Gene Details



EDARADD and homologs in 7 species are found in 622 GeneSets:


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

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Mouse MP 1087 Genes GS165707: MP:0000428 abnormal craniofacial morphology
Expand Tier I Mouse GO 7747 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Human 386 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier II Mouse 25 Genes GS33882: Striatum Gene expression correlates of Distance traveled (cm) during the first five minutes after ethanol in Males BXD
Expand Tier I Human 130 Genes GS175744: HP:0001231 Abnormality of the fingernails
Expand Tier II Human 9028 Genes GS241666: [MeSH] Sequence Homology, Amino Acid : D017386
Expand Tier I Human 878 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Mouse MP 1190 Genes GS164220: MP:0002882 abnormal neuron morphology
Expand Tier I Mouse MP 1081 Genes GS166412: MP:0002118 abnormal lipid homeostasis
Expand Tier II Human 177 Genes GS238706: [MeSH] Blood Coagulation Disorders : D001778
Expand Tier III Human 1743 Genes GS246374: Differential Expression Hippocampus Human Cocaine Addicts
Expand Tier I Human 78 Genes GS227601: MSigDB Geneset - AGGGCCA,MIR-328
Expand Tier II Mouse 524 Genes GS136891: voluntary alcohol consumption QTL 5 (Vacq5, Published QTL Chr 13)
Expand Tier I Human GO 7611 Genes GS201949: GO:0044699 single-organism process
Expand Tier II Human 352 Genes GS237774: [MeSH] RNA Caps : D012315
Expand Tier II Human 9751 Genes GS244084: [MeSH] Phenotype : D010641
Expand Tier I Mouse 193 Genes GS228856: MSigDB Geneset - GSE24142_EARLY_THYMIC_PROGENITOR_VS_DN2_THYMOCYTE_DN
Expand Tier I Human CTD 817 Genes GS251896: Bortezomib interacting with Homo sapiens associated genes (MeSH:D000069286) in CTD
Expand Tier II Human 604 Genes GS237797: [MeSH] Transition Elements : D028561
Expand Tier I Human 58 Genes GS172176: HP:0000232 Everted lower lip vermilion
Expand Tier I Human 274 Genes GS170962: HP:0000159 Abnormality of the lip
Expand Tier I Mouse MP 9 Genes GS165082: MP:0006365 absent guard hair
Expand Tier II Human 4818 Genes GS238504: [MeSH] Tissues : D014024
Expand Tier I Human 1177 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 258 Genes GS229962: MSigDB Geneset - V$AML1_Q6
Expand Tier II Human 3562 Genes GS237717: [MeSH] Tissue Distribution : D014018
Expand Tier II Human 70 Genes GS235926: [MeSH] Dental Enamel : D003743
Expand Tier II Human 5070 Genes GS243926: [MeSH] Exons : D005091
Expand Tier I Mouse 170 Genes GS228141: MSigDB Geneset - ESC_J1_UP_EARLY.V1_UP
Expand Tier I Mouse MP 397 Genes GS167151: MP:0000454 abnormal jaw morphology
Expand Tier I Mouse GO 15 Genes GS187094: GO:0060438 trachea development
Expand Tier II Human 8948 Genes GS244882: [MeSH] Epithelial Cells : D004847
Expand Tier I Human 259 Genes GS232376: PC Geneset - "V$AML1_01" pathway genes
Expand Tier II Human 169 Genes GS244782: [MeSH] Blood Platelet Disorders : D001791
Expand Tier I Human CTD 4420 Genes GS124185: Plant Extracts interacting with Homo sapiens associated genes (MeSH:D010936) in CTD
Expand Tier II Human 6241 Genes GS236947: [MeSH] Brain : D001921
Expand Tier I Human 3 Genes GS173979: HP:0001106 Periorbital hyperpigmentation
Expand Tier II Human 17829 Genes GS235234: [MeSH] Biochemical Phenomena : D001669
Expand Tier II Human 14843 Genes GS237114: [MeSH] Regulatory Elements, Transcriptional : D050436
Expand Tier II Human 1743 Genes GS243816: [MeSH] Organogenesis : D038081
Expand Tier I Mouse MP 463 Genes GS167149: MP:0000452 abnormal mouth morphology
Expand Tier II Mouse 102 Genes GS35797: Striatum Gene expression correlates of Cocaine CPP- Time (s) in drug-paired compartment a in Females & Males BXD
Expand Tier II Mouse 370 Genes GS135384: body weight 1 (Bdw1, Published QTL Chr 13)
Expand Tier II Human 74 Genes GS239619: [MeSH] Manganese : D008345
Expand Tier I Mouse CTD 3927 Genes GS256188: Valinomycin interacting with Mus musculus associated genes (MeSH:D014634) in CTD
Expand Tier I Mouse 187 Genes GS229230: MSigDB Geneset - GSE24142_EARLY_THYMIC_PROGENITOR_VS_DN2_THYMOCYTE_ADULT_DN
Expand Tier II Human 6978 Genes GS245264: [MeSH] Nervous System : D009420
Expand Tier II Human 9308 Genes GS234359: [MeSH] Reproduction : D012098
Expand Tier II Human 529 Genes GS243881: [MeSH] MAP Kinase Kinase Kinases : D020930
Expand Tier II Human 4853 Genes GS239764: [MeSH] Glycoproteins : D006023
Expand Tier I Human 376 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier II Human 17829 Genes GS238030: [MeSH] Chemical Phenomena : D055598
Expand Tier I Human GO 2649 Genes GS207797: GO:0030154 cell differentiation
Expand Tier I Mouse MP 16 Genes GS168383: MP:0000417 short hair
Expand Tier I Human 97 Genes GS227949: MSigDB Geneset - chr1q42
Expand Tier I Human GO 4064 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier II Mouse 374 Genes GS136884: testis weight QTL 1 (Twq1, Published QTL Chr 13)
Expand Tier I Mouse MP 97 Genes GS169664: MP:0001314 corneal opacity
Expand Tier I Mouse MP 309 Genes GS166753: MP:0001935 decreased litter size
Expand Tier I Human 55 Genes GS174818: HP:0007495 Prematurely aged appearance
Expand Tier I Human GO 261 Genes GS197298: GO:0042303 molting cycle
Expand Tier II Human 112 Genes GS238847: [MeSH] Tail : D013623
Expand Tier II Human 1562 Genes GS245025: [MeSH] Receptors, Cytokine : D018121
Expand Tier I Human GO 4016 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human 783 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 637 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Mouse MP 17 Genes GS163139: MP:0005252 abnormal Meibomian gland morphology
Expand Tier II Human 11234 Genes GS236481: [MeSH] Enzymes : D004798
Expand Tier I Human 392 Genes GS229256: MSigDB Geneset - SMTTTTGT_UNKNOWN
Expand Tier I Human CTD 1798 Genes GS251956: C646 compound interacting with Homo sapiens associated genes (MeSH:C584509) in CTD
Expand Tier I Mouse MP 258 Genes GS165800: MP:0001923 reduced female fertility
Expand Tier I Mouse 194 Genes GS230671: MSigDB Geneset - GSE30083_SP1_VS_SP4_THYMOCYTE_UP
Expand Tier I Mouse MP 637 Genes GS168389: MP:0001186 pigmentation phenotype
Expand Tier I Mouse MP 8 Genes GS168354: MP:0006400 decreased molar number
Expand Tier I Mouse MP 2295 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier I Mouse MP 1879 Genes GS165528: MP:0005379 endocrine/exocrine gland phenotype
Expand Tier II Human 2522 Genes GS241084: [MeSH] Purine Nucleotides : D011685
Expand Tier I Human 22 Genes GS171992: HP:0011363 Abnormality of hair growth rate
Expand Tier I Mouse MP 1902 Genes GS169835: MP:0005389 reproductive system phenotype
Expand Tier I Mouse MP 41 Genes GS168627: MP:0000379 decreased hair follicle number
Expand Tier I Mouse 188 Genes GS227181: MSigDB Geneset - GSE24142_EARLY_THYMIC_PROGENITOR_VS_DN2_THYMOCYTE_FETAL_DN
Expand Tier II Human 2386 Genes GS234275: [MeSH] Heterozygote : D006579
Expand Tier I Human 34 Genes GS172053: HP:0000966 Hypohidrosis
Expand Tier II Rat 272 Genes GS223818: Glucose level QTL 49 (Gluco49 Published QTL Chr 17)
Expand Tier I Human 1219 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier II Human 43 Genes GS244391: [MeSH] Ectodysplasins : D053331
Expand Tier II Human 1770 Genes GS244236: [MeSH] Homozygote : D006720
Expand Tier I Human 736 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier III Mouse 80 Genes GS34965: Whole Brain Gene expression correlates of Open Field - Total distance traveled 5-10 minutes [Basal Behavior] in Females BXD
Expand Tier I Human 266 Genes GS229353: MSigDB Geneset - V$GR_Q6_01
Expand Tier I Mouse GO 3076 Genes GS177265: GO:0048731 system development
Expand Tier I Human GO 12166 Genes GS201251: GO:0044424 intracellular part
Expand Tier II Human 938 Genes GS235841: [MeSH] Peripheral Nerves : D010525
Expand Tier I Mouse 194 Genes GS230685: MSigDB Geneset - GSE30083_SP3_VS_SP4_THYMOCYTE_UP
Expand Tier II Human 4976 Genes GS243100: [MeSH] Protein-Serine-Threonine Kinases : D017346
Expand Tier I Mouse GO 3592 Genes GS188142: GO:0048856 anatomical structure development
Expand Tier I Mouse MP 727 Genes GS165874: MP:0002133 abnormal respiratory system physiology
Expand Tier I Mouse MP 1091 Genes GS165228: MP:0005382 craniofacial phenotype
Expand Tier II Human 300 Genes GS241760: [MeSH] Nerve Tissue : D009417
Expand Tier II Human 514 Genes GS237532: [MeSH] Extremities : D005121
Expand Tier II Human 4598 Genes GS244871: [MeSH] Time Factors : D013997
Expand Tier II Human 6064 Genes GS237183: [MeSH] Growth and Development : D048788
Expand Tier II Human 4862 Genes GS244627: [MeSH] Biological Processes : D055694
Expand Tier I Mouse MP 778 Genes GS166660: MP:0001731 abnormal postnatal growth
Expand Tier II Human 14167 Genes GS240208: [MeSH] Amino Acid Sequence : D000595
Expand Tier II Human 9588 Genes GS240239: [MeSH] Sequence Homology : D017385
Expand Tier I Mouse 190 Genes GS227723: MSigDB Geneset - GSE27786_BCELL_VS_NKCELL_UP
Expand Tier II Human 14336 Genes GS238002: [MeSH] Antisense Elements (Genetics) : D016375
Expand Tier I Human GO 3 Genes GS203211: GO:0061153 trachea gland development
Expand Tier I Mouse MP 280 Genes GS169082: MP:0002073 abnormal hair growth
Expand Tier I Mouse GO 118 Genes GS191736: GO:0022405 hair cycle process
Expand Tier I Mouse MP 614 Genes GS163226: MP:0003312 abnormal locomotor coordination
Expand Tier I Human 125 Genes GS230109: MSigDB Geneset - GTGCAAA,MIR-507
Expand Tier I Mouse MP 2 Genes GS163444: MP:0009825 cornea ulcer
Expand Tier I Human CTD 560 Genes GS123943: Curcumin interacting with Homo sapiens associated genes (MeSH:D003474) in CTD
Expand Tier I Mouse GO 65 Genes GS180717: GO:0042475 odontogenesis of dentin-containing tooth
Expand Tier II Human 2173 Genes GS234926: [MeSH] Epithelium : D004848
Expand Tier I Human 451 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human 52 Genes GS176598: HP:0000668 Hypodontia
Expand Tier II Human 13572 Genes GS242639: [MeSH] Metabolic Phenomena : D055754
