Gene Details



H19 and homologs in 2 species are found in 565 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 Mouse MP 1350 Genes GS165707: MP:0000428 abnormal craniofacial morphology
Expand Tier I Human 187 Genes GS171907: HP:0004299 Hernia of the abdominal wall
Expand Tier I Mouse MP 519 Genes GS170662: MP:0000274 enlarged heart
Expand Tier I Mouse MP 1051 Genes GS166825: MP:0000462 abnormal digestive system morphology
Expand Tier I Mouse MP 545 Genes GS167188: MP:0001264 increased body size
Expand Tier I Mouse MP 453 Genes GS170247: MP:0002038 carcinoma
Expand Tier I Mouse MP 10 Genes GS164505: MP:0001699 increased embryo size
Expand Tier I Human 271 Genes GS176826: HP:0000202 Oral cleft
Expand Tier I Human 72 Genes GS176436: HP:0000047 Hypospadias
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Mouse MP 1055 Genes GS166120: MP:0002106 abnormal muscle physiology
Expand Tier I Mouse MP 223 Genes GS167526: MP:0000157 abnormal sternum morphology
Expand Tier I Mouse MP 55 Genes GS170769: MP:0003567 abnormal fetal cardiomyocyte proliferation
Expand Tier I Mouse MP 302 Genes GS167687: MP:0011099 complete lethality throughout fetal growth and development
Expand Tier I Mouse MP 96 Genes GS169577: MP:0010224 abnormal heart ventricle outflow tract morphology
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Mouse 874 Genes GS136784: seizure severity 2 (Szv2, Published QTL Chr 7)
Expand Tier I Mouse MP 467 Genes GS168549: MP:0000477 abnormal intestine morphology
Expand Tier I Human 54 Genes GS176464: HP:0100242 Sarcoma
Expand Tier I Human 100 Genes GS175101: HP:0000280 Coarse facial features
Expand Tier I Human 282 Genes GS175900: HP:0009118 Aplasia/Hypoplasia of the mandible
Expand Tier I Human 1 Genes GS173270: HP:0005461 Craniofacial disproportion
Expand Tier I Mouse MP 44 Genes GS164451: MP:0010352 gastrointestinal tract polyps
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Human 8 Genes GS175574: HP:0002884 Hepatoblastoma
Expand Tier I Mouse MP 3631 Genes GS169830: MP:0005384 cellular phenotype
Expand Tier I Human 125 Genes GS173384: HP:0002750 Delayed skeletal maturation
Expand Tier I Mouse MP 264 Genes GS166949: MP:0009308 adenocarcinoma
Expand Tier I Mouse MP 151 Genes GS170667: MP:0010080 abnormal hepatocyte physiology
Expand Tier I Human 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Mouse 874 Genes GS136339: nicotine induced locomotor activity 4 (Nilac4, Published QTL Chr 7)
Expand Tier I Human 170 Genes GS174488: HP:0000525 Abnormality of the iris
Expand Tier I Human 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human CTD 2424 Genes GS123265: Estradiol interacting genes (MeSH:D004958) in CTD
Expand Tier I Mouse MP 1386 Genes GS169973: MP:0002006 tumorigenesis
Expand Tier I Human 24 Genes GS175787: HP:0002898 Embryonal neoplasm
Expand Tier I Mouse MP 552 Genes GS167149: MP:0000452 abnormal mouth morphology
Expand Tier I Mouse MP 521 Genes GS165382: MP:0001260 increased body weight
Expand Tier I Human 68 Genes GS173148: HP:0003712 Muscle hypertrophy
Expand Tier I Mouse MP 469 Genes GS165308: MP:0004848 abnormal liver size
Expand Tier I Human 189 Genes GS176004: HP:0100656 Thoracoabdominal wall defects
Expand Tier I Mouse GO 2678 Genes GS181892: GO:0048523 negative regulation of cellular process
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Mouse 454 Genes GS136306: myocardial infarction 1 (Myci1, Published QTL Chr 7)
Expand Tier I Human 7 Genes GS176667: HP:0004220 Short middle phalanx of the 5th finger
Expand Tier I Human 21 Genes GS171123: HP:0003006 Neuroblastoma
Expand Tier I Mouse MP 385 Genes GS166406: MP:0002110 abnormal digit morphology
Expand Tier I Human 138 Genes GS174644: HP:0000953 Hyperpigmentation of the skin
Expand Tier I Mouse MP 349 Genes GS166162: MP:0011090 partial perinatal lethality
Expand Tier I Human 374 Genes GS175815: HP:0011025 Abnormality of cardiovascular system physiology
Expand Tier I Mouse MP 100 Genes GS165360: MP:0004625 abnormal rib attachment
Expand Tier I Mouse MP 20 Genes GS164296: MP:0003269 colon polyps
Expand Tier I Human CTD 2780 Genes GS123332: 7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxide interacting genes (MeSH:D015123) in CTD
Expand Tier I Mouse MP 242 Genes GS167156: MP:0000459 abnormal presacral vertebrae morphology
Expand Tier I Human 52 Genes GS171623: HP:0008055 Aplasia/Hypoplasia affecting the uvea
Expand Tier I Human 120 Genes GS172358: HP:0003117 Abnormality of circulating hormone level
Expand Tier I Human 135 Genes GS170969: HP:0000157 Abnormality of the tongue
Expand Tier I Human 602 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Mouse MP 1628 Genes GS163852: MP:0001544 abnormal cardiovascular system physiology
Expand Tier I Human 168 Genes GS170916: HP:0008056 Aplasia/Hypoplasia affecting the eye
