182703: GO:0051171 regulation of nitrogen compound metabolic process
Expand Tier I Human 32 Genes GS176375: HP:0000269 Prominent occiput
Expand Tier I Mouse GO 496 Genes GS192779: GO:0000122 negative regulation of transcription from RNA polymerase II promoter
Expand Tier I Mouse GO 4500 Genes GS186790: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Mouse 2963 Genes GS127934: Retrohippocampal region - Allen Mouse Brain Atlas
Expand Tier I Human GO 5452 Genes GS194111: GO:0097159 organic cyclic compound binding
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 Human GO 432 Genes GS205645: GO:0008134 transcription factor binding
Expand Tier I Mouse MP 80 Genes GS164488: MP:0005225 abnormal vertebrae development
Expand Tier I Mouse GO 8386 Genes GS189751: GO:0050794 regulation of cellular process
Expand Tier I Mouse GO 92 Genes GS192057: GO:0007219 Notch signaling pathway
Expand Tier I Mouse GO 809 Genes GS185258: GO:0051253 negative regulation of RNA metabolic process
Expand Tier I Mouse GO 2588 Genes GS187343: GO:0006351 transcription, DNA-dependent
Expand Tier I Human 148 Genes GS172906: HP:0003319 Abnormality of the cervical spine
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 403 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I 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 GO 3401 Genes GS200312: GO:0019219 regulation of nucleobase-containing compound metabolic process
Expand Tier I Human 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Mouse MP 1460 Genes GS164264: MP:0002082 postnatal lethality
Expand Tier I Mouse 1281 Genes GS129115: collagen induced arthritis 40 (Cia40 Published QTL Chr 11)
Expand Tier I Human GO 4314 Genes GS204746: GO:0080090 regulation of primary metabolic process
Expand Tier I Mouse MP 3437 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Mouse 870 Genes GS135519: body weight at necropsy 3 (Bwtn3, Published QTL Chr 11)
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
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 3626 Genes GS198456: GO:0019438 aromatic compound biosynthetic process
Expand Tier I Mouse MP 60 Genes GS164514: MP:0001690 failure of somite differentiation
Expand Tier I Human GO 3310 Genes GS194088: GO:0003676 nucleic acid binding
Expand Tier I Human 298 Genes GS174145: HP:0005918 Abnormality of phalanx of finger
Expand Tier I Mouse MP 4173 Genes GS165527: MP:0005378 growth/size phenotype
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Mouse 3267 Genes GS127938: Striatum - Allen Mouse Brain Atlas
Expand Tier I Mouse GO 933 Genes GS178813: GO:0046983 protein dimerization activity
Expand Tier I Mouse 1061 Genes GS136477: periosteal circumference 2 (Pcir2, Published QTL Chr 11)
Expand Tier I Human 384 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Human 384 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human 221 Genes GS172288: HP:0000358 Posteriorly rotated ears
Expand Tier I Mouse 761 Genes GS135686: C. trachomatis resistance QTL 3 (Ctrq3, Published QTL Chr 11)
Expand Tier I Mouse MP 181 Genes GS169017: MP:0002932 abnormal joint morphology
Expand Tier I Mouse 999 Genes GS135823: ethanol conditioned taste aversion 9 (Etohcta9, Published QTL Chr 11)
Expand Tier I Mouse GO 3978 Genes GS188506: GO:0010467 gene expression
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Mouse MP 74 Genes GS165484: MP:0001706 abnormal left-right axis patterning
Expand Tier I Mouse 1004 Genes GS135766: experimental allergic encephalomyelitis susceptibility 7 (Eae7, Published QTL Chr 11)
Expand Tier I Human GO 5369 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier I Mouse GO 4218 Genes GS192073: GO:1901576 organic substance biosynthetic process