Expand Tier II Mouse 26 Genes GS36412: Whole Brain Gene expression correlates of Open Field - Total rears 5-10 minutes in Females BXD
Expand Tier II Human 31 Genes GS241640: [MeSH] Toes : D014034
Expand Tier II Human 6336 Genes GS238872: [MeSH] Central Nervous System : D002490
Expand Tier II Human 2556 Genes GS241025: [MeSH] Ribonucleotides : D012265
Expand Tier I Mouse MP 1894 Genes GS163824: MP:0001259 abnormal body weight
Expand Tier II Rat 288 Genes GS224084: Body weight QTL 151 (Bw151 Published QTL Chr 17)
Expand Tier I Mouse MP 60 Genes GS170552: MP:0000876 Purkinje cell degeneration
Expand Tier II Human 3604 Genes GS240446: [MeSH] Pharmacokinetics : D010599
Expand Tier I Human CTD 69 Genes GS126426: 3,5-bis(2-fluorobenzylidene)piperidin-4-one interacting with Homo sapiens associated genes (MeSH:C524042) in CTD
Expand Tier I Mouse MP 246 Genes GS163926: MP:0004097 abnormal cerebellar cortex morphology
Expand Tier I Rat CTD 1207 Genes GS263577: Estradiol interacting with Rattus norvegicus associated genes (MeSH:D004958) in CTD
Expand Tier II Mouse 35 Genes GS36427: Whole Brain Gene expression correlates of Open Field - Total number of Rears in Females BXD
Expand Tier I Human CTD 486 Genes GS121843: 2,6-dinitrotoluene interacting with Colinus virginianus associated genes (MeSH:C023514) in CTD
Expand Tier II Human 16597 Genes GS235287: [MeSH] Proteins : D011506
Expand Tier II Human 802 Genes GS243625: [MeSH] Sex Chromosomes : D012730
Expand Tier II Human 16030 Genes GS243659: [MeSH] RNA, Messenger : D012333
Expand Tier II Mouse 507 Genes GS136779: systolic blood pressure 2 (Sysbp2, Published QTL Chr 13)
Expand Tier II Human 17816 Genes GS235305: [MeSH] DNA, Complementary : D018076
Expand Tier II Human 10126 Genes GS237194: [MeSH] Physiological Phenomena : D010829
Expand Tier II Human 3993 Genes GS239079: [MeSH] Cell Membrane : D002462
Expand Tier I Mouse GO 758 Genes GS188757: GO:0009887 organ morphogenesis
Expand Tier I Human 9 Genes GS176415: HP:0100678 Premature skin wrinkling
Expand Tier II Human 1454 Genes GS238126: [MeSH] Integumentary System : D034582
Expand Tier II Human 3665 Genes GS239266: [MeSH] Morphogenesis : D009024
Expand Tier II Human 11962 Genes GS245976: [MeSH] Cellular Structures : D022082
Expand Tier II Human 1141 Genes GS236278: [MeSH] Chromosome Aberrations : D002869
Expand Tier II Human 18212 Genes GS240572: [MeSH] DNA : D004247
Expand Tier II Human 11733 Genes GS241930: [MeSH] Mutation : D009154
Expand Tier I Mouse MP 2000 Genes GS168476: MP:0005451 abnormal body composition
Expand Tier I Mouse MP 18 Genes GS165441: MP:0000382 underdeveloped hair follicles
Expand Tier II Human 1358 Genes GS243025: [MeSH] Neuroglia : D009457
Expand Tier I Human 402 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier II Human 11248 Genes GS237794: [MeSH] Oligodeoxyribonucleotides : D009838
Expand Tier I Mouse MP 1251 Genes GS166409: MP:0002114 abnormal axial skeleton morphology
Expand Tier II Human 15234 Genes GS236911: [MeSH] Transcription, Genetic : D014158
Expand Tier II Human 16814 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier II Rat 288 Genes GS223917: Body weight QTL 140 (Bw140 Published QTL Chr 17)
Expand Tier II Human 309 Genes GS239040: [MeSH] Tumor Necrosis Factor Receptor-Associated Peptides and Proteins : D047988
Expand Tier I Human 22 Genes GS170891: HP:0006480 Premature loss of teeth
Expand Tier I Human GO 177 Genes GS201227: GO:0060541 respiratory system development
Expand Tier I Human GO 5627 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Mouse MP 196 Genes GS168408: MP:0000585 kinked tail
Expand Tier I Mouse MP 212 Genes GS166799: MP:0009956 abnormal cerebellar layer morphology
Expand Tier II Human 372 Genes GS242475: [MeSH] Schwann Cells : D012583
Expand Tier I Mouse MP 557 Genes GS167070: MP:0001921 reduced fertility
Expand Tier I Mouse MP 3256 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier II Human 7529 Genes GS239132: [MeSH] Gene Expression Regulation, Developmental : D018507
Expand Tier II Mouse 30 Genes GS35901: Cerebellum Gene expression correlates of Number of entries into open arms of plus maze in Males BXD
Expand Tier II Human 2191 Genes GS243603: [MeSH] 3T3 Cells : D016475
Expand Tier II Human 7336 Genes GS238771: [MeSH] Transferases : D014166
Expand Tier I Human 211 Genes GS174189: HP:0001597 Abnormality of the nail
Expand Tier II Human 28 Genes GS234900: [MeSH] Sex Chromosome Aberrations : D012729
Expand Tier II Human 19180 Genes GS243722: [MeSH] Genetic Structures : D040342
Expand Tier II Human 17454 Genes GS241889: [MeSH] Molecular Structure : D015394
Expand Tier II Mouse 374 Genes GS136221: mandible length 13 (Manln13, Published QTL Chr 13)
Expand Tier II Mouse 378 Genes GS136005: hapatic PMN infiltration 1 (Hpi1, Published QTL Chr 13)
Expand Tier I Human 12 Genes GS174782: HP:0002047 Malignant hyperthermia
Expand Tier II Human 4260 Genes GS234648: [MeSH] Alleles : D000483
