Gene Details



IL1RAPL1 and homologs in 4 species are found in 339 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 GO 66 Genes GS197352: GO:0050773 regulation of dendrite development
Expand Tier I Human 32 Genes GS173773: HP:0000194 Open mouth
Expand Tier I Human GO 408 Genes GS199582: GO:0016044 cellular membrane organization
Expand Tier I Human GO 691 Genes GS210096: GO:0032940 secretion by cell
Expand Tier II Mouse 319 Genes GS84318: METH responses for chewing (Published QTL, Chr X)
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human GO 217 Genes GS196320: GO:0060627 regulation of vesicle-mediated transport
Expand Tier I Human GO 412 Genes GS201052: GO:0061024 membrane organization
Expand Tier I Human 379 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human 491 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Human GO 187 Genes GS197672: GO:0010769 regulation of cell morphogenesis involved in differentiation
Expand Tier I Human 786 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human GO 215 Genes GS196883: GO:0097060 synaptic membrane
Expand Tier I Human GO 126 Genes GS206435: GO:0016358 dendrite development
Expand Tier I Mouse GO 774 Genes GS181423: GO:0022891 substrate-specific transmembrane transporter activity
Expand Tier I Human GO 954 Genes GS195976: GO:0007155 cell adhesion
Expand Tier I Human GO 440 Genes GS209602: GO:0051960 regulation of nervous system development
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 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Mouse GO 3615 Genes GS178359: GO:0071840 cellular component organization or biogenesis
Expand Tier I Mouse GO 3597 Genes GS188142: GO:0048856 anatomical structure development
Expand Tier I Human GO 1010 Genes GS196988: GO:0045595 regulation of cell differentiation
Expand Tier I Mouse GO 4001 Genes GS183543: GO:0051179 localization
Expand Tier I Mouse GO 2762 Genes GS178357: GO:0071842 cellular component organization at cellular level
Expand Tier I Mouse GO 446 Genes GS192944: GO:0050767 regulation of neurogenesis
Expand Tier I Mouse GO 124 Genes GS184856: GO:0072509 divalent inorganic cation transmembrane transporter activity
Expand Tier I Human GO 4371 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Mouse 323 Genes GS135526: body weight QTL (Bywq, Published QTL Chr X)
Expand Tier I Mouse MP 695 Genes GS168579: MP:0003635 abnormal synaptic transmission
Expand Tier I Human 453 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human GO 213 Genes GS197927: GO:0010975 regulation of neuron projection development
Expand Tier I Mouse GO 240 Genes GS181136: GO:0010975 regulation of neuron projection development
Expand Tier I Mouse GO 292 Genes GS178254: GO:0031344 regulation of cell projection organization
Expand Tier I Mouse GO 912 Genes GS179236: GO:0048699 generation of neurons
Expand Tier I Human GO 687 Genes GS197017: GO:0032990 cell part morphogenesis
Expand Tier I Human GO 793 Genes GS196790: GO:0046903 secretion
Expand Tier I Human 210 Genes GS174857: HP:0200006 Slanting of the palpebral fissure
Expand Tier I Mouse MP 375 Genes GS163926: MP:0004097 abnormal cerebellar cortex morphology
Expand Tier I Human 348 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier I Human GO 439 Genes GS202796: GO:0051046 regulation of secretion
Expand Tier I Mouse 290 Genes GS136285: modifier of Odc2 (Moo2, Published QTL Chr X)
Expand Tier I Human GO 1639 Genes GS204106: GO:0060089 molecular transducer activity
Expand Tier I Human 39 Genes GS174016: HP:0000717 Autism
Expand Tier I Human 397 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier I Mouse GO 1366 Genes GS193632: GO:0051649 establishment of localization in cell
Expand Tier I Human GO 393 Genes GS196169: GO:0005216 ion channel activity
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 1770 Genes GS194455: GO:0051239 regulation of multicellular organismal process
Expand Tier I Mouse 3319 Genes GS127931: Olfactory bulb - Allen Mouse Brain Atlas
Expand Tier I Human GO 533 Genes GS208131: GO:0045087 innate immune response
Expand Tier I Human GO 682 Genes GS205338: GO:0051094 positive regulation of developmental process
Expand Tier I Human GO 786 Genes GS195226: GO:0015075 ion transmembrane transporter activity
Expand Tier I Mouse GO 1064 Genes GS179401: GO:0005215 transporter activity
Expand Tier I Human GO 1096 Genes GS208716: GO:2000026 regulation of multicellular organismal development
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Mouse MP 334 Genes GS166799: MP:0009956 abnormal cerebellar layer morphology
Expand Tier I Human GO 270 Genes GS207070: GO:0051051 negative regulation of transport
Expand Tier I Human GO 700 Genes GS205439: GO:0031175 neuron projection development
Expand Tier I Human GO 302 Genes GS205812: GO:0022836 gated channel activity
Expand Tier I Human GO 2833 Genes GS198684: GO:0048523 negative regulation of cellular process
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human GO 2050 Genes GS203406: GO:0009653 anatomical structure morphogenesis
Expand Tier I Human GO 1972 Genes GS210586: GO:0051641 cellular localization
Expand Tier I Human 403 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Mouse GO 6473 Genes GS184448: GO:0044425 membrane part
Expand Tier I Mouse GO 639 Genes GS192628: GO:0048666 neuron development
Expand Tier I Human 39 Genes GS174048: HP:0000729 Autism spectrum disorder
Expand Tier I Human GO 471 Genes GS198213: GO:0022890 inorganic cation transmembrane transporter activity
Expand Tier I Human GO 4097 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Mouse MP 3716 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Human GO 993 Genes GS209525: GO:0032989 cellular component morphogenesis
Expand Tier I Human 446 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier I Human GO 4144 Genes GS200341: GO:0051179 localization
Expand Tier I Mouse MP 482 Genes GS163429: MP:0000849 abnormal cerebellum morphology
Expand Tier I Mouse GO 617 Genes GS178700: GO:0060341 regulation of cellular localization
Expand Tier I Mouse GO 8386 Genes GS189751: GO:0050794 regulation of cellular process
Expand Tier I Mouse GO 663 Genes GS180021: GO:0046903 secretion
Expand Tier I Human GO 112 Genes GS208041: GO:0015085 calcium ion transmembrane transporter activity
Expand Tier I Mouse GO 93 Genes GS191617: GO:0017157 regulation of exocytosis
Expand Tier I Human 46 Genes GS173611: HP:0002219 Facial hypertrichosis
Expand Tier I Human GO 80 Genes GS208549: GO:0017157 regulation of exocytosis
Expand Tier I Human 104 Genes GS173512: HP:0000306 Abnormality of the chin
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human GO 302 Genes GS205816: GO:0022839 ion gated channel activity
Expand Tier I Mouse GO 8942 Genes GS185492: GO:0050789 regulation of biological process
Expand Tier I Mouse GO 781 Genes GS184010: GO:0030030 cell projection organization
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Mouse GO 5892 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier I Mouse GO 825 Genes GS187237: GO:0030182 neuron differentiation
Expand Tier I Human GO 8622 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human GO 9 Genes GS208817: GO:0097090 presynaptic membrane organization
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Mouse GO 256 Genes GS182559: GO:0005261 cation channel activity
Expand Tier I Human 76 Genes GS171608: HP:0011338 Abnormality of mouth shape
Expand Tier I Human 232 Genes GS173288: HP:0000316 Hypertelorism
Expand Tier I Mouse GO 3614 Genes GS180229: GO:0005886 plasma membrane
Expand Tier I Human GO 1724 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Mouse GO 1166 Genes GS191779: GO:2000026 regulation of multicellular organismal development
Expand Tier I Human GO 285 Genes GS202125: GO:0030424 axon
Expand Tier I Human GO 271 Genes GS203896: GO:0006887 exocytosis
Expand Tier I Human GO 3104 Genes GS203058: GO:0048519 negative regulation of biological process
Expand Tier I Human GO 3513 Genes GS193991: GO:0048731 system development
Expand Tier I Human GO 10 Genes GS198645: GO:0045920 negative regulation of exocytosis
Expand Tier I Human GO 474 Genes GS200117: GO:0051130 positive regulation of cellular component organization
