Gene Details



FANCB and homologs in 7 species are found in 756 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 II Human 5314 Genes GS244604: [MeSH] Neoplasms : D009369
Expand Tier II Human 68 Genes GS235574: [MeSH] Genes, BRCA2 : D024522
Expand Tier II Human 1228 Genes GS234139: [MeSH] Biophysical Processes : D055597
Expand Tier I Human 83 Genes GS172224: HP:0001770 Toe syndactyly
Expand Tier I Mouse MP 29 Genes GS169546: MP:0008391 abnormal primordial germ cell morphology
Expand Tier I Human 17 Genes GS173775: HP:0005344 Abnormality of the carotid arteries
Expand Tier I Mouse GO 1621 Genes GS336812: GO:0019219 regulation of nucleobase-containing compound metabolic process
Expand Tier I Human GO 12429 Genes GS313464: GO:0044464 cell part
Expand Tier I Mouse MP 439 Genes GS166812: MP:0002209 decreased germ cell number
Expand Tier I Human 1177 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 212 Genes GS232486: PC Geneset - "V$AHR_Q5" pathway genes
Expand Tier I Mouse MP 76 Genes GS166956: MP:0001153 small seminiferous tubules
Expand Tier II Human 1388 Genes GS236574: [MeSH] Methylation : D008745
Expand Tier I Human GO 10354 Genes GS308945: GO:0044424 intracellular part
Expand Tier I Mouse GO 335 Genes GS332577: GO:0014070 response to organic cyclic compound
Expand Tier I Human 99 Genes GS173687: HP:0001643 Patent ductus arteriosus
Expand Tier II Human 1400 Genes GS243347: [MeSH] Alkylation : D000478
Expand Tier I Mouse GO 3249 Genes GS336483: GO:0051716 cellular response to stimulus
Expand Tier I Mouse GO 5764 Genes GS331745: GO:0065007 biological regulation
Expand Tier I Human 202 Genes GS175802: HP:0003272 Abnormality of the hip bone
Expand Tier II Human 8948 Genes GS244882: [MeSH] Epithelial Cells : D004847
Expand Tier II Human 2207 Genes GS239579: [MeSH] Blood Coagulation Factors : D001779
Expand Tier II Human 3901 Genes GS240775: [MeSH] Blood Proteins : D001798
Expand Tier II Human 75 Genes GS237718: [MeSH] Fanconi Anemia : D005199
Expand Tier II Human 6611 Genes GS234210: [MeSH] HeLa Cells : D006367
Expand Tier I Mouse MP 3142 Genes GS169830: MP:0005384 cellular phenotype
Expand Tier I Human 31 Genes GS170875: HP:0009619 Accessory phalanx of the thumb
Expand Tier I Human 179 Genes GS175391: HP:0011004 Abnormality of the systemic arterial tree
Expand Tier I Mouse GO 1477 Genes GS338744: GO:0010604 positive regulation of macromolecule metabolic process
Expand Tier I Mouse GO 8920 Genes GS331753: GO:0008150 biological_process
Expand Tier I Human 642 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 241 Genes GS231680: PC Geneset - "V$DR1_Q3" pathway genes
Expand Tier I Rat CTD 708 Genes GS264420: 2,2',4,4'-tetrabromodiphenyl ether interacting with Rattus norvegicus associated genes (MeSH:C511295) in CTD
Expand Tier I Human 319 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier II Rat 985 Genes GS224236: Collagen induced arthritis QTL 18 (Cia18 Published QTL Chr X)
Expand Tier I Human 170 Genes GS174488: HP:0000525 Abnormality of the iris
Expand Tier I Mouse GO 718 Genes GS332491: GO:0009719 response to endogenous stimulus
Expand Tier I Human 841 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Mouse GO 40 Genes GS334223: GO:0051053 negative regulation of DNA metabolic process
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 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 Zebrafish CTD 115 Genes GS261561: Thapsigargin interacting with Danio rerio associated genes (MeSH:D019284) in CTD
Expand Tier I Human CTD 5877 Genes GS121789: (6-(4-(2-piperidin-1-ylethoxy)phenyl))-3-pyridin-4-ylpyrazolo(1,5-a)pyrimidine interacting with Homo sapiens associated genes (MeSH:C516138) in CTD
Expand Tier I Human GO 4654 Genes GS311710: GO:0005634 nucleus
Expand Tier I Human 117 Genes GS173868: HP:0002143 Abnormality of the spinal cord
Expand Tier II Human 7246 Genes GS234071: [MeSH] Protein Modification, Translational : D046188
Expand Tier I Human 137 Genes GS174644: HP:0000953 Hyperpigmentation of the skin
Expand Tier I Mouse MP 832 Genes GS165493: MP:0000653 abnormal sex gland morphology