Expand Tier I Human GO 9089 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 160 Genes GS230378: MSigDB Geneset - GSE13485_DAY1_VS_DAY3_YF17D_VACCINE_PBMC_UP
Expand Tier I Human GO 2047 Genes GS203406: GO:0009653 anatomical structure morphogenesis
Expand Tier II Human 17923 Genes GS234621: [MeSH] Chemical Actions and Uses : D020164
Expand Tier II Human 16633 Genes GS235061: [MeSH] Amino Acids, Peptides, and Proteins : D000602
Expand Tier I Human 25 Genes GS172624: HP:0000653 Sparse eyelashes
Expand Tier II Mouse 578 Genes GS84267: nicotine sensitivity (Published QTL, Chr 13)
Expand Tier I Human 402 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Human 311 Genes GS176642: HP:0011355 Localized skin lesion
Expand Tier I Mouse CTD 3927 Genes GS256187: Valproic Acid interacting with Mus musculus associated genes (MeSH:D014635) in CTD
Expand Tier I Mouse MP 482 Genes GS167656: MP:0001943 abnormal respiration
Expand Tier I Mouse GO 118 Genes GS191735: GO:0022404 molting cycle process
Expand Tier II Human 4880 Genes GS240252: [MeSH] Intercellular Signaling Peptides and Proteins : D036341
Expand Tier I Human 175 Genes GS173540: HP:0002115 Sparse or absent hair
Expand Tier II Human 10170 Genes GS235056: [MeSH] Peptides : D010455
Expand Tier II Human 15712 Genes GS236298: [MeSH] Gene Expression : D015870
Expand Tier I Mouse MP 98 Genes GS163177: MP:0000852 small cerebellum
Expand Tier I Mouse MP 5 Genes GS166950: MP:0000017 big ears
Expand Tier I Mouse MP 206 Genes GS167970: MP:0001340 abnormal eyelid morphology
Expand Tier I Mouse MP 2915 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier II Human 4608 Genes GS243806: [MeSH] Time : D013995
Expand Tier I Mouse MP 322 Genes GS163429: MP:0000849 abnormal cerebellum morphology
Expand Tier I Mouse MP 1562 Genes GS165386: MP:0001262 decreased body weight
Expand Tier II Human 13540 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier I Mouse MP 790 Genes GS168336: MP:0000367 abnormal coat/ hair morphology
Expand Tier I Human 71 Genes GS171600: HP:0000168 Abnormality of the gingiva
Expand Tier II Human 15098 Genes GS236076: [MeSH] Protein Conformation : D011487
Expand Tier I Human 1021 Genes GS232236: PC Geneset - "TGACCTY_V$ERR1_Q2" pathway genes
Expand Tier II Human 7493 Genes GS236470: [MeSH] DNA-Binding Proteins : D004268
Expand Tier II Human 5292 Genes GS239596: [MeSH] Expressed Sequence Tags : D020224
Expand Tier II Human 367 Genes GS234070: [MeSH] Skin Diseases, Genetic : D012873
Expand Tier I Human 121 Genes GS170890: HP:0006483 Abnormal number of teeth
Expand Tier II Human 9339 Genes GS234761: [MeSH] Reproductive Physiological Processes : D055704
Expand Tier I Mouse MP 2315 Genes GS169391: MP:0002066 abnormal motor capabilities/coordination/movement
Expand Tier II Human 748 Genes GS235487: [MeSH] Stomatognathic Diseases : D009057
Expand Tier I Human 1288 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 1069 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier II Human 335 Genes GS235950: [MeSH] Hair Follicle : D018859
Expand Tier II Human 290 Genes GS239475: [MeSH] Zinc : D015032
Expand Tier I Human 2115 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier II Human 711 Genes GS234729: [MeSH] Nutritional Physiological Phenomena : D009747
Expand Tier I Human 94 Genes GS176573: HP:0008065 Aplasia/Hypoplasia of the skin
Expand Tier I Mouse GO 5884 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier I Human GO 8581 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Mouse 195 Genes GS230290: MSigDB Geneset - GSE24142_EARLY_THYMIC_PROGENITOR_VS_DN3_THYMOCYTE_FETAL_DN
Expand Tier I Human 38 Genes GS268656: GWAS Catalog Data for urate measurement, body mass index in up to 15,007 European ancestry male individuals, up to 16,943 European ancestry female individuals
Expand Tier I Human GO 255 Genes GS194492: GO:0001942 hair follicle development
Expand Tier II Human 1694 Genes GS244083: [MeSH] Tumor Necrosis Factors : D048069
Expand Tier I Mouse 195 Genes GS229123: MSigDB Geneset - GSE36392_TYPE_2_MYELOID_VS_MAC_IL25_TREATED_LUNG_UP
Expand Tier I Mouse MP 6 Genes GS167366: MP:0001950 abnormal respiratory sounds
Expand Tier I Mouse GO 253 Genes GS177266: GO:0048732 gland development
Expand Tier II Human 5099 Genes GS244797: [MeSH] Disease Susceptibility : D004198
Expand Tier I Mouse MP 49 Genes GS169071: MP:0000418 focal hair loss
Expand Tier I Mouse MP 184 Genes GS169205: MP:0003717 pallor
Expand Tier I Mouse MP 834 Genes GS169389: MP:0002060 abnormal skin morphology
Expand Tier II Human 17259 Genes GS239769: [MeSH] Gene Library : D015723
Expand Tier I Mouse MP 1026 Genes GS164264: MP:0002082 postnatal lethality
Expand Tier II Human 16451 Genes GS242107: [MeSH] Chemical Processes : D055599
Expand Tier II Human 15903 Genes GS243578: [MeSH] Reading Frames : D016364
Expand Tier I Mouse MP 2874 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Zebrafish CTD 209 Genes GS261704: Equilin interacting with Danio rerio associated genes (MeSH:D004857) in CTD
Expand Tier II Rat 274 Genes GS223117: Gastrointestinal inflammation QTL 3 (Ginf3 Published QTL Chr 17)
Expand Tier II Human 11159 Genes GS237597: [MeSH] Cell Physiological Processes : D055648
Expand Tier II Human 756 Genes GS240201: [MeSH] Epidermis : D004817
Expand Tier I Human GO 3507 Genes GS193991: GO:0048731 system development
Expand Tier I Mouse MP 9 Genes GS168147: MP:0006236 absent Meibomian glands
Expand Tier I Mouse 194 Genes GS230089: MSigDB Geneset - GSE27786_BCELL_VS_ERYTHROBLAST_UP
Expand Tier I Mouse MP 21 Genes GS165264: MP:0000397 abnormal guard hair morphology
Expand Tier I Human GO 68 Genes GS197514: GO:0042475 odontogenesis of dentin-containing tooth
Expand Tier II Human 8835 Genes GS240544: [MeSH] Pregnancy : D011247
Expand Tier I Mouse MP 16 Genes GS167616: MP:0003932 abnormal molar crown morphology
Expand Tier I Human CTD 533 Genes GS127285: nickel chloride interacting with Homo sapiens associated genes (MeSH:C022838) in CTD
Expand Tier I Human GO 277 Genes GS193992: GO:0048732 gland development
Expand Tier II Human 11230 Genes GS237820: [MeSH] DNA Primers : D017931
Expand Tier I Mouse MP 425 Genes GS166123: MP:0002102 abnormal ear morphology
Expand Tier I Mouse MP 3960 Genes GS165527: MP:0005378 growth/size/body region phenotype
Expand Tier II Human 9485 Genes GS235276: [MeSH] Signal Transduction : D015398
Expand Tier I Human 3 Genes GS171449: HP:0000607 Periorbital wrinkles
Expand Tier I Human 2365 Genes GS175529: HP:0000001 All
Expand Tier I Mouse MP 4387 Genes GS165524: MP:0010769 abnormal survival
Expand Tier I Human GO 4064 Genes GS209199: GO:0007165 signal transduction
Expand Tier I Human CTD 1460 Genes GS124711: Genistein interacting with Homo sapiens associated genes (MeSH:D019833) in CTD
Expand Tier II Human 4 Genes GS234425: [MeSH] Edar-Associated Death Domain Protein : D053362
Expand Tier II Human 563 Genes GS237818: [MeSH] Diet : D004032
Expand Tier II Human 3864 Genes GS235095: [MeSH] Digestive System : D004064
Expand Tier II Human 6986 Genes GS237339: [MeSH] Regulatory Sequences, Nucleic Acid : D012045
Expand Tier I Human CTD 2771 Genes GS253114: ICG 001 interacting with Homo sapiens associated genes (MeSH:C492448) in CTD
Expand Tier II Human 3172 Genes GS236727: [MeSH] Skin and Connective Tissue Diseases : D017437
Expand Tier II Human 155 Genes GS240613: [MeSH] TNF Receptor-Associated Factor 6 : D048029
Expand Tier I Human GO 4699 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human 85 Genes GS175086: HP:0008388 Abnormality of the toenails
Expand Tier I Mouse MP 481 Genes GS164448: MP:0005193 abnormal anterior eye segment morphology
Expand Tier II Human 439 Genes GS244062: [MeSH] Oligodendroglia : D009836
Expand Tier I Human 908 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Mouse MP 3894 Genes GS165243: MP:0010770 preweaning lethality
Expand Tier I Mouse MP 2672 Genes GS169767: MP:0002396 abnormal hematopoietic system morphology/development
Expand Tier II Human 6493 Genes GS236576: [MeSH] Promoter Regions, Genetic : D011401
Expand Tier I Mouse MP 50 Genes GS167618: MP:0003930 abnormal tooth hard tissue morphology
Expand Tier II Human 18339 Genes GS238575: [MeSH] Nucleic Acids : D009696
Expand Tier I Human 122 Genes GS176258: HP:0004370 Abnormality of temperature regulation
Expand Tier II Human 1600 Genes GS237854: [MeSH] Peripheral Nervous System : D017933
Expand Tier I Mouse MP 53 Genes GS163553: MP:0003704 abnormal hair follicle development
Expand Tier I Human GO 6547 Genes GS209863: GO:0050896 response to stimulus
Expand Tier II Human 31 Genes GS235888: [MeSH] Edar Receptor : D053339
Expand Tier I Mouse MP 34 Genes GS167118: MP:0005287 narrow eye opening
Expand Tier II Human 10961 Genes GS242691: [MeSH] Embryonic Structures : D004628
Expand Tier I Human 93 Genes GS174190: HP:0001596 Alopecia
Expand Tier I Human CTD 840 Genes GS124274: Particulate Matter interacting with Homo sapiens associated genes (MeSH:D052638) in CTD
Expand Tier I Mouse MP 393 Genes GS163436: MP:0000841 abnormal hindbrain morphology
Expand Tier II Human 5491 Genes GS241654: [MeSH] Disease Attributes : D020969
Expand Tier II Human 1665 Genes GS239484: [MeSH] Gastrointestinal Tract : D041981
Expand Tier II Human 17884 Genes GS239502: [MeSH] Nucleic Acid Probes : D015341
Expand Tier I Human GO 2540 Genes GS203335: GO:0048513 organ development
Expand Tier II Mouse 437 Genes GS136440: peak bone density 2 (Pbd2, Published QTL Chr 13)
Expand Tier I Human 258 Genes GS227840: MSigDB Geneset - V$AML1_01
Expand Tier II Human 737 Genes GS239890: [MeSH] Mouth : D009055
Expand Tier I Mouse GO 22819 Genes GS180164: GO:0008150 biological_process
Expand Tier II Human 8777 Genes GS244835: [MeSH] Chromosomes : D002875
Expand Tier II Human 155 Genes GS234790: [MeSH] Tooth Components : D019589
Expand Tier II Mouse 28 Genes GS36379: Striatum Gene expression correlates of Open Field - Total rears 10-15 minutes in Females BXD
Expand Tier II Human 2091 Genes GS237069: [MeSH] Congenital Abnormalities : D000013
Expand Tier I Mouse MP 1361 Genes GS166712: MP:0002161 abnormal fertility/fecundity
Expand Tier II Human 5184 Genes GS241851: [MeSH] Receptors, Cell Surface : D011956
Expand Tier I Mouse MP 639 Genes GS165437: MP:0000438 abnormal cranium morphology
Expand Tier II Human 15271 Genes GS242059: [MeSH] Cells : D002477
Expand Tier I Human 61 Genes GS171609: HP:0011339 Abnormality of upper lip vermillion
Expand Tier II Human 2500 Genes GS238149: [MeSH] Metals : D008670
Expand Tier II Human 169 Genes GS241884: [MeSH] Suppression, Genetic : D013489
Expand Tier I Mouse GO 184 Genes GS184422: GO:0060541 respiratory system development
Expand Tier I Human 5 Genes GS174822: HP:0010803 Everted upper lip vermilion
Expand Tier I Human GO 255 Genes GS208672: GO:0022404 molting cycle process
Expand Tier I Mouse MP 115 Genes GS165949: MP:0000416 sparse hair
Expand Tier I Human GO 3 Genes GS203212: GO:0061152 trachea submucosa development
Expand Tier II Human 18365 Genes GS244482: [MeSH] Nucleic Acids, Nucleotides, and Nucleosides : D009706
Expand Tier I Mouse MP 140 Genes GS163970: MP:0002095 abnormal skin pigmentation
Expand Tier I Mouse GO 1849 Genes GS186562: GO:0009653 anatomical structure morphogenesis
Expand Tier I Human 470 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Human CTD 1571 Genes GS124037: Oxygen interacting with Homo sapiens associated genes (MeSH:D010100) in CTD
Expand Tier II Human 1853 Genes GS237007: [MeSH] Cell Membrane Structures : D021961
Expand Tier I Human GO 14550 Genes GS208012: GO:0044464 cell part
Expand Tier I Human 30 Genes GS170892: HP:0006481 Abnormality of primary teeth
Expand Tier I Human GO 16873 Genes GS210212: GO:0005575 cellular_component
Expand Tier II Human 474 Genes GS241696: [MeSH] Wound Healing : D014945
Expand Tier II Human 8178 Genes GS243735: [MeSH] Biological Factors : D001685
Expand Tier II Human 2705 Genes GS245493: [MeSH] Purines : D011687
Expand Tier II Human 17873 Genes GS235797: [MeSH] DNA Probes : D015342
Expand Tier II Human 14315 Genes GS237296: [MeSH] RNA, Antisense : D016372
Expand Tier I Human 59 Genes GS175262: HP:0000964 Eczema
Expand Tier II Human 5214 Genes GS242147: [MeSH] Fibroblasts : D005347
Expand Tier I Mouse MP 19 Genes GS164498: MP:0009535 abnormal skin sebaceous gland morphology
Expand Tier I Mouse GO 1203 Genes GS188763: GO:0009888 tissue development
Expand Tier I Mouse MP 1583 Genes GS165465: MP:0003633 abnormal nervous system physiology
Expand Tier II Human 11214 Genes GS242332: [MeSH] Cell Physiological Phenomena : D002468
Expand Tier I Human 217 Genes GS228551: MSigDB Geneset - ACTGCCT,MIR-34B
Expand Tier II Human 13809 Genes GS234192: [MeSH] Gene Expression Regulation : D005786
Expand Tier II Human 16448 Genes GS235242: [MeSH] Biochemical Processes : D055438
Expand Tier II Human 948 Genes GS234269: [MeSH] Guanine Nucleotides : D006150
Expand Tier I Human 565 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human GO 7653 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier I Mouse MP 320 Genes GS163635: MP:0001933 abnormal litter size
Expand Tier II Human 16145 Genes GS245685: [MeSH] RNA : D012313
Expand Tier I Human CTD 2162 Genes GS122305: resveratrol interacting with Homo sapiens associated genes (MeSH:C059514) in CTD
Expand Tier I Mouse GO 125 Genes GS178016: GO:0042633 hair cycle
Expand Tier I Human 168 Genes GS170980: HP:0011362 Abnormal hair quantity
Expand Tier II Human 11279 Genes GS239302: [MeSH] Oligonucleotides : D009841
Expand Tier I Mouse MP 6 Genes GS165041: MP:0009267 abnormal cerebellum fissure morphology
Expand Tier I Mouse MP 96 Genes GS166031: MP:0005358 abnormal incisor morphology
Expand Tier I Human GO 1436 Genes GS205623: GO:0009888 tissue development
Expand Tier II Human 7589 Genes GS242551: [MeSH] Physiological Processes : D055705
Expand Tier II Human 145 Genes GS236416: [MeSH] Death Domain Receptor Signaling Adaptor Proteins : D053418
Expand Tier II Mouse 80 Genes GS34955: Whole Brain Gene expression correlates of Open Field - Total distance traveled 5-10 minutes in Females BXD
Expand Tier II Mouse 359 Genes GS135550: CD4 T cell subset 6 (Cd4ts6, Published QTL Chr 13)
Expand Tier I Mouse MP 404 Genes GS166194: MP:0009931 abnormal skin appearance
Expand Tier I Human 1206 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Mouse MP 1105 Genes GS166719: MP:0010678 abnormal skin adnexa morphology
Expand Tier II Human 4554 Genes GS241940: [MeSH] Urogenital System : D014566
Expand Tier II Human 1402 Genes GS237932: [MeSH] Skin : D012867
Expand Tier I Human 231 Genes GS176771: HP:0001000 Abnormality of skin pigmentation
Expand Tier II Mouse 30 Genes GS36868: Cerebellum Gene expression correlates of Percentage of entries into open arms of plus maze in Males BXD
Expand Tier II Human 463 Genes GS239997: [MeSH] Hemorrhagic Disorders : D006474
