Gene Details



ADAMTSL2 and homologs in 3 species are found in 333 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 GO 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Mouse GO 335 Genes GS193273: GO:0005578 proteinaceous extracellular matrix
Expand Tier I Human 99 Genes GS172242: HP:0004930 Abnormality of the pulmonary vasculature
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human 146 Genes GS171320: HP:0100360 Contractures of the joints of the upper limbs
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Mouse 537 Genes GS136604: spinal bone mineral density 2 (Sbmd2, Published QTL Chr 2)
Expand Tier I Human 275 Genes GS170962: HP:0000159 Abnormality of the lip
Expand Tier I Human GO 871 Genes GS198861: GO:0007167 enzyme linked receptor protein signaling pathway
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 7 Genes GS171530: HP:0001702 Abnormality of the tricuspid valve
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Mouse GO 171 Genes GS182225: GO:0008237 metallopeptidase activity
Expand Tier I Mouse 545 Genes GS135847: femoral cross-sectional area 5 (Fcsa5, Published QTL Chr 2)
Expand Tier I Mouse GO 3537 Genes GS192041: GO:0043169 cation binding
Expand Tier I Human 125 Genes GS173384: HP:0002750 Delayed skeletal maturation
Expand Tier I Human 181 Genes GS175391: HP:0011004 Abnormality of the systemic arterial tree
Expand Tier I Human 182 Genes GS174612: HP:0001600 Abnormality of the larynx
Expand Tier I Human 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 322 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier I Human 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 150 Genes GS174586: HP:0005930 Abnormality of the epiphyses
Expand Tier I Human 176 Genes GS175103: HP:0000288 Abnormality of the philtrum
Expand Tