Gene Details



FANCB and homologs in 7 species are found in 604 GeneSets:


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

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Human 187 Genes GS171907: HP:0004299 Hernia of the abdominal wall
Expand Tier I Human 6 Genes GS173591: HP:0008517 Aplasia/Hypoplasia of the sacrum
Expand Tier II Human 8052 Genes GS244604: [MeSH] Neoplasms : D009369
Expand Tier II Human 2152 Genes GS234139: [MeSH] Biophysical Processes : D055597
Expand Tier II Human 77 Genes GS235574: [MeSH] Genes, BRCA2 : D024522
Expand Tier I Mouse GO 5650 Genes GS183848: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 83 Genes GS172224: HP:0001770 Toe syndactyly
Expand Tier II Human 109 Genes GS236044: [MeSH] BRCA2 Protein : D024682
Expand Tier I Human 17 Genes GS173775: HP:0005344 Abnormality of the carotid arteries
Expand Tier II Human 19440 Genes GS241666: [MeSH] Sequence Homology, Amino Acid : D017386
Expand Tier I Human 270 Genes GS176826: HP:0000202 Oral cleft
Expand Tier II Human 19667 Genes GS245646: [MeSH] Hydrolases : D006867
Expand Tier I Human 877 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human GO 602 Genes GS202362: GO:0006974 response to DNA damage stimulus
Expand Tier III Rat 177 Genes GS224554: Memory QTL 2 (Memor2 Published QTL Chr X)
Expand Tier II Human 4141 Genes GS237911: [MeSH] Immunoglobulins : D007136
Expand Tier I Human 42 Genes GS176725: HP:0011425 Fetal ultrasound soft marker
Expand Tier II Human 22403 Genes GS244084: [MeSH] Phenotype : D010641
Expand Tier I Human GO 5184 Genes GS208954: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Mouse GO 778 Genes GS186526: GO:0005654 nucleoplasm
Expand Tier I Human 215 Genes GS232486: PC Geneset - "V$AHR_Q5" pathway genes
Expand Tier I Human 280 Genes GS175900: HP:0009118 Aplasia/Hypoplasia of the mandible
Expand Tier II Human 2235 Genes GS236574: [MeSH] Methylation : D008745
Expand Tier I Human 99 Genes GS173687: HP:0001643 Patent ductus arteriosus
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier II Human 2253 Genes GS243347: [MeSH] Alkylation : D000478
Expand Tier I Mouse GO 8630 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 201 Genes GS175802: HP:0003272 Abnormality of the hip bone
Expand Tier II Human 4326 Genes GS239579: [MeSH] Blood Coagulation Factors : D001779
Expand Tier II Human 14353 Genes GS244882: [MeSH] Epithelial Cells : D004847
Expand Tier II Human 8563 Genes GS234210: [MeSH] HeLa Cells : D006367
Expand Tier II Human 108 Genes GS237718: [MeSH] Fanconi Anemia : D005199
Expand Tier II Human 7112 Genes GS240775: [MeSH] Blood Proteins : D001798
Expand Tier I Mouse GO 8650 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier I Human 31 Genes GS170875: HP:0009619 Accessory phalanx of the thumb
Expand Tier I Human GO 2921 Genes GS210507: GO:0006950 response to stress
Expand Tier I Human 179 Genes GS175391: HP:0011004 Abnormality of the systemic arterial tree
Expand Tier I Human 247 Genes GS231680: PC Geneset - "V$DR1_Q3" pathway genes
Expand Tier I Human 641 Genes GS172294: HP:0001510 Growth delay
Expand Tier III Rat 985 Genes GS224236: Collagen induced arthritis QTL 18 (Cia18 Published QTL Chr X)
Expand Tier I Human 318 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier I Human 170 Genes GS174488: HP:0000525 Abnormality of the iris
Expand Tier I Human 840 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier II Human 70216 Genes GS235234: [MeSH] Biochemical Phenomena : D001669
Expand Tier II Human 31959 Genes GS237114: [MeSH] Regulatory Elements, Transcriptional : D050436
Expand Tier I Human 189 Genes GS176004: HP:0100656 Thoracoabdominal wall defects
Expand Tier I Human 48 Genes GS171928: HP:0100577 Urinary bladder inflammation
Expand Tier I Mouse GO 23778 Genes GS193268: GO:0005575 cellular_component
Expand Tier II Human 10106 Genes GS234071: [MeSH] Protein Modification, Translational : D046188
Expand Tier I Mouse GO 4887 Genes GS188190: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human 116 Genes GS173868: HP:0002143 Abnormality of the spinal cord
Expand Human 2063 Genes GS219980: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human 137 Genes GS174644: HP:0000953 Hyperpigmentation of the skin
Expand Tier II Human 70252 Genes GS238030: [MeSH] Chemical Phenomena : D055598
Expand Tier I Human 104 Genes GS176638: HP:0011603 Congenital malformation of the great arteries
Expand Tier I Human 10 Genes GS174464: HP:0002410 Aqueductal stenosis
Expand Tier I Human 52 Genes GS171623: HP:0008055 Aplasia/Hypoplasia affecting the uvea
