Gene Details



KCNQ1OT1 and homologs in 2 species are found in 297 GeneSets:


- Entrez   - Ensembl   - GeneNetwork   - STRING   - Allen Brain Atlas   - Comparative Toxicogenomics Database  

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Human 187 Genes GS171907: HP:0004299 Hernia of the abdominal wall
Expand Tier I Mouse GO 2982 Genes GS183514: GO:0019219 regulation of nucleobase-containing compound metabolic process
Expand Tier I Mouse GO 5650 Genes GS183848: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Mouse MP 94 Genes GS163028: MP:0003402 decreased liver weight
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 Mouse GO 1392 Genes GS184458: GO:0009892 negative regulation of metabolic process
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal 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 Mouse GO 204 Genes GS190176: GO:0051052 regulation of DNA metabolic process
Expand Tier I Mouse MP 599 Genes GS164506: MP:0001698 decreased embryo size
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 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 24 Genes GS175787: HP:0002898 Embryonal neoplasm
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 Human 21 Genes GS171123: HP:0003006 Neuroblastoma
Expand Tier II Mouse 211 Genes GS35397: Hippocampus Gene expression correlates of Zero Maze - Total Activity count; number of beam breaks in Females & Males BXD
Expand Tier I Mouse GO 4887 Genes GS188190: GO:0006807 nitrogen compound metabolic process
Expand Tier I Mouse GO 10 Genes GS179745: GO:0044030 regulation of DNA methylation
Expand Tier I Mouse GO 5 Genes GS192060: GO:0044027 hypermethylation of CpG island
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 GO 4619 Genes GS191019: GO:0034641 cellular nitrogen compound metabolic process
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 Mouse GO 3776 Genes GS187887: GO:0080090 regulation of primary metabolic process
Expand Tier I Human 426 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Mouse GO 727 Genes GS179950: GO:0006259 DNA metabolic process
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 Human 149 Genes GS176098: HP:0000927 Abnormality of skeletal maturation
Expand Tier I Human 66 Genes GS176033: HP:0011039 Abnormality of the helix
Expand Tier I Mouse GO 4353 Genes GS192017: GO:0006139 nucleobase-containing compound metabolic process
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 40 Genes GS186474: GO:0006306 DNA methylation
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 3599 Genes GS186227: GO:0090304 nucleic acid metabolic process
Expand Tier I Mouse GO 3865 Genes GS193238: GO:0031323 regulation of cellular metabolic process
Expand Tier I Mouse MP 870 Genes GS168593: MP:0002088 abnormal embryonic growth/weight/body size
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 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 Human 392 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Mouse MP 1082 Genes GS166660: MP:0001731 abnormal postnatal growth
Expand Tier I Human 239 Genes GS174066: HP:0100737 Abnormality of the hard palate
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 GO 40 Genes GS186475: GO:0006305 DNA alkylation
Expand Tier III Mouse 64 Genes GS34580: Hippocampus Gene expression correlates of Novel environment distance (cm) travelled minutes 0-15 in BXD Females & Males
Expand Tier I Mouse MP 2357 Genes GS163824: MP:0001259 abnormal body weight
Expand Tier I Mouse MP 1038 Genes GS169114: MP:0004196 abnormal prenatal growth/weight/body size
Expand Tier I Human 10 Genes GS173197: HP:0012094 Abnormal pancreas size
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 Mouse GO 228 Genes GS192206: GO:0032259 methylation
Expand Tier I Mouse MP 165 Genes GS164953: MP:0002707 abnormal kidney weight
Expand Tier I Human 741 Genes GS175601: HP:0002086 Abnormality of the respiratory system
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 II Mouse 64 Genes GS34565: Hippocampus Gene expression correlates of Novel environment distance (cm) travelled minutes 0-15 in Females & Males BXD
Expand Tier I Human 492 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human 33 Genes GS173194: HP:0012090 Abnormality of pancreas morphology