Expand Tier I Mouse MP 715 Genes GS167063: MP:0001929 abnormal gametogenesis
Expand Tier II Human 17829 Genes GS238030: [MeSH] Chemical Phenomena : D055598
Expand Tier I Mouse GO 2460 Genes GS337904: GO:0080090 regulation of primary metabolic process
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 Mouse GO 225 Genes GS338784: GO:0071407 cellular response to organic cyclic compound
Expand Tier I Human 52 Genes GS171623: HP:0008055 Aplasia/Hypoplasia affecting the uvea
Expand Tier I Human 358 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human 283 Genes GS171902: HP:0010987 Abnormality of cellular immune system
Expand Tier II Human 899 Genes GS241253: [MeSH] Protein Folding : D017510
Expand Tier I Human 598 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Human 1207 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Mouse 194 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 8168 Genes GS238718: [MeSH] Peptide Biosynthesis : D010452
Expand Tier I Human 168 Genes GS170916: HP:0008056 Aplasia/Hypoplasia affecting the eye
Expand Tier I Human 106 Genes GS175048: HP:0006824 Cranial nerve paralysis
Expand Tier I Human 783 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 531 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier II Rat 178 Genes GS224840: Glucose level QTL 34 (Gluco34 Published QTL Chr X)
Expand Tier I Human 263 Genes GS173014: HP:0010936 Abnormality of the lower urinary tract
Expand Tier I Human 174 Genes GS172293: HP:0001511 Intrauterine growth retardation
Expand Tier I Human 637 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier II Human 384 Genes GS236986: [MeSH] Anemia : D000740
Expand Tier I Human 222 Genes GS173995: HP:0000508 Ptosis
Expand Tier II Human 11234 Genes GS236481: [MeSH] Enzymes : D004798
Expand Tier I Mouse GO 12 Genes GS338787: GO:2000779 regulation of double-strand break repair
Expand Tier I Human 87 Genes GS176142: HP:0001034 Hypermelanotic macule
Expand Tier I Human 488 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Human 80 Genes GS172726: HP:0000268 Dolichocephaly
Expand Tier I Mouse 192 Genes GS229085: MSigDB Geneset - GSE13306_TREG_RA_VS_TCONV_RA_DN
Expand Tier II Human 93 Genes GS234087: [MeSH] Thromboplastin : D013925
Expand Tier II Human 8166 Genes GS241165: [MeSH] Protein Biosynthesis : D014176
Expand Tier I Human 423 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Mouse GO 1060 Genes GS336557: GO:0051172 negative regulation of nitrogen compound metabolic process
Expand Tier II Human 89 Genes GS234408: [MeSH] Intracranial Hypertension : D019586
Expand Tier I Mouse GO 342 Genes GS338167: GO:0042493 response to drug
Expand Tier I Human 276 Genes GS231649: PC Geneset - "DNA Repair" pathway genes
Expand Tier I Mouse MP 1879 Genes GS165528: MP:0005379 endocrine/exocrine gland phenotype
Expand Tier I Mouse GO 295 Genes GS335669: GO:0071417 cellular response to organonitrogen compound
Expand Tier I Human CTD 1813 Genes GS126685: Methotrexate interacting with Homo sapiens associated genes (MeSH:D008727) in CTD
Expand Tier I Human GO 4602 Genes GS314485: GO:0070013 intracellular organelle lumen
Expand Tier I Human 323 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Mouse MP 1902 Genes GS169835: MP:0005389 reproductive system phenotype
Expand Tier I Human 243 Genes GS232089: PC Geneset - "V$PBX1_01" pathway genes
Expand Tier I Human 16 Genes GS173779: HP:0010293 Aplasia/Hypoplasia of the uvula
Expand Tier I Human GO 2437 Genes GS311223: GO:0006950 response to stress
Expand Tier I Human 118 Genes GS174314: HP:0002973 Abnormality of the forearm
Expand Tier II Human 3757 Genes GS239838: [MeSH] Luminescent Proteins : D008164
Expand Tier I Human 121 Genes GS172789: HP:0001537 Umbilical hernia
Expand Tier I Human GO 10738 Genes GS315285: GO:0005488 binding
Expand Tier I Human 1219 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 35 Genes GS175326: HP:0001217 Clubbing
Expand Human 188 Genes GS222320: Genes associated with high risk of intellectual disability.