Expand Tier I Human GO 2711 Genes GS199273: GO:0043233 organelle lumen
Expand Tier I Human 282 Genes GS171902: HP:0010987 Abnormality of cellular immune system
Expand Tier I Human 357 Genes GS172701: HP:0002650 Scoliosis
Expand Tier II Human 1685 Genes GS241253: [MeSH] Protein Folding : D017510
Expand Tier I Human 598 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Mouse GO 4619 Genes GS191019: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Mouse 199 Genes GS230127: MSigDB Geneset - GSE27786_LSK_VS_NKTCELL_UP
Expand Tier I Human 18 Genes GS176340: HP:0001549 Abnormality of the ileum
Expand Tier II Human 13741 Genes GS238718: [MeSH] Peptide Biosynthesis : D010452
Expand Tier I Human 167 Genes GS170916: HP:0008056 Aplasia/Hypoplasia affecting the eye
Expand Tier I Human 106 Genes GS175048: HP:0006824 Cranial nerve paralysis
Expand Tier III Rat 178 Genes GS224840: Glucose level QTL 34 (Gluco34 Published QTL Chr X)
Expand Tier I Human 530 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 174 Genes GS172293: HP:0001511 Intrauterine growth retardation
Expand Tier I Human 263 Genes GS173014: HP:0010936 Abnormality of the lower urinary tract
Expand Tier I Human 636 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier II Human 548 Genes GS236986: [MeSH] Anemia : D000740
Expand Tier I Human 222 Genes GS173995: HP:0000508 Ptosis
Expand Tier II Human 30225 Genes GS236481: [MeSH] Enzymes : D004798
Expand Tier I Human 87 Genes GS176142: HP:0001034 Hypermelanotic macule
Expand Tier I Human 487 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Human 80 Genes GS172726: HP:0000268 Dolichocephaly
Expand Tier I Mouse 200 Genes GS229085: MSigDB Geneset - GSE13306_TREG_RA_VS_TCONV_RA_DN
Expand Tier II Human 139 Genes GS234087: [MeSH] Thromboplastin : D013925
Expand Human 2063 Genes GS219986: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier II Human 13737 Genes GS241165: [MeSH] Protein Biosynthesis : D014176
Expand Tier I Human 423 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier II Human 102 Genes GS234408: [MeSH] Intracranial Hypertension : D019586
Expand Tier I Mouse GO 727 Genes GS179950: GO:0006259 DNA metabolic process
Expand Tier I Human 278 Genes GS231649: PC Geneset - "DNA Repair" pathway genes
Expand Tier I Human 323 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Human 247 Genes GS232089: PC Geneset - "V$PBX1_01" pathway genes
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Human 2063 Genes GS219964: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Mouse GO 4353 Genes GS192017: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human 16 Genes GS173779: HP:0010293 Aplasia/Hypoplasia of the uvula
Expand Tier I Human 118 Genes GS174314: HP:0002973 Abnormality of the forearm
Expand Tier II Human 7025 Genes GS239838: [MeSH] Luminescent Proteins : D008164
Expand Tier I Human 121 Genes GS172789: HP:0001537 Umbilical hernia
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 35 Genes GS175326: HP:0001217 Clubbing
Expand Human 195 Genes GS222320: Genes associated with high risk of intellectual disability.
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 736 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human 73 Genes GS171188: HP:0000415 Abnormality of the choanae
Expand Tier I Mouse GO 3599 Genes GS186227: GO:0090304 nucleic acid metabolic process
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human 590 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human 300 Genes GS172416: HP:0002242 Abnormality of the intestine
Expand Tier I Human 2005 Genes GS232341: PC Geneset - "TTGTTT_V$FOXO4_01" pathway genes
Expand Tier I Human 484 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human 389 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Human 273 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier II Human 17266 Genes GS244627: [MeSH] Biological Processes : D055694
Expand Tier I Human 181 Genes GS175907: HP:0004349 Reduced bone mineral density
Expand Tier I Human GO 2092 Genes GS209551: GO:0031981 nuclear lumen
Expand Tier II Human 37746 Genes GS240208: [MeSH] Amino Acid Sequence : D000595
Expand Tier II Human 21236 Genes GS240239: [MeSH] Sequence Homology : D017385
Expand Tier II Human 4782 Genes GS239103: [MeSH] Serum Globulins : D012712
Expand Tier II Human 7666 Genes GS239503: [MeSH] Ubiquitination : D054875
Expand Tier I Human 200 Genes GS176242: HP:0004207 Abnormality of the 5th finger
Expand Tier I Human GO 2756 Genes GS194555: GO:0031974 membrane-enclosed lumen
Expand Tier II Human 30100 Genes GS238002: [MeSH] Antisense Elements (Genetics) : D016375
