Gene Details



SLX4 and homologs in 6 species are found in 699 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 Mouse MP 1246 Genes GS165707: MP:0000428 abnormal craniofacial morphology
Expand Tier I Mouse MP 167 Genes GS164444: MP:0005197 abnormal uvea morphology
Expand Tier I Human 83 Genes GS172224: HP:0001770 Toe syndactyly
Expand Tier I Mouse MP 31 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 MP 985 Genes GS169127: MP:0002445 abnormal mononuclear cell differentiation
Expand Tier I Mouse MP 124 Genes GS166501: MP:0003189 fused joints
Expand Tier I Mouse MP 255 Genes GS165814: MP:0001922 reduced male fertility
Expand Tier I Mouse MP 469 Genes GS166812: MP:0002209 decreased germ cell number
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 99 Genes GS173687: HP:0001643 Patent ductus arteriosus
Expand Tier I Mouse MP 384 Genes GS166257: MP:0005291 abnormal glucose tolerance
Expand Tier I Mouse MP 3520 Genes GS169830: MP:0005384 cellular phenotype
Expand Tier I Human 641 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 318 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier I Human 840 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Mouse 296 Genes GS135249: adiposity 17 (Adip17, Published QTL Chr 16)
Expand Tier I Human 48 Genes GS171928: HP:0100577 Urinary bladder inflammation
Expand Tier I Mouse MP 766 Genes GS167063: MP:0001929 abnormal gametogenesis
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 Mouse GO 232 Genes GS180671: GO:0044454 nuclear chromosome part
Expand Tier I Human GO 2711 Genes GS199273: GO:0043233 organelle lumen
Expand Tier I Mouse MP 334 Genes GS166753: MP:0001935 decreased litter size
Expand Tier I Human 357 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Mouse GO 4619 Genes GS191019: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Mouse MP 75 Genes GS168818: MP:0005431 decreased oocyte number
Expand Tier I Human 18 Genes GS176340: HP:0001549 Abnormality of the ileum
Expand Tier I Mouse MP 1362 Genes GS168334: MP:0002619 abnormal lymphocyte morphology
Expand Tier I Human 167 Genes GS170916: HP:0008056 Aplasia/Hypoplasia affecting the eye
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 174 Genes GS172293: HP:0001511 Intrauterine growth retardation
Expand Tier I Human 222 Genes GS173995: HP:0000508 Ptosis
Expand Tier I Mouse MP 295 Genes GS165800: MP:0001923 reduced female fertility
Expand Tier I Human 423 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Mouse MP 2220 Genes GS166858: MP:0000685 abnormal immune system morphology
Expand Tier I Mouse GO 727 Genes GS179950: GO:0006259 DNA metabolic process
Expand Tier I Mouse MP 1254 Genes GS163965: MP:0011182 decreased hematopoietic cell number
Expand Tier I Human 323 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Mouse MP 1045 Genes GS163010: MP:0011181 increased hematopoietic cell number
Expand Tier I Mouse MP 113 Genes GS167216: MP:0001322 abnormal iris morphology
Expand Tier I Mouse GO 4353 Genes GS192017: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human 16 Genes GS173779: HP:0010293 Aplasia/Hypoplasia of the uvula
Expand Tier I Mouse MP 14 Genes GS163744: MP:0000439 enlarged cranium
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 GO 145 Genes GS194417: GO:0000790 nuclear chromatin
Expand Tier I Human 35 Genes GS175326: HP:0001217 Clubbing
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 73 Genes GS171188: HP:0000415 Abnormality of the choanae
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Mouse MP 1246 Genes GS165228: MP:0005382 craniofacial phenotype
Expand Tier I Mouse MP 100 Genes GS164349: MP:0010094 abnormal chromosome stability
Expand Tier I Mouse 320 Genes GS136205: lung tumor shape-determining 7 (Ltsd7, Published QTL Chr 16)
Expand Tier I Mouse MP 99 Genes GS169763: MP:0008866 chromosomal instability
Expand Tier I Human 389 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Human 273 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier I Human 181 Genes GS175907: HP:0004349 Reduced bone mineral density
Expand Tier I Human GO 2092 Genes GS209551: GO:0031981 nuclear lumen
Expand Tier I Mouse MP 1015 Genes GS166660: MP:0001731 abnormal postnatal growth
Expand Tier I Human 200 Genes GS176242: HP:0004207 Abnormality of the 5th finger
Expand Tier III Rat 334 Genes GS223213: Bone structure and strength QTL 63 (Bss63 Published QTL Chr 10)
Expand Tier I Mouse MP 321 Genes GS169040: MP:0005559 increased circulating glucose level
Expand Tier I Mouse MP 65 Genes GS166334: MP:0001134 absent corpus luteum
Expand Tier I Human 454 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Mouse MP 2070 Genes GS163824: MP:0001259 abnormal body weight