Expand Tier I Mouse GO 7644 Genes GS188399: GO:0044238 primary metabolic process
Expand Tier I Mouse GO 4478 Genes GS184435: GO:0046483 heterocycle metabolic process
Expand Tier I Human GO 1439 Genes GS205623: GO:0009888 tissue development
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 545 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Mouse GO 4651 Genes GS177310: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Mouse 998 Genes GS136543: periosteal circumference 2 (Pstc2, Published QTL Chr 11)
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 MP 3110 Genes GS167020: MP:0003956 abnormal body size
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 908 Genes GS191157: GO:0010558 negative regulation of macromolecule biosynthetic process
Expand Tier I Mouse GO 2835 Genes GS191151: GO:0010556 regulation of macromolecule biosynthetic process
Expand Tier I Mouse GO 3757 Genes GS189460: GO:0060255 regulation of macromolecule metabolic process
Expand Tier I Human 189 Genes GS176745: HP:0010866 Abdominal wall defect
Expand Tier I Mouse 3096 Genes GS127928: Lateral septal complex - Allen Mouse Brain Atlas
Expand Tier I Mouse MP 1989 Genes GS169530: MP:0005390 skeleton phenotype
Expand Tier I Mouse GO 5247 Genes GS178448: GO:0005634 nucleus
Expand Tier I Human 291 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier I Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 110 Genes GS173939: HP:0006101 Finger syndactyly
Expand Tier I Mouse MP 11 Genes GS165075: MP:0005227 abnormal vertebral body development
Expand Tier I Mouse MP 2485 Genes GS168012: MP:0010832 lethality during fetal growth through weaning
Expand Tier I Mouse MP 10 Genes GS164623: MP:0004612 fusion of vertebral bodies
Expand Tier I Human 112 Genes GS172569: HP:0000343 Long philtrum
Expand Tier I Mouse MP 304 Genes GS168013: MP:0010831 partial lethality
Expand Tier I Human 285 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier I Mouse 2918 Genes GS127935: Striatum dorsal region - Allen Mouse Brain Atlas
Expand Tier I Human 378 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier I Mouse 848 Genes GS135593: P. chabaudi malaria resistance QTL 8 (Char8, Published QTL Chr 11)
Expand Tier I Human GO 3199 Genes GS208061: GO:0010556 regulation of macromolecule biosynthetic process
Expand Tier I Mouse GO 2536 Genes GS178537: GO:0006355 regulation of transcription, DNA-dependent
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
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 848 Genes GS136907: vertebral morphology and mechanical traits 12 (Vmmt12, Published QTL Chr 11)
Expand Tier I Mouse MP 63 Genes GS167224: MP:0000141 abnormal vertebral body morphology
Expand Tier I Human 941 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Mouse MP 14488 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Mouse 848 Genes GS136161: leishmaniasis resistance 15 (Lmr15, Published QTL Chr 11)
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 Mouse GO 3136 Genes GS187045: GO:0016070 RNA metabolic process
Expand Tier I Mouse GO 926 Genes GS192344: GO:0010629 negative regulation of gene expression
Expand Tier I Mouse 988 Genes GS136337: nicotine induced locomotor activity 2 (Nilac2, Published QTL Chr 11)
Expand Tier I Human GO 4377 Genes GS210182: GO:0031323 regulation of cellular metabolic process
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
Expand Tier I Mouse 1039 Genes GS136708: semilethal sex-restricted (Slthsr, Published QTL Chr 11)
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier III Mouse 629 Genes GS37187: Positional candidate on chromosome 11 (59-79Mb) for overdominant effect for 24-hour, 2 bottle choice 30g/kg EtOH excessive consumption.