Expand Tier I Human 342 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human GO 818 Genes GS197472: GO:0044451 nucleoplasm part
Expand Tier I Mouse 51 Genes GS233472: KEGG Geneset - "Fanconi anemia pathway" pathway genes
Expand Tier I Human 238 Genes GS174066: HP:0100737 Abnormality of the hard palate
Expand Tier II Human 35836 Genes GS242639: [MeSH] Metabolic Phenomena : D055754
Expand Tier II Human 9151 Genes GS238044: [MeSH] Acid Anhydride Hydrolases : D017766
Expand Tier I Human 454 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Human 607 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human GO 12 Genes GS195427: GO:0043240 Fanconi anaemia nuclear complex
Expand Tier I Human 110 Genes GS173580: HP:0011994 Abnormality of the atrial septum
Expand Tier I Human 242 Genes GS175909: HP:0004348 Abnormality of bone mineral density
Expand Tier I Human 207 Genes GS174857: HP:0200006 Slanting of the palpebral fissure
Expand Tier I Human 346 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier I Mouse GO 8414 Genes GS185585: GO:0044710 single-organism metabolic process
Expand Tier I Human 75 Genes GS173155: HP:0005561 Abnormality of bone marrow cell morphology
Expand Tier II Human 737 Genes GS243991: [MeSH] Protein Multimerization : D055503
Expand Tier II Human 61866 Genes GS235287: [MeSH] Proteins : D011506
Expand Tier II Human 15855 Genes GS239444: [MeSH] Biological Evolution : D005075
Expand Tier I Human 395 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier I Human 397 Genes GS172134: HP:0000639 Nystagmus
Expand Tier II Human 46864 Genes GS243659: [MeSH] RNA, Messenger : D012333
Expand Tier I Human 737 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 487 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human 220 Genes GS176632: HP:0001903 Anemia
Expand Tier II Human 15116 Genes GS243569: [MeSH] Macromolecular Substances : D046911
Expand Tier II Human 56846 Genes GS235305: [MeSH] DNA, Complementary : D018076
Expand Tier II Human 12802 Genes GS237481: [MeSH] Recombination, Genetic : D011995
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier II Human 6533 Genes GS244610: [MeSH] Nervous System Diseases : D009422
Expand Tier I Human 532 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier II Human 4450 Genes GS236040: [MeSH] Nutritional and Metabolic Diseases : D009750
Expand Tier I Human 489 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier II Human 67553 Genes GS240572: [MeSH] DNA : D004247
Expand Tier II Human 31495 Genes GS241930: [MeSH] Mutation : D009154
Expand Tier I Mouse 199 Genes GS229769: MSigDB Geneset - GSE15750_WT_VS_TRAF6KO_DAY10_EFF_CD8_TCELL_UP
Expand Tier I Human 532 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human 401 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 177 Genes GS174214: HP:0009466 Radial deviation of finger
Expand Tier II Human 43280 Genes GS236911: [MeSH] Transcription, Genetic : D014158
Expand Tier II Human 65203 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier I Human 234 Genes GS175523: HP:0000008 Abnormality of female internal genitalia
Expand Tier I Mouse 198 Genes GS227278: MSigDB Geneset - GSE14308_INDUCED_VS_NATURAL_TREG_UP
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier II Human 79329 Genes GS243722: [MeSH] Genetic Structures : D040342
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human 184 Genes GS173740: HP:0009485 Radial deviation of the hand or of fingers of the hand
Expand Tier II Human 67130 Genes GS241889: [MeSH] Molecular Structure : D015394
Expand Tier I Human 576 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human 121 Genes GS176672: HP:0000980 Pallor
Expand Tier I Human 57 Genes GS171016: HP:0011893 Abnormal leukocyte count
Expand Tier II Human 460 Genes GS236432: [MeSH] Immunoglobulin Fab Fragments : D007140
Expand Tier II Human 4098 Genes GS235532: [MeSH] Central Nervous System Diseases : D002493
Expand Tier I Mouse GO 4500 Genes GS186790: GO:0006725 cellular aromatic compound metabolic process
Expand Tier II Human 5833 Genes GS242178: [MeSH] Neoplasms by Site : D009371
Expand Tier II Human 59585 Genes GS234621: [MeSH] Chemical Actions and Uses : D020164
Expand Tier II Human 62071 Genes GS235061: [MeSH] Amino Acids, Peptides, and Proteins : D000602
Expand Tier I Human 361 Genes GS232347: PC Geneset - "CATTGTYY_V$SOX9_B1" pathway genes
Expand Tier I Human 232 Genes GS170999: HP:0000082 Abnormality of renal physiology
Expand Tier I Human 310 Genes GS176642: HP:0011355 Localized skin lesion
Expand Tier II Human 23706 Genes GS235056: [MeSH] Peptides : D010455