Expand Tier I Human 736 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human 951 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Mouse GO 1243 Genes GS332824: GO:0009892 negative regulation of metabolic process
Expand Tier I Human GO 4002 Genes GS310623: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Human 73 Genes GS171188: HP:0000415 Abnormality of the choanae
Expand Tier I Human 590 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human 301 Genes GS172416: HP:0002242 Abnormality of the intestine
Expand Tier I Human 1971 Genes GS232341: PC Geneset - "TTGTTT_V$FOXO4_01" pathway genes
Expand Tier I Human CTD 3339 Genes GS126466: Quercetin interacting with Homo sapiens associated genes (MeSH:D011794) in CTD
Expand Tier I Human 484 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human GO 6923 Genes GS312233: GO:0044238 primary metabolic process
Expand Tier I Human CTD 3845 Genes GS126898: Methyl Methanesulfonate interacting with Homo sapiens associated genes (MeSH:D008741) in CTD
Expand Tier I Human 274 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier I Human 389 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier II Human 4862 Genes GS244627: [MeSH] Biological Processes : D055694
Expand Tier I Human GO 3801 Genes GS308943: GO:0044428 nuclear part
Expand Tier I Human 181 Genes GS175907: HP:0004349 Reduced bone mineral density
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 II Human 2845 Genes GS239103: [MeSH] Serum Globulins : D012712
Expand Tier II Human 6268 Genes GS239503: [MeSH] Ubiquitination : D054875
Expand Tier I Human 200 Genes GS176242: HP:0004207 Abnormality of the 5th finger
Expand Tier II Human 14336 Genes GS238002: [MeSH] Antisense Elements (Genetics) : D016375
Expand Tier I Zebrafish 52 Genes GS282211: KEGG Geneset - "Fanconi anemia pathway" pathway genes
Expand Tier I Human CTD 2002 Genes GS123157: Carbamazepine interacting with Homo sapiens associated genes (MeSH:D002220) in CTD
Expand Tier I Human 342 Genes GS174378: HP:0000518 Cataract
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 13572 Genes GS242639: [MeSH] Metabolic Phenomena : D055754
Expand Tier II Human 3848 Genes GS238044: [MeSH] Acid Anhydride Hydrolases : D017766
Expand Tier I Mouse GO 29 Genes GS334051: GO:0000724 double-strand break repair via homologous recombination
Expand Tier I Mouse GO 58 Genes GS334222: GO:0051054 positive regulation of DNA metabolic process
Expand Tier I Mouse CTD 979 Genes GS257004: Succimer interacting with Mus musculus associated genes (MeSH:D004113) in CTD
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 Mouse GO 2393 Genes GS336556: GO:0051171 regulation of nitrogen compound metabolic process
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 Mouse GO 947 Genes GS333993: GO:0048584 positive regulation of response to stimulus
Expand Tier I Mouse MP 971 Genes GS168710: MP:0001648 abnormal apoptosis
Expand Tier I Human 243 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 Mouse GO 8412 Genes GS185585: GO:0044710 single-organism metabolic process
Expand Tier I Human 347 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier I Human 76 Genes GS173155: HP:0005561 Abnormality of bone marrow cell morphology
Expand Tier II Human 538 Genes GS243991: [MeSH] Protein Multimerization : D055503
Expand Tier I Mouse MP 118 Genes GS169705: MP:0006380 abnormal spermatid morphology
Expand Tier I Human GO 8550 Genes GS309495: GO:0043229 intracellular organelle
Expand Tier II Human 4189 Genes GS239444: [MeSH] Biological Evolution : D005075
Expand Tier II Human 16597 Genes GS235287: [MeSH] Proteins : D011506
Expand Tier I Human 396 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier I Mouse GO 8 Genes GS336883: GO:0045739 positive regulation of DNA repair
Expand Tier I Human CTD 5877 Genes GS126658: 2,3-dimethylhydroquinone interacting with Homo sapiens associated genes (MeSH:C516077) in CTD
Expand Tier I Human GO 3663 Genes GS314003: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Human 397 Genes GS172134: HP:0000639 Nystagmus
Expand Tier II Human 16030 Genes GS243659: [MeSH] RNA, Messenger : D012333
Expand Tier I Human CTD 484 Genes GS121731: Diclofenac interacting with Homo sapiens associated genes (MeSH:D004008) in CTD
Expand Tier I Human 738 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 488 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human 221 Genes GS176632: HP:0001903 Anemia
Expand Tier II Human 7005 Genes GS243569: [MeSH] Macromolecular Substances : D046911
Expand Tier II Human 17816 Genes GS235305: [MeSH] DNA, Complementary : D018076
Expand Tier II Human 6916 Genes GS237481: [MeSH] Recombination, Genetic : D011995