Expand Tier I Mouse MP 679 Genes GS170021: MP:0011087 complete neonatal lethality
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 Mouse MP 115 Genes GS165522: MP:0009674 decreased birth weight
Expand Tier I Human CTD 1201 Genes GS123595: Progesterone interacting genes (MeSH:D011374) in CTD
Expand Tier I Human 88 Genes GS176142: HP:0001034 Hypermelanotic macule
Expand Tier I Mouse MP 282 Genes GS165049: MP:0004857 abnormal heart weight
Expand Tier I Mouse MP 254 Genes GS165859: MP:0000351 increased cell proliferation
Expand Tier I Human 490 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Mouse MP 257 Genes GS165839: MP:0009701 abnormal birth body size
Expand Tier I Mouse 427 Genes GS136460: postnatal body weight growth 3 (Pbwg3, Published QTL Chr 7)
Expand Tier I Mouse MP 55 Genes GS163529: MP:0002957 intestinal adenocarcinoma
Expand Tier I Human 426 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Mouse MP 1941 Genes GS165528: MP:0005379 endocrine/exocrine gland phenotype
Expand Tier I Human 189 Genes GS172471: HP:0001744 Splenomegaly
Expand Tier I Human 61 Genes GS172737: HP:0010991 Abnormality of the abdominal musculature
Expand Tier I Mouse MP 13 Genes GS169099: MP:0004920 increased placenta weight
Expand Tier I Human 149 Genes GS176098: HP:0000927 Abnormality of skeletal maturation
Expand Tier I Mouse MP 1292 Genes GS166706: MP:0002166 altered tumor susceptibility
Expand Tier I Human 66 Genes GS176033: HP:0011039 Abnormality of the helix
Expand Tier I Human 96 Genes GS175036: HP:0009767 Aplasia/Hypoplasia of the phalanges of the hand
Expand Tier I Mouse MP 235 Genes GS168906: MP:0011117 abnormal susceptibility to weight gain
Expand Tier I Human 473 Genes GS171893: HP:0011458 Abdominal symptom
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 Mouse GO 13186 Genes GS191106: GO:0044464 cell part
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 Mouse GO 2994 Genes GS186215: GO:0048519 negative regulation of biological process
Expand Tier I Mouse GO 8406 Genes GS177404: GO:0005737 cytoplasm
Expand Tier I Human CTD 2047 Genes GS127205: Tamoxifen interacting genes (MeSH:D013629) in CTD
Expand Tier I Mouse MP 870 Genes GS168593: MP:0002088 abnormal embryonic growth/weight/body size
Expand Tier I Mouse MP 792 Genes GS170024: MP:0011086 partial postnatal lethality
Expand Tier I Mouse MP 700 Genes GS165194: MP:0001533 abnormal skeleton physiology
Expand Tier I Mouse MP 1350 Genes GS165228: MP:0005382 craniofacial phenotype
Expand Tier I Human 4 Genes GS171064: HP:0006277 Pancreatic hyperplasia
Expand Tier I Human 46 Genes GS174296: HP:0010787 Genital neoplasm
Expand Tier I Mouse MP 22 Genes GS164073: MP:0004678 split xiphoid process
Expand Tier I Mouse MP 257 Genes GS170425: MP:0004508 abnormal pectoral girdle bone morphology
Expand Tier I Mouse MP 1008 Genes GS164333: MP:0000516 abnormal renal/urinary system morphology
Expand Tier I Human 117 Genes GS172063: HP:0000107 Renal cysts
Expand Tier I Human 486 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Mouse MP 876 Genes GS165866: MP:0000350 abnormal cell proliferation
Expand Tier I Human 392 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Mouse MP 1172 Genes GS162953: MP:0002020 increased tumor incidence
Expand Tier I Mouse MP 985 Genes GS167025: MP:0003953 abnormal hormone level
Expand Tier I Human 202 Genes GS176242: HP:0004207 Abnormality of the 5th finger
Expand Tier I Human CTD 578 Genes GS123943: Curcumin interacting genes (MeSH:D003474) in CTD
Expand Tier I Human 12 Genes GS176159: HP:0009237 Short 5th finger
Expand Tier I Mouse MP 39 Genes GS162971: MP:0008011 intestine polyps
Expand Tier I Mouse MP 306 Genes GS169962: MP:0001286 abnormal eye development
Expand Tier I Mouse MP 749 Genes GS167833: MP:0001784 abnormal fluid regulation
Expand Tier I Human 239 Genes GS174066: HP:0100737 Abnormality of the hard palate
Expand Tier I Mouse MP 520 Genes GS165595: MP:0010545 abnormal heart layer morphology
Expand Tier I Human 456 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Human 93 Genes GS174098: HP:0011792 Neoplasm by histology
Expand Tier I Human 157 Genes GS176612: HP:0000272 Malar flattening
Expand Tier I Mouse MP 2357 Genes GS163824: MP:0001259 abnormal body weight
Expand Tier I Mouse 426 Genes GS135396: body growth early QTL 6 (Bgeq6, Published QTL Chr 7)
Expand Tier I Mouse MP 1038 Genes GS169114: MP:0004196 abnormal prenatal growth/weight/body size
Expand Tier I Human 51 Genes GS172933: HP:0003745 Sporadic
Expand Tier I Human 10 Genes GS173197: HP:0012094 Abnormal pancreas size
Expand Tier I Human 11 Genes GS174931: HP:0009161 Aplasia/Hypoplasia of the middle phalanx of the 5th finger
Expand Tier I Human 348 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier I Mouse GO 8414 Genes GS185585: GO:0044710 single-organism metabolic process
Expand Tier I Human 177 Genes GS173048: HP:0005557 Abnormality of the zygomatic arch
Expand Tier I Human 397 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier I Mouse MP 165 Genes GS164953: MP:0002707 abnormal kidney weight
Expand Tier I Mouse MP 994 Genes GS168502: MP:0002058 neonatal lethality
Expand Tier I Human 741 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier II Mouse 880 Genes GS84196: alcohol preference locus (Published QTL, Chr 7)
Expand Tier I Mouse MP 49 Genes GS164178: MP:0000480 increased rib number
Expand Tier I Human 489 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human 115 Genes GS170850: HP:0006265 Aplasia/Hypoplasia of fingers
Expand Tier I Mouse MP 6 Genes GS163766: MP:0009432 increased fetal weight
Expand Tier I Human 47 Genes GS171564: HP:0000383 Abnormality of periauricular region
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Mouse MP 272 Genes GS167805: MP:0000150 abnormal rib morphology
Expand Tier I Mouse DRG 919 Genes provisional GS87378: Table S2: The data provided represent genes showing differential expression using ANOVA. (Whole Table) [DRG]
Expand Tier I Mouse MP 486 Genes GS169630: MP:0001785 edema
Expand Tier I Human 492 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Mouse 577 Genes GS136899: ventral midbrain iron content 3 (Vmbic3, Published QTL Chr 7)
Expand Tier I Mouse MP 11 Genes GS164804: MP:0004199 increased fetal size
Expand Tier I Human 33 Genes GS173194: HP:0012090 Abnormality of pancreas morphology
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 Mouse MP 570 Genes GS164042: MP:0002018 malignant tumors
Expand Tier I Mouse MP 49 Genes GS166390: MP:0008877 abnormal DNA methylation
Expand Tier I Human 179 Genes GS174214: HP:0009466 Radial deviation of finger
Expand Tier I Mouse MP 1183 Genes GS166409: MP:0002114 abnormal axial skeleton morphology
Expand Tier I Human 22 Genes GS173089: HP:0004376 Neuroblastic tumors
Expand Tier I Human 32 Genes GS172787: HP:0001539 Omphalocele
Expand Tier I Mouse MP 207 Genes GS169118: MP:0004198 abnormal fetal size
Expand Tier I Mouse MP 56 Genes GS163544: MP:0011390 abnormal fetal cardiomyocyte physiology
Expand Tier I Mouse MP 738 Genes GS168826: MP:0005294 abnormal heart ventricle morphology
Expand Tier I Mouse MP 241 Genes GS164183: MP:0000488 abnormal intestinal epithelium morphology
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Mouse MP 146 Genes GS164669: MP:0010292 increased alimentary system tumor incidence
Expand Tier II Mouse 657 Genes GS84199: METH responses for body temperature (Published QTL, Chr 7)
Expand Tier III Mouse 6105 Genes GS213074: Genes with suggestive difference in (B6PF1) vs (PB6F1 + B6 + PWD) comparison
Expand Tier I Human 186 Genes GS173740: HP:0009485 Radial deviation of the hand or of fingers of the hand
Expand Tier I Mouse 716 Genes GS135272: "alcohol preference locus 12, male specific" (Alcp12, Published QTL Chr 7)
Expand Tier I Human 15 Genes GS174100: HP:0011794 Embryonal renal neoplasm
Expand Tier III Mouse 8003 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampal tissue
Expand Tier I Mouse 852 Genes GS135542: cerebellar cAMP 5 (Ccmp5, Published QTL Chr 7)
Expand Tier I Human 2 Genes GS176165: HP:0009239 Aplasia/Hypoplasia of the distal phalanx of the 5th finger
Expand Tier I Mouse MP 1402 Genes GS169832: MP:0005381 digestive/alimentary phenotype
Expand Tier I Human 579 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human 32 Genes GS176375: HP:0000269 Prominent occiput
Expand Tier I Human 105 Genes GS171199: HP:0001943 Hypoglycemia
Expand Tier I Mouse MP 558 Genes GS170680: MP:0003744 abnormal orofacial morphology
Expand Tier I Mouse MP 365 Genes GS168326: MP:0002706 abnormal kidney size
Expand Tier I Human 4 Genes GS171665: HP:0000796 Urethral obstruction
Expand Tier I Mouse MP 86 Genes GS169103: MP:0003257 abnormal abdominal wall morphology
Expand Tier I Human 19 Genes GS171480: HP:0100555 Asymmetric growth
Expand Tier I Mouse MP 1041 Genes GS168683: MP:0000598 abnormal liver morphology
Expand Tier I Mouse 870 Genes GS136924: VPA induced neural tube defect (Vpantd, Published QTL Chr 7)
Expand Tier I Human 74 Genes GS175265: HP:0002733 Abnormality of the lymph nodes
Expand Tier I Human 266 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier I Human 313 Genes GS176642: HP:0011355 Localized skin lesion
Expand Tier I Human 37 Genes GS173744: HP:0000995 Pigmented nevi
Expand Tier I Mouse 868 Genes GS136937: vertebral trabecular bone trait 4 (Vtbt4, Published QTL Chr 7)
Expand Tier I Mouse MP 857 Genes GS166118: MP:0002109 abnormal limb morphology
Expand Tier I Mouse MP 307 Genes GS167970: MP:0001340 abnormal eyelid morphology
Expand Tier I Human 282 Genes GS172572: HP:0000347 Micrognathia
Expand Tier I Mouse MP 343 Genes GS167907: MP:0003921 abnormal heart left ventricle morphology