Expand Tier I Human 311 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human 253 Genes GS171634: HP:0008050 Abnormality of the palpebral fissures
Expand Tier I Human GO 493 Genes GS200286: GO:0060284 regulation of cell development
Expand Tier I Human GO 133 Genes GS200620: GO:0022843 voltage-gated cation channel activity
Expand Tier I Human GO 8 Genes GS199335: GO:0097105 presynaptic membrane assembly
Expand Tier I Mouse GO 397 Genes GS178812: GO:0015267 channel activity
Expand Tier I Human GO 6585 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Mouse GO 2872 Genes GS178360: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Human 77 Genes GS174230: HP:0000303 Mandibular prognathia
Expand Tier I Human GO 488 Genes GS205674: GO:0045202 synapse
Expand Tier I Human GO 76 Genes GS204424: GO:0048813 dendrite morphogenesis
Expand Tier I Human GO 608 Genes GS195457: GO:0060341 regulation of cellular localization
Expand Tier I Human 61 Genes GS171609: HP:0011339 Abnormality of upper lip vermillion
Expand Tier I Human 160 Genes GS175806: HP:0001417 X-linked inheritance
Expand Tier I Human 474 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Mouse GO 384 Genes GS188954: GO:0022838 substrate-specific channel activity
Expand Tier I Human GO 135 Genes GS202025: GO:0031346 positive regulation of cell projection organization
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Mouse GO 415 Genes GS181424: GO:0022890 inorganic cation transmembrane transporter activity
Expand Tier I Human GO 6151 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human GO 139 Genes GS201669: GO:0072509 divalent inorganic cation transmembrane transporter activity
Expand Tier I Mouse GO 15 Genes GS181852: GO:0045920 negative regulation of exocytosis
Expand Tier I Mouse 323 Genes GS136255: modifier of muscularity 6 (Mdmsc6, Published QTL Chr X)
Expand Tier I Mouse GO 790 Genes GS177334: GO:0016192 vesicle-mediated transport
Expand Tier I Human GO 121 Genes GS209893: GO:0050769 positive regulation of neurogenesis
Expand Tier I Human GO 7689 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier I Human 168 Genes GS170980: HP:0011362 Abnormal hair quantity
Expand Tier I Mouse GO 339 Genes GS181532: GO:0046873 metal ion transmembrane transporter activity
Expand Tier I Human GO 3409 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Mouse GO 1221 Genes GS187576: GO:0051128 regulation of cellular component organization
Expand Tier I Human GO 1456 Genes GS205144: GO:0048468 cell development
Expand Tier I Human GO 184 Genes GS201313: GO:0045211 postsynaptic membrane
Expand Tier I Mouse GO 509 Genes GS192789: GO:0008324 cation transmembrane transporter activity
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 15 Genes GS173040: HP:0010804 Tented upper lip vermilion
Expand Tier I Human GO 579 Genes GS204425: GO:0048812 neuron projection morphogenesis
Expand Tier I Human 83 Genes GS172098: HP:0000582 Upslanted palpebral fissure
Expand Tier I Human GO 14 Genes GS197346: GO:0050775 positive regulation of dendrite morphogenesis
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Mouse GO 280 Genes GS188949: GO:0022836 gated channel activity
Expand Tier I Human GO 1544 Genes GS195733: GO:0022607 cellular component assembly
Expand Tier I Mouse GO 886 Genes GS181425: GO:0022892 substrate-specific transporter activity
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Human GO 5436 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human 411 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human GO 1067 Genes GS196002: GO:0048699 generation of neurons
Expand Tier I Human 32 Genes GS172028: HP:0000363 Abnormality of earlobe
Expand Tier I Human GO 401 Genes GS205817: GO:0022838 substrate-specific channel activity
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 13 Genes GS171055: HP:0002342 Intellectual disability, moderate
Expand Tier I Human 139 Genes GS171397: HP:0000177 Abnormality of upper lip
Expand Tier III Mouse 8107 Genes GS213076: Genes with suggestive difference in (B6) vs (B6PF1 + PB6F1 + PWD) comparison