Expand Tier I Human 1163 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier II Human 3924 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 I Human GO 3833 Genes GS311351: GO:1901360 organic cyclic compound metabolic process
Expand Tier II Human 2605 Genes GS236040: [MeSH] Nutritional and Metabolic Diseases : D009750
Expand Tier I Human GO 5610 Genes GS315635: GO:0050896 response to stimulus
Expand Tier I Human 489 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier II Human 18212 Genes GS240572: [MeSH] DNA : D004247
Expand Tier I Human GO 10188 Genes GS308991: GO:0005515 protein binding
Expand Tier II Human 11733 Genes GS241930: [MeSH] Mutation : D009154
Expand Tier I Mouse 192 Genes GS229769: MSigDB Geneset - GSE15750_WT_VS_TRAF6KO_DAY10_EFF_CD8_TCELL_UP
Expand Tier I Mouse MP 1108 Genes GS168063: MP:0000313 abnormal cell death
Expand Tier I Human 402 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 532 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human 177 Genes GS174214: HP:0009466 Radial deviation of finger
Expand Tier I Rat CTD 1030 Genes GS266883: sodium bichromate interacting with Rattus norvegicus associated genes (MeSH:C016104) in CTD
Expand Tier II Human 15234 Genes GS236911: [MeSH] Transcription, Genetic : D014158
Expand Tier I Human GO 7151 Genes GS312238: GO:0044237 cellular metabolic process
Expand Tier II Human 16814 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier I Mouse GO 7482 Genes GS335497: GO:0009987 cellular process
Expand Tier I Human 234 Genes GS175523: HP:0000008 Abnormality of female internal genitalia
Expand Tier I Human GO 3513 Genes GS310296: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Mouse GO 59 Genes GS336792: GO:0006302 double-strand break repair
Expand Tier I Mouse 190 Genes GS227278: MSigDB Geneset - GSE14308_INDUCED_VS_NATURAL_TREG_UP
Expand Tier II Human 19180 Genes GS243722: [MeSH] Genetic Structures : D040342
Expand Tier I Human GO 9158 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human CTD 4695 Genes GS125893: Tetradecanoylphorbol Acetate interacting with Oryctolagus cuniculus associated genes (MeSH:D013755) in CTD
Expand Tier I Human 184 Genes GS173740: HP:0009485 Radial deviation of the hand or of fingers of the hand
Expand Tier II Human 17454 Genes GS241889: [MeSH] Molecular Structure : D015394
Expand Tier I Mouse GO 1747 Genes GS333994: GO:0048583 regulation of response to stimulus
Expand Tier I Mouse GO 2 Genes GS331009: GO:0072757 cellular response to camptothecin
Expand Tier I Human 577 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 338 Genes GS236432: [MeSH] Immunoglobulin Fab Fragments : D007140
Expand Tier II Human 2544 Genes GS235532: [MeSH] Central Nervous System Diseases : D002493
Expand Tier I Mouse GO 7 Genes GS336015: GO:2000780 negative regulation of double-strand break repair
Expand Tier I Mouse MP 542 Genes GS167061: MP:0002210 abnormal sex determination
Expand Tier I Mouse GO 2610 Genes GS337479: GO:0048519 negative regulation of biological process
Expand Tier II Human 4234 Genes GS242178: [MeSH] Neoplasms by Site : D009371
Expand Tier I Mouse CTD 2896 Genes GS256531: Phenobarbital interacting with Mus musculus associated genes (MeSH:D010634) in CTD
Expand Tier II Human 16633 Genes GS235061: [MeSH] Amino Acids, Peptides, and Proteins : D000602
Expand Tier II Human 17923 Genes GS234621: [MeSH] Chemical Actions and Uses : D020164
Expand Tier I Human 358 Genes GS232347: PC Geneset - "CATTGTYY_V$SOX9_B1" pathway genes
Expand Tier I Human GO 3047 Genes GS314962: GO:0090304 nucleic acid metabolic process
Expand Tier I Human 232 Genes GS170999: HP:0000082 Abnormality of renal physiology
Expand Tier I Human 311 Genes GS176642: HP:0011355 Localized skin lesion
Expand Tier I Mouse GO 2326 Genes GS332190: GO:0048523 negative regulation of cellular process
Expand Tier I Mouse MP 48 Genes GS164435: MP:0001149 testicular hyperplasia
Expand Tier I Human GO 598 Genes GS313619: GO:0006974 cellular response to DNA damage stimulus
Expand Tier I Mouse GO 2146 Genes GS337639: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Mouse MP 61 Genes GS167176: MP:0002784 abnormal Sertoli cell morphology
Expand Tier II Human 15712 Genes GS236298: [MeSH] Gene Expression : D015870
Expand Tier II Human 10170 Genes GS235056: [MeSH] Peptides : D010455
Expand Tier I Human 45 Genes GS231942: PC Geneset - "Fanconi anemia pathway" pathway genes
Expand Tier I Rat CTD 3210 Genes GS263517: Flutamide interacting with Rattus norvegicus associated genes (MeSH:D005485) in CTD
Expand Tier I Mouse GO 4862 Genes GS334126: GO:0050794 regulation of cellular process