Expand Tier I Mouse MP 1856 Genes GS165386: MP:0001262 decreased body weight
Expand Tier I Mouse MP 384 Genes GS165361: MP:0004624 abnormal thoracic cage morphology
Expand Tier I Mouse GO 8386 Genes GS189751: GO:0050794 regulation of cellular process
Expand Tier I Mouse MP 1966 Genes GS166590: MP:0002873 normal phenotype
Expand Tier I Mouse MP 1222 Genes GS165535: MP:0005370 liver/biliary system phenotype
Expand Tier I Mouse MP 1420 Genes GS163052: MP:0000266 abnormal heart morphology
Expand Tier I Mouse MP 207 Genes GS164323: MP:0000511 abnormal intestinal mucosa morphology
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human 22 Genes GS171342: HP:0001738 Exocrine pancreatic insufficiency
Expand Tier I Mouse 852 Genes GS135817: ethanol induced thermoregulation 3 (Ethm3, Published QTL Chr 7)
Expand Tier I Human CTD 765 Genes GS123769: 2-(1'H-indolo-3'-carbonyl)thiazole-4-carboxylic acid methyl ester interacting genes (MeSH:C548651) in CTD
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 14 Genes GS171393: HP:0002667 Nephroblastoma (Wilms tumor)
Expand Tier I Mouse GO 8942 Genes GS185492: GO:0050789 regulation of biological process
Expand Tier I Human 544 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Mouse MP 1 Genes GS170046: MP:0009430 increased embryo weight
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Mouse MP 104 Genes GS164405: MP:0003385 abnormal body wall morphology
Expand Tier I Mouse MP 19 Genes GS168200: MP:0010601 thick pulmonary valve
Expand Tier I Human 7 Genes GS173760: HP:0100620 Germinoma
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 76 Genes GS171608: HP:0011338 Abnormality of mouth shape
Expand Tier I Human 75 Genes GS175886: HP:0007378 Neoplasm of the gastrointestinal tract
Expand Tier I Mouse 868 Genes GS135577: cystic fibrosis lung disease 4 (Cfld4, Published QTL Chr 7)
Expand Tier I Human CTD 168 Genes GS126756: tobacco tar interacting genes (MeSH:C024746) in CTD
Expand Tier I Mouse MP 54 Genes GS167479: MP:0003052 omphalocele
Expand Tier I Mouse MP 1460 Genes GS164264: MP:0002082 postnatal lethality
Expand Tier I Human 61 Genes GS174375: HP:0002027 Abdominal pain
Expand Tier I Mouse MP 85 Genes GS165970: MP:0002746 abnormal semilunar valve morphology
Expand Tier I Mouse MP 401 Genes GS166640: MP:0000609 abnormal liver physiology
Expand Tier I Human 266 Genes GS172415: HP:0002240 Hepatomegaly
Expand Tier I Mouse MP 3437 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Mouse MP 1086 Genes GS165869: MP:0002138 abnormal hepatobiliary system morphology
Expand Tier I Human 19 Genes GS175076: HP:0001402 Hepatocellular carcinoma
Expand Tier I Human 302 Genes GS176029: HP:0009116 Aplasia/Hypoplasia involving bones of the skull
Expand Tier I Mouse MP 127 Genes GS163083: MP:0010279 increased gastrointestinal tumor incidence
Expand Tier I Human 73 Genes GS176571: HP:0008067 Abnormally lax or hyperextensible skin
Expand Tier I Human 114 Genes GS175593: HP:0011015 Abnormality of blood glucose concentration
Expand Tier I Mouse MP 290 Genes GS168654: MP:0000111 cleft palate
Expand Tier I Human 311 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier I Mouse MP 303 Genes GS166272: MP:0000288 abnormal pericardium morphology
Expand Tier I Mouse MP 68 Genes GS167513: MP:0000159 abnormal xiphoid process morphology
Expand Tier I Mouse 523 Genes GS135440: bone mineral density 9 (Bmd9, Published QTL Chr 7)
Expand Tier I Mouse 426 Genes GS136732: susceptibility to lung cancer 8 (Sluc8, Published QTL Chr 7)
Expand Tier I Human 12 Genes GS172301: HP:0000105 Enlarged kidneys
Expand Tier I Human 298 Genes GS174145: HP:0005918 Abnormality of phalanx of finger
Expand Tier I Human 271 Genes GS174948: HP:0100763 Abnormality of the lymphatic system
Expand Tier I Mouse GO 3090 Genes GS188511: GO:0010468 regulation of gene expression
Expand Tier I Mouse MP 4173 Genes GS165527: MP:0005378 growth/size phenotype
Expand Tier I Mouse MP 114 Genes GS163899: MP:0000495 abnormal colon morphology
Expand Tier I Human 43 Genes GS171179: HP:0003764 Nevus
Expand Tier I Human 73 Genes GS175158: HP:0011747 Abnormality of the anterior pituitary
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human 13 Genes GS173175: HP:0004219 Abnormality of the middle phalanx of the 5th finger
Expand Tier I Human 55 Genes GS174648: HP:0000957 Cafe-au-lait spot
Expand Tier I Mouse MP 28 Genes GS169385: MP:0004320 split sternum
Expand Tier I Human 4 Genes GS172817: HP:0003247 Overgrowth of external genitalia
Expand Tier I Human 30 Genes GS170949: HP:0005616 Accelerated skeletal maturation
Expand Tier I Mouse MP 8 Genes GS166163: MP:0010591 enlarged aortic valve
Expand Tier I Mouse MP 491 Genes GS164448: MP:0005193 abnormal anterior eye segment morphology
