Gene Details



SLX4 and homologs in 1 species are found in 392 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 83 Genes GS172224: HP:0001770 Toe syndactyly
Expand Tier I Human 64 Genes GS175226: HP:0008713 Genitourinary tract malformation
Expand Tier I Human 17 Genes GS173775: HP:0005344 Abnormality of the carotid arteries
Expand Tier I Human GO 11 Genes GS202038: GO:0000738 DNA catabolic process, exonucleolytic
Expand Tier I Human 271 Genes GS176826: HP:0000202 Oral cleft
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human 140 Genes GS175471: HP:0001172 Abnormality of the thumb
Expand Tier I Human GO 606 Genes GS202362: GO:0006974 response to DNA damage stimulus
Expand Tier I Human 103 Genes GS173507: HP:0000520 Proptosis
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 124 Genes GS172403: HP:0011873 Abnormal platelet count
Expand Tier I Human 101 Genes GS176684: HP:0008678 Renal hypoplasia/aplasia
Expand Tier I Human 232 Genes GS176771: HP:0001000 Abnormality of skin pigmentation
Expand Tier I Human GO 5216 Genes GS208954: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human 30 Genes GS172414: HP:0002246 Abnormality of the duodenum
Expand Human 60 Genes GS220970: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_P53_SIGNALING_PATHWAY
Expand Tier I Human 414 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human 83 Genes GS172098: HP:0000582 Upslanted palpebral fissure
Expand Tier I Human GO 396 Genes GS208602: GO:0006281 DNA repair
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human GO 111 Genes GS200247: GO:0006302 double-strand break repair
Expand Human 184 Genes GS219855: http://www.broadinstitute.org/gsea/msigdb/cards/CELL_CYCLE_PROCESS
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human 282 Genes GS175900: HP:0009118 Aplasia/Hypoplasia of the mandible
Expand Tier I Human GO 77 Genes GS208605: GO:0006289 nucleotide-excision repair
Expand Tier I Human 68 Genes GS176574: HP:0008062 Aplasia/Hypoplasia affecting the anterior segment of the eye
Expand Tier I Human GO 13 Genes GS201553: GO:0000109 nucleotide-excision repair complex
Expand Tier I Human 99 Genes GS173687: HP:0001643 Patent ductus arteriosus
Expand Tier I Human 163 Genes GS176478: HP:0002119 Ventriculomegaly
Expand Tier I Human 203 Genes GS175802: HP:0003272 Abnormality of the hip bone
Expand Tier I Human GO 790 Genes GS208912: GO:0046700 heterocycle catabolic process
Expand Tier I Human 31 Genes GS170875: HP:0009619 Accessory phalanx of the thumb
Expand Tier I Human 553 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human GO 2940 Genes GS210507: GO:0006950 response to stress
Expand Tier I Human 411 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human 181 Genes GS175391: HP:0011004 Abnormality of the systemic arterial tree
Expand Tier I Human 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 322 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier I Human 189 Genes GS176745: HP:0010866 Abdominal wall defect
Expand Tier I Human 170 Genes GS174488: HP:0000525 Abnormality of the iris
Expand Tier I Human GO 3861 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Human 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 291 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier I Human GO 215 Genes GS198948: GO:0006310 DNA recombination
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier III Human 3178 Genes GS137407: Supplementary Table 2. Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Human GO 1 Genes GS210723: GO:0070522 ERCC4-ERCC1 complex
Expand Tier I Human 110 Genes GS173939: HP:0006101 Finger syndactyly
Expand Tier I Human 489 Genes GS171461: HP:0011121 Abnormality of skin morphology
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 Human 145 Genes GS171586: HP:0001560 Abnormality of the amniotic fluid
Expand Tier I Human 285 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier I Human 139 Genes GS171000: HP:0000083 Renal insufficiency
Expand Tier I Human 117 Genes GS173868: HP:0002143 Abnormality of the spinal cord
Expand Tier I Human 160 Genes GS174814: HP:0001639 Hypertrophic cardiomyopathy
Expand Tier I Human 138 Genes GS174644: HP:0000953 Hyperpigmentation of the skin
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 81 Genes GS175635: HP:0002251 Aganglionic megacolon
Expand Tier I Human 148 Genes GS173537: HP:0001872 Abnormality of thrombocytes
Expand Tier I Human 104 Genes GS176638: HP:0011603 Congenital malformation of the great arteries
Expand Tier I Human GO 3 Genes GS195760: GO:0010792 DNA double-strand break processing involved in repair via single-strand annealing
Expand Tier I Human 52 Genes GS171623: HP:0008055 Aplasia/Hypoplasia affecting the uvea
Expand Tier I Human 108 Genes GS171228: HP:0002823 Abnormality of the femur
Expand Tier I Human GO 2719 Genes GS199273: GO:0043233 organelle lumen
Expand Tier I Human 285 Genes GS171902: HP:0010987 Abnormality of cellular immune system
Expand Tier I Human 360 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human 941 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human 602 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 40 Genes GS204011: GO:0016893 endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human 54 Genes GS172571: HP:0000340 Sloping forehead
Expand Tier I Human GO 741 Genes GS208043: GO:0016788 hydrolase activity, acting on ester bonds
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human 18 Genes GS176340: HP:0001549 Abnormality of the ileum
Expand Tier I Human GO 1668 Genes GS202188: GO:0044248 cellular catabolic process
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 533 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Human 786 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 177 Genes GS172293: HP:0001511 Intrauterine growth retardation
Expand Tier I Human 264 Genes GS173014: HP:0010936 Abnormality of the lower urinary tract
Expand Tier I Human 639 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human 189 Genes GS176449: HP:0001671 Abnormality of the cardiac septa
Expand Tier I Human GO 241 Genes GS197470: GO:0044454 nuclear chromosome part
Expand Tier I Human 222 Genes GS173995: HP:0000508 Ptosis
Expand Tier I Human 498 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Human 88 Genes GS176142: HP:0001034 Hypermelanotic macule
Expand Tier I Human 115 Genes GS172500: HP:0007400 Irregular hyperpigmentation
Expand Tier I Human 490 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Human 81 Genes GS172726: HP:0000268 Dolichocephaly
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human 212 Genes GS171106: HP:0006496 Aplasia/Hypoplasia involving bones of the upper limbs
Expand Tier I Human 525 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Human 426 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Human 150 Genes GS176233: HP:0004209 Clinodactyly of the 5th finger
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 324 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Human 405 Genes GS173743: HP:0001999 Abnormal facial shape
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 470 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Human GO 1799 Genes GS196933: GO:0065009 regulation of molecular function
Expand Tier I Human GO 283 Genes GS203238: GO:0000228 nuclear chromosome
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 1 Genes GS209585: GO:0048476 Holliday junction resolvase complex
Expand Tier I Human 16 Genes GS173779: HP:0010293 Aplasia/Hypoplasia of the uvula
Expand Tier I Human 64 Genes GS176161: HP:0100589 Urogenital fistula
Expand Tier I Human 118 Genes GS174314: HP:0002973 Abnormality of the forearm
Expand Tier I Human 121 Genes GS172789: HP:0001537 Umbilical hernia
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human GO 145 Genes GS194417: GO:0000790 nuclear chromatin
Expand Tier I Human 35 Genes GS175326: HP:0001217 Clubbing
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 409 Genes GS175670: HP:0007364 Aplasia/Hypoplasia of the cerebrum
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 739 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human GO 3275 Genes GS199267: GO:0043234 protein complex
Expand Tier I Human 192 Genes GS174579: HP:0002031 Abnormality of the esophagus
Expand Tier I Human 73 Genes GS171188: HP:0000415 Abnormality of the choanae
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human GO 4811 Genes GS204612: GO:0019222 regulation of metabolic process
Expand Tier I Human 303 Genes GS172416: HP:0002242 Abnormality of the intestine
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 189 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier I Human GO 1425 Genes GS206620: GO:0050790 regulation of catalytic activity
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human GO 56 Genes GS206363: GO:0000725 recombinational repair
Expand Tier I Human 486 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human GO 67 Genes GS209296: GO:0090305 nucleic acid phosphodiester bond hydrolysis
Expand Tier I Human 52 Genes GS174291: HP:0002575 Tracheoesophageal fistula
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Human 60 Genes GS221219: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_P53_SIGNALING_PATHWAY
Expand Tier I Human 392 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Human 275 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier I Human GO 3125 Genes GS199272: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Human 184 Genes GS175907: HP:0004349 Reduced bone mineral density
Expand Tier I Human GO 2098 Genes GS209551: GO:0031981 nuclear lumen
Expand Tier I Human 114 Genes GS173262: HP:0000864 Abnormality of the hypothalamus-pituitary axis
Expand Tier I Human 59 Genes GS172412: HP:0002244 Abnormality of the small intestine
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human 202 Genes GS176242: HP:0004207 Abnormality of the 5th finger
Expand Tier I Human GO 2764 Genes GS194555: GO:0031974 membrane-enclosed lumen
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 273 Genes GS172516: HP:0001347 Hyperreflexia
Expand Tier I Human 237 Genes GS171395: HP:0000175 Cleft palate
Expand Tier I Human 545 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human 87 Genes GS173838: HP:0002778 Abnormality of the trachea
Expand Tier I Human 36 Genes GS173892: HP:0005528 Bone marrow hypocellularity
Expand Tier I Human 344 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human 160 Genes GS175096: HP:0000286 Epicanthus
Expand Tier I Human 26 Genes GS175175: HP:0003220 Abnormality of chromosome stability
Expand Tier I Human GO 5962 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human 83 Genes GS171875: HP:0002997 Abnormality of the ulna
Expand Tier I Human 239 Genes GS174066: HP:0100737 Abnormality of the hard palate
Expand Tier I Human 110 Genes GS175595: HP:0011017 Abnormality of cell physiology
Expand Tier I Human 737 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human 150 Genes GS175149: HP:0009179 Deviation of the 5th finger
Expand Human 60 Genes GS219635: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_P53_SIGNALING_PATHWAY
Expand Tier I Human 456 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human 63 Genes GS175660: HP:0006501 Aplasia/Hypoplasia of the radius
Expand Tier I Human 81 Genes GS173031: HP:0004362 Abnormality of the enteric ganglia
Expand Tier I Human 111 Genes GS173580: HP:0011994 Abnormality of the atrial septum
Expand Tier I Human 69 Genes GS176623: HP:0000453 Choanal atresia
Expand Tier I Human GO 624 Genes GS202775: GO:0005694 chromosome
Expand Tier I Human GO 748 Genes GS203608: GO:0034655 nucleobase-containing compound catabolic process
Expand Tier I Human GO 890 Genes GS207863: GO:0009057 macromolecule catabolic process
Expand Tier I Human 246 Genes GS175909: HP:0004348 Abnormality of bone mineral density
Expand Tier I Human 210 Genes GS174857: HP:0200006 Slanting of the palpebral fissure
Expand Tier I Human 397 Genes GS171067: HP:0002664 Neoplasm
Expand Tier I Human 348 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier I Human 78 Genes GS173155: HP:0005561 Abnormality of bone marrow cell morphology
Expand Tier I Human GO 8702 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 990 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier III Human 2403 Genes GS137413: Supplementary Table 2. CNA Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Human 315 Genes GS176568: HP:0000486 Strabismus
Expand Tier I Human 474 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Human 319 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Human 397 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier I Human 398 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human 64 Genes GS171273: HP:0100542 Abnormal localization of kidneys
Expand Tier I Human GO 821 Genes GS194041: GO:1901361 organic cyclic compound catabolic process
Expand Tier I Human GO 52 Genes GS198862: GO:0000781 chromosome, telomeric region
Expand Tier I Human 433 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 212 Genes GS176185: HP:0100790 Hernia
Expand Tier I Human 518 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human GO 5369 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier I Human 487 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Human 741 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 74 Genes GS171850: HP:0002414 Spina bifida
Expand Tier I Human 489 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human 223 Genes GS176632: HP:0001903 Anemia
Expand Tier I Human GO 2 Genes GS195411: GO:0048257 3'-flap endonuclease activity
Expand Tier I Human GO 164 Genes GS208951: GO:0004518 nuclease activity
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 25 Genes GS176991: HP:0100867 Duodenal stenosis
Expand Tier I Human 514 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human GO 895 Genes GS200867: GO:0043085 positive regulation of catalytic activity
Expand Tier I Human GO 5321 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human 289 Genes GS173167: HP:0100491 Abnormality of the joints of the lower limbs
Expand Tier I Human GO 5 Genes GS201326: GO:0017108 5'-flap endonuclease activity
Expand Tier I Human 115 Genes GS171171: HP:0005607 Abnormality of the tracheobronchial system
Expand Tier I Human 578 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human 76 Genes GS172219: HP:0010301 Spinal dysraphism
Expand Tier I Human 258 Genes GS175602: HP:0002087 Abnormality of the upper respiratory tract
Expand Human 306 Genes GS222211: http://www.broadinstitute.org/gsea/msigdb/cards/CELL_CYCLE_GO_0007049
Expand Tier I Human GO 792 Genes GS201002: GO:0044270 cellular nitrogen compound catabolic process
Expand Tier I Human 39 Genes GS171399: HP:0000172 Abnormality of the uvula
Expand Human 184 Genes GS220857: http://www.broadinstitute.org/gsea/msigdb/cards/CELL_CYCLE_PROCESS
Expand Tier I Human GO 6 Genes GS208386: GO:0016889 endodeoxyribonuclease activity, producing 3'-phosphomonoesters
Expand Tier I Human 492 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human 51 Genes GS171628: HP:0008053 Aplasia/Hypoplasia of the iris
Expand Tier I Human 601 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 438 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier I Human 174 Genes GS173901: HP:0002007 Frontal bossing
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human 534 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human 403 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 179 Genes GS174214: HP:0009466 Radial deviation of finger
Expand Tier I Human GO 3125 Genes GS197892: GO:0043228 non-membrane-bounded organelle
Expand Tier I Human 153 Genes GS175067: HP:0001159 Syndactyly
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 229 Genes GS171908: HP:0004298 Abnormality of the abdominal wall
Expand Tier I Human 558 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Human GO 3 Genes GS208826: GO:0045002 double-strand break repair via single-strand annealing
Expand Tier I Human 235 Genes GS175523: HP:0000008 Abnormality of female internal genitalia
Expand Tier I Human GO 69 Genes GS203330: GO:0006308 DNA catabolic process
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human GO 296 Genes GS198866: GO:0000785 chromatin
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human 67 Genes GS171115: HP:0001053 Hypopigmented skin patches
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human 186 Genes GS173740: HP:0009485 Radial deviation of the hand or of fingers of the hand
Expand Tier I Human GO 22 Genes GS204227: GO:0016894 endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 3'-phosphomonoesters
Expand Tier I Human 142 Genes GS171178: HP:0000238 Hydrocephalus
Expand Tier I Human 114 Genes GS174643: HP:0005120 Abnormality of cardiac atrium
Expand Tier I Human GO 1087 Genes GS203482: GO:0044093 positive regulation of molecular function
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human 579 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human 123 Genes GS176672: HP:0000980 Pallor
Expand Tier I Human 57 Genes GS171016: HP:0011893 Abnormal leukocyte count
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 8137 Genes GS202316: GO:0050789 regulation of biological process
Expand Tier I Human 112 Genes GS173465: HP:0001654 Abnormality of the heart valves
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human 599 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human 37 Genes GS172691: HP:0100026 Arteriovenous malformation
Expand Tier I Human GO 7 Genes GS196942: GO:0048256 flap endonuclease activity
Expand Tier I Human 80 Genes GS173498: HP:0001763 Pes planus
Expand Tier I Human 324 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Human 129 Genes GS173090: HP:0004377 Hematological neoplasm
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 13 Genes GS208387: GO:0016888 endodeoxyribonuclease activity, producing 5'-phosphomonoesters
Expand Tier I Human 232 Genes GS170999: HP:0000082 Abnormality of renal physiology
Expand Tier I Human 313 Genes GS176642: HP:0011355 Localized skin lesion
Expand Tier I Human 42 Genes GS175750: HP:0000010 Recurrent urinary tract infections
Expand Tier I Human 398 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human 285 Genes GS175119: HP:0001881 Abnormality of leukocytes
Expand Tier I Human 19 Genes GS176709: HP:0100587 Abnormality of the preputium
Expand Tier I Human 258 Genes GS172272: HP:0001197 Abnormality of prenatal development or birth
Expand Tier I Human 195 Genes GS174813: HP:0001638 Cardiomyopathy
Expand Tier I Human 263 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier I Human GO 5948 Genes GS195199: GO:0005634 nucleus
Expand Human 306 Genes GS219820: http://www.broadinstitute.org/gsea/msigdb/cards/CELL_CYCLE_GO_0007049
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 282 Genes GS172572: HP:0000347 Micrognathia
Expand Tier I Human 33 Genes GS171079: HP:0001882 Leukopenia
Expand Tier I Human 358 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human 472 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human GO 4446 Genes GS203072: GO:0090304 nucleic acid metabolic process
Expand Tier I Human 56 Genes GS173053: HP:0000324 Facial asymmetry
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 246 Genes GS173534: HP:0001877 Abnormality of erythrocytes
Expand Tier I Human GO 529 Genes GS201253: GO:0044427 chromosomal part
Expand Tier I Human 551 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 337 Genes GS174076: HP:0009122 Aplasia/Hypoplasia affecting bones of the axial skeleton
Expand Tier I Human 364 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human GO 1852 Genes GS209010: GO:1901575 organic substance catabolic process
Expand Tier I Human 136 Genes GS175524: HP:0000009 Functional abnormality of the bladder
Expand Tier I Human 263 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 I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 18 Genes GS172413: HP:0002245 Meckel diverticulum
Expand Tier I Human 426 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Human 699 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human 403 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Human 544 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 52 Genes GS176559: HP:0000483 Astigmatism
Expand Tier I Human 95 Genes GS176560: HP:0001010 Hypopigmentation of the skin
Expand Tier I Human GO 2673 Genes GS205543: GO:0070013 intracellular organelle lumen
Expand Tier I Human 75 Genes GS172096: HP:0000581 Blepharophimosis
Expand Tier I Human 48 Genes GS174811: HP:0001636 Tetralogy of Fallot
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 975 Genes GS201034: GO:0030234 enzyme regulator activity
Expand Tier I Human 144 Genes GS175754: HP:0000014 Abnormality of the bladder
Expand Tier I Human GO 8622 Genes GS196930: GO:0065007 biological regulation
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 869 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 162 Genes GS175958: HP:0000795 Abnormality of the urethra
Expand Tier I Human GO 29 Genes GS204575: GO:0004520 endodeoxyribonuclease activity
Expand Tier I Human 588 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 59 Genes GS171588: HP:0001562 Oligohydramnios
Expand Tier I Human 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 435 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
Expand Tier I Human GO 103 Genes GS208952: GO:0004519 endonuclease activity
Expand Tier I Human GO 17 Genes GS206362: GO:0000726 non-recombinational repair
Expand Human 184 Genes GS222212: http://www.broadinstitute.org/gsea/msigdb/cards/CELL_CYCLE_PROCESS
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Human 60 Genes GS220172: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_P53_SIGNALING_PATHWAY
Expand Tier I Human 232 Genes GS173288: HP:0000316 Hypertelorism
Expand Tier I Human GO 4983 Genes GS199124: GO:0051716 cellular response to stimulus
Expand Tier I Human GO 6651 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 123 Genes GS171384: HP:0001551 Abnormality of the umbilicus
Expand Tier I Human 128 Genes GS171035: HP:0002620 Systemic artery abnormality
Expand Tier I Human GO 2486 Genes GS201249: GO:0044428 nuclear part
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human 174 Genes GS171148: HP:0011218 Abnormal shape of the frontal region
Expand Tier I Human GO 5379 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Human 421 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human 626 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human 302 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 5601 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Human 360 Genes GS174099: HP:0011793 Neoplasm by anatomical site
Expand Tier I Human 311 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier I Human 46 Genes GS170867: HP:0100736 Abnormality of the soft palate
Expand Tier I Human 111 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 I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human 346 Genes GS171309: HP:0000252 Microcephaly
Expand Tier I Human 240 Genes GS172433: HP:0002644 Abnormality of pelvic girdle bone morphology
Expand Tier I Human GO 5558 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human GO 9 Genes GS206365: GO:0000729 DNA double-strand break processing
Expand Tier I Human GO 3 Genes GS206254: GO:0008821 crossover junction endodeoxyribonuclease activity
Expand Tier I Human 55 Genes GS171305: HP:0012145 Abnormality of multiple cell lineages in the bone marrow
Expand Tier I Human GO 55 Genes GS206364: GO:0000724 double-strand break repair via homologous recombination
Expand Tier I Human 298 Genes GS174145: HP:0005918 Abnormality of phalanx of finger
Expand Tier I Human 36 Genes GS174128: HP:0002863 Myelodysplasia
Expand Tier I Human GO 1189 Genes GS197275: GO:0033554 cellular response to stress
Expand Tier I Human GO 38 Genes GS200250: GO:0004536 deoxyribonuclease activity
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human 445 Genes GS175423: HP:0010461 Abnormality of the male genitalia
Expand Tier I Human 55 Genes GS174648: HP:0000957 Cafe-au-lait spot
Expand Tier I Human GO 2353 Genes GS208037: GO:0016787 hydrolase activity
Expand Tier I Human GO 2 Genes GS197274: GO:0033557 Slx1-Slx4 complex
Expand Tier I Human 88 Genes GS173938: HP:0001679 Abnormality of the aorta
Expand Tier I Human 253 Genes GS171634: HP:0008050 Abnormality of the palpebral fissures
Expand Tier I Human 224 Genes GS175459: HP:0009484 Deviation of the hand or of fingers of the hand
Expand Tier I Human 358 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Human GO 1993 Genes GS207862: GO:0009056 catabolic process
Expand Tier I Human GO 793 Genes GS198455: GO:0019439 aromatic compound catabolic process
Expand Tier I Human 397 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human GO 7311 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human 394 Genes GS172362: HP:0004325 Decreased body weight
Expand Human 306 Genes GS220859: http://www.broadinstitute.org/gsea/msigdb/cards/CELL_CYCLE_GO_0007049
Expand Tier I Human GO 405 Genes GS207716: GO:0008047 enzyme activator activity
Expand Tier I Human 384 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 6585 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 202 Genes GS171413: HP:0004097 Deviation of finger
Expand Tier I Human 121 Genes GS173538: HP:0001873 Thrombocytopenia
Expand Tier I Human 60 Genes GS172311: HP:0100691 Abnormality of the curvature of the cornea
Expand Tier I Human 271 Genes GS172637: HP:0010460 Abnormality of the female genitalia
Expand Tier I Human 62 Genes GS173692: HP:0001646 Abnormality of the aortic valve
Expand Tier I Human 103 Genes GS171478: HP:0002818 Abnormality of the radius
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human 24 Genes GS174728: HP:0100760 Clubbing of toes
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 GO 24 Genes GS198867: GO:0000784 nuclear chromosome, telomeric region
Expand Tier I Human 384 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human 58 Genes GS172829: HP:0001824 Weight loss
Expand Tier I Human 200 Genes GS174812: HP:0001637 Abnormality of the myocardium
Expand Tier I Human GO 692 Genes GS208575: GO:0044265 cellular macromolecule catabolic process
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 137 Genes GS171202: HP:0100627 Displacement of the external urethral meatus
Expand Tier I Human 48 Genes GS171755: HP:0001710 Conotruncal defect
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human 71 Genes GS175658: HP:0006503 Aplasia/Hypoplasia involving forearm bones