Expand Tier I Mouse MP 100 Genes GS167943: MP:0006254 thin cerebral cortex
Expand Tier I Human 242 Genes GS175909: HP:0004348 Abnormality of bone mineral density
Expand Tier III Rat 602 Genes GS224603: Hypercalciuria QTL 4 (Hc4 Published QTL Chr 10)
Expand Tier I Human 207 Genes GS174857: HP:0200006 Slanting of the palpebral fissure
Expand Tier I Human 346 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier I Human 737 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Mouse MP 133 Genes GS168084: MP:0006410 abnormal common myeloid progenitor cell morphology
Expand Tier III Rat 2054 Genes GS224162: Mammary tumor resistance QTL 7 (Mamtr7 Published QTL Chr 10)
Expand Tier I Human 532 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Mouse MP 104 Genes GS164406: MP:0004609 vertebral fusion
Expand Tier III Rat 542 Genes GS224828: Bone structure and strength QTL 40 (Bss40 Published QTL Chr 10)
Expand Tier I Human 489 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Mouse MP 141 Genes GS166757: MP:0001931 abnormal oogenesis
Expand Tier I Mouse MP 575 Genes GS170733: MP:0000188 abnormal circulating glucose level
Expand Tier I Mouse GO 31 Genes GS186483: GO:0006308 DNA catabolic process
Expand Tier I Mouse MP 1408 Genes GS168063: MP:0000313 abnormal cell death
Expand Tier I Human 401 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 177 Genes GS174214: HP:0009466 Radial deviation of finger
Expand Tier I Mouse MP 1052 Genes GS166409: MP:0002114 abnormal axial skeleton morphology
Expand Tier I Human GO 3 Genes GS208826: GO:0045002 double-strand break repair via single-strand annealing
Expand Tier I Human GO 69 Genes GS203330: GO:0006308 DNA catabolic process
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Mouse MP 627 Genes GS167070: MP:0001921 reduced fertility
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Human 184 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 GO 1082 Genes GS203482: GO:0044093 positive regulation of molecular function
Expand Tier I Human 57 Genes GS171016: HP:0011893 Abnormal leukocyte count
Expand Tier I Mouse MP 543 Genes GS170680: MP:0003744 abnormal orofacial morphology
Expand Tier I Mouse GO 4500 Genes GS186790: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Mouse MP 855 Genes GS169075: MP:0002078 abnormal glucose homeostasis
Expand Tier I Human 232 Genes GS170999: HP:0000082 Abnormality of renal physiology
Expand Tier I Mouse MP 101 Genes GS166338: MP:0001130 abnormal ovarian folliculogenesis
Expand Human 324 Genes GS219820: http://www.broadinstitute.org/gsea/msigdb/cards/CELL_CYCLE_GO_0007049
Expand Tier I Human 33 Genes GS171079: HP:0001882 Leukopenia
Expand Tier I Human 356 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human 65 Genes GS171085: HP:0009602 Abnormality of the phalanges of the thumb
Expand Tier I Human 243 Genes GS173534: HP:0001877 Abnormality of erythrocytes
Expand Tier I Human GO 1853 Genes GS209010: GO:1901575 organic substance catabolic process
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 1068 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 18 Genes GS172413: HP:0002245 Meckel diverticulum
Expand Tier I Human 401 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Human 47 Genes GS174811: HP:0001636 Tetralogy of Fallot
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Mouse GO 1777 Genes GS184445: GO:0044428 nuclear part
Expand Tier I Mouse GO 45 Genes GS189493: GO:0000724 double-strand break repair via homologous recombination
Expand Tier I Human GO 970 Genes GS201034: GO:0030234 enzyme regulator activity
Expand Tier I Human GO 8578 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human GO 29 Genes GS204575: GO:0004520 endodeoxyribonuclease activity
Expand Tier I Mouse MP 239 Genes GS166294: MP:0011109 partial lethality throughout fetal growth and development
Expand Tier I Human 780 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 433 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
Expand Tier I Human GO 17 Genes GS206362: GO:0000726 non-recombinational repair
Expand Human 64 Genes GS220172: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_P53_SIGNALING_PATHWAY
Expand Tier I Human 231 Genes GS173288: HP:0000316 Hypertelorism
Expand Tier I Human 127 Genes GS171035: HP:0002620 Systemic artery abnormality
Expand Tier I Mouse MP 3051 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Mouse MP 352 Genes GS167360: MP:0002200 abnormal brain ventricle/choroid plexus morphology
Expand Tier I Human GO 2479 Genes GS201249: GO:0044428 nuclear part