Expand Tier I Human 224 Genes GS175459: HP:0009484 Deviation of the hand or of fingers of the hand
Expand Tier I Human 913 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human 188 Genes GS171167: HP:0000235 Abnormality of the fontanelles and cranial sutures
Expand Tier III Mouse 8392 Genes GS128199: Alcohol Preference union of 86 Gene Sets
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Human 397 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Mouse MP 40 Genes GS167496: MP:0008146 asymmetric rib-sternum attachment
Expand Tier I Human 96 Genes GS174884: HP:0009381 Short finger
Expand Tier I Mouse MP 931 Genes GS163080: MP:0010273 increased classified tumor incidence
Expand Tier I Mouse 627 Genes GS136663: skin tumor susceptibility 2 (Skts2, Published QTL Chr 7)
Expand Tier I Mouse MP 83 Genes GS163863: MP:0004258 abnormal placenta size
Expand Tier I Human 236 Genes GS174257: HP:0000309 Abnormality of the midface
Expand Tier I Human 384 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human 137 Genes GS171202: HP:0100627 Displacement of the external urethral meatus
Expand Tier I Human CTD 870 Genes GS123911: Ozone interacting genes (MeSH:D010126) in CTD
Expand Tier I Mouse GO 3978 Genes GS188506: GO:0010467 gene expression
Expand Tier I Mouse MP 1267 Genes GS164534: MP:0002019 abnormal tumor incidence
Expand Tier I Human 8 Genes GS176216: HP:0100641 Neoplasm of the adrenal cortex
Expand Tier I Mouse MP 217 Genes GS166609: MP:0002833 increased heart weight
Expand Tier I Human 40 Genes GS171823: HP:0000113 Polycystic kidney dysplasia
Expand Tier I Human 52 Genes GS176460: HP:0000790 Hematuria
Expand Tier I Human 514 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human CTD 908 Genes GS124805: decitabine interacting genes (MeSH:C014347) in CTD
Expand Tier I Human 44 Genes GS174200: HP:0009726 Renal neoplasm
Expand Tier III Mouse 1964 Genes GS865: Sey_Pax6_Age_Reduced_Linear_Incr
Expand Tier I Human 211 Genes GS175164: HP:0011927 Short digit
Expand Tier I Mouse 612 Genes GS135999: hepatic lipase activity in BSB 1 (Hlbsb1, Published QTL Chr 7)
Expand Tier I Human 72 Genes GS175885: HP:0007379 Neoplasm of the genitourinary tract
Expand Tier I Mouse MP 62 Genes GS169428: MP:0010429 abnormal heart left ventricle outflow tract morphology
Expand Tier I Mouse MP 93 Genes GS170392: MP:0005545 abnormal lens development
Expand Tier I Mouse MP 231 Genes GS162925: MP:0010383 increased adenoma incidence
Expand Tier I Mouse MP 1416 Genes GS164261: MP:0002081 perinatal lethality
Expand Tier I Human 64 Genes GS175226: HP:0008713 Genitourinary tract malformation
Expand Tier I Mouse 868 Genes GS136272: multigenic obesity QTL 1 (Mobq1, Published QTL Chr 7)
Expand Tier I Human CTD 1541 Genes GS125445: Phenobarbital interacting genes (MeSH:D010634) in CTD
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 Mouse MP 99 Genes GS167525: MP:0000154 rib fusion
Expand Tier I Human 232 Genes GS176771: HP:0001000 Abnormality of skin pigmentation
Expand Tier I Human 40 Genes GS174330: HP:0002714 Downturned corners of mouth
Expand Tier I Human 175 Genes GS174377: HP:0005927 Aplasia/Hypoplasia involving bones of the hand
Expand Tier I Human CTD 4423 Genes GS123718: Ethinyl Estradiol interacting genes (MeSH:D004997) in CTD
Expand Tier I Mouse MP 249 Genes GS168505: MP:0002052 decreased tumor incidence
Expand Tier I Human 33 Genes GS176282: HP:0009833 Abnormality of the middle phalanges of the hand
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
Expand Tier I Human 26 Genes GS173686: HP:0001640 Cardiomegaly
Expand Tier I Human 545 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Mouse MP 1817 Genes GS168149: MP:0005508 abnormal skeleton morphology
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier II Mouse 875 Genes GS84197: alcohol preference locus 14, female specific (Alcp14, Published QTL, Chr 7)
Expand Tier I Mouse MP 3110 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Mouse MP 2099 Genes GS165616: MP:0002127 abnormal cardiovascular system morphology
Expand Tier I Mouse MP 132 Genes GS169887: MP:0008272 abnormal endochondral bone ossification
Expand Tier I Human 68 Genes GS176574: HP:0008062 Aplasia/Hypoplasia affecting the anterior segment of the eye
Expand Tier I Mouse MP 61 Genes GS169427: MP:0010428 abnormal heart right ventricle outflow tract morphology
Expand Tier I Human 38 Genes GS171851: HP:0000592 Blue sclerae
Expand Tier I Mouse MP 1615 Genes GS165789: MP:0005369 muscle phenotype
Expand Tier I Human 51 Genes GS176092: HP:0100006 Neoplasm of the central nervous system
Expand Tier I Mouse MP 1692 Genes GS169833: MP:0005380 embryogenesis phenotype
Expand Tier I Mouse MP 323 Genes GS170380: MP:0003755 abnormal palate morphology
Expand Tier I Human 12 Genes GS171257: HP:0009376 Aplasia/Hypoplasia of the phalanges of the 5th finger
