Gene Details



FANCB and homologs in 7 species are found in 698 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 Human 6 Genes GS173591: HP:0008517 Aplasia/Hypoplasia of the sacrum
Expand Tier I Human 187 Genes GS171907: HP:0004299 Hernia of the abdominal wall
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 CTD 2637 Genes GS122408: vorinostat interacting with Homo sapiens associated genes (MeSH:C111237) in CTD
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 86 Genes GS236044: [MeSH] BRCA2 Protein : D024682
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 II Human 9028 Genes GS241666: [MeSH] Sequence Homology, Amino Acid : D017386
Expand Tier I Human 270 Genes GS176826: HP:0000202 Oral cleft
Expand Tier II Human 8283 Genes GS245646: [MeSH] Hydrolases : D006867
Expand Tier I Human 878 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 II Rat 177 Genes GS224554: Memory QTL 2 (Memor2 Published QTL Chr X)
Expand Tier I Mouse MP 590 Genes GS166951: MP:0001156 abnormal spermatogenesis
Expand Tier II Human 2535 Genes GS237911: [MeSH] Immunoglobulins : D007136
Expand Tier I Human 42 Genes GS176725: HP:0011425 Fetal ultrasound soft marker
Expand Tier II Human 9751 Genes GS244084: [MeSH] Phenotype : D010641
Expand Tier I Mouse MP 439 Genes GS166812: MP:0002209 decreased germ cell number
Expand Tier I Human GO 5182 Genes GS208954: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Mouse GO 778 Genes GS186526: GO:0005654 nucleoplasm
Expand Tier I Human 1177 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 212 Genes GS232486: PC Geneset - "V$AHR_Q5" pathway genes
Expand Tier I Mouse MP 76 Genes GS166956: MP:0001153 small seminiferous tubules
Expand Tier I Human 281 Genes GS175900: HP:0009118 Aplasia/Hypoplasia of the mandible
Expand Tier II Human 1388 Genes GS236574: [MeSH] Methylation : D008745
Expand Tier I Human CTD 104 Genes GS127151: nickel acetate interacting with Homo sapiens associated genes (MeSH:C119536) in CTD
Expand Tier I Mouse GO 13255 Genes GS178461: GO:0009987 cellular process
Expand Tier I Human 99 Genes GS173687: HP:0001643 Patent ductus arteriosus
Expand Tier II Human 1400 Genes GS243347: [MeSH] Alkylation : D000478
Expand Tier I Mouse GO 8629 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 202 Genes GS175802: HP:0003272 Abnormality of the hip bone
Expand Tier II Human 8948 Genes GS244882: [MeSH] Epithelial Cells : D004847
Expand Tier II Human 2207 Genes GS239579: [MeSH] Blood Coagulation Factors : D001779
Expand Tier II Human 3901 Genes GS240775: [MeSH] Blood Proteins : D001798
Expand Tier II Human 75 Genes GS237718: [MeSH] Fanconi Anemia : D005199
Expand Tier II Human 6611 Genes GS234210: [MeSH] HeLa Cells : D006367
Expand Tier I Mouse GO 8649 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse MP 3142 Genes GS169830: MP:0005384 cellular phenotype
Expand Tier I Human GO 2923 Genes GS210507: GO:0006950 response to stress
Expand Tier I Human 31 Genes GS170875: HP:0009619 Accessory phalanx of the thumb
Expand Tier I Human 179 Genes GS175391: HP:0011004 Abnormality of the systemic arterial tree
Expand Tier I Human 642 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 241 Genes GS231680: PC Geneset - "V$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 Human 841 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
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 Mouse GO 22753 Genes GS193268: GO:0005575 cellular_component
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 Mouse GO 4886 Genes GS188190: GO:0006807 nitrogen compound metabolic process
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 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 2712 Genes GS199273: GO:0043233 organelle lumen
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 Mouse GO 4618 Genes GS191019: GO:0034641 cellular nitrogen compound metabolic process
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 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 727 Genes GS179950: GO:0006259 DNA metabolic process
Expand Tier II Human 89 Genes GS234408: [MeSH] Intracranial Hypertension : D019586
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 Human CTD 1813 Genes GS126685: Methotrexate interacting with Homo sapiens associated genes (MeSH:D008727) in CTD
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$PBX1_01" pathway genes
Expand Tier I Human GO 8951 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Mouse GO 4352 Genes GS192017: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human 16 Genes GS173779: HP:0010293 Aplasia/Hypoplasia of the uvula
Expand Tier I Human 118 Genes GS174314: HP:0002973 Abnormality of the forearm
Expand Tier II Human 3757 Genes GS239838: [MeSH] Luminescent Proteins : D008164
Expand Tier I Human 121 Genes GS172789: HP:0001537 Umbilical hernia
Expand Tier I Human 1219 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 35 Genes GS175326: HP:0001217 Clubbing
Expand Human 188 Genes GS222320: Genes associated with high risk of intellectual disability.
Expand Tier I Mouse GO 13184 Genes GS191106: GO:0044464 cell part
Expand Tier I Human 736 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human 951 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Mouse GO 3599 Genes GS186227: GO:0090304 nucleic acid metabolic process
Expand Tier I Human GO 12166 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human 73 Genes GS171188: HP:0000415 Abnormality of the choanae
Expand Tier I Human 590 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human 301 Genes GS172416: HP:0002242 Abnormality of the intestine
Expand Tier I Human 1971 Genes GS232341: PC Geneset - "TTGTTT_V$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 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 2093 Genes GS209551: GO:0031981 nuclear lumen
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 GO 2757 Genes GS194555: GO:0031974 membrane-enclosed lumen
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 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 Human GO 817 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 13572 Genes GS242639: [MeSH] Metabolic Phenomena : D055754
Expand Tier II Human 3848 Genes GS238044: [MeSH] Acid Anhydride Hydrolases : D017766
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 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 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 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 Human CTD 5877 Genes GS126658: 2,3-dimethylhydroquinone interacting with Homo sapiens associated genes (MeSH:C516077) in CTD
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 II Human 2605 Genes GS236040: [MeSH] Nutritional and Metabolic Diseases : D009750
Expand Tier I Human 489 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier II Human 18212 Genes GS240572: [MeSH] DNA : D004247
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 II Human 16814 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier I Human 234 Genes GS175523: HP:0000008 Abnormality of female internal genitalia
Expand Tier I Mouse 190 Genes GS227278: MSigDB Geneset - GSE14308_INDUCED_VS_NATURAL_TREG_UP
Expand Tier I Mouse GO 9739 Genes GS186744: GO:0043226 organelle
Expand Tier I Mouse GO 11363 Genes GS182835: GO:0005622 intracellular
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 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 MP 542 Genes GS167061: MP:0002210 abnormal sex determination
Expand Tier I Mouse GO 4499 Genes GS186790: GO:0006725 cellular aromatic compound metabolic 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 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 MP 48 Genes GS164435: MP:0001149 testicular hyperplasia
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 Human GO 5911 Genes GS195199: GO:0005634 nucleus
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 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 Human 12 Genes GS171124: HP:0010881 Abnormality of the umbilical cord
Expand Tier I Human CTD 1267 Genes GS123763: Testolactone interacting with Homo sapiens associated genes (MeSH:D013738) in CTD
Expand Tier II Human 3048 Genes GS237959: [MeSH] Ubiquitin-Protein Ligases : D044767
Expand Tier I Mouse GO 5652 Genes GS182325: GO:0051716 cellular response to stimulus
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 I Human 550 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 336 Genes GS174076: HP:0009122 Aplasia/Hypoplasia affecting bones of the axial skeleton
Expand Tier II Human 4260 Genes GS238232: [MeSH] Nucleoproteins : D009698
Expand Tier I Mouse MP 75 Genes GS166953: MP:0001154 seminiferous tubule degeneration
Expand Tier II Human 3332 Genes GS236303: [MeSH] Ligases : D008025
Expand Tier I Human 362 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Mouse MP 79 Genes GS163518: MP:0006307 abnormal seminiferous tubule size
Expand Tier I Human CTD 3934 Genes GS126584: Tetrachlorodibenzodioxin interacting with Oryzias latipes associated genes (MeSH:D013749) in CTD
Expand Tier I Human GO 1475 Genes GS203369: GO:0005654 nucleoplasm
Expand Tier I Human 136 Genes GS175524: HP:0000009 Functional abnormality of the bladder