Expand Tier II Rat 411 Genes GS224329: Insulin dependent diabetes mellitus QTL 5 (Iddm5 Published QTL Chr X)
Expand Tier I Human 281 Genes GS172572: HP:0000347 Micrognathia
Expand Tier I Human 356 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human 33 Genes GS171079: HP:0001882 Leukopenia
Expand Tier I Mouse GO 23 Genes GS338489: GO:2001021 negative regulation of response to DNA damage stimulus
Expand Tier I Human 471 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Mouse MP 495 Genes GS165820: MP:0001116 small gonad
Expand Tier II Human 13540 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier I Human 65 Genes GS171085: HP:0009602 Abnormality of the phalanges of the thumb
Expand Tier I Mouse GO 121 Genes GS334224: GO:0051052 regulation of DNA metabolic process
Expand Tier I Human 244 Genes GS173534: HP:0001877 Abnormality of erythrocytes
Expand Tier II Human 15098 Genes GS236076: [MeSH] Protein Conformation : D011487
Expand Tier II Human 7493 Genes GS236470: [MeSH] DNA-Binding Proteins : D004268
Expand Tier II Human 4260 Genes GS238232: [MeSH] Nucleoproteins : D009698
Expand Tier II Human 3332 Genes GS236303: [MeSH] Ligases : D008025
Expand Tier I Human 362 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human CTD 3934 Genes GS126584: Tetrachlorodibenzodioxin interacting with Oryzias latipes associated genes (MeSH:D013749) in CTD
Expand Tier I Mouse GO 35 Genes GS332477: GO:0043279 response to alkaloid
Expand Tier I Human 18 Genes GS172413: HP:0002245 Meckel diverticulum
Expand Tier I Human 1069 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier II Human 2389 Genes GS245455: [MeSH] Metabolic Diseases : D008659
Expand Tier I Human 541 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 402 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Human 90 Genes GS171587: HP:0001561 Polyhydramnios
Expand Tier II Human 2362 Genes GS235626: [MeSH] Brain Diseases : D001927
Expand Tier I Human 47 Genes GS174811: HP:0001636 Tetralogy of Fallot
Expand Tier I Human 511 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier II Human 43 Genes GS241949: [MeSH] Genes, X-Linked : D050172
Expand Tier I Mouse GO 2053 Genes GS334151: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Mouse GO 649 Genes GS335350: GO:0071495 cellular response to endogenous stimulus
Expand Tier I Human 98 Genes GS170997: HP:0000080 Abnormality of genital physiology
Expand Tier I Human GO 8004 Genes GS309497: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse GO 1599 Genes GS335046: GO:0006950 response to stress
Expand Tier I Human 434 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
Expand Tier I Human 781 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Mouse MP 87 Genes GS168770: MP:0011750 abnormal seminiferous tubule epithelium morphology
Expand Tier II Human 5099 Genes GS244797: [MeSH] Disease Susceptibility : D004198
Expand Tier I Human 232 Genes GS173288: HP:0000316 Hypertelorism
Expand Tier I Human 127 Genes GS171035: HP:0002620 Systemic artery abnormality
Expand Tier II Human 17259 Genes GS239769: [MeSH] Gene Library : D015723
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 GO 3989 Genes GS335998: GO:0044237 cellular metabolic process
Expand Tier I Mouse MP 2874 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Human GO 654 Genes GS307860: GO:0006259 DNA metabolic process
Expand Tier I Human 53 Genes GS173835: HP:0003422 Vertebral segmentation defect
Expand Tier II Human 11159 Genes GS237597: [MeSH] Cell Physiological Processes : D055648
Expand Tier II Human 2865 Genes GS236987: [MeSH] Tumor Suppressor Proteins : D025521
Expand Tier I Human 301 Genes GS176029: HP:0009116 Aplasia/Hypoplasia involving bones of the skull
Expand Tier I Mouse GO 4 Genes GS331016: GO:1990414 replication-born double-strand break repair via sister chromatid exchange
Expand Tier I Human 310 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier II Rat 336 Genes GS223965: Non-insulin dependent diabetes mellitus QTL 16 (Niddm16 Published QTL Chr X)
Expand Tier II Human 1054 Genes GS241516: [MeSH] DNA Methylation : D019175
Expand Tier I Mouse CTD 2495 Genes GS256068: Aflatoxin B1 interacting with Mus musculus associated genes (MeSH:D016604) in CTD
Expand Tier I Mouse MP 606 Genes GS167074: MP:0001925 male infertility
Expand Tier I Mouse 612 Genes GS128586: Rotarod Baseline Chr# X
Expand Tier I Human 239 Genes GS172433: HP:0002644 Abnormality of pelvic girdle bone morphology
Expand Tier I Human 53 Genes GS171305: HP:0012145 Abnormality of multiple cell lineages in the bone marrow
Expand Tier I Mouse MP 737 Genes GS163427: MP:0009205 abnormal internal male genitalia morphology