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 9 Genes GS206365: GO:0000729 DNA double-strand break processing
Expand Tier I Mouse GO 16 Genes GS189491: GO:0000726 non-recombinational repair
Expand Tier I Human GO 3 Genes GS206254: GO:0008821 crossover junction endodeoxyribonuclease activity
Expand Tier I Human 53 Genes GS171305: HP:0012145 Abnormality of multiple cell lineages in the bone marrow
Expand Tier I Human 296 Genes GS174145: HP:0005918 Abnormality of phalanx of finger
Expand Tier I Mouse MP 3761 Genes GS165527: MP:0005378 growth/size phenotype
Expand Tier I Human GO 38 Genes GS200250: GO:0004536 deoxyribonuclease activity
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 250 Genes GS171634: HP:0008050 Abnormality of the palpebral fissures
Expand Tier I Mouse 476 Genes GS136684: skull morphology 23 (Skull23, Published QTL Chr 16)
Expand Tier I Mouse MP 472 Genes GS164448: MP:0005193 abnormal anterior eye segment morphology
Expand Tier I Mouse MP 117 Genes GS164445: MP:0005194 abnormal anterior uvea morphology
Expand Tier I Human 382 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Mouse MP 1332 Genes GS169777: MP:0002398 abnormal bone marrow cell morphology/development
Expand Tier I Human 24 Genes GS174728: HP:0100760 Clubbing of toes
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Mouse GO 6 Genes GS189494: GO:0000729 DNA double-strand break processing
Expand Tier I Human 31 Genes GS172259: HP:0001199 Triphalangeal thumb
Expand Tier I Human 86 Genes GS174858: HP:0200007 Abnormal size of the palpebral fissures
Expand Tier I Human 381 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier III Rat 1893 Genes GS224230: Collagen induced arthritis QTL 16 (Cia16 Published QTL Chr 10)
Expand Tier III Rat 1375 Genes GS224287: Vascular elastic tissue fragility QTL 10 (Vetf10 Published QTL Chr 10)
Expand Tier I Mouse MP 1634 Genes GS166250: MP:0008247 abnormal mononuclear cell morphology
Expand Tier I Human 313 Genes GS176568: HP:0000486 Strabismus
Expand Tier I Mouse MP 178 Genes GS169017: MP:0002932 abnormal joint morphology
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 5337 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier I Mouse GO 7644 Genes GS188399: GO:0044238 primary metabolic process
Expand Tier I Mouse 335 Genes GS136334: nicotine induced locomotor activity 10 (Nilac10, Published QTL Chr 16)
Expand Tier I Human GO 891 Genes GS200867: GO:0043085 positive regulation of catalytic activity
Expand Tier I Mouse GO 4478 Genes GS184435: GO:0046483 heterocycle metabolic process
Expand Tier I Mouse MP 1811 Genes GS168422: MP:0000716 abnormal immune system cell morphology
Expand Tier I Mouse MP 112 Genes GS167461: MP:0002792 abnormal retinal vasculature morphology
Expand Tier I Mouse MP 896 Genes GS168295: MP:0003698 abnormal male reproductive system physiology
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 122 Genes GS172403: HP:0011873 Abnormal platelet count
Expand Tier I Human 231 Genes GS176771: HP:0001000 Abnormality of skin pigmentation
Expand Human 64 Genes GS220970: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_P53_SIGNALING_PATHWAY
Expand Tier I Mouse MP 215 Genes GS170240: MP:0001297 microphthalmia
Expand Tier I Mouse MP 1210 Genes GS166711: MP:0002160 abnormal reproductive system morphology
Expand Tier I Mouse GO 4651 Genes GS177310: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Mouse MP 2788 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Mouse MP 2551 Genes GS169535: MP:0005397 hematopoietic system phenotype
Expand Tier I Mouse MP 130 Genes GS164917: MP:0008280 male germ cell apoptosis
Expand Tier I Mouse MP 622 Genes GS167367: MP:0002208 abnormal germ cell morphology
Expand Tier I Human 163 Genes GS176478: HP:0002119 Ventriculomegaly
Expand Tier I Human 550 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human 407 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human 189 Genes GS176745: HP:0010866 Abdominal wall defect
Expand Tier I Mouse GO 8 Genes GS185219: GO:0000738 DNA catabolic process, exonucleolytic
Expand Tier I Human GO 3853 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Mouse MP 1674 Genes GS169530: MP:0005390 skeleton phenotype
Expand Tier I Mouse GO 5247 Genes GS178448: GO:0005634 nucleus
Expand Tier I Human GO 211 Genes GS198948: GO:0006310 DNA recombination
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human GO 1 Genes GS210723: GO:0070522 ERCC4-ERCC1 complex
Expand Tier I Human 486 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Mouse 396 Genes GS135719: determination of interleukin 4 commitment 1 (Dice1, Published QTL Chr 16)
Expand Tier I Human 144 Genes GS171586: HP:0001560 Abnormality of the amniotic fluid