Expand Tier II Human 47536 Genes GS236298: [MeSH] Gene Expression : D015870
Expand Tier I Human 47 Genes GS231942: PC Geneset - "Fanconi anemia pathway" pathway genes
Expand Tier I Human 257 Genes GS172272: HP:0001197 Abnormality of prenatal development or birth
Expand Tier I Human 193 Genes GS174813: HP:0001638 Cardiomyopathy
Expand Tier I Human 64 Genes GS175020: HP:0001622 Premature birth
Expand Tier I Human 262 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier II Human 33265 Genes GS237679: [MeSH] Genetic Code : D005815
Expand Tier I Human GO 5908 Genes GS195199: GO:0005634 nucleus
Expand Tier I Mouse GO 9049 Genes GS180166: GO:0008152 metabolic process
Expand Tier II Human 2405 Genes GS238714: [MeSH] Hemic and Lymphatic Diseases : D006425
Expand Tier III Rat 411 Genes GS224329: Insulin dependent diabetes mellitus QTL 5 (Iddm5 Published QTL Chr X)
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 22 Genes GS172271: HP:0001194 Abnormalities of placenta and umbilical cord
Expand Tier I Mouse GO 480 Genes GS185536: GO:0006974 response to DNA damage stimulus
Expand Tier II Human 35136 Genes GS240987: [MeSH] Metabolism : D008660
Expand Tier I Human 280 Genes GS172572: HP:0000347 Micrognathia
Expand Tier I Human 33 Genes GS171079: HP:0001882 Leukopenia
Expand Tier I Human 356 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Mouse GO 690 Genes GS180673: GO:0044451 nucleoplasm part
Expand Tier I Human 471 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human GO 4415 Genes GS203072: GO:0090304 nucleic acid metabolic process
Expand Tier II Human 20622 Genes GS237310: [MeSH] Biological Phenomena : D001686
Expand Tier II Human 61 Genes GS239432: [MeSH] Fanconi Anemia Complementation Group D2 Protein : D052236
Expand Tier I Human 56 Genes GS173053: HP:0000324 Facial asymmetry
Expand Tier II Human 36279 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier I Human 58 Genes GS174923: HP:0008572 External ear malformation
Expand Tier I Human 65 Genes GS171085: HP:0009602 Abnormality of the phalanges of the thumb
Expand Tier I Human 12 Genes GS171124: HP:0010881 Abnormality of the umbilical cord
Expand Tier II Human 4869 Genes GS237959: [MeSH] Ubiquitin-Protein Ligases : D044767
Expand Tier I Mouse GO 5654 Genes GS182325: GO:0051716 cellular response to stimulus
Expand Tier I Human 243 Genes GS173534: HP:0001877 Abnormality of erythrocytes
Expand Tier II Human 38809 Genes GS236076: [MeSH] Protein Conformation : D011487
Expand Tier II Human 19302 Genes GS236470: [MeSH] DNA-Binding Proteins : D004268
Expand Tier I Human 550 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 335 Genes GS174076: HP:0009122 Aplasia/Hypoplasia affecting bones of the axial skeleton
Expand Tier II Human 21260 Genes GS238232: [MeSH] Nucleoproteins : D009698
Expand Tier II Human 5702 Genes GS236303: [MeSH] Ligases : D008025
Expand Tier I Human 361 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human GO 1476 Genes GS203369: GO:0005654 nucleoplasm
Expand Tier I Human 136 Genes GS175524: HP:0000009 Functional abnormality of the bladder
Expand Tier I Human 261 Genes GS176692: HP:0009815 Aplasia/Hypoplasia of the extremities
Expand Tier I Human 390 Genes GS175537: HP:0011277 Abnormality of the urinary system physiology
Expand Tier II Human 18 Genes GS240658: [MeSH] Fanconi Anemia Complementation Group L Protein : D052240
Expand Tier I Human 1068 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 18 Genes GS172413: HP:0002245 Meckel diverticulum
Expand Tier I Human 423 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier II Human 3936 Genes GS245455: [MeSH] Metabolic Diseases : D008659
Expand Tier I Human 401 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Human 541 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier II Mouse 174 Genes GS34913: Hippocampus Gene expression correlates of Open Field - Total distance traveled 0-5 minutes in Males BXD
Expand Tier I Human 90 Genes GS171587: HP:0001561 Polyhydramnios
Expand Tier I Human 51 Genes GS176559: HP:0000483 Astigmatism
Expand Tier I Human 94 Genes GS176560: HP:0001010 Hypopigmentation of the skin
Expand Tier I Human GO 2665 Genes GS205543: GO:0070013 intracellular organelle lumen
Expand Tier II Human 3784 Genes GS235626: [MeSH] Brain Diseases : D001927
Expand Tier I Human 75 Genes GS172096: HP:0000581 Blepharophimosis
Expand Tier I Human 47 Genes GS174811: HP:0001636 Tetralogy of Fallot
Expand Tier I Mouse GO 1777 Genes GS184445: GO:0044428 nuclear part
Expand Tier I Human 510 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier II Human 71 Genes GS241949: [MeSH] Genes, X-Linked : D050172