Expand Tier I Human 403 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Mouse GO 7 Genes GS184617: GO:0010216 maintenance of DNA methylation
Expand Tier I Mouse MP 49 Genes GS166390: MP:0008877 abnormal DNA methylation
Expand Tier I Mouse GO 5 Genes GS192059: GO:0044026 DNA hypermethylation
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 32 Genes GS168268: MP:0003122 maternal imprinting
Expand Tier I Human 15 Genes GS174100: HP:0011794 Embryonal renal neoplasm
Expand Tier I Mouse GO 3021 Genes GS182703: GO:0051171 regulation of nitrogen compound metabolic process
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 GO 4500 Genes GS186790: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Mouse MP 365 Genes GS168326: MP:0002706 abnormal kidney size
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 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 Mouse GO 15 Genes GS185886: GO:0006349 regulation of gene expression by genetic imprinting
Expand Tier I Human 37 Genes GS173744: HP:0000995 Pigmented nevi
Expand Tier I Mouse GO 148 Genes GS182939: GO:0040029 regulation of gene expression, epigenetic
Expand Tier I Mouse MP 1856 Genes GS165386: MP:0001262 decreased body weight
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 III Mouse 62 Genes GS34933: Hippocampus Gene expression correlates of Open Field - Total distance traveled 10-15 minutes [Basal Behavior] in Males BXD
Expand Tier I Human 22 Genes GS171342: HP:0001738 Exocrine pancreatic insufficiency
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 Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 75 Genes GS175886: HP:0007378 Neoplasm of the gastrointestinal tract
Expand Tier I Mouse MP 24 Genes GS162930: MP:0005631 decreased lung weight
Expand Tier I Human 39 Genes GS175738: HP:0011732 Abnormality of adrenal morphology
Expand Tier II Mouse 62 Genes GS34923: Hippocampus Gene expression correlates of Open Field - Total distance traveled 10-15 minutes in Males BXD
Expand Tier I Human 123 Genes GS171384: HP:0001551 Abnormality of the umbilicus
Expand Tier I Mouse MP 750 Genes GS170442: MP:0010866 abnormal prenatal body size
Expand Tier I Mouse MP 497 Genes GS165388: MP:0001263 weight loss
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 11 Genes GS171174: HP:0001540 Diastasis recti
Expand Tier I Human 421 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human 60 Genes GS174720: HP:0000775 Abnormality of the diaphragm
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 Human 120 Genes GS171607: HP:0011337 Abnormality of mouth size
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 Mouse MP 34 Genes GS167206: MP:0003787 abnormal imprinting
Expand Tier II Mouse 79 Genes GS35930: Striatum Gene expression correlates of Handling induced convulsions 7 hrs after ethanol in Females & Males BXD
Expand Tier I Human 12 Genes GS172301: HP:0000105 Enlarged kidneys
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 229 Genes GS170701: MP:0004847 abnormal liver weight
Expand Tier I Human 43 Genes GS171179: HP:0003764 Nevus
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 4 Genes GS172817: HP:0003247 Overgrowth of external genitalia
Expand Tier I Human 30 Genes GS170949: HP:0005616 Accelerated skeletal maturation
Expand Tier II Mouse 240 Genes GS36123: Hippocampus Gene expression correlates of Activity during 1st tone shock pairing in Females & Males BXD
Expand Tier I Human 50 Genes GS174295: HP:0010786 Urinary tract neoplasm
Expand Tier I Human 913 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human 79 Genes GS172284: HP:0000821 Hypothyroidism
Expand Tier I Human 188 Genes GS171167: HP:0000235 Abnormality of the fontanelles and cranial sutures
Expand Tier I Mouse GO 140 Genes GS177600: GO:0043414 macromolecule methylation
Expand Tier I Human 358 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Human 397 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human 13 Genes GS171993: HP:0100631 Neoplasm of the adrenal gland
Expand Tier I Human 320 Genes GS175597: HP:0011013 Abnormality of carbohydrate metabolism/homeostasis
Expand Tier I Mouse GO 7552 Genes GS180452: GO:0044237 cellular metabolic process
Expand Tier I Mouse MP 118 Genes GS164729: MP:0003641 small lung
Expand Tier I Mouse MP 83 Genes GS163863: MP:0004258 abnormal placenta size
Expand Tier I Mouse GO 2303 Genes GS177598: GO:0043412 macromolecule modification
Expand Tier I Mouse MP 1316 Genes GS165798: MP:0005367 renal/urinary system phenotype
Expand Tier I Human 102 Genes GS173545: HP:0010647 Abnormal elasticity of skin
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
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 200 Genes GS174812: HP:0001637 Abnormality of the myocardium
Expand Tier I Human 67 Genes GS173092: HP:0004375 Neoplasm of the nervous system
Expand Tier I Mouse GO 6435 Genes GS177531: GO:0043170 macromolecule metabolic process
Expand Tier I Human 990 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human 5 Genes GS172541: HP:0001528 Hemihypertrophy
Expand Tier I Mouse MP 80 Genes GS170048: MP:0005629 abnormal lung weight
Expand Tier I Mouse GO 3978 Genes GS188506: GO:0010467 gene expression
Expand Tier I Human 8 Genes GS176216: HP:0100641 Neoplasm of the adrenal cortex
Expand Tier I Human 40 Genes GS171823: HP:0000113 Polycystic kidney dysplasia
Expand Tier I Human 433 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Mouse MP 610 Genes GS164511: MP:0001697 abnormal embryo size
Expand Tier I Mouse GO 7644 Genes GS188399: GO:0044238 primary metabolic process
Expand Tier I Human 514 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Mouse GO 8072 Genes GS184218: GO:0071704 organic substance metabolic process
Expand Tier I Human 44 Genes GS174200: HP:0009726 Renal neoplasm
Expand Tier I Mouse GO 4478 Genes GS184435: GO:0046483 heterocycle metabolic process
Expand Tier I Human 72 Genes GS175885: HP:0007379 Neoplasm of the genitourinary tract
Expand Tier I Human 64 Genes GS175226: HP:0008713 Genitourinary tract malformation
Expand Tier I Human 103 Genes GS173507: HP:0000520 Proptosis
Expand Tier II Mouse 389 Genes GS36133: Hippocampus Gene expression correlates of Activity during 1st tone shock pairing in Males BXD
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 232 Genes GS176771: HP:0001000 Abnormality of skin pigmentation
Expand Tier I Human 26 Genes GS173686: HP:0001640 Cardiomegaly
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Mouse GO 4651 Genes GS177310: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Mouse MP 3110 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Mouse GO 25 Genes GS180747: GO:0071514 genetic imprinting
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 II Mouse 219 Genes GS36477: Whole Brain Gene expression correlates of Morphine - Severity of ptosis in Males BXD
Expand Tier I Mouse MP 651 Genes GS167563: MP:0001175 abnormal lung morphology
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 Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human 489 Genes GS171461: HP:0011121 Abnormality of skin morphology
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 II Mouse 65 Genes GS34213: Hippocampus Gene expression correlates of Light Dark Box Total distance traveled in dark compartment in Females & Males BXD
Expand Tier I Human 285 Genes GS175125: HP:0000028 Cryptorchidism
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 II Mouse 56 Genes GS36043: Hippocampus Gene expression correlates of Light-Dark Box Total distance traveled in light and dark compartments in Males BXD
Expand Tier I Mouse GO 327 Genes GS187984: GO:0003682 chromatin binding
Expand Tier I Mouse MP 71 Genes GS168265: MP:0003121 genetic imprinting
Expand Tier I Mouse MP 72 Genes GS168172: MP:0003918 decreased kidney weight
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 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 Mouse GO 926 Genes GS192344: GO:0010629 negative regulation of gene expression
Expand Tier I Human 525 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
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 Mouse GO 50 Genes GS181807: GO:0044728 DNA methylation or demethylation
Expand Tier I Human 60 Genes GS170970: HP:0000154 Wide mouth
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 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 820 Genes GS165875: MP:0002132 abnormal respiratory system morphology
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 MP 67 Genes GS163864: MP:0004259 small placenta