Expand Tier I Mouse GO 322 Genes GS190813: GO:0008047 enzyme activator activity
Expand Tier I Human 283 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier I Mouse GO 629 Genes GS186758: GO:0034655 nucleobase-containing compound catabolic process
Expand Tier III Rat 663 Genes GS224281: Food consumption QTL 17 (Foco17 Published QTL Chr 10)
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 80 Genes GS175635: HP:0002251 Aganglionic megacolon
Expand Tier III Mouse 8151 Genes GS213076: Genes with suggestive difference in (B6) vs (B6PF1 + PB6F1 + PWD) comparison
Expand Tier I Mouse 339 Genes GS135974: wound healing/regeneration 11 (Heal11, Published QTL Chr 16)
Expand Tier I Mouse MP 108 Genes GS166635: MP:0001125 abnormal oocyte morphology
Expand Tier I Mouse 476 Genes GS135444: bone length and organs 10 (Bod10, Published QTL Chr 16)
Expand Tier I Human 146 Genes GS173537: HP:0001872 Abnormality of thrombocytes
Expand Tier I Human 107 Genes GS171228: HP:0002823 Abnormality of the femur
Expand Tier I Mouse MP 547 Genes GS169161: MP:0006362 abnormal male germ cell morphology
Expand Tier I Human 936 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 36 Genes GS204011: GO:0016893 endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters
Expand Tier I Human 53 Genes GS172571: HP:0000340 Sloping forehead
Expand Tier I Human GO 731 Genes GS208043: GO:0016788 hydrolase activity, acting on ester bonds
Expand Tier I Mouse MP 183 Genes GS167518: MP:0001312 abnormal cornea morphology
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Mouse MP 11449 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Mouse 315 Genes GS136792: TallyHo associated non-insulin dependent diabetes mellitus 3 (Tanidd3, Published QTL Chr 16)
Expand Tier I Mouse 476 Genes GS136669: skin tumor susceptibility 9 (Skts9, Published QTL Chr 16)
Expand Tier I Human 187 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 496 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Human 114 Genes GS172500: HP:0007400 Irregular hyperpigmentation
Expand Tier I Human GO 6347 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human 210 Genes GS171106: HP:0006496 Aplasia/Hypoplasia involving bones of the upper limbs
Expand Tier I Human 521 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Mouse MP 26 Genes GS164311: MP:0004805 absent oocytes
Expand Tier I Mouse MP 1073 Genes GS163026: MP:0000221 decreased leukocyte cell number
Expand Tier I Human 148 Genes GS176233: HP:0004209 Clinodactyly of the 5th finger
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Tier I Mouse MP 257 Genes GS163987: MP:0000822 abnormal brain ventricle morphology
Expand Tier I Mouse MP 225 Genes GS164122: MP:0000228 abnormal thrombopoiesis
Expand Tier I Human 404 Genes GS173743: HP:0001999 Abnormal facial shape
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Mouse MP 2204 Genes GS165615: MP:0002123 abnormal hematopoiesis
Expand Tier I Human 468 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Human GO 1794 Genes GS196933: GO:0065009 regulation of molecular function
Expand Tier I Rat 299 Genes GS128032: Alcohol consumption QTL 9 (Alc9, Published QTL, Chr 10)
Expand Tier I Human GO 1 Genes GS209585: GO:0048476 Holliday junction resolvase complex
Expand Tier I Human 64 Genes GS176161: HP:0100589 Urogenital fistula
Expand Tier I Human 886 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 407 Genes GS175670: HP:0007364 Aplasia/Hypoplasia of the cerebrum
Expand Tier I Mouse MP 486 Genes GS166636: MP:0001124 abnormal gametes
Expand Tier III Rat 1156 Genes GS223265: Neuroinflammation QTL 9 (Neuinf9 Published QTL Chr 10)
Expand Tier I Human GO 3271 Genes GS199267: GO:0043234 protein complex
Expand Tier I Human 189 Genes GS174579: HP:0002031 Abnormality of the esophagus
Expand Tier I Mouse MP 2219 Genes GS168551: MP:0002429 abnormal blood cell morphology/development
Expand Tier I Mouse GO 4224 Genes GS193059: GO:0044446 intracellular organelle part
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier III Rat 772 Genes GS224203: Stress response QTL 21 (Stresp21 Published QTL Chr 10)
Expand Tier I Human 187 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier I Human GO 1421 Genes GS206620: GO:0050790 regulation of catalytic activity
Expand Tier I Mouse MP 7 Genes GS169058: MP:0000917 obstructive hydrocephaly
Expand Tier I Mouse 480 Genes GS135263: acute functional tolerance to ethanol QTL 2 (Afteq2, Published QTL Chr 16)
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human GO 56 Genes GS206363: GO:0000725 recombinational repair
Expand Tier I Mouse MP 3168 Genes GS169827: MP:0005387 immune system phenotype
Expand Tier I Human 51 Genes GS174291: HP:0002575 Tracheoesophageal fistula
Expand Tier I Mouse MP 1235 Genes GS170198: MP:0001614 abnormal blood vessel morphology
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human GO 3116 Genes GS199272: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Mouse MP 918 Genes GS165427: MP:0000432 abnormal head morphology
Expand Tier I Human 113 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 III Rat 1280 Genes GS224751: Blood pressure QTL 133 (Bp133 Published QTL Chr 10)
Expand Tier I Human 525 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human 837 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Mouse GO 681 Genes GS184065: GO:0043085 positive regulation of catalytic activity
Expand Tier I Mouse MP 1444 Genes GS163297: MP:0000217 abnormal leukocyte cell number
Expand Tier I Human 273 Genes GS172516: HP:0001347 Hyperreflexia
Expand Tier I Human 236 Genes GS171395: HP:0000175 Cleft palate
Expand Tier I Human 542 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human 85 Genes GS173838: HP:0002778 Abnormality of the trachea
Expand Tier I Human 34 Genes GS173892: HP:0005528 Bone marrow hypocellularity
Expand Tier I Human 159 Genes GS175096: HP:0000286 Epicanthus
Expand Tier I Human 25 Genes GS175175: HP:0003220 Abnormality of chromosome stability
Expand Tier I Human GO 5928 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 108 Genes GS175595: HP:0011017 Abnormality of cell physiology
Expand Tier I Mouse MP 832 Genes GS167759: MP:0000787 abnormal telencephalon morphology
Expand Tier I Mouse MP 245 Genes GS168843: MP:0005293 impaired glucose tolerance
Expand Tier I Human 733 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human 148 Genes GS175149: HP:0009179 Deviation of the 5th finger
Expand Human 64 Genes GS219635: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_P53_SIGNALING_PATHWAY
Expand Tier I Human 63 Genes GS175660: HP:0006501 Aplasia/Hypoplasia of the radius
Expand Tier I Human 80 Genes GS173031: HP:0004362 Abnormality of the enteric ganglia
Expand Tier I Mouse MP 1327 Genes GS163971: MP:0002092 abnormal eye morphology
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 Mouse MP 192 Genes GS165821: MP:0001117 absent gametes
Expand Tier I Human GO 890 Genes GS207863: GO:0009057 macromolecule catabolic process
Expand Tier I Mouse MP 605 Genes GS169421: MP:0002447 abnormal erythrocyte morphology
Expand Tier I Human 392 Genes GS171067: HP:0002664 Neoplasm
Expand Tier I Mouse MP 311 Genes GS166634: MP:0001126 abnormal ovary morphology
Expand Tier I Mouse GO 9323 Genes GS180152: GO:0065007 biological regulation
Expand Tier II Mouse 599 Genes GS84293: METH responses for home cage activity (Published QTL, Chr 16)
Expand Tier I Mouse MP 33 Genes GS164465: MP:0003671 abnormal eyelid aperture
Expand Tier III Human 2273 Genes GS137413: Supplementary Table 2. CNA Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Mouse MP 1093 Genes GS165536: MP:0005371 limbs/digits/tail phenotype
Expand Tier I Human 317 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Mouse MP 2489 Genes GS165397: MP:0001265 decreased body size
Expand Tier I Mouse MP 3396 Genes GS170601: MP:0005621 abnormal cell physiology
Expand Tier I Mouse GO 1395 Genes GS185366: GO:0044248 cellular catabolic process
Expand Tier I Mouse MP 16 Genes GS166898: MP:0001333 absent optic nerve
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 212 Genes GS176185: HP:0100790 Hernia
Expand Tier I Human 483 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier III Rat 329 Genes GS224900: Alcohol consumption QTL 9 (Alc9 Published QTL Chr 10)
Expand Tier I Mouse MP 222 Genes GS166121: MP:0002100 abnormal tooth morphology
Expand Tier I Human 25 Genes GS176991: HP:0100867 Duodenal stenosis
Expand Tier I Mouse MP 68 Genes GS167556: MP:0009364 abnormal mature ovarian follicle morphology
Expand Tier I Human GO 5 Genes GS201326: GO:0017108 5'-flap endonuclease activity
Expand Tier I Human 113 Genes GS171171: HP:0005607 Abnormality of the tracheobronchial system
Expand Tier I Human 576 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 256 Genes GS175602: HP:0002087 Abnormality of the upper respiratory tract
Expand Tier I Mouse MP 240 Genes GS170627: MP:0001586 abnormal erythrocyte cell number
Expand Tier I Human GO 792 Genes GS201002: GO:0044270 cellular nitrogen compound catabolic process
Expand Tier I Mouse MP 229 Genes GS170688: MP:0002697 abnormal eye size
Expand Tier I Human GO 6 Genes GS208386: GO:0016889 endodeoxyribonuclease activity, producing 3'-phosphomonoesters
Expand Tier I Human 51 Genes GS171628: HP:0008053 Aplasia/Hypoplasia of the iris
Expand Tier I Human 598 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 435 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier I Human 173 Genes GS173901: HP:0002007 Frontal bossing
Expand Tier I Mouse MP 611 Genes GS163101: MP:0008540 abnormal cerebrum morphology
Expand Tier I Mouse MP 438 Genes GS163418: MP:0009208 abnormal female genitalia morphology
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Mouse GO 872 Genes GS186633: GO:0044093 positive regulation of molecular function
Expand Tier I Human GO 10576 Genes GS203594: GO:0043226 organelle
Expand Tier I Mouse MP 120 Genes GS166386: MP:0008871 abnormal ovarian follicle number
Expand Tier III Rat 314 Genes GS224904: Alcohol consumption QTL 5 (Alc5 Published QTL Chr 10)
Expand Tier I Human 153 Genes GS175067: HP:0001159 Syndactyly
Expand Tier I Mouse MP 442 Genes GS165816: MP:0001119 abnormal female reproductive system morphology
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 228 Genes GS171908: HP:0004298 Abnormality of the abdominal wall
Expand Tier I Mouse MP 1798 Genes GS164022: MP:0008246 abnormal leukocyte morphology
Expand Tier I Human 554 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Mouse MP 4019 Genes GS165537: MP:0005376 homeostasis/metabolism phenotype
Expand Tier I Mouse MP 88 Genes GS166246: MP:0002759 abnormal caudal vertebrae morphology
Expand Tier I Mouse MP 105 Genes GS167442: MP:0000440 domed cranium
Expand Tier I Human 676 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Mouse MP 553 Genes GS167217: MP:0001325 abnormal retina morphology
Expand Tier I Mouse MP 1765 Genes GS167622: MP:0002152 abnormal brain morphology
Expand Tier I Human GO 296 Genes GS198866: GO:0000785 chromatin
Expand Tier I Mouse GO 662 Genes GS184198: GO:0044270 cellular nitrogen compound catabolic process
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse GO 2876 Genes GS181102: GO:0043228 non-membrane-bounded organelle
Expand Tier I Mouse MP 155 Genes GS163986: MP:0000823 abnormal lateral ventricle morphology
Expand Tier I Human 66 Genes GS171115: HP:0001053 Hypopigmented skin patches
Expand Tier I Mouse GO 666 Genes GS191973: GO:0046700 heterocycle catabolic process
Expand Tier I Mouse MP 983 Genes GS164742: MP:0001732 postnatal growth retardation
Expand Tier I Mouse MP 500 Genes GS166405: MP:0002111 abnormal tail morphology
Expand Tier I Human 142 Genes GS171178: HP:0000238 Hydrocephalus
Expand Tier I Human 113 Genes GS174643: HP:0005120 Abnormality of cardiac atrium
Expand Tier I Mouse MP 219 Genes GS168584: MP:0004720 abnormal platelet morphology
Expand Tier I Human GO 6256 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 8094 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 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human 596 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Mouse MP 474 Genes GS170351: MP:0006208 lethality throughout fetal growth and development
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 Mouse MP 794 Genes GS169062: MP:0000913 abnormal brain development
Expand Tier I Human 80 Genes GS173498: HP:0001763 Pes planus
Expand Tier I Human 322 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Mouse MP 602 Genes GS166407: MP:0002116 abnormal craniofacial bone morphology
Expand Tier I Human 126 Genes GS173090: HP:0004377 Hematological neoplasm
Expand Tier I Mouse GO 23359 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Mouse 475 Genes GS136288: modifier of polycystic kidney disease progression 2 (Mopkd2, Published QTL Chr 16)
Expand Tier I Mouse 339 Genes GS136314: non-HDL QTL 10 (Nhdlq10, Published QTL Chr 16)
Expand Tier I Human GO 13 Genes GS208387: GO:0016888 endodeoxyribonuclease activity, producing 5'-phosphomonoesters
Expand Tier I Human 42 Genes GS175750: HP:0000010 Recurrent urinary tract infections
Expand Tier I Human 395 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Mouse 415 Genes GS135361: B.burgdorferi-associated arthritis 19 (Bbaa19, Published QTL Chr 16)
Expand Tier I Mouse MP 148 Genes GS166808: MP:0003179 decreased platelet cell number
Expand Tier I Mouse MP 112 Genes GS169200: MP:0006361 abnormal female germ cell morphology
Expand Tier I Human 282 Genes GS175119: HP:0001881 Abnormality of leukocytes
Expand Tier I Human 19 Genes GS176709: HP:0100587 Abnormality of the preputium
Expand Tier I Mouse MP 728 Genes GS170683: MP:0003743 abnormal facial morphology
Expand Tier I Human 257 Genes GS172272: HP:0001197 Abnormality of prenatal development or birth
Expand Tier I Human 193 Genes GS174813: HP:0001638 Cardiomyopathy
Expand Tier I Human 262 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier I Mouse GO 9049 Genes GS180166: GO:0008152 metabolic process
Expand Tier I Mouse MP 623 Genes GS164446: MP:0005195 abnormal posterior eye segment morphology
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Mouse GO 480 Genes GS185536: GO:0006974 response to DNA damage stimulus
Expand Tier I Human GO 4415 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 GO 529 Genes GS201253: GO:0044427 chromosomal part
Expand Tier I Human 550 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 335 Genes GS174076: HP:0009122 Aplasia/Hypoplasia affecting bones of the axial skeleton
Expand Tier I Human 136 Genes GS175524: HP:0000009 Functional abnormality of the bladder
Expand Tier I Human 261 Genes GS176692: HP:0009815 Aplasia/Hypoplasia of the extremities
Expand Tier I Mouse MP 66 Genes GS163811: MP:0004643 abnormal vertebrae number
Expand Tier I Mouse MP 1415 Genes GS169531: MP:0005391 vision/eye phenotype
Expand Tier I Human 390 Genes GS175537: HP:0011277 Abnormality of the urinary system physiology
Expand Tier I Human 423 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Human 51 Genes GS176559: HP:0000483 Astigmatism
Expand Tier I Human 94 Genes GS176560: HP:0001010 Hypopigmentation of the skin
Expand Tier I Human GO 2665 Genes GS205543: GO:0070013 intracellular organelle lumen
Expand Tier I Human 75 Genes GS172096: HP:0000581 Blepharophimosis
Expand Tier I Mouse 431 Genes GS136591: radiation induced thymic lymphoma susceptibility (Ritls, Published QTL Chr 16)
Expand Tier I Human 144 Genes GS175754: HP:0000014 Abnormality of the bladder
Expand Tier I Mouse 476 Genes GS136653: skeletal size (tail length) 7 (Skl7, Published QTL Chr 16)
Expand Tier I Mouse MP 569 Genes GS165809: MP:0002864 abnormal ocular fundus morphology
Expand Tier I Human 263 Genes GS176477: HP:0002118 Abnormality of the cerebral ventricles
Expand Tier I Mouse GO 4518 Genes GS187751: GO:0019222 regulation of metabolic process
Expand Tier I Mouse GO 35 Genes GS191670: GO:0006289 nucleotide-excision repair
Expand Tier I Human GO 864 Genes GS196719: GO:0006259 DNA metabolic process
Expand Tier I Human 48 Genes GS174251: HP:0010161 Abnormality of the phalanges of the toes
Expand Tier I Mouse MP 636 Genes GS169663: MP:0004703 abnormal vertebral column morphology
Expand Tier I Human 161 Genes GS175958: HP:0000795 Abnormality of the urethra
Expand Tier I Human 583 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human 776 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 58 Genes GS171588: HP:0001562 Oligohydramnios
Expand Tier I Human GO 99 Genes GS208952: GO:0004519 endonuclease activity
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse 296 Genes GS136457: postnatal body weight growth 19 (Pbwg19, Published QTL Chr 16)
Expand Tier I Mouse MP 3424 Genes GS163934: MP:0001764 abnormal homeostasis
Expand Tier I Mouse GO 4333 Genes GS184452: GO:0044422 organelle part
Expand Tier I Human GO 4960 Genes GS199124: GO:0051716 cellular response to stimulus
Expand Tier I Human GO 6605 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 123 Genes GS171384: HP:0001551 Abnormality of the umbilicus
Expand Tier I Mouse MP 4902 Genes GS165525: MP:0010768 mortality/aging
Expand Tier I Mouse GO 1662 Genes GS180155: GO:0065009 regulation of molecular function
Expand Tier I Human 173 Genes GS171148: HP:0011218 Abnormal shape of the frontal region
Expand Tier I Human GO 5347 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Mouse MP 71 Genes GS163983: MP:0000826 abnormal third ventricle morphology
Expand Tier I Human 418 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Mouse MP 1626 Genes GS168174: MP:0001919 abnormal reproductive system physiology
Expand Tier I Human 621 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human 120 Genes GS177000: HP:0001291 Abnormality of the cranial nerves
Expand Tier I Human GO 5567 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Human 356 Genes GS174099: HP:0011793 Neoplasm by anatomical site
Expand Tier I Human 46 Genes GS170867: HP:0100736 Abnormality of the soft palate
Expand Tier I Human 110 Genes GS174806: HP:0001631 Defect in the atrial septum
Expand Tier I Human 31 Genes GS175137: HP:0000025 Functional abnormality of male internal genitalia
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human 344 Genes GS171309: HP:0000252 Microcephaly
Expand Tier I Human GO 5526 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Mouse GO 46 Genes GS189492: GO:0000725 recombinational repair
Expand Tier III Rat 334 Genes GS223250: Bone mineral density QTL 71 (Bmd71 Published QTL Chr 10)
Expand Tier I Human GO 55 Genes GS206364: GO:0000724 double-strand break repair via homologous recombination
Expand Tier I Mouse GO 6947 Genes GS192918: GO:0050896 response to stimulus
Expand Tier I Human 35 Genes GS174128: HP:0002863 Myelodysplasia
Expand Tier I Human GO 1184 Genes GS197275: GO:0033554 cellular response to stress
Expand Tier I Mouse MP 4624 Genes GS165524: MP:0010769 abnormal survival
Expand Tier I Human 442 Genes GS175423: HP:0010461 Abnormality of the male genitalia
Expand Tier I Human GO 2331 Genes GS208037: GO:0016787 hydrolase activity
Expand Tier I Human 87 Genes GS173938: HP:0001679 Abnormality of the aorta
Expand Tier I Mouse MP 391 Genes GS169234: MP:0000137 abnormal vertebrae morphology
Expand Tier I Mouse MP 3714 Genes GS165243: MP:0010770 preweaning lethality
Expand Tier I Human 356 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Mouse GO 1 Genes GS180481: GO:0033557 Slx1-Slx4 complex
Expand Tier I Human GO 7259 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human 393 Genes GS172362: HP:0004325 Decreased body weight
Expand Tier I Mouse GO 7552 Genes GS180452: GO:0044237 cellular metabolic process
Expand Tier I Mouse MP 57 Genes GS168565: MP:0008813 decreased common myeloid progenitor cell number
Expand Tier I Human GO 402 Genes GS207716: GO:0008047 enzyme activator activity
Expand Tier I Human 203 Genes GS174706: HP:0000553 Abnormality of the uvea
Expand Tier I Mouse MP 406 Genes GS168923: MP:0002673 abnormal sperm number
Expand Tier I Human 200 Genes GS171413: HP:0004097 Deviation of finger
Expand Tier I Human 119 Genes GS173538: HP:0001873 Thrombocytopenia
Expand Tier I Human 59 Genes GS172311: HP:0100691 Abnormality of the curvature of the cornea
Expand Tier I Human 270 Genes GS172637: HP:0010460 Abnormality of the female genitalia
Expand Tier I Mouse GO 2991 Genes GS182469: GO:0043234 protein complex
Expand Tier I Mouse MP 308 Genes GS163706: MP:0000830 abnormal diencephalon morphology
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 Mouse GO 54 Genes GS192360: GO:0090305 nucleic acid phosphodiester bond hydrolysis
Expand Tier I Human 1046 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Mouse GO 23849 Genes GS180164: GO:0008150 biological_process
Expand Tier I Human GO 24 Genes GS198867: GO:0000784 nuclear chromosome, telomeric region
Expand Tier I Human 58 Genes GS172829: HP:0001824 Weight loss
Expand Tier I Human 198 Genes GS174812: HP:0001637 Abnormality of the myocardium
Expand Tier I Human GO 692 Genes GS208575: GO:0044265 cellular macromolecule catabolic process
Expand Tier I Mouse MP 2337 Genes GS168995: MP:0009642 abnormal blood homeostasis
Expand Tier I Human 917 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Mouse GO 6435 Genes GS177531: GO:0043170 macromolecule metabolic process
Expand Tier I Human 47 Genes GS171755: HP:0001710 Conotruncal defect
Expand Tier I Mouse MP 583 Genes GS165437: MP:0000438 abnormal cranium morphology
Expand Tier I Human 71 Genes GS175658: HP:0006503 Aplasia/Hypoplasia involving forearm bones
Expand Tier I Mouse MP 93 Genes GS170238: MP:0001293 anophthalmia
Expand Tier I Human GO 8645 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Mouse MP 2465 Genes GS169829: MP:0005385 cardiovascular system phenotype
Expand Tier I Human 985 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Mouse GO 3583 Genes GS180236: GO:0032991 macromolecular complex
Expand Tier I Mouse GO 334 Genes GS191667: GO:0006281 DNA repair
Expand Tier I Mouse GO 935 Genes GS180482: GO:0033554 cellular response to stress
Expand Tier I Mouse MP 357 Genes GS167748: MP:0000788 abnormal cerebral cortex morphology
Expand Tier I Human 64 Genes GS171273: HP:0100542 Abnormal localization of kidneys
Expand Tier I Human 430 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Mouse MP 2211 Genes GS164262: MP:0002080 prenatal lethality
Expand Tier I Human 74 Genes GS171850: HP:0002414 Spina bifida
Expand Tier I Human GO 159 Genes GS208951: GO:0004518 nuclease activity
Expand Tier I Mouse GO 1648 Genes GS190954: GO:0009056 catabolic process
Expand Tier III Rat 334 Genes GS223278: Bone structure and strength QTL 64 (Bss64 Published QTL Chr 10)
Expand Tier I Mouse MP 60 Genes GS164404: MP:0008008 early cellular replicative senescence
Expand Tier I Human GO 5280 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Mouse MP 346 Genes GS163635: MP:0001933 abnormal litter size
Expand Tier I Mouse MP 416 Genes GS168520: MP:0004901 decreased male germ cell number
Expand Tier I Human 286 Genes GS173167: HP:0100491 Abnormality of the joints of the lower limbs
Expand Tier I Mouse GO 1628 Genes GS177813: GO:0031974 membrane-enclosed lumen