Expand Tier I 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 845 Genes GS198212: GO:0022891 substrate-specific transmembrane transporter activity
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Mouse MP 81 Genes GS166861: MP:0002945 abnormal inhibitory postsynaptic currents
Expand Tier I Mouse MP 14488 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Mouse MP 605 Genes GS167357: MP:0002206 abnormal CNS synaptic transmission
Expand Tier I Mouse GO 2538 Genes GS190893: GO:0030154 cell differentiation
Expand Tier I Human GO 4283 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Human GO 569 Genes GS209735: GO:0008324 cation transmembrane transporter activity
Expand Tier I Human 122 Genes GS173563: HP:0000692 Misalignment of teeth
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 Mouse GO 29 Genes GS191472: GO:0005245 voltage-gated calcium channel activity
Expand Tier I Human GO 331 Genes GS206569: GO:0045664 regulation of neuron differentiation
Expand Tier I Human GO 2824 Genes GS209411: GO:0048869 cellular developmental process
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Mouse GO 3605 Genes GS190682: GO:0007275 multicellular organismal development
Expand Tier I Human GO 273 Genes GS199357: GO:0005261 cation channel activity
Expand Tier I Human GO 3307 Genes GS195110: GO:0071842 cellular component organization at cellular level
Expand Tier I Human GO 956 Genes GS200151: GO:0022610 biological adhesion
Expand Tier I Human GO 419 Genes GS195569: GO:0015267 channel activity
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 Human GO 986 Genes GS204095: GO:0030182 neuron differentiation
Expand Tier I Mouse GO 980 Genes GS188826: GO:0022008 neurogenesis
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 61 Genes GS175740: HP:0010747 Medial flaring of the eyebrow
Expand Tier I Human GO 964 Genes GS202799: GO:0051049 regulation of transport
Expand Tier I Human GO 3318 Genes GS209452: GO:0006810 transport
Expand Tier I Mouse GO 167 Genes GS184303: GO:0005244 voltage-gated ion channel activity
Expand Tier I Human GO 355 Genes GS202124: GO:0030425 dendrite
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 2 Genes GS176939: HP:0009909 Uplifted earlobe
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 699 Genes GS210236: GO:0000904 cell morphogenesis involved in differentiation
Expand Tier I Human GO 590 Genes GS195737: GO:0022603 regulation of anatomical structure morphogenesis
Expand Tier I Human 203 Genes GS171621: HP:0100851 Abnormal emotion/affect behavior
Expand Tier I Human GO 3372 Genes GS194459: GO:0051234 establishment of localization
Expand Tier I Human 148 Genes GS171552: HP:0001382 Joint hypermobility
Expand Tier I Mouse GO 9323 Genes GS180152: GO:0065007 biological regulation
Expand Tier I Human GO 1639 Genes GS202760: GO:0004871 signal transducer activity
Expand Tier I Mouse GO 83 Genes GS185183: GO:0005262 calcium channel activity
Expand Tier I Mouse GO 397 Genes GS186078: GO:0022803 passive transmembrane transporter activity
Expand Tier I Human GO 794 Genes GS209568: GO:0048666 neuron development
Expand Tier I Mouse MP 486 Genes GS163438: MP:0000847 abnormal metencephalon morphology
Expand Tier I Mouse GO 371 Genes GS189692: GO:0045664 regulation of neuron differentiation
Expand Tier I Human GO 1539 Genes GS202759: GO:0004872 receptor activity
Expand Tier I Human GO 123 Genes GS202798: GO:0051048 negative regulation of secretion
Expand Tier I Mouse 25 Genes GS127948: Olfactory bulb only - Allen Mouse Brain Atlas
Expand Tier I Human 601 Genes GS172021: HP:0001367 Abnormal joint morphology
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 Human GO 1213 Genes GS204438: GO:0051128 regulation of cellular component organization
Expand Tier I Human GO 44 Genes GS206772: GO:0048814 regulation of dendrite morphogenesis
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human GO 1790 Genes GS194586: GO:0002376 immune system process
Expand Tier I Human GO 1336 Genes GS209622: GO:0038023 signaling receptor activity
Expand Tier I Mouse GO 97 Genes GS191133: GO:0015085 calcium ion transmembrane transporter activity
Expand Tier I Mouse GO 442 Genes GS185958: GO:0051046 regulation of secretion