Expand Tier I Human 144 Genes GS175754: HP:0000014 Abnormality of the bladder
Expand Tier II Human 6195 Genes GS243775: [MeSH] Genetic Predisposition to Disease : D020022
Expand Tier II Human 8558 Genes GS241064: [MeSH] Ubiquitins : D014452
Expand Tier I Human 263 Genes GS176477: HP:0002118 Abnormality of the cerebral ventricles
Expand Tier I Human 98 Genes GS170997: HP:0000080 Abnormality of genital physiology
Expand Tier I Human GO 864 Genes GS196719: GO:0006259 DNA metabolic process
Expand Tier I Human 48 Genes GS174251: HP:0010161 Abnormality of the phalanges of the toes
Expand Tier I Human 161 Genes GS175958: HP:0000795 Abnormality of the urethra
Expand Tier II Human 30749 Genes GS236775: [MeSH] RNA, Untranslated : D022661
Expand Tier II Human 5957 Genes GS240584: [MeSH] Green Fluorescent Proteins : D049452
Expand Tier I Human 583 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human 776 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 58 Genes GS171588: HP:0001562 Oligohydramnios
Expand Tier I Human 780 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 433 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
Expand Tier II Human 14234 Genes GS242721: [MeSH] Physical Phenomena : D055585
Expand Tier II Mouse 16 Genes GS35423: Hippocampus Gene expression correlates of Distance traveled (cm) during the second five minute bin after saline in Females & Males BXD
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier II Human 6250 Genes GS244797: [MeSH] Disease Susceptibility : D004198
Expand Tier I Human 231 Genes GS173288: HP:0000316 Hypertelorism
Expand Tier I Mouse GO 4333 Genes GS184452: GO:0044422 organelle part
Expand Tier I Human 48 Genes GS171726: HP:0005107 Abnormality of the sacrum
Expand Tier I Human GO 4960 Genes GS199124: GO:0051716 cellular response to stimulus
Expand Tier I Human GO 6605 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 123 Genes GS171384: HP:0001551 Abnormality of the umbilicus
Expand Tier II Human 28680 Genes GS238990: [MeSH] Mathematical Concepts : D055641
Expand Tier I Human 127 Genes GS171035: HP:0002620 Systemic artery abnormality
Expand Tier II Human 50108 Genes GS239769: [MeSH] Gene Library : D015723
Expand Tier II Human 26319 Genes GS238348: [MeSH] Cell Line : D002460
Expand Human 2063 Genes GS219747: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier II Human 174 Genes GS239555: [MeSH] Sister Chromatid Exchange : D012854
Expand Tier II Human 58105 Genes GS242107: [MeSH] Chemical Processes : D055599
Expand Tier II Human 32929 Genes GS243578: [MeSH] Reading Frames : D016364
Expand Tier I Human GO 2479 Genes GS201249: GO:0044428 nuclear part
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human 173 Genes GS171148: HP:0011218 Abnormal shape of the frontal region
Expand Tier I Human GO 5347 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Human 53 Genes GS173835: HP:0003422 Vertebral segmentation defect
Expand Tier II Human 4761 Genes GS236987: [MeSH] Tumor Suppressor Proteins : D025521
Expand Tier II Human 29996 Genes GS237597: [MeSH] Cell Physiological Processes : D055648
Expand Tier I Human 418 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human 621 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human 300 Genes GS176029: HP:0009116 Aplasia/Hypoplasia involving bones of the skull
Expand Tier I Human 120 Genes GS177000: HP:0001291 Abnormality of the cranial nerves
Expand Tier I Human GO 5567 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Rat 50 Genes GS233103: KEGG Geneset - "Fanconi anemia pathway" pathway genes
Expand Tier III Rat 336 Genes GS223965: Non-insulin dependent diabetes mellitus QTL 16 (Niddm16 Published QTL Chr X)
Expand Tier I Human 356 Genes GS174099: HP:0011793 Neoplasm by anatomical site
Expand Tier I Human 309 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier II Human 2373 Genes GS236826: [MeSH] Genes, Neoplasm : D052138
Expand Tier II Human 1488 Genes GS241516: [MeSH] DNA Methylation : D019175
Expand Tier I Human 46 Genes GS170867: HP:0100736 Abnormality of the soft palate
Expand Tier II Human 83226 Genes GS241072: [MeSH] Genetic Phenomena : D055614
Expand Tier I Human 110 Genes GS174806: HP:0001631 Defect in the atrial septum
Expand Tier I Human 31 Genes GS175137: HP:0000025 Functional abnormality of male internal genitalia
Expand Tier II Human 60093 Genes GS243325: [MeSH] Base Sequence : D001483
Expand Tier I Mouse 627 Genes GS128586: Rotarod Baseline Chr# X
Expand Tier I Human 344 Genes GS171309: HP:0000252 Microcephaly
Expand Tier I Human 238 Genes GS172433: HP:0002644 Abnormality of pelvic girdle bone morphology