Expand Tier I Human CTD 1267 Genes GS123759: Testosterone interacting with Homo sapiens associated genes (MeSH:D013739) in CTD
Expand Tier I Mouse MP 757 Genes GS163916: MP:0009198 abnormal male genitalia morphology
Expand Tier I Human 297 Genes GS174145: HP:0005918 Abnormality of phalanx of finger
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 II Human 3472 Genes GS241451: [MeSH] Phosphoproteins : D010750
Expand Tier II Human 9704 Genes GS244426: [MeSH] Tumor Cells, Cultured : D014407
Expand Tier I Human 2365 Genes GS175529: HP:0000001 All
Expand Tier I Human 55 Genes GS174648: HP:0000957 Cafe-au-lait spot
Expand Tier I Human CTD 5902 Genes GS124700: 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide interacting with Homo sapiens associated genes (MeSH:C459179) in CTD
Expand Tier I Human 250 Genes GS171634: HP:0008050 Abnormality of the palpebral fissures
Expand Tier I Human 222 Genes GS175459: HP:0009484 Deviation of the hand or of fingers of the hand
Expand Tier II Human 5312 Genes GS237745: [MeSH] Epigenesis, Genetic : D044127
Expand Tier II Human 6493 Genes GS236576: [MeSH] Promoter Regions, Genetic : D011401
Expand Tier II Rat 426 Genes GS224012: Urinary albumin excretion QTL 27 (Uae27 Published QTL Chr X)
Expand Tier I Human 395 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human 382 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Mouse GO 3 Genes GS328903: GO:1901563 response to camptothecin
Expand Tier II Mouse 310 Genes GS136739: small testis weight 2 (Smtw2, Published QTL Chr X)
Expand Tier I Human 254 Genes GS231731: PC Geneset - "V$SOX5_01" pathway genes
Expand Tier II Human 483 Genes GS240567: [MeSH] Bone Marrow Diseases : D001855
Expand Tier I Mouse GO 3602 Genes GS335221: GO:0043170 macromolecule metabolic process
Expand Tier II Human 201 Genes GS240134: [MeSH] DNA Repair-Deficiency Disorders : D049914
Expand Tier II Human 17884 Genes GS239502: [MeSH] Nucleic Acid Probes : D015341
Expand Tier I Human 24 Genes GS174728: HP:0100760 Clubbing of toes
Expand Tier I Human 86 Genes GS174858: HP:0200007 Abnormal size of the palpebral fissures
Expand Tier I Human 31 Genes GS172259: HP:0001199 Triphalangeal thumb
Expand Tier I Human 381 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Mouse MP 1361 Genes GS166712: MP:0002161 abnormal fertility/fecundity
Expand Tier I Mouse GO 654 Genes GS336004: GO:0033554 cellular response to stress
Expand Tier I Human 604 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human 136 Genes GS171202: HP:0100627 Displacement of the external urethral meatus
Expand Tier I Mouse GO 5375 Genes GS337271: GO:0050789 regulation of biological process
Expand Tier II Human 1432 Genes GS239652: [MeSH] Genes, Recessive : D005808
Expand Tier I Mouse MP 85 Genes GS164281: MP:0008058 abnormal DNA repair
Expand Tier I Human 314 Genes GS176568: HP:0000486 Strabismus
Expand Tier II Human 18365 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 Human CTD 1571 Genes GS124037: Oxygen interacting with Homo sapiens associated genes (MeSH:D010100) in CTD
Expand Tier I Human 470 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier II Human 960 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 515 Genes GS174081: HP:0004322 Short stature
Expand Tier II Human 14315 Genes GS237296: [MeSH] RNA, Antisense : D016372
Expand Tier II Human 17873 Genes GS235797: [MeSH] DNA Probes : D015342
Expand Tier I Human GO 5850 Genes GS311412: GO:0043170 macromolecule metabolic process
Expand Tier II Human 13809 Genes GS234192: [MeSH] Gene Expression Regulation : D005786
Expand Tier I Human 511 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier II Human 16145 Genes GS245685: [MeSH] RNA : D012313
Expand Tier I Human 76 Genes GS172219: HP:0010301 Spinal dysraphism
Expand Tier II Human 1023 Genes GS236295: [MeSH] Isomerases : D007535
Expand Tier II Human 2266 Genes GS242720: [MeSH] Breast Neoplasms : D001943
Expand Tier II Human 5163 Genes GS234406: [MeSH] Multiprotein Complexes : D046912
Expand Tier I Human GO 3615 Genes GS310967: GO:0031981 nuclear lumen
Expand Tier I Human GO 12430 Genes GS308571: GO:0005623 cell
Expand Tier I Human 64 Genes GS175226: HP:0008713 Genitourinary tract malformation
Expand Tier I Mouse MP 40 Genes GS169796: MP:0010948 abnormal double-strand DNA break repair
Expand Tier I Human GO 4602 Genes GS312757: GO:0043233 organelle lumen
Expand Tier I Human CTD 835 Genes GS127327: troglitazone interacting with Homo sapiens associated genes (MeSH:C057693) in CTD
Expand Tier II Rat 413 Genes GS224776: Estrogen-dependent pituitary mass QTL 12 (Edpm12 Published QTL Chr X)