Expand Tier I Human 262 Genes GS176692: HP:0009815 Aplasia/Hypoplasia of the extremities
Expand Tier I Human 391 Genes GS175537: HP:0011277 Abnormality of the urinary system physiology
Expand Tier II Human 14 Genes GS240658: [MeSH] Fanconi Anemia Complementation Group L Protein : D052240
Expand Tier I Human 424 Genes GS175268: HP:0001167 Abnormality of finger
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 I Human 51 Genes GS176559: HP:0000483 Astigmatism
Expand Tier I Human GO 2666 Genes GS205543: GO:0070013 intracellular organelle lumen
Expand Tier I Human 94 Genes GS176560: HP:0001010 Hypopigmentation of the skin
Expand Tier II Human 2362 Genes GS235626: [MeSH] Brain Diseases : D001927
Expand Tier I Mouse GO 1777 Genes GS184445: GO:0044428 nuclear part
Expand Tier I Human 47 Genes GS174811: HP:0001636 Tetralogy of Fallot
Expand Tier I Human 75 Genes GS172096: HP:0000581 Blepharophimosis
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 Human 144 Genes GS175754: HP:0000014 Abnormality of the bladder
Expand Tier I Mouse MP 27 Genes GS165345: MP:0006378 abnormal spermatogonia morphology
Expand Tier II Human 5088 Genes GS243775: [MeSH] Genetic Predisposition to Disease : D020022
Expand Tier II Human 6208 Genes GS241064: [MeSH] Ubiquitins : D014452
Expand Tier I Human 263 Genes GS176477: HP:0002118 Abnormality of the cerebral ventricles
Expand Tier I Human GO 862 Genes GS196719: GO:0006259 DNA metabolic process
Expand Tier I Human 98 Genes GS170997: HP:0000080 Abnormality of genital physiology
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 3239 Genes GS240584: [MeSH] Green Fluorescent Proteins : D049452
Expand Tier II Human 14403 Genes GS236775: [MeSH] RNA, Untranslated : D022661
Expand Tier I Human 584 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human 777 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
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 Human 58 Genes GS171588: HP:0001562 Oligohydramnios
Expand Tier II Human 6299 Genes GS242721: [MeSH] Physical Phenomena : D055585
Expand Tier I Mouse MP 87 Genes GS168770: MP:0011750 abnormal seminiferous tubule epithelium morphology
Expand Tier I Human GO 12781 Genes GS195214: GO:0009987 cellular process
Expand Tier II Human 5099 Genes GS244797: [MeSH] Disease Susceptibility : D004198
Expand Tier I Mouse GO 4333 Genes GS184452: GO:0044422 organelle part
Expand Tier I Human 232 Genes GS173288: HP:0000316 Hypertelorism
Expand Tier I Human 49 Genes GS171726: HP:0005107 Abnormality of the sacrum
Expand Tier I Human GO 4958 Genes GS199124: GO:0051716 cellular response to stimulus
Expand Tier I Human GO 6609 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 123 Genes GS171384: HP:0001551 Abnormality of the umbilicus
Expand Tier I Mouse MP 67 Genes GS167280: MP:0001148 enlarged testis
Expand Tier II Human 14645 Genes GS238990: [MeSH] Mathematical Concepts : D055641
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 12777 Genes GS238348: [MeSH] Cell Line : D002460
Expand Tier II Human 16451 Genes GS242107: [MeSH] Chemical Processes : D055599
Expand Tier II Human 71 Genes GS239555: [MeSH] Sister Chromatid Exchange : D012854
Expand Tier II Human 15903 Genes GS243578: [MeSH] Reading Frames : D016364
Expand Tier I Mouse MP 594 Genes GS167270: MP:0001146 abnormal testis morphology
Expand Tier I Mouse MP 2874 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Human GO 2480 Genes GS201249: GO:0044428 nuclear part
Expand Tier I Human GO 8546 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 5345 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Human 174 Genes GS171148: HP:0011218 Abnormal shape of the frontal region
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 Mouse MP 1026 Genes GS169225: MP:0000358 abnormal cell morphology
Expand Tier I Human 419 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Mouse MP 1544 Genes GS168174: MP:0001919 abnormal reproductive system physiology
Expand Tier I Human 301 Genes GS176029: HP:0009116 Aplasia/Hypoplasia involving bones of the skull
Expand Tier I Human 622 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human GO 5565 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Human 120 Genes GS177000: HP:0001291 Abnormality of the cranial nerves