Expand Tier I Human 470 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Mouse 1061 Genes GS136560: QTL for body weight independent of sex 3 (Qbis3, Published QTL Chr 11)
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 1061 Genes GS136086: kidney weight QTL 15 (Kwq15, Published QTL Chr 11)
Expand Tier I Mouse GO 2981 Genes GS177761: GO:0044271 cellular nitrogen compound biosynthetic process
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 Human 3 Genes GS172686: HP:0003305 Block vertebrae
Expand Tier I Human 210 Genes GS175990: HP:0000463 Anteverted nares
Expand Tier I Mouse 340 Genes GS129152: immunity to S. typhimurium 2b (Ity2b Published QTL Chr 11)
Expand Tier I Mouse MP 273 Genes GS167796: MP:0008770 decreased survivor rate
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse 799 Genes GS136611: colon tumor susceptibility 15 (Scc15, Published QTL Chr 11)
Expand Tier I Mouse 999 Genes GS136048: insulin dependent diabetes susceptibility 4 (Idd4, Published QTL Chr 11)
Expand Tier I Human GO 2957 Genes GS202080: GO:0051252 regulation of RNA metabolic process
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 180 Genes GS175902: HP:0003468 Abnormality of the vertebrae
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Mouse 848 Genes GS135430: bone mineral density 11 (Bmd11, Published QTL Chr 11)
Expand Tier I Mouse 885 Genes GS136502: proteoglycan induced arthritis 7 (Pgia7, Published QTL Chr 11)
Expand Tier I Mouse 856 Genes GS135919: graft-versus host disease 4 (Gvhd4, Published QTL Chr 11)
Expand Tier I Mouse MP 51 Genes GS170334: MP:0003345 decreased rib number
Expand Tier I Mouse GO 19 Genes GS192357: GO:0036342 post-anal tail morphogenesis
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 Mouse GO 954 Genes GS184460: GO:0009890 negative regulation of biosynthetic process
Expand Tier I Mouse 1077 Genes GS135507: body weight QTL 4 (Bw4, Published QTL Chr 11)
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 III Mouse 3192 Genes GS213073: Genes with suggestive difference in (PB6F1) vs (B6PF1 + B6 + PWD) comparison
Expand Tier I Human GO 5962 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Mouse MP 226 Genes GS167806: MP:0000164 abnormal cartilage development
Expand Tier I Mouse GO 6204 Genes GS184629: GO:0005515 protein binding
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 988 Genes GS136566: retinoic acid induced forelimb autopod reduction (Rafar, Published QTL Chr 11)
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 5221 Genes GS179211: GO:0007154 cell communication
Expand Tier I Mouse GO 4725 Genes GS192265: GO:0007165 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 768 Genes GS136219: mandible length 11 (Manln11, Published QTL Chr 11)
Expand Tier I Mouse MP 1211 Genes GS165536: MP:0005371 limbs/digits/tail phenotype
Expand Tier I Mouse 861 Genes GS136302: modifier of Salmonella typhimurium susceptibility 3 (Msts3, Published QTL Chr 11)
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 Human 212 Genes GS176185: HP:0100790 Hernia
Expand Tier I Mouse 1077 Genes GS135366: B.burgdorferi-associated arthritis 4 (Bbaa4, Published QTL Chr 11)
Expand Tier I Mouse MP 21 Genes GS164624: MP:0004613 fusion of vertebral arches
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 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 Mouse 883 Genes GS128596: Change in rotarod latency over training trials Chr#11
Expand Tier I Mouse 1142 Genes GS129196: Tmc1 modifier 2 (Tmc1m2 Published QTL Chr 11)
Expand Tier II Mouse 1002 Genes GS84253: alcohol preference locus (Published QTL, Chr 11)
Expand Tier I Mouse 3375 Genes GS127927: Hypothalamus - Allen Mouse Brain Atlas
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human 530 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human GO 4713 Genes GS205364: GO:0010467 gene expression
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 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 Human GO 5152 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier I Mouse GO 4286 Genes GS190949: GO:0009058 biosynthetic process
Expand Tier I Mouse MP 63 Genes GS164392: MP:0003050 abnormal sacral vertebrae morphology
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier III Mouse 1654 Genes GS37188: Positional candidate on Chromosome 11 (30-110 Mb) for dominant deviation measuring EtOH consumption during DID, 24 hour access and BEC.
Expand Tier I Mouse 870 Genes GS136651: skeletal size (tail length) 5 (Skl5, Published QTL Chr 11)
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse GO 3005 Genes GS177308: GO:1901362 organic cyclic compound biosynthetic process
Expand Tier I Mouse 990 Genes GS136439: peak bone density 1 (Pbd1, Published QTL Chr 11)
Expand Tier I Mouse MP 544 Genes GS166405: MP:0002111 abnormal tail morphology
Expand Tier I Mouse GO 1298 Genes GS183756: GO:0010605 negative regulation of macromolecule metabolic process
Expand Tier I Mouse 3289 Genes GS127924: Cerebral cortex - Allen Mouse Brain Atlas
Expand Tier I Mouse 3384 Genes GS127925: Hippocampal formation - Allen Mouse Brain Atlas
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 Mouse 768 Genes GS136398: organ weight 7 (Org7, Published QTL Chr 11)
Expand Tier I Human 324 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Mouse GO 1763 Genes GS178885: GO:0003677 DNA binding
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Mouse 996 Genes GS135295: acute lung injury QTL 1 (Aliq1, Published QTL Chr 11)
Expand Tier I Mouse GO 1466 Genes GS180001: GO:0048646 anatomical structure formation involved in morphogenesis
Expand Tier I Mouse GO 4588 Genes GS177309: GO:1901363 heterocyclic compound binding
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 2595 Genes GS188410: GO:0032774 RNA biosynthetic process
Expand Tier I Mouse GO 9049 Genes GS180166: GO:0008152 metabolic process
Expand Tier I Mouse 861 Genes GS136741: spermatocyte heat stress resistance 2 (Sphsr2, Published QTL Chr 11)
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 4446 Genes GS203072: GO:0090304 nucleic acid metabolic process
Expand Tier I Human 54 Genes GS176964: HP:0011217 Abnormal shape of the occiput
Expand Tier II Mouse 1017 Genes GS84254: nicotine sensitivity (Published QTL,Chr 11)
Expand Tier I Mouse 1004 Genes GS136517: platelet count 2 (Pltct2, Published QTL Chr 11)
Expand Tier I Mouse GO 4637 Genes GS177382: GO:0097159 organic cyclic compound binding
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 2944 Genes GS127937: Striatum-like amygdalar nuclei - Allen Mouse Brain Atlas
Expand Tier I Mouse 861 Genes GS136753: susceptibility to Salmonella typhimurium antigens 4 (Ssta4, Published QTL Chr 11)
Expand Tier I Human 426 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Mouse 2962 Genes GS127936: Striatum ventral region - Allen Mouse Brain Atlas
Expand Tier I Mouse 715 Genes GS128585: Rotarod Baseline Chr# 11
Expand Tier II Mouse 746 Genes GS84251: chronic alcohol withdrawal severity (Published QTL, Chr 11)
Expand Tier I Human 186 Genes GS171144: HP:0005280 Depressed nasal bridge
Expand Tier I Mouse GO 4518 Genes GS187751: GO:0019222 regulation of metabolic process
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 Mouse 848 Genes GS135349: Alzheimer's disease modifier 1 (Azdm1, Published QTL Chr 11)
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human GO 3201 Genes GS204204: GO:0006351 transcription, DNA-dependent
Expand Tier I Mouse GO 4073 Genes GS180034: GO:0032502 developmental process
Expand Tier I Human GO 6651 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
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 GO 2598 Genes GS185259: GO:0051252 regulation of RNA metabolic process
Expand Tier I Human GO 5379 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Mouse 996 Genes GS135461: bone mineral density 7 (Bomd7, Published QTL Chr 11)
Expand Tier I Human 421 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human 60 Genes GS174720: HP:0000775 Abnormality of the diaphragm
Expand Tier I Human GO 5601 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human 346 Genes GS171309: HP:0000252 Microcephaly
Expand Tier I Human GO 5558 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Mouse 763 Genes GS135765: experimental allergic encephalomyelitis susceptibility 6b (Eae6b, Published QTL Chr 11)
Expand Tier I Mouse GO 6947 Genes GS192918: GO:0050896 response to stimulus
Expand Tier I Human 17 Genes GS173373: HP:0002937 Hemivertebrae
Expand Tier I Mouse GO 2917 Genes GS190067: GO:0018130 heterocycle biosynthetic process
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 Mouse MP 30 Genes GS167522: MP:0000153 rib bifurcation