Expand Tier I Human GO 1751 Genes GS210579: GO:0051649 establishment of localization in cell
Expand Tier I Mouse MP 1848 Genes GS167622: MP:0002152 abnormal brain morphology
Expand Tier I Human GO 370 Genes GS197471: GO:0044456 synapse part
Expand Tier I Human GO 178 Genes GS205810: GO:0022832 voltage-gated channel activity
Expand Tier I Human 43 Genes GS172862: HP:0000664 Synophrys
Expand Tier I Mouse GO 143 Genes GS185960: GO:0051048 negative regulation of secretion
Expand Tier I Mouse GO 280 Genes GS188953: GO:0022839 ion gated channel activity
Expand Tier I Human GO 36 Genes GS208399: GO:0005245 voltage-gated calcium channel activity
Expand Tier I Human GO 397 Genes GS209887: GO:0050767 regulation of neurogenesis
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 404 Genes GS204214: GO:0016337 cell-cell adhesion
Expand Tier I Human GO 419 Genes GS202908: GO:0022803 passive transmembrane transporter activity
Expand Tier I Human 251 Genes GS171793: HP:0000377 Abnormality of the pinna
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human GO 5320 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Mouse GO 1860 Genes GS177717: GO:0051239 regulation of multicellular organismal process
Expand Tier I Mouse GO 2710 Genes GS192471: GO:0048869 cellular developmental process
Expand Tier I Human GO 256 Genes GS195002: GO:0031344 regulation of cell projection organization
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Mouse GO 725 Genes GS178474: GO:0015075 ion transmembrane transporter activity
Expand Tier I Mouse 307 Genes GS135846: femoral cross-sectional area 4 (Fcsa4, Published QTL Chr X)
Expand Tier I Human GO 1126 Genes GS195108: GO:0071844 cellular component assembly at cellular level
Expand Tier I Human GO 925 Genes GS197610: GO:0022857 transmembrane transporter activity
Expand Tier I Mouse 336 Genes GS136813: testis weight 1 (Tesw1, Published QTL Chr X)
Expand Tier I Human GO 1242 Genes GS204740: GO:0004888 transmembrane signaling receptor activity
Expand Tier I Mouse GO 3211 Genes GS192509: GO:0006810 transport
Expand Tier I Human GO 1100 Genes GS206909: GO:0006952 defense response
Expand Tier I Human GO 75 Genes GS202196: GO:0007416 synapse assembly
Expand Tier I Human 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Mouse GO 239 Genes GS179556: GO:0060627 regulation of vesicle-mediated transport
Expand Tier I Human GO 1685 Genes GS199112: GO:0044085 cellular component biogenesis
Expand Tier I Human GO 940 Genes GS194065: GO:0016192 vesicle-mediated transport
Expand Tier I Mouse GO 8145 Genes GS190714: GO:0016020 membrane
Expand Tier I Mouse GO 549 Genes GS183491: GO:0060284 regulation of cell development
Expand Tier I Human GO 1055 Genes GS209480: GO:0006955 immune response
Expand Tier I Human 588 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Mouse GO 1075 Genes GS185961: GO:0051049 regulation of transport
Expand Tier I Mouse 323 Genes GS136824: thymocyte count 1 (Thyct1, Published QTL Chr X)
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 4213 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human 543 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Mouse GO 1608 Genes GS193639: GO:0051641 cellular localization
Expand Tier I Human GO 1195 Genes GS196168: GO:0005215 transporter activity
Expand Tier I Human GO 97 Genes GS201997: GO:0005262 calcium channel activity
Expand Tier I Human CTD 221 Genes GS125002: Topotecan interacting genes (MeSH:D019772) in CTD
Expand Tier I Mouse GO 852 Genes GS180817: GO:0022857 transmembrane transporter activity
Expand Tier I Human GO 374 Genes GS198322: GO:0046873 metal ion transmembrane transporter activity
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 649 Genes GS207805: GO:0043005 neuron projection
Expand Tier I Human GO 930 Genes GS200809: GO:0030030 cell projection organization
Expand Tier I Human 198 Genes GS174236: HP:0000534 Abnormality of the eyebrow
Expand Tier II Mouse 342 Genes GS35779: Neocortex Gene expression correlates of CPP - Time (s) in drug-paired compartment a in Males BXD
Expand Tier I Human 41 Genes GS173096: HP:0000678 Dental crowding