Expand Tier I Mouse MP 162 Genes GS167608: MP:0000285 abnormal heart valve morphology
Expand Tier I Mouse MP 8 Genes GS168199: MP:0010600 enlarged pulmonary valve
Expand Tier I Mouse 491 Genes GS135492: behavioral response to methamphetamines 6 (Brmth6, Published QTL Chr 7)
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Human 132 Genes GS171835: HP:0011329 Abnormality of cranial sutures
Expand Tier I Human 553 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human CTD 7 Genes GS121593: 2-amino-4-phosphonobutyric acid interacting genes (MeSH:C012729) in CTD
Expand Tier I Human 6 Genes GS175276: HP:0006744 Adrenocortical carcinoma
Expand Tier I Mouse GO 3757 Genes GS189460: GO:0060255 regulation of macromolecule metabolic process
Expand Tier I Human 189 Genes GS176745: HP:0010866 Abdominal wall defect
Expand Tier I Human 32 Genes GS172028: HP:0000363 Abnormality of earlobe
Expand Tier I Mouse MP 1989 Genes GS169530: MP:0005390 skeleton phenotype
Expand Tier I Human 291 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier I Mouse 716 Genes GS136716: susceptibility to lung cancer 19 (Sluc19, Published QTL Chr 7)
Expand Tier I Mouse MP 185 Genes GS164411: MP:0000562 polydactyly
Expand Tier I Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier II Mouse 882 Genes GS84198: METH responses for home cage activity (Published QTL, Chr 7)
Expand Tier I Human 489 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Mouse 852 Genes GS135854: femoral bone morphometry 3 (Fembm3, Published QTL Chr 7)
Expand Tier I Human 56 Genes GS173195: HP:0012091 Abnormality of pancreas physiology
Expand Tier I Human 56 Genes GS175070: HP:0000973 Cutis laxa
Expand Tier I Mouse MP 4 Genes GS165039: MP:0009265 delayed eyelid fusion
Expand Tier I Mouse MP 2485 Genes GS168012: MP:0010832 lethality during fetal growth through weaning
Expand Tier I Human 87 Genes GS176903: HP:0009803 Short phalanx of finger
Expand Tier I Human 285 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier I Mouse MP 1740 Genes GS166710: MP:0002163 abnormal gland morphology
Expand Tier I Human 160 Genes GS174814: HP:0001639 Hypertrophic cardiomyopathy
Expand Tier I Human 378 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier I Mouse MP 20 Genes GS166369: MP:0010594 thick aortic valve
Expand Tier III Mouse 8107 Genes GS213076: Genes with suggestive difference in (B6) vs (B6PF1 + PB6F1 + PWD) comparison
Expand Tier I Mouse MP 1020 Genes GS163077: MP:0010274 increased organ/body region tumor incidence
Expand Tier I Mouse MP 21 Genes GS168267: MP:0003123 paternal imprinting
Expand Tier I Mouse MP 71 Genes GS168265: MP:0003121 genetic imprinting
Expand Tier I Human CTD 1697 Genes GS122142: Dietary Fats interacting genes (MeSH:D004041) in CTD
Expand Tier I Mouse MP 72 Genes GS168172: MP:0003918 decreased kidney weight
Expand Tier I Mouse MP 290 Genes GS168682: MP:0000599 enlarged liver
Expand Tier I Human 941 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human 34 Genes GS174298: HP:0010785 Gonadal neoplasm
Expand Tier I Mouse MP 399 Genes GS165567: MP:0008271 abnormal bone ossification
Expand Tier I Mouse MP 14488 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Human 49 Genes GS173398: HP:0000776 Congenital diaphragmatic hernia
Expand Tier I Mouse MP 663 Genes GS163398: MP:0005266 abnormal metabolism
Expand Tier I Human 115 Genes GS172500: HP:0007400 Irregular hyperpigmentation
Expand Tier I Mouse 812 Genes GS136596: resistance to thymic deletion 1 (Rthyd1, Published QTL Chr 7)
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 150 Genes GS176233: HP:0004209 Clinodactyly of the 5th finger
Expand Tier I Human 405 Genes GS173743: HP:0001999 Abnormal facial shape
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 60 Genes GS170970: HP:0000154 Wide mouth
Expand Tier I Mouse 432 Genes GS136261: "murine leukemia virus infection QTL, 1" (Mlviq1, Published QTL Chr 7)
Expand Tier I Human 9 Genes GS172308: HP:0001998 Neonatal hypoglycemia
Expand Tier I Mouse MP 396 Genes GS165214: MP:0001711 abnormal placenta morphology
Expand Tier I Mouse MP 652 Genes GS170577: MP:0005406 abnormal heart size
Expand Tier I Human 60 Genes GS171207: HP:0000098 Tall stature
Expand Tier I Human 64 Genes GS176161: HP:0100589 Urogenital fistula
Expand Tier I Human 81 Genes GS173600: HP:0002926 Abnormality of thyroid physiology
Expand Tier I Human 287 Genes GS175594: HP:0011014 Abnormal glucose homeostasis
Expand Tier I Mouse MP 442 Genes GS165868: MP:0002139 abnormal hepatobiliary system physiology
Expand Tier I Human 114 Genes GS172283: HP:0000820 Abnormality of the thyroid gland
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 316 Genes GS170825: HP:0002167 Neurological speech impairment
Expand Tier I Mouse 501 Genes GS136843: thymic lymphoma susceptible 1 (Tlsm1, Published QTL Chr 7)