Expand Tier I Human GO 3287 Genes GS205266: GO:0032774 RNA biosynthetic process
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 Mouse MP 35 Genes GS164513: MP:0001691 abnormal somite shape
Expand Tier I Mouse 811 Genes GS136508: prion incubation determinant 3 (Pid3, Published QTL Chr 11)
Expand Tier I Mouse GO 55 Genes GS185983: GO:0001756 somitogenesis
Expand Tier I Mouse 850 Genes GS135939: HDL level 39 (Hdl39, Published QTL Chr 11)
Expand Tier I Human GO 7311 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human GO 5047 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Tier I Mouse GO 7552 Genes GS180452: GO:0044237 cellular metabolic process
Expand Tier I Mouse 3315 Genes GS127939: Thalamus - Allen Mouse Brain Atlas
Expand Tier I Mouse MP 18 Genes GS166593: MP:0005223 abnormal anterior-posterior polarity of the somites
Expand Tier I Human 271 Genes GS172637: HP:0010460 Abnormality of the female genitalia
Expand Tier I Human GO 969 Genes GS195570: GO:0046983 protein dimerization activity
Expand Tier I Human GO 3640 Genes GS206953: GO:0018130 heterocycle biosynthetic process
Expand Tier I Mouse 870 Genes GS135399: body growth early QTL 9 (Bgeq9, Published QTL Chr 11)
Expand Tier I Mouse MP 13 Genes GS165027: MP:0005229 abnormal intervertebral disk development
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human GO 3721 Genes GS194499: GO:0044271 cellular nitrogen compound biosynthetic process
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Mouse GO 2595 Genes GS177357: GO:0003676 nucleic acid binding
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Mouse GO 6435 Genes GS177531: GO:0043170 macromolecule metabolic process
Expand Tier I Human GO 8702 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 990 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Mouse GO 1208 Genes GS177214: GO:0006366 transcription from RNA polymerase II promoter
Expand Tier I Mouse GO 1850 Genes GS186562: GO:0009653 anatomical structure morphogenesis
Expand Tier I Human GO 4276 Genes GS207858: GO:0009059 macromolecule biosynthetic process
Expand Tier I Human 250 Genes GS172246: HP:0001371 Flexion contracture
Expand Tier I Human 433 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Mouse 3343 Genes GS127930: Midbrain - Allen Mouse Brain Atlas
Expand Tier I Mouse 3329 Genes GS127933: Pons - Allen Mouse Brain Atlas
Expand Tier I Mouse GO 871 Genes GS186097: GO:2000113 negative regulation of cellular macromolecule biosynthetic process
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 Mouse GO 8072 Genes GS184218: GO:0071704 organic substance metabolic process
Expand Tier I Mouse GO 370 Genes GS193610: GO:0007389 pattern specification process
Expand Tier I Human 187 Genes GS171907: HP:0004299 Hernia of the abdominal wall
Expand Tier I Human 387 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Mouse GO 2982 Genes GS183514: GO:0019219 regulation of nucleobase-containing compound metabolic process
Expand Tier I Mouse GO 5650 Genes GS183848: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Mouse GO 2855 Genes GS186757: GO:0034654 nucleobase-containing compound biosynthetic process
Expand Tier I Mouse 763 Genes GS135990: Hfe modifier 3 (Hfem3, Published QTL Chr 11)
Expand Tier I Mouse MP 969 Genes GS164257: MP:0002085 abnormal embryonic tissue morphology
Expand Tier I Mouse GO 880 Genes GS186179: GO:0045934 negative regulation of nucleobase-containing compound metabolic process
Expand Tier I Human 271 Genes GS176826: HP:0000202 Oral cleft
Expand Tier I Mouse MP 55 Genes GS163548: MP:0001689 incomplete somite formation
Expand Tier I Mouse MP 412 Genes GS167813: MP:0000163 abnormal cartilage morphology
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Mouse 850 Genes GS135637: cytokine induced activation 1 (Cinda1, Published QTL Chr 11)
Expand Tier I Human GO 5216 Genes GS208954: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Mouse GO 3473 Genes GS190950: GO:0009059 macromolecule biosynthetic process
Expand Tier I Mouse GO 1187 Genes GS181568: GO:0006357 regulation of transcription from RNA polymerase II promoter
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Mouse GO 8630 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse GO 8650 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse 990 Genes GS136605: spinal bone mineral density 4 (Sbmd4, Published QTL Chr 11)