Expand Tier I Human 358 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Mouse GO 167 Genes GS188947: GO:0022832 voltage-gated channel activity
Expand Tier I Human GO 1136 Genes GS205691: GO:0022008 neurogenesis
Expand Tier I Human GO 980 Genes GS198214: GO:0022892 substrate-specific transporter activity
Expand Tier I Mouse MP 562 Genes GS163436: MP:0000841 abnormal hindbrain morphology
Expand Tier I Human GO 3446 Genes GS203057: GO:0048518 positive regulation of biological process
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Mouse GO 118 Genes GS183821: GO:0022843 voltage-gated cation channel activity
Expand Tier I Mouse GO 1378 Genes GS188287: GO:0048468 cell development
Expand Tier I Human 82 Genes GS175765: HP:0001419 X-linked recessive inheritance
Expand Tier I Human GO 498 Genes GS196986: GO:0045597 positive regulation of cell differentiation
Expand Tier I Mouse GO 1463 Genes GS189746: GO:0050793 regulation of developmental process
Expand Tier I Human GO 178 Genes GS201111: GO:0005244 voltage-gated ion channel activity
Expand Tier I Human GO 1324 Genes GS207293: GO:0032879 regulation of localization
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 GO 27 Genes GS206357: GO:0007157 heterophilic cell-cell adhesion
Expand Tier I Human GO 492 Genes GS195213: GO:0009986 cell surface
Expand Tier I Mouse GO 533 Genes GS188578: GO:0031175 neuron projection development
Expand Tier I Human GO 134 Genes GS198495: GO:0050808 synapse organization
Expand Tier I Human 433 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Mouse GO 3268 Genes GS177721: GO:0051234 establishment of localization
Expand Tier I Human GO 1211 Genes GS195176: GO:0005102 receptor binding
Expand Tier I Human GO 1224 Genes GS208482: GO:0042995 cell projection
Expand Tier I Mouse MP 2200 Genes GS165465: MP:0003633 abnormal nervous system physiology
Expand Tier I Human 567 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human GO 675 Genes GS204996: GO:0048858 cell projection morphogenesis
Expand Tier I Human GO 3121 Genes GS198685: GO:0048522 positive regulation of cellular process
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Mouse GO 1435 Genes GS190397: GO:0032879 regulation of localization
Expand Tier I Human 275 Genes GS170962: HP:0000159 Abnormality of the lip
Expand Tier I Mouse GO 3706 Genes GS188641: GO:0071944 cell periphery
Expand Tier I Human GO 571 Genes GS209569: GO:0048667 cell morphogenesis involved in neuron differentiation
Expand Tier I Mouse GO 293 Genes GS190177: GO:0051051 negative regulation of transport
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Mouse GO 375 Genes GS179402: GO:0005216 ion channel activity
Expand Tier I Human 166 Genes GS171901: HP:0010985 Gonosomal inheritance
Expand Tier I Human GO 2940 Genes GS210507: GO:0006950 response to stress
Expand Tier I Mouse 337 Genes GS136376: obesity QTL 22 (Obq22, Published QTL Chr X)
Expand Tier I Mouse GO 188 Genes GS187033: GO:0006887 exocytosis
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 Mouse GO 582 Genes GS193151: GO:0032940 secretion by cell
Expand Tier I Human GO 2661 Genes GS207797: GO:0030154 cell differentiation
Expand Tier I Human GO 4070 Genes GS207581: GO:0007275 multicellular organismal development
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 119 Genes GS172170: HP:0003196 Short nose
Expand Tier I Mouse GO 5734 Genes GS190713: GO:0016021 integral to membrane
Expand Tier I Human 639 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human GO 300 Genes GS195731: GO:0022604 regulation of cell morphogenesis
Expand Tier I Human 80 Genes GS172801: HP:0000752 Hyperactivity
Expand Tier I Mouse MP 3019 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier I Human GO 938 Genes GS210237: GO:0000902 cell morphogenesis
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 136 Genes GS173751: HP:0000998 Hypertrichosis
Expand Tier I Mouse MP 76 Genes GS170261: MP:0000889 abnormal cerebellar molecular layer
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier I Mouse GO 3493 Genes GS177570: GO:0016043 cellular component organization