Expand Tier I Mouse GO 4 Genes GS338485: GO:2000781 positive regulation of double-strand break repair
Expand Tier I Mouse MP 7 Genes GS167195: MP:0002776 Sertoli cell hyperplasia
Expand Tier I Human 140 Genes GS175471: HP:0001172 Abnormality of the thumb
Expand Tier II Human 5393 Genes GS243396: [MeSH] Neoplasm Proteins : D009363
Expand Tier I Mouse CTD 67 Genes GS258220: CPG-oligonucleotide interacting with Mus musculus associated genes (MeSH:C408982) in CTD
Expand Tier I Human 102 Genes GS173507: HP:0000520 Proptosis
Expand Tier I Mouse MP 885 Genes GS168295: MP:0003698 abnormal male reproductive system physiology
Expand Tier I Mouse MP 220 Genes GS163015: MP:0002687 oligozoospermia
Expand Tier I Mouse GO 2 Genes GS329778: GO:1905168 positive regulation of double-strand break repair via homologous recombination
Expand Tier I Human 1206 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier II Human 9375 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 1229 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 13275 Genes GS238592: [MeSH] Cells, Cultured : D002478
Expand Tier I Human 412 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Mouse MP 451 Genes GS167269: MP:0001147 small testis
Expand Tier I Human 82 Genes GS172098: HP:0000582 Upslanted palpebral fissure
Expand Tier I Mouse MP 302 Genes GS167066: MP:0002216 abnormal seminiferous tubule morphology
Expand Tier I Human CTD 7995 Genes GS123916: Aflatoxin B1 interacting with Homo sapiens associated genes (MeSH:D016604) in CTD
Expand Tier I Human 542 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Human 1563 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Mouse GO 29 Genes GS334050: GO:0000725 recombinational repair
Expand Tier I Mouse MP 1210 Genes GS166711: MP:0002160 abnormal reproductive system morphology
Expand Tier I Human 1223 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Mouse MP 2557 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Human 68 Genes GS176574: HP:0008062 Aplasia/Hypoplasia affecting the anterior segment of the eye
Expand Tier II Human 6771 Genes GS237257: [MeSH] Pathologic Processes : D010335
Expand Tier I Mouse MP 130 Genes GS164917: MP:0008280 abnormal male germ cell apoptosis
Expand Tier I Mouse MP 599 Genes GS167367: MP:0002208 abnormal germ cell morphology
Expand Tier I Human 163 Genes GS176478: HP:0002119 Ventriculomegaly
Expand Tier I Mouse MP 480 Genes GS170746: MP:0004849 abnormal testis size
Expand Tier I Mouse GO 1383 Genes GS336558: GO:0051173 positive regulation of nitrogen compound metabolic process
Expand Tier II Human 382 Genes GS239438: [MeSH] Immunoglobulin Fragments : D007128
Expand Tier I Human 551 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human GO 3068 Genes GS307944: GO:0032991 protein-containing complex
Expand Tier I Human CTD 2385 Genes GS126764: Calcitriol interacting with Homo sapiens associated genes (MeSH:D002117) in CTD
Expand Tier I Human 408 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Mouse GO 628 Genes GS328403: GO:1901701 cellular response to oxygen-containing compound
Expand Tier I Human 189 Genes GS176745: HP:0010866 Abdominal wall defect
Expand Tier II Human 7908 Genes GS245804: [MeSH] Transcription Factors : D014157
Expand Tier I Human 143 Genes GS232225: PC Geneset - "V$AHRARNT_01" pathway genes
Expand Tier II Human 9890 Genes GS235538: [MeSH] Protein Binding : D011485
Expand Tier I Human 288 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier II Human 6014 Genes GS245560: [MeSH] Ubiquitin : D025801
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 I Human GO 3209 Genes GS313104: GO:0005654 nucleoplasm
Expand Tier II Human 1449 Genes GS242366: [MeSH] Inheritance Patterns : D040582
Expand Tier I Human 144 Genes GS171586: HP:0001560 Abnormality of the amniotic fluid
Expand Tier I Mouse 195 Genes GS230531: MSigDB Geneset - GSE27786_NKTCELL_VS_MONO_MAC_DN
Expand Tier I Human 283 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier I Human GO 5180 Genes GS313168: GO:0044260 cellular macromolecule metabolic process
Expand Tier II Human 329 Genes GS235247: [MeSH] BRCA1 Protein : D019313
Expand Tier I Mouse MP 1717 Genes GS166710: MP:0002163 abnormal gland morphology
Expand Tier I Human 159 Genes GS174814: HP:0001639 Hypertrophic cardiomyopathy
Expand Tier I Human 139 Genes GS171000: HP:0000083 Renal insufficiency
Expand Tier I Human 163 Genes GS228826: MSigDB Geneset - GSE18791_CTRL_VS_NEWCASTLE_VIRUS_DC_1H_UP
Expand Tier I Human GO 7060 Genes GS308950: GO:0044422 organelle part
Expand Tier I Mouse MP 822 Genes GS167075: MP:0001924 infertility
Expand Tier II Human 1978 Genes GS239789: [MeSH] Adenosine Triphosphatases : D000251