Expand Tier I Mouse 763 Genes GS136658: skeletal muscle weight 17 (Skmw17, Published QTL Chr 11)
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 GO 5400 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Human 117 Genes GS173868: HP:0002143 Abnormality of the spinal cord
Expand Tier I Mouse GO 4887 Genes GS188190: GO:0006807 nitrogen compound metabolic process
Expand Tier I Mouse MP 120 Genes GS164196: MP:0009768 impaired somite development
Expand Tier I Mouse 3109 Genes GS127923: Cerebellum - Allen Mouse Brain Atlas
Expand Tier I Human GO 4070 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Mouse 1061 Genes GS136798: total body bone mineral density 5 (Tbbmd5, Published QTL Chr 11)
Expand Tier I Human 602 Genes GS176718: HP:0000078 Abnormality of the genital system
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 Mouse 1061 Genes GS136208: liver weight QTL 9 (Lwq9, Published QTL Chr 11)
Expand Tier I Human 533 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Human 264 Genes GS173014: HP:0010936 Abnormality of the lower urinary tract
Expand Tier I Human 639 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human 490 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Human GO 5223 Genes GS207857: GO:0009058 biosynthetic process
Expand Tier I Mouse GO 3311 Genes GS192279: GO:0007166 cell surface receptor signaling pathway
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 19 Genes GS172915: HP:0003310 Abnormality of the odontoid process
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier I Mouse GO 3599 Genes GS186227: GO:0090304 nucleic acid metabolic process
Expand Tier I Human 165 Genes GS171654: HP:0003121 Limb joint contracture
Expand Tier I Human GO 4811 Genes GS204612: GO:0019222 regulation of metabolic process
Expand Tier I Mouse MP 6 Genes GS165065: MP:0005224 abnormal left-right axis symmetry of the somites
Expand Tier I Mouse 590 Genes GS136646: serum IGFBP-5 level QTL 5 (Si5lq5, Published QTL Chr 11)
Expand Tier I Mouse 609 Genes GS135718: despair 2 (Desp2, Published QTL Chr 11)
Expand Tier I Human 486 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human 239 Genes GS174066: HP:0100737 Abnormality of the hard palate
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human GO 3573 Genes GS203607: GO:0034654 nucleobase-containing compound biosynthetic process
Expand Tier I Mouse 1047 Genes GS136901: ventral midbrain iron content 6 (Vmbic6, Published QTL Chr 11)
Expand Tier I Mouse GO 8414 Genes GS185585: GO:0044710 single-organism metabolic process
Expand Tier I Mouse 870 Genes GS136877: tooth shape 10 (Tshp10, Published QTL Chr 11)
Expand Tier I Mouse MP 994 Genes GS168502: MP:0002058 neonatal lethality
Expand Tier I Mouse MP 261 Genes GS168497: MP:0001256 abnormal body length
Expand Tier I Mouse MP 272 Genes GS167805: MP:0000150 abnormal rib morphology
Expand Tier I Human 34 Genes GS170804: HP:0003298 Spina bifida occulta
Expand Tier I Mouse 765 Genes GS136325: non-insulin-dependent diabetes mellitus 1 in NSY (Nidd1n, Published QTL Chr 11)
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 Human GO 2332 Genes GS195643: GO:0003677 DNA binding
Expand Tier I Mouse 763 Genes GS135793: ethanol induced low dose activation 1 (Elda1, Published QTL Chr 11)
Expand Tier I Human 235 Genes GS175523: HP:0000008 Abnormality of female internal genitalia
Expand Tier I Mouse GO 903 Genes GS184317: GO:0009790 embryo development
Expand Tier I Human 129 Genes GS172916: HP:0003312 Abnormal form of the vertebral bodies
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human GO 3118 Genes GS206544: GO:2000112 regulation of cellular macromolecule biosynthetic process
Expand Tier I Human 249 Genes GS176844: HP:0000429 Abnormality of the nasal alae
Expand Tier I Mouse 3289 Genes GS127932: Pallidum - Allen Mouse Brain Atlas
Expand Tier I Human 579 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human 281 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human 403 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Mouse GO 588 Genes GS184318: GO:0009792 embryo development ending in birth or egg hatching
Expand Tier I Human GO 4151 Genes GS206329: GO:0060255 regulation of macromolecule metabolic process