Expand Tier I Human 2 Genes GS231356: OMIM Geneset - Genes with known associations to "Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive"
Expand Tier II Human 17 Genes GS235110: [MeSH] Tooth, Supernumerary : D014096
Expand Tier II Human 13275 Genes GS238592: [MeSH] Cells, Cultured : D002478
Expand Tier II Human 848 Genes GS242322: [MeSH] Stomatognathic System : D013284
Expand Tier I Human GO 261 Genes GS194762: GO:0042633 hair cycle
Expand Tier I Mouse MP 1961 Genes GS168149: MP:0005508 abnormal skeleton morphology
Expand Tier I Human 49 Genes GS174713: HP:0002213 Fine hair
Expand Tier I Human 1223 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human CTD 3849 Genes GS252195: (+)-JQ1 compound interacting with Homo sapiens associated genes (MeSH:C561695) in CTD
Expand Tier I Mouse MP 2557 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Mouse MP 655 Genes GS168294: MP:0003699 abnormal female reproductive system physiology
Expand Tier I Mouse MP 952 Genes GS164263: MP:0002083 premature death
Expand Tier I Mouse MP 3063 Genes GS169535: MP:0005397 hematopoietic system phenotype
Expand Tier II Human 6771 Genes GS237257: [MeSH] Pathologic Processes : D010335
Expand Tier I Human 14 Genes GS173874: HP:0006323 Premature loss of primary teeth
Expand Tier II Human 295 Genes GS241551: [MeSH] Stomatognathic System Abnormalities : D018640
Expand Tier I Human 408 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human 90 Genes GS170889: HP:0006482 Abnormality of dental morphology
Expand Tier II Human 7908 Genes GS245804: [MeSH] Transcription Factors : D014157
Expand Tier I Mouse MP 2061 Genes GS169530: MP:0005390 skeleton phenotype
Expand Tier II Human 9890 Genes GS235538: [MeSH] Protein Binding : D011485
Expand Tier II Human 5776 Genes GS235960: [MeSH] Connective Tissue Cells : D003239
Expand Tier I Human GO 12490 Genes GS199635: GO:0005622 intracellular
Expand Tier II Human 4645 Genes GS238960: [MeSH] Membrane Glycoproteins : D008562
Expand Tier I Human 486 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier II Human 33 Genes GS235336: [MeSH] Receptors, Ectodysplasin : D053338
Expand Tier I Mouse MP 1893 Genes GS168012: MP:0010832 lethality during fetal growth through weaning
Expand Tier I Human 114 Genes GS176227: HP:0010719 Abnormality of hair texture
Expand Tier II Human 1449 Genes GS242366: [MeSH] Inheritance Patterns : D040582
Expand Tier II Human 279 Genes GS242283: [MeSH] Myelin Sheath : D009186
Expand Tier I Mouse MP 1717 Genes GS166710: MP:0002163 abnormal gland morphology
Expand Tier II Human 4038 Genes GS235744: [MeSH] Neurons : D009474
Expand Tier I Mouse MP 302 Genes GS165390: MP:0003224 neuron degeneration
Expand Tier II Human 5524 Genes GS245439: [MeSH] Protein Kinases : D011494
Expand Tier I Human 139 Genes GS171397: HP:0000177 Abnormality of upper lip
Expand Tier III Mouse 7391 Genes GS213076: Genes with suggestive difference in (C57BL/6) vs [(C57BL/6 x PWD)F1 + (PWD x C57BL/6)F1 + PWD] comparison
Expand Tier I Mouse 184 Genes GS228821: MSigDB Geneset - AKT_UP.V1_DN
Expand Tier I Human 1002 Genes GS227646: MSigDB Geneset - TGACCTY_V$ERR1_Q2
Expand Tier I Mouse MP 43 Genes GS163008: MP:0002689 abnormal molar morphology
Expand Tier I Mouse MP 386 Genes GS169080: MP:0002075 abnormal coat/hair pigmentation
Expand Tier I Human 259 Genes GS231678: PC Geneset - "V$AML1_Q6" pathway genes
Expand Tier II Human 17895 Genes GS243866: [MeSH] Laboratory Chemicals : D019995
Expand Tier II Human 281 Genes GS234814: [MeSH] Salivary Glands : D012469
Expand Tier II Human 1591 Genes GS242618: [MeSH] Apoptosis Regulatory Proteins : D051017
Expand Tier I Mouse MP 1870 Genes GS165244: MP:0010771 integument phenotype
Expand Tier I Human 11971 Genes GS232685: PC Geneset - "Homo sapiens" pathway genes
Expand Tier I Human 937 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14517 Genes GS196941: GO:0008150 biological_process
Expand Tier I Mouse MP 191 Genes GS167518: MP:0001312 abnormal cornea morphology
Expand Tier I Human GO 14551 Genes GS199634: GO:0005623 cell
Expand Tier II Mouse 229 Genes GS35824: Neocortex Gene expression correlates of Cocaine CPP - Time (s) in saline paired compartment a in Males BXD
Expand Tier II Human 420 Genes GS234441: [MeSH] Hair : D006197
Expand Tier I Mouse MP 11231 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier II Human 9296 Genes GS237836: [MeSH] Carrier Proteins : D002352
Expand Tier II Human 91 Genes GS239668: [MeSH] Tooth Diseases : D014076
Expand Tier I Human CTD 840 Genes GS251230: Ionic Liquids interacting with Physella acuta associated genes (MeSH:D052578) in CTD
Expand Tier I Human 80 Genes GS174550: HP:0000958 Dry skin
Expand Tier I Human CTD 1468 Genes GS122847: nickel sulfate interacting with Homo sapiens associated genes (MeSH:C029938) in CTD
Expand Tier I Mouse MP 269 Genes GS166150: MP:0001577 anemia
Expand Tier II Human 7086 Genes GS239275: [MeSH] Intracellular Signaling Peptides and Proteins : D047908