Expand Tier II Mouse 113 Genes GS36078: Hippocampus Gene expression correlates of Activity in altered context in fear conditioning apparatus in Females & Males BXD
Expand Tier I Human 35 Genes GS176360: HP:0100836 Malignant neoplasm of the central nervous system
Expand Tier I Human 46 Genes GS170961: HP:0000158 Macroglossia
Expand Tier I Human 4 Genes GS174116: HP:0008186 Adrenocortical cytomegaly
Expand Tier II Mouse 115 Genes GS34958: Hippocampus Gene expression correlates of Open Field - Total distance traveled 5-10 minutes in Males BXD
Expand Tier I Human 310 Genes GS175805: HP:0003271 Visceromegaly
Expand Tier II Mouse 73 Genes GS36033: Hippocampus Gene expression correlates of Light-Dark Box Total distance traveled in light and dark compartments in Females & Males BXD
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Mouse MP 692 Genes GS163620: MP:0002086 abnormal extraembryonic tissue morphology
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 GO 6204 Genes GS184629: GO:0005515 protein binding
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 Human 87 Genes GS172544: HP:0000834 Abnormality of the adrenal glands
Expand Tier I Human 397 Genes GS171067: HP:0002664 Neoplasm
Expand Tier I Mouse GO 9323 Genes GS180152: GO:0065007 biological regulation
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 GO 104 Genes GS180247: GO:0016458 gene silencing
Expand Tier I Mouse MP 1344 Genes GS169836: MP:0005388 respiratory system phenotype
Expand Tier II Mouse 78 Genes GS35958: Striatum Gene expression correlates of Handling induced convulsion score in Females & Males BXD
Expand Tier I Mouse MP 1963 Genes GS166718: MP:0002169 no abnormal phenotype detected
Expand Tier I Human 438 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human 530 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human 94 Genes GS174879: HP:0002104 Apnea
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 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 Mouse MP 201 Genes GS164746: MP:0000601 small liver
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 Mouse MP 1007 Genes GS164742: MP:0001732 postnatal growth retardation
Expand Tier I Mouse GO 1298 Genes GS183756: GO:0010605 negative regulation of macromolecule metabolic process
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 251 Genes GS171793: HP:0000377 Abnormality of the pinna
Expand Tier I Mouse GO 57 Genes GS186476: GO:0006304 DNA modification
Expand Tier I Mouse MP 245 Genes GS168428: MP:0002989 small kidney
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
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 195 Genes GS174813: HP:0001638 Cardiomyopathy
Expand Tier II Mouse 84 Genes GS35018: Hippocampus Gene expression correlates of Open Field Total distance traveled in Females & Males BXD
Expand Tier I Mouse GO 9049 Genes GS180166: GO:0008152 metabolic process
Expand Tier III Mouse 115 Genes GS34968: Hippocampus Gene expression correlates of Open Field - Total distance traveled 5-10 minutes [Basal Behavior] in Males BXD
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 8 Genes GS171963: HP:0000150 Gonadoblastoma
Expand Tier I Mouse MP 190 Genes GS166365: MP:0004881 abnormal lung size
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 II Mouse 163 Genes GS36088: Hippocampus Gene expression correlates of Activity in altered context in fear conditioning apparatus in Males BXD
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 II Mouse 97 Genes GS33937: Whole Brain Gene expression correlates of Total distance traveled (cm) following ethanol in Males BXD
Expand Tier II Mouse 158 Genes GS36093: Hippocampus Gene expression correlates of Baseline activity in fear conditioning apparatus in Females & Males BXD
Expand Tier I Mouse MP 940 Genes GS165876: MP:0002135 abnormal kidney morphology
Expand Tier I Human 228 Genes GS172470: HP:0001743 Abnormality of the spleen
Expand Tier I Mouse GO 4518 Genes GS187751: GO:0019222 regulation of metabolic process
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 II Mouse 48 Genes GS34247: Hippocampus Gene expression correlates of Activity in altered context during presentation of cue in Females BXD