Expand Tier I Human GO 5526 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human 53 Genes GS171305: HP:0012145 Abnormality of multiple cell lineages in the bone marrow
Expand Tier I Human 265 Genes GS231920: PC Geneset - "V$GR_Q6" pathway genes
Expand Tier II Human 24024 Genes GS240200: [MeSH] Transcription Initiation Site : D024363
Expand Tier II Human 12489 Genes GS241292: [MeSH] Pathological Conditions, Signs and Symptoms : D013568
Expand Tier I Human 296 Genes GS174145: HP:0005918 Abnormality of phalanx of finger
Expand Tier I Mouse GO 6947 Genes GS192918: GO:0050896 response to stimulus
Expand Tier II Human 23569 Genes GS235276: [MeSH] Signal Transduction : D015398
Expand Tier II Human 6405 Genes GS241451: [MeSH] Phosphoproteins : D010750
Expand Tier I Human 35 Genes GS174128: HP:0002863 Myelodysplasia
Expand Tier I Human GO 1184 Genes GS197275: GO:0033554 cellular response to stress
Expand Tier II Human 14819 Genes GS244426: [MeSH] Tumor Cells, Cultured : D014407
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 442 Genes GS175423: HP:0010461 Abnormality of the male genitalia
Expand Tier I Human 55 Genes GS174648: HP:0000957 Cafe-au-lait spot
Expand Tier II Human 15964 Genes GS237339: [MeSH] Regulatory Sequences, Nucleic Acid : D012045
Expand Tier I Human 87 Genes GS173938: HP:0001679 Abnormality of the aorta
Expand Tier I Human 250 Genes GS171634: HP:0008050 Abnormality of the palpebral fissures
Expand Tier II Human 4291 Genes GS236727: [MeSH] Skin and Connective Tissue Diseases : D017437
Expand Tier I Human 222 Genes GS175459: HP:0009484 Deviation of the hand or of fingers of the hand
Expand Tier II Human 12251 Genes GS237745: [MeSH] Epigenesis, Genetic : D044127
Expand Tier I Human 356 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier II Human 12343 Genes GS236576: [MeSH] Promoter Regions, Genetic : D011401
Expand Tier II Human 73736 Genes GS238575: [MeSH] Nucleic Acids : D009696
Expand Tier III Rat 426 Genes GS224012: Urinary albumin excretion QTL 27 (Uae27 Published QTL Chr X)
Expand Tier I Human 308 Genes GS172100: HP:0000587 Abnormality of the optic nerve
Expand Tier I Monkey 55 Genes GS232907: KEGG Geneset - "Fanconi anemia pathway" pathway genes
Expand Tier I Human 394 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human GO 7259 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human 393 Genes GS172362: HP:0004325 Decreased body weight
Expand Tier I Mouse GO 7552 Genes GS180452: GO:0044237 cellular metabolic process
Expand Tier I Human 382 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Human 203 Genes GS174706: HP:0000553 Abnormality of the uvea
Expand Tier I Human GO 6548 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 513 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Mouse 310 Genes GS136739: small testis weight 2 (Smtw2, Published QTL Chr X)
Expand Tier I Human 200 Genes GS171413: HP:0004097 Deviation of finger
Expand Tier I Human 119 Genes GS173538: HP:0001873 Thrombocytopenia
Expand Tier I Human 59 Genes GS172311: HP:0100691 Abnormality of the curvature of the cornea
Expand Tier I Human 257 Genes GS231731: PC Geneset - "V$SOX5_01" pathway genes
Expand Tier I Human 270 Genes GS172637: HP:0010460 Abnormality of the female genitalia
Expand Tier I Mouse GO 2991 Genes GS182469: GO:0043234 protein complex
Expand Tier I Human 62 Genes GS173692: HP:0001646 Abnormality of the aortic valve
Expand Tier II Human 620 Genes GS240567: [MeSH] Bone Marrow Diseases : D001855
Expand Tier I Human 103 Genes GS171478: HP:0002818 Abnormality of the radius
Expand Tier II Human 4808 Genes GS234116: [MeSH] Globulins : D005916
Expand Tier II Human 7218 Genes GS241654: [MeSH] Disease Attributes : D020969
Expand Tier I Human 8 Genes GS171299: HP:0001195 Single umbilical artery
Expand Tier II Human 58261 Genes GS239502: [MeSH] Nucleic Acid Probes : D015341
Expand Tier II Human 314 Genes GS240134: [MeSH] DNA Repair-Deficiency Disorders : D049914
Expand Tier I Mouse GO 1582 Genes GS188684: GO:0070013 intracellular organelle lumen
Expand Tier I Human 1046 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human 24 Genes GS174728: HP:0100760 Clubbing of toes
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Mouse GO 23849 Genes GS180164: GO:0008150 biological_process
Expand Tier I Human 31 Genes GS172259: HP:0001199 Triphalangeal thumb
Expand Tier I Human 86 Genes GS174858: HP:0200007 Abnormal size of the palpebral fissures
Expand Tier I Human 381 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human 58 Genes GS172829: HP:0001824 Weight loss