Expand Tier I Human 134 Genes GS227140: MSigDB Geneset - chrxp22
Expand Tier I Human 81 Genes GS175635: HP:0002251 Aganglionic megacolon
Expand Tier I Human GO 6956 Genes GS311091: GO:0044446 intracellular organelle part
Expand Tier I Human 146 Genes GS173537: HP:0001872 Abnormality of thrombocytes
Expand Tier II Human 140 Genes GS243274: [MeSH] Fanconi Anemia Complementation Group Proteins : D051856
Expand Tier II Human 17895 Genes GS243866: [MeSH] Laboratory Chemicals : D019995
Expand Tier I Human 107 Genes GS171228: HP:0002823 Abnormality of the femur
Expand Tier I Mouse MP 533 Genes GS169161: MP:0006362 abnormal male germ cell morphology
Expand Tier I Human 937 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Mouse CTD 1100 Genes GS260311: benzo(b)fluoranthene interacting with Mus musculus associated genes (MeSH:C006703) in CTD
Expand Tier II Human 2656 Genes GS244204: [MeSH] Immunoproteins : D007162
Expand Tier I Human 53 Genes GS172571: HP:0000340 Sloping forehead
Expand Tier I Mouse MP 11231 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Rat CTD 2307 Genes GS266190: furan interacting with Rattus norvegicus associated genes (MeSH:C039281) in CTD
Expand Tier I Human 188 Genes GS176449: HP:0001671 Abnormality of the cardiac septa
Expand Tier I Human 192 Genes GS230822: MSigDB Geneset - GSE14000_TRANSLATED_RNA_VS_MRNA_DC_UP
Expand Tier II Human 17896 Genes GS243233: [MeSH] Specialty Uses of Chemicals : D020313
Expand Tier I Mouse CTD 1018 Genes GS255822: Magnetite Nanoparticles interacting with Mus musculus associated genes (MeSH:D058185) in CTD
Expand Tier I Human 496 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Mouse MP 557 Genes GS163398: MP:0005266 abnormal metabolism
Expand Tier I Human 114 Genes GS172500: HP:0007400 Irregular hyperpigmentation
Expand Tier I Human 211 Genes GS171106: HP:0006496 Aplasia/Hypoplasia involving bones of the upper limbs
Expand Tier I Human GO 7591 Genes GS307924: GO:0008152 metabolic process
Expand Tier I Human 522 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier II Human 1445 Genes GS235299: [MeSH] Physical Processes : D055586
Expand Tier I Mouse GO 19 Genes GS338833: GO:0006282 regulation of DNA repair
Expand Tier I Human 194 Genes GS230650: MSigDB Geneset - GSE7460_CTRL_VS_TGFB_TREATED_ACT_CD8_TCELL_UP
Expand Tier II Human 2881 Genes GS243242: [MeSH] Skin Diseases : D012871
Expand Tier I Human 148 Genes GS176233: HP:0004209 Clinodactyly of the 5th finger
Expand Tier I Human 405 Genes GS173743: HP:0001999 Abnormal facial shape
Expand Tier I Human 1099 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier II Human 5108 Genes GS236666: [MeSH] Gene Silencing : D020868
Expand Tier I Human 468 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier II Human 14808 Genes GS236241: [MeSH] Protein Structure, Tertiary : D017434
Expand Tier I Human 64 Genes GS176161: HP:0100589 Urogenital fistula
Expand Tier I Human 407 Genes GS175670: HP:0007364 Aplasia/Hypoplasia of the cerebrum
Expand Tier I Human 887 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Mouse MP 472 Genes GS166636: MP:0001124 abnormal gametes
Expand Tier I Human GO 3269 Genes GS199267: GO:0043234 protein complex
Expand Tier I Human 190 Genes GS174579: HP:0002031 Abnormality of the esophagus
Expand Tier I Human 51 Genes GS233662: KEGG Geneset - "Fanconi anemia pathway" pathway genes
Expand Tier I Mouse CTD 892 Genes GS259676: 1,4-bis(2-(3,5-dichloropyridyloxy))benzene interacting with Mus musculus associated genes (MeSH:C028474) in CTD
Expand Tier II Human 10244 Genes GS244735: [MeSH] Mutagenesis : D016296
Expand Tier II Human 1637 Genes GS239331: [MeSH] Histones : D006657
Expand Tier I Mouse GO 26 Genes GS331262: GO:0045911 positive regulation of DNA recombination
Expand Tier I Mouse MP 25 Genes GS169545: MP:0008392 decreased primordial germ cell number
Expand Tier I Human 188 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier I Mouse GO 112 Genes GS336446: GO:0006310 DNA recombination
Expand Tier I Human 1056 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier II Human 120 Genes GS235575: [MeSH] Genes, BRCA1 : D019398
Expand Tier I Human 51 Genes GS174291: HP:0002575 Tracheoesophageal fistula
Expand Tier I Human 698 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 179 Genes GS175902: HP:0003468 Abnormality of the vertebrae
Expand Tier I Human CTD 4465 Genes GS121383: Ionomycin interacting with Oryctolagus cuniculus associated genes (MeSH:D015759) in CTD
Expand Tier I Mouse GO 1557 Genes GS332825: GO:0009893 positive regulation of metabolic process
Expand Tier II Human 4822 Genes GS241962: [MeSH] RNA Interference : D034622