Expand Tier I Human 54 Genes GS172298: HP:0001518 Small for gestational age
Expand Tier I Human 67 Genes GS174328: HP:0002716 Lymphadenopathy
Expand Tier I Human 35 Genes GS176360: HP:0100836 Malignant neoplasm of the central nervous system
Expand Tier I Mouse MP 256 Genes GS165811: MP:0009703 decreased birth body size
Expand Tier I Mouse MP 87 Genes GS167830: MP:0001787 pericardial edema
Expand Tier I Human 47 Genes GS172542: HP:0000830 Anterior hypopituitarism
Expand Tier I Human 46 Genes GS170961: HP:0000158 Macroglossia
Expand Tier I Human 4 Genes GS174116: HP:0008186 Adrenocortical cytomegaly
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 3 Genes GS176665: HP:0004225 Abnormality of the distal phalanx of the 5th finger
Expand Tier I Human 310 Genes GS175805: HP:0003271 Visceromegaly
Expand Tier I Human CTD 175 Genes GS121386: Zearalenone interacting genes (MeSH:D015025) in CTD
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 9 Genes GS172092: HP:0010788 Testicular neoplasm
Expand Tier I Human CTD 1468 Genes GS125062: palm oil interacting genes (MeSH:C041786) in CTD
Expand Tier I Mouse MP 692 Genes GS163620: MP:0002086 abnormal extraembryonic tissue morphology
Expand Tier I Mouse MP 951 Genes GS165427: MP:0000432 abnormal head morphology
Expand Tier I Mouse MP 221 Genes GS167553: MP:0003448 altered tumor morphology
Expand Tier I Human 114 Genes GS173262: HP:0000864 Abnormality of the hypothalamus-pituitary axis
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 17 Genes GS173343: HP:0001548 Overgrowth
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 Mouse MP 28 Genes GS168788: MP:0002044 increased colonic adenoma incidence
Expand Tier I Mouse MP 87 Genes GS170106: MP:0003721 increased tumor growth/size
Expand Tier I Mouse DRG 516 Genes provisional GS87101: Table S4: List of Saline-Treated HDAC5 KO vs. Saline-Treated WT Significantly Regulated Genes. [DRG]
Expand Tier I Mouse MP 213 Genes GS167908: MP:0003920 abnormal heart right ventricle morphology
Expand Tier I Mouse MP 1692 Genes GS169603: MP:0001672 abnormal embryogenesis/ development
Expand Tier I Human 737 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Mouse 716 Genes GS135273: "alcohol preference locus 14, female specific" (Alcp14, Published QTL Chr 7)
Expand Tier I Human 150 Genes GS175149: HP:0009179 Deviation of the 5th finger
Expand Tier I Human 87 Genes GS172544: HP:0000834 Abnormality of the adrenal glands
Expand Tier I Mouse MP 267 Genes GS169111: MP:0004197 abnormal fetal growth/weight/body size
Expand Tier I Mouse MP 1385 Genes GS163971: MP:0002092 abnormal eye morphology
Expand Tier I Mouse MP 511 Genes GS164555: MP:0005329 abnormal myocardium layer morphology
Expand Tier I Human 397 Genes GS171067: HP:0002664 Neoplasm
Expand Tier I Mouse 673 Genes GS135720: determination of interleukin 4 commitment 2 (Dice2, Published QTL Chr 7)
Expand Tier I Mouse GO 9323 Genes GS180152: GO:0065007 biological regulation
Expand Tier I Mouse MP 33 Genes GS163866: MP:0004257 abnormal placenta weight
Expand Tier I Mouse MP 1211 Genes GS165536: MP:0005371 limbs/digits/tail phenotype
Expand Tier I Mouse MP 119 Genes GS168479: MP:0005455 increased susceptibility to weight gain
Expand Tier I Mouse DRG 919 Genes provisional GS86984: Table S2: The data provided represent genes showing differential expression using ANOVA. A. Genes showing main effect of strain. [DRG]
Expand Tier I Human 319 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Mouse MP 2606 Genes GS165397: MP:0001265 decreased body size
Expand Tier I Mouse MP 3494 Genes GS170601: MP:0005621 abnormal cell physiology
Expand Tier I Human 212 Genes GS176185: HP:0100790 Hernia
Expand Tier I Human 487 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Mouse MP 25 Genes GS165037: MP:0009263 abnormal eyelid fusion
Expand Tier I Human 68 Genes GS176281: HP:0009832 Abnormality of the distal phalanx of finger
Expand Tier I Mouse MP 62 Genes GS167030: MP:0002747 abnormal aortic valve morphology
Expand Tier I Mouse MP 1963 Genes GS166718: MP:0002169 no abnormal phenotype detected
Expand Tier I Mouse MP 40 Genes GS167351: MP:0003893 increased hepatocyte proliferation
Expand Tier I Human 78 Genes GS175969: HP:0000069 Abnormality of the ureter
Expand Tier I Human 28 Genes GS175494: HP:0100526 Neoplasm of the lungs
Expand Tier I Human 51 Genes GS171628: HP:0008053 Aplasia/Hypoplasia of the iris
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 Mouse MP 59 Genes GS167995: MP:0002404 increased intestinal adenoma incidence
Expand Tier I Mouse MP 149 Genes GS164108: MP:0008019 increased liver tumor incidence
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Mouse MP 200 Genes GS164182: MP:0000489 abnormal large intestine morphology
Expand Tier I Human 530 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Mouse MP 47 Genes GS165979: MP:0002748 abnormal pulmonary valve morphology