Expand Tier I Human 198 Genes GS174812: HP:0001637 Abnormality of the myocardium
Expand Tier III Rat 324 Genes GS223599: Blood pressure QTL 64 (Bp64 Published QTL Chr X)
Expand Tier I Human 917 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 136 Genes GS171202: HP:0100627 Displacement of the external urethral meatus
Expand Tier I Human 47 Genes GS171755: HP:0001710 Conotruncal defect
Expand Tier I Human 604 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier II Human 52165 Genes GS242059: [MeSH] Cells : D002477
Expand Tier I Human 71 Genes GS175658: HP:0006503 Aplasia/Hypoplasia involving forearm bones
Expand Tier II Human 2272 Genes GS239652: [MeSH] Genes, Recessive : D005808
Expand Tier I Human GO 8645 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 985 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Mouse GO 3583 Genes GS180236: GO:0032991 macromolecular complex
Expand Tier I Mouse GO 334 Genes GS191667: GO:0006281 DNA repair
Expand Tier I Human 313 Genes GS176568: HP:0000486 Strabismus
Expand Tier I Mouse GO 935 Genes GS180482: GO:0033554 cellular response to stress
Expand Tier II Human 73996 Genes GS244482: [MeSH] Nucleic Acids, Nucleotides, and Nucleosides : D009706
Expand Tier I Human 8 Genes GS171023: HP:0010948 Abnormality of the fetal cardiovascular system
Expand Tier I Mouse GO 1587 Genes GS182475: GO:0043233 organelle lumen
Expand Tier I Human 469 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier II Human 1446 Genes GS244926: [MeSH] Genes, Tumor Suppressor : D016147
Expand Tier I Human 32 Genes GS173586: HP:0008518 Aplasia/Hypoplasia involving the vertebral column
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human 64 Genes GS171273: HP:0100542 Abnormal localization of kidneys
Expand Tier I Human 192 Genes GS229940: MSigDB Geneset - GSE18791_CTRL_VS_NEWCASTLE_VIRUS_DC_2H_UP
Expand Tier I Human 430 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier II Human 18456 Genes GS243735: [MeSH] Biological Factors : D001685
Expand Tier I Human 514 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human GO 5337 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier II Human 58105 Genes GS235797: [MeSH] DNA Probes : D015342
Expand Tier II Human 29719 Genes GS237296: [MeSH] RNA, Antisense : D016372
Expand Tier I Human 74 Genes GS171850: HP:0002414 Spina bifida
Expand Tier I Mouse GO 7644 Genes GS188399: GO:0044238 primary metabolic process
Expand Tier II Human 30298 Genes GS242332: [MeSH] Cell Physiological Phenomena : D002468
Expand Tier II Human 41481 Genes GS234192: [MeSH] Gene Expression Regulation : D005786
Expand Tier II Human 58023 Genes GS235242: [MeSH] Biochemical Processes : D055438
Expand Tier I Human 511 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human 286 Genes GS173167: HP:0100491 Abnormality of the joints of the lower limbs
Expand Tier I Mouse GO 1628 Genes GS177813: GO:0031974 membrane-enclosed lumen
Expand Tier I Mouse GO 8072 Genes GS184218: GO:0071704 organic substance metabolic process
Expand Tier II Human 52588 Genes GS245685: [MeSH] RNA : D012313
Expand Tier I Mouse GO 1381 Genes GS192610: GO:0031981 nuclear lumen
Expand Tier I Human 75 Genes GS172219: HP:0010301 Spinal dysraphism
Expand Tier I Human 39 Genes GS171399: HP:0000172 Abnormality of the uvula
Expand Tier II Human 2161 Genes GS236295: [MeSH] Isomerases : D007535
Expand Tier I Mouse GO 4478 Genes GS184435: GO:0046483 heterocycle metabolic process
Expand Tier I Mouse GO 2101 Genes GS193563: GO:0006950 response to stress
Expand Tier II Human 2692 Genes GS242720: [MeSH] Breast Neoplasms : D001943
Expand Tier II Human 10324 Genes GS234406: [MeSH] Multiprotein Complexes : D046912
Expand Tier I Human 64 Genes GS175226: HP:0008713 Genitourinary tract malformation
Expand Tier III Rat 413 Genes GS224776: Estrogen-dependent pituitary mass QTL 12 (Edpm12 Published QTL Chr X)
Expand Tier I Human 140 Genes GS175471: HP:0001172 Abnormality of the thumb
Expand Tier II Human 10034 Genes GS243396: [MeSH] Neoplasm Proteins : D009363
Expand Tier I Human 102 Genes GS173507: HP:0000520 Proptosis
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier II Human 13987 Genes GS237817: [MeSH] Cell Line, Tumor : D045744
Expand Tier I Human 122 Genes GS172403: HP:0011873 Abnormal platelet count
Expand Tier I Human 100 Genes GS176684: HP:0008678 Renal hypoplasia/aplasia
Expand Tier II Human 3229 Genes GS243331: [MeSH] DNA Replication : D004261
Expand Tier I Human 231 Genes GS176771: HP:0001000 Abnormality of skin pigmentation
Expand Tier I Human 30 Genes GS172414: HP:0002246 Abnormality of the duodenum
Expand Tier II Human 28877 Genes GS238592: [MeSH] Cells, Cultured : D002478
Expand Tier I Human 411 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human 82 Genes GS172098: HP:0000582 Upslanted palpebral fissure
Expand Tier I Human 541 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Human GO 394 Genes GS208602: GO:0006281 DNA repair
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Mouse GO 4651 Genes GS177310: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human 68 Genes GS176574: HP:0008062 Aplasia/Hypoplasia affecting the anterior segment of the eye
Expand Tier II Human 11221 Genes GS237257: [MeSH] Pathologic Processes : D010335
Expand Tier I Human 163 Genes GS176478: HP:0002119 Ventriculomegaly
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier II Human 517 Genes GS239438: [MeSH] Immunoglobulin Fragments : D007128
Expand Tier I Human 550 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human 407 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human 189 Genes GS176745: HP:0010866 Abdominal wall defect
Expand Tier II Human 20775 Genes GS245804: [MeSH] Transcription Factors : D014157
Expand Tier I Human 144 Genes GS232225: PC Geneset - "V$AHRARNT_01" pathway genes
Expand Tier I Human GO 3853 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Mouse GO 5247 Genes GS178448: GO:0005634 nucleus
Expand Tier II Human 23211 Genes GS235538: [MeSH] Protein Binding : D011485
Expand Tier I Human 288 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier II Human 8081 Genes GS245560: [MeSH] Ubiquitin : D025801
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 110 Genes GS173939: HP:0006101 Finger syndactyly
Expand Tier I Human 486 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier II Human 2555 Genes GS242366: [MeSH] Inheritance Patterns : D040582
Expand Tier I Human 144 Genes GS171586: HP:0001560 Abnormality of the amniotic fluid
Expand Tier I Mouse 199 Genes GS230531: MSigDB Geneset - GSE27786_NKTCELL_VS_MONO_MAC_DN
Expand Tier I Human 283 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier II Human 370 Genes GS235247: [MeSH] BRCA1 Protein : D019313
Expand Tier I Human 167 Genes GS228826: MSigDB Geneset - GSE18791_CTRL_VS_NEWCASTLE_VIRUS_DC_1H_UP
Expand Tier I Human 139 Genes GS171000: HP:0000083 Renal insufficiency
Expand Tier I Human 158 Genes GS174814: HP:0001639 Hypertrophic cardiomyopathy
Expand Tier II Human 4906 Genes GS239789: [MeSH] Adenosine Triphosphatases : D000251
Expand Tier I Human 138 Genes GS227140: MSigDB Geneset - chrxp22
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 80 Genes GS175635: HP:0002251 Aganglionic megacolon
Expand Tier I Human 146 Genes GS173537: HP:0001872 Abnormality of thrombocytes
Expand Tier II Human 186 Genes GS243274: [MeSH] Fanconi Anemia Complementation Group Proteins : D051856
Expand Tier II Human 58766 Genes GS243866: [MeSH] Laboratory Chemicals : D019995
Expand Tier I Human 107 Genes GS171228: HP:0002823 Abnormality of the femur
Expand Tier I Human 936 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier II Human 4405 Genes GS244204: [MeSH] Immunoproteins : D007162
Expand Tier I Human 53 Genes GS172571: HP:0000340 Sloping forehead
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human 200 Genes GS230822: MSigDB Geneset - GSE14000_TRANSLATED_RNA_VS_MRNA_DC_UP
Expand Tier I Human 187 Genes GS176449: HP:0001671 Abnormality of the cardiac septa
Expand Tier II Mouse 41 Genes GS36375: Hippocampus Gene expression correlates of Open Field - Total rears 10-15 minutes in Females & Males BXD
Expand Tier II Human 58901 Genes GS243233: [MeSH] Specialty Uses of Chemicals : D020313
Expand Tier I Human 496 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Human 114 Genes GS172500: HP:0007400 Irregular hyperpigmentation
Expand Tier I Human GO 6347 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human 210 Genes GS171106: HP:0006496 Aplasia/Hypoplasia involving bones of the upper limbs
Expand Tier I Human 521 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier II Human 2584 Genes GS235299: [MeSH] Physical Processes : D055586
Expand Tier I Human 200 Genes GS230650: MSigDB Geneset - GSE7460_CTRL_VS_TGFB_TREATED_ACT_CD8_TCELL_UP
Expand Tier II Human 3803 Genes GS243242: [MeSH] Skin Diseases : D012871
Expand Tier I Human 148 Genes GS176233: HP:0004209 Clinodactyly of the 5th finger
Expand Tier I Human 404 Genes GS173743: HP:0001999 Abnormal facial shape
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier II Human 11797 Genes GS236666: [MeSH] Gene Silencing : D020868
Expand Tier I Human 468 Genes