Expand Tier I Human GO 5948 Genes GS195199: GO:0005634 nucleus
Expand Tier I Mouse 850 Genes GS135966: HDL QTL 37 (Hdlq37, Published QTL Chr 11)
Expand Tier I Mouse GO 2540 Genes GS189240: GO:2001141 regulation of RNA biosynthetic process
Expand Tier I Mouse MP 384 Genes GS165361: MP:0004624 abnormal thoracic cage morphology
Expand Tier I Mouse GO 1223 Genes GS190386: GO:0031324 negative regulation of cellular metabolic process
Expand Tier I Mouse GO 5654 Genes GS182325: GO:0051716 cellular response to stimulus
Expand Tier I Mouse 1061 Genes GS136119: body length 6 (Lgth6, Published QTL Chr 11)
Expand Tier I Mouse GO 8942 Genes GS185492: GO:0050789 regulation of biological process
Expand Tier I Mouse 1061 Genes GS136528: prion disease incubation time 3 (Prdt3, Published QTL Chr 11)
Expand Tier I Mouse 1068 Genes GS136388: autoimmune orchitis resistance 3 (Orch3, Published QTL Chr 11)
Expand Tier III Mouse 5726 Genes GS213077: Genes with suggestive difference in (PWD) vs (PB6F1 + B6PF1 + B6) comparison
Expand Tier I Human 112 Genes GS171616: HP:0100490 Camptodactyly of finger
Expand Tier I Mouse MP 176 Genes GS168687: MP:0000592 short tail
Expand Tier I Mouse MP 247 Genes GS163546: MP:0001688 abnormal somite development
Expand Tier I Mouse 3395 Genes GS127929: Medulla - Allen Mouse Brain Atlas
Expand Tier I Mouse GO 2907 Genes GS181667: GO:0019438 aromatic compound biosynthetic process
Expand Tier I Mouse GO 583 Genes GS190900: GO:0043009 chordate embryonic development
Expand Tier I Mouse GO 3090 Genes GS188511: GO:0010468 regulation of gene expression
Expand Tier I Mouse GO 290 Genes GS193014: GO:0003002 regionalization
Expand Tier I Human 130 Genes GS173970: HP:0009473 Joint contracture of the hand
Expand Tier I Mouse 848 Genes GS135868: fat induced adiposity 1 (Fina1, Published QTL Chr 11)
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Mouse GO 2947 Genes GS193236: GO:0031326 regulation of cellular biosynthetic process
Expand Tier I Human 397 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Mouse GO 3382 Genes GS191021: GO:0034645 cellular macromolecule biosynthetic process
Expand Tier I Human GO 3487 Genes GS199499: GO:0051171 regulation of nitrogen compound metabolic process
Expand Tier I Human 17 Genes GS171717: HP:0005108 Abnormality of the intervertebral disk
Expand Tier I Human 137 Genes GS171202: HP:0100627 Displacement of the external urethral meatus
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human 39 Genes GS172815: HP:0000337 Broad forehead
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 GO 2875 Genes GS195291: GO:0006355 regulation of transcription, DNA-dependent
Expand Tier I Human 28 Genes GS173311: HP:0010651 Abnormality of the meninges
Expand Tier I Mouse 770 Genes GS136444: peak bone mineral density 4 (Pbmd4, Published QTL Chr 11)
Expand Tier I Human GO 3344 Genes GS205369: GO:0010468 regulation of gene expression
Expand Tier I Mouse GO 2984 Genes GS188762: GO:0009889 regulation of biosynthetic process
Expand Tier I Human GO 7689 Genes GS206623: GO:0050794 regulation of cellular process
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 112 Genes GS171810: HP:0005651 Flexion contracture of finger
Expand Tier I Human GO 110 Genes GS203402: GO:0007498 mesoderm development
Expand Tier I Mouse MP 1416 Genes GS164261: MP:0002081 perinatal lethality
Expand Tier I Human 64 Genes GS175226: HP:0008713 Genitourinary tract malformation
Expand Tier I Human GO 3737 Genes GS194038: GO:1901362 organic cyclic compound biosynthetic process
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 GO 937 Genes GS193235: GO:0031327 negative regulation of cellular biosynthetic process
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Mouse MP 1817 Genes GS168149: MP:0005508 abnormal skeleton morphology
Expand Tier I Mouse 762 Genes GS136864: T cell receptor induced activation 1 (Tria1, Published QTL Chr 11)
Expand Tier I Human GO 3324 Genes GS210180: GO:0031326 regulation of cellular biosynthetic process
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Human GO 3354 Genes GS205622: GO:0009889 regulation of biosynthetic process
Expand Tier I Mouse 1071 Genes GS135702: dopamine uptake transporter binding 4 (Dautb4, Published QTL Chr 11)