Expand Tier II Human 17896 Genes GS243233: [MeSH] Specialty Uses of Chemicals : D020313
Expand Tier I Mouse MP 454 Genes GS163664: MP:0005274 abnormal viscerocranium morphology
Expand Tier I Human 50 Genes GS173561: HP:0000691 Microdontia
Expand Tier I Human 111 Genes GS176907: HP:0009804 Reduced number of teeth
Expand Tier I Human CTD 1798 Genes GS251957: 3-(2-benzyloxyphenyl)-5-chloromethylisoxazole interacting with nan associated genes (MeSH:C584469) in CTD
Expand Tier I Mouse MP 74 Genes GS165413: MP:0000647 abnormal sebaceous gland morphology
Expand Tier I Human GO 791 Genes GS205616: GO:0009887 organ morphogenesis
Expand Tier I Human CTD 111 Genes GS125827: lipopolysaccharide, E. coli O26-B6 interacting with Homo sapiens associated genes (MeSH:C433788) in CTD
Expand Tier II Mouse 215 Genes GS35807: Striatum Gene expression correlates of Cocaine CPP- Time (s) in drug-paired compartment a in Males BXD
Expand Tier I Human 17 Genes GS176773: HP:0001006 Hypotrichosis
Expand Tier I Human GO 4573 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Human GO 255 Genes GS208673: GO:0022405 hair cycle process
Expand Tier II Human 1970 Genes GS238775: [MeSH] Animal Structures : D000825
Expand Tier II Human 2881 Genes GS243242: [MeSH] Skin Diseases : D012871
Expand Tier I Human 1099 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 72 Genes GS170824: HP:0002164 Nail dysplasia
Expand Tier II Human 9373 Genes GS241444: [MeSH] Reproductive Physiological Phenomena : D055703
Expand Tier II Human 14808 Genes GS236241: [MeSH] Protein Structure, Tertiary : D017434
Expand Tier II Human 3394 Genes GS235807: [MeSH] Cytokines : D016207
Expand Tier I Human 44 Genes GS172038: HP:0000963 Thin skin
Expand Tier I Human GO 2812 Genes GS209411: GO:0048869 cellular developmental process
Expand Tier I Mouse MP 173 Genes GS170555: MP:0000875 abnormal cerebellar Purkinje cell layer
Expand Tier I Mouse MP 727 Genes GS165875: MP:0002132 abnormal respiratory system morphology
Expand Tier I Mouse GO 5871 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Mouse GO 3601 Genes GS190682: GO:0007275 multicellular organismal development
Expand Tier II Rat 179 Genes GS223916: Body weight QTL 141 (Bw141 Published QTL Chr 17)
Expand Tier I Mouse MP 147 Genes GS168630: MP:0000377 abnormal hair follicle morphology
Expand Tier I Mouse GO 125 Genes GS180505: GO:0042303 molting cycle
Expand Tier I Mouse MP 865 Genes GS168551: MP:0002429 abnormal blood cell morphology/development
Expand Tier I Mouse MP 137 Genes GS169362: MP:0000920 abnormal myelination
Expand Tier I Mouse 189 Genes GS229056: MSigDB Geneset - GSE28237_FOLLICULAR_VS_LATE_GC_BCELL_UP
Expand Tier II Human 331 Genes GS242426: [MeSH] Dentition : D003817
Expand Tier II Human 10244 Genes GS244735: [MeSH] Mutagenesis : D016296
Expand Tier II Mouse 507 Genes GS136029: hypertension (Hypt, Published QTL Chr 13)
Expand Tier I Mouse MP 129 Genes GS167028: MP:0002177 abnormal outer ear morphology
Expand Tier II Mouse 221 Genes GS129100: bone mineral density 3 (Bmd3 Published QTL Chr 13)
Expand Tier II Human 891 Genes GS239437: [MeSH] Keratinocytes : D015603
Expand Tier II Human 3949 Genes GS240624: [MeSH] Adaptor Proteins, Signal Transducing : D048868
Expand Tier II Human 3530 Genes GS234348: [MeSH] Inorganic Chemicals : D007287
Expand Tier I Mouse MP 25 Genes GS165371: MP:0002277 abnormal respiratory mucosa morphology
Expand Tier I Mouse MP 1022 Genes GS163853: MP:0001547 abnormal lipid level
Expand Tier I Human 698 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Mouse MP 30 Genes GS166210: MP:0000402 abnormal zigzag hair morphology
Expand Tier I Mouse MP 834 Genes GS165427: MP:0000432 abnormal head morphology
Expand Tier II Human 31 Genes GS233957: [MeSH] Forefoot, Human : D005545
Expand Tier II Human 3527 Genes GS237484: [MeSH] Congenital, Hereditary, and Neonatal Diseases and Abnormalities : D009358
Expand Tier II Human 18573 Genes GS238415: [MeSH] Genome Components : D040481
Expand Tier II Human 653 Genes GS242067: [MeSH] Metals, Heavy : D019216
Expand Tier II Human 892 Genes GS243817: [MeSH] Abnormalities, Multiple : D000015
Expand Tier I Mouse MP 71 Genes GS169363: MP:0000921 demyelination
Expand Tier I Human GO 5595 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human 70 Genes GS171136: HP:0100840 Aplasia/Hypoplasia of the eyebrow
Expand Tier I Mouse MP 1422 Genes GS165260: MP:0001392 abnormal locomotor behavior
Expand Tier II Human 15107 Genes GS238930: [MeSH] Molecular Conformation : D008968
Expand Tier I Mouse MP 242 Genes GS164482: MP:0001216 abnormal epidermal layer morphology
Expand Tier II Human 17884 Genes GS240750: [MeSH] Molecular Probes : D015335
Expand Tier I Mouse MP 192 Genes GS168118: MP:0001191 abnormal skin condition
Expand Tier I Mouse MP 1358 Genes GS163971: MP:0002092 abnormal eye morphology
Expand Tier I Human GO 13 Genes GS203953: GO:0060438 trachea development
Expand Tier II Human 2729 Genes GS234130: [MeSH] Genetic Diseases, Inborn : D030342
Expand Tier II