Expand Tier I Rat 48 Genes GS233103: KEGG Geneset - "Fanconi anemia pathway" pathway genes
Expand Tier I Human 310 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier I Human 357 Genes GS174099: HP:0011793 Neoplasm by anatomical site
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 II Human 1452 Genes GS236826: [MeSH] Genes, Neoplasm : D052138
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 Human 46 Genes GS170867: HP:0100736 Abnormality of the soft palate
Expand Tier II Human 19359 Genes GS241072: [MeSH] Genetic Phenomena : D055614
Expand Tier I Human 31 Genes GS175137: HP:0000025 Functional abnormality of male internal genitalia
Expand Tier I Human 110 Genes GS174806: HP:0001631 Defect in the atrial septum
Expand Tier II Human 16876 Genes GS243325: [MeSH] Base Sequence : D001483
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 344 Genes GS171309: HP:0000252 Microcephaly
Expand Tier I Human GO 5524 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 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 II Human 7110 Genes GS241292: [MeSH] Pathological Conditions, Signs and Symptoms : D013568
Expand Tier II Human 14014 Genes GS240200: [MeSH] Transcription Initiation Site : D024363
Expand Tier I Human 260 Genes GS231920: PC Geneset - "V$GR_Q6" pathway genes
Expand Tier I Mouse GO 6943 Genes GS192918: GO:0050896 response to stimulus
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 I Human GO 1183 Genes GS197275: GO:0033554 cellular response to stress
Expand Tier I Human 35 Genes GS174128: HP:0002863 Myelodysplasia
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 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 6986 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 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 II Human 3172 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 5312 Genes GS237745: [MeSH] Epigenesis, Genetic : D044127
Expand Tier I Mouse GO 11123 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Human 357 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier II Human 6493 Genes GS236576: [MeSH] Promoter Regions, Genetic : D011401
Expand Tier II Human 18339 Genes GS238575: [MeSH] Nucleic Acids : D009696
Expand Tier II 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 Human GO 7265 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human 395 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Monkey 56 Genes GS232907: KEGG Geneset - "Fanconi anemia pathway" pathway genes
Expand Tier I Mouse GO 7551 Genes GS180452: GO:0044237 cellular metabolic process
Expand Tier I Human 393 Genes GS172362: HP:0004325 Decreased body weight
Expand Tier I Human GO 6547 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 203 Genes GS174706: HP:0000553 Abnormality of the uvea
Expand Tier I Human 382 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Human 514 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Mouse MP 391 Genes GS168923: MP:0002673 abnormal sperm number
Expand Tier II 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 Mouse GO 2991 Genes GS182469: GO:0043234 protein complex
Expand Tier I Human 270 Genes GS172637: HP:0010460 Abnormality of the female genitalia
Expand Tier I Human 254 Genes GS231731: PC Geneset - "V$SOX5_01" pathway genes
Expand Tier I Human 62 Genes GS173692: HP:0001646 Abnormality of the aortic valve
Expand Tier II Human 483 Genes GS240567: [MeSH] Bone Marrow Diseases : D001855
Expand Tier I Human 103 Genes GS171478: HP:0002818 Abnormality of the radius
Expand Tier II Human 5491 Genes GS241654: [MeSH] Disease Attributes : D020969
Expand Tier II Human 2856 Genes GS234116: [MeSH] Globulins : D005916
Expand Tier I Human 8 Genes GS171299: HP:0001195 Single umbilical artery
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 Mouse GO 1582 Genes GS188684: GO:0070013 intracellular organelle lumen
Expand Tier I Mouse GO 9716 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Human 24 Genes GS174728: HP:0100760 Clubbing of toes
Expand Tier I Human 1047 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Mouse GO 22819 Genes GS180164: GO:0008150 biological_process
Expand Tier I Human CTD 7249 Genes GS123768: Cyclosporine interacting with Homo sapiens associated genes (MeSH:D016572) in CTD
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 Human 199 Genes GS174812: HP:0001637 Abnormality of the myocardium
Expand Tier I Human 58 Genes GS172829: HP:0001824 Weight loss
Expand Tier I Mouse GO 6435 Genes GS177531: GO:0043170 macromolecule metabolic process
Expand Tier I Human 918 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier II Rat 324 Genes GS223599: Blood pressure QTL 64 (Bp64 Published QTL Chr X)
Expand Tier I Human 604 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human 47 Genes GS171755: HP:0001710 Conotruncal defect
Expand Tier I Human 136 Genes GS171202: HP:0100627 Displacement of the external urethral meatus
Expand Tier II Human 15271 Genes GS242059: [MeSH] Cells : D002477
Expand Tier I Human 71 Genes GS175658: HP:0006503 Aplasia/Hypoplasia involving forearm bones
Expand Tier II Human 1432 Genes GS239652: [MeSH] Genes, Recessive : D005808
Expand Tier I Mouse MP 508 Genes GS167062: MP:0002211 abnormal primary sex determination
Expand Tier I Human GO 8649 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 986 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 Mouse MP 85 Genes GS164281: MP:0008058 abnormal DNA repair
Expand Tier I Mouse GO 935 Genes GS180482: GO:0033554 cellular response to stress
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 Mouse GO 1587 Genes GS182475: GO:0043233 organelle lumen
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 GO 14550 Genes GS208012: GO:0044464 cell part
Expand Tier I Human 32 Genes GS173586: HP:0008518 Aplasia/Hypoplasia involving the vertebral column
Expand Tier I Human 64 Genes GS171273: HP:0100542 Abnormal localization of kidneys
Expand Tier I Human GO 16873 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 431 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Human 187 Genes GS229940: MSigDB Geneset - GSE18791_CTRL_VS_NEWCASTLE_VIRUS_DC_2H_UP
Expand Tier II Human 8178 Genes GS243735: [MeSH] Biological Factors : D001685
Expand Tier I Human GO 5335 Genes GS201239: GO:0046483 heterocycle metabolic process
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 74 Genes GS171850: HP:0002414 Spina bifida
Expand Tier I Mouse GO 7642 Genes GS188399: GO:0044238 primary metabolic process
Expand Tier II Human 11214 Genes GS242332: [MeSH] Cell Physiological Phenomena : D002468
Expand Tier I Mouse CTD 2495 Genes GS256069: Trimetrexate interacting with Mus musculus associated genes (MeSH:D016597) in CTD
Expand Tier II Human 16448 Genes GS235242: [MeSH] Biochemical Processes : D055438
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 I Mouse GO 8070 Genes GS184218: GO:0071704 organic substance metabolic process
Expand Tier I Mouse GO 1628 Genes GS177813: GO:0031974 membrane-enclosed lumen
Expand Tier I Mouse MP 397 Genes GS168520: MP:0004901 decreased male germ cell number
Expand Tier I Human 287 Genes GS173167: HP:0100491 Abnormality of the joints of the lower limbs
Expand Tier II Human 16145 Genes GS245685: [MeSH] RNA : D012313
Expand Tier I Mouse GO 1381 Genes GS192610: GO:0031981 nuclear lumen
Expand Tier I Human 76 Genes GS172219: HP:0010301 Spinal dysraphism
Expand Tier I Human CTD 10572 Genes GS125506: Valproic Acid interacting with Homo sapiens associated genes (MeSH:D014635) in CTD
Expand Tier I Human 39 Genes GS171399: HP:0000172 Abnormality of the uvula
Expand Tier II Human 1023 Genes GS236295: [MeSH] Isomerases : D007535
Expand Tier I Mouse GO 4477 Genes GS184435: GO:0046483 heterocycle metabolic process
Expand Tier I Mouse GO 2100 Genes GS193563: GO:0006950 response to stress
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 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 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 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 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 GO 394 Genes GS208602: GO:0006281 DNA repair
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 4650 Genes GS177310: GO:1901360 organic cyclic compound metabolic process
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