Expand Tier I Human 94 Genes GS174879: HP:0002104 Apnea
Expand Tier I Mouse MP 115 Genes GS165509: MP:0009672 abnormal birth weight
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 2 Genes GS176666: HP:0004227 Short distal phalanx of the 5th finger
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 Mouse MP 30 Genes GS169296: MP:0009651 abnormal eyelid development
Expand Tier I Human 6 Genes GS171272: HP:0009908 Anterior creases of earlobe
Expand Tier I Mouse MP 4592 Genes GS165537: MP:0005376 homeostasis/metabolism phenotype
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human 39 Genes GS171701: HP:0100568 Neoplasm of the endocrine system
Expand Tier I Human 51 Genes GS176287: HP:0009835 Aplasia/Hypoplasia of the distal phalanges of the hand
Expand Tier I Mouse 577 Genes GS135632: collagen induced arthritis 42 (Cia42, Published QTL Chr 7)
Expand Tier I Mouse 491 Genes GS136763: soft tissue heal 7 (Stheal7, Published QTL Chr 7)
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 599 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Mouse MP 478 Genes GS170351: MP:0006208 lethality throughout fetal growth and development
Expand Tier I Human 32 Genes GS174665: HP:0001428 Somatic mutation
Expand Tier I Human 251 Genes GS171793: HP:0000377 Abnormality of the pinna
Expand Tier I Human 324 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Mouse MP 245 Genes GS168428: MP:0002989 small kidney
Expand Tier I Mouse MP 151 Genes GS163902: MP:0000490 abnormal crypts of Lieberkuhn morphology
Expand Tier I Mouse MP 49 Genes GS167524: MP:0000155 asymmetric rib attachment
Expand Tier I Mouse GO 466 Genes GS191722: GO:0008285 negative regulation of cell proliferation
Expand Tier I Mouse MP 465 Genes GS164665: MP:0000572 abnormal autopod morphology
Expand Tier I Human 36 Genes GS175798: HP:0002896 Neoplasm of the liver
Expand Tier I Human 80 Genes GS171836: HP:0011328 Abnormality of fontanelles
Expand Tier I Human 27 Genes GS175156: HP:0009843 Aplasia/Hypoplasia of the middle phalanges of the hand
Expand Tier I Mouse MP 756 Genes GS170683: MP:0003743 abnormal facial morphology
Expand Tier I Human 195 Genes GS174813: HP:0001638 Cardiomyopathy
Expand Tier I Mouse MP 151 Genes GS164672: MP:0010297 increased hepatobiliary system tumor incidence
Expand Tier I Mouse GO 9049 Genes GS180166: GO:0008152 metabolic process
Expand Tier I Mouse GO 1322 Genes GS191727: GO:0008283 cell proliferation
Expand Tier I Human 6 Genes GS170807: HP:0003162 Fasting hypoglycemia
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Mouse MP 40 Genes GS167394: MP:0003237 abnormal lens epithelium morphology
Expand Tier I Human 29 Genes GS176614: HP:0000270 Delayed cranial suture closure
Expand Tier I Human 8 Genes GS171963: HP:0000150 Gonadoblastoma
Expand Tier I Mouse MP 114 Genes GS164970: MP:0000639 abnormal adrenal gland morphology
Expand Tier I Human 66 Genes GS174788: HP:0000239 Large fontanelles
Expand Tier I Human 54 Genes GS176964: HP:0011217 Abnormal shape of the occiput
Expand Tier I Human 106 Genes GS171336: HP:0001732 Abnormality of the pancreas
Expand Tier I Human 58 Genes GS171822: HP:0000112 Nephropathy
Expand Tier I Human 18 Genes GS173820: HP:0100728 Germ cell neoplasia
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 23 Genes GS176475: HP:0005819 Short middle phalanx of finger
Expand Tier I Human 14 Genes GS176444: HP:0004213 Abnormality of the phalanges of the 5th finger
Expand Tier I Human 263 Genes GS176692: HP:0009815 Aplasia/Hypoplasia of the extremities
Expand Tier I Mouse MP 1476 Genes GS169531: MP:0005391 vision/eye phenotype
Expand Tier I Human 391 Genes GS175537: HP:0011277 Abnormality of the urinary system physiology
Expand Tier I Human 141 Genes GS172281: HP:0000822 Hypertension
Expand Tier I Human 426 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Mouse MP 309 Genes GS167795: MP:0001303 abnormal lens morphology
Expand Tier I Mouse MP 940 Genes GS165876: MP:0002135 abnormal kidney morphology
Expand Tier I Human 20 Genes GS172286: HP:0000824 Growth hormone deficiency
Expand Tier I Human 228 Genes GS172470: HP:0001743 Abnormality of the spleen
Expand Tier I Mouse MP 136 Genes GS164110: MP:0003049 abnormal lumbar vertebrae morphology
Expand Tier I Human 13 Genes GS170851: HP:0006262 Aplasia/Hypoplasia of the 5th finger
Expand Tier I Mouse GO 4518 Genes GS187751: GO:0019222 regulation of metabolic process
Expand Tier I Mouse 491 Genes GS136142: lithogenic gene 22 (Lith22, Published QTL Chr 7)
Expand Tier I Mouse MP 684 Genes GS169663: MP:0004703 abnormal vertebral column morphology
Expand Tier I Human 162 Genes GS175958: HP:0000795 Abnormality of the urethra
Expand Tier I Human 588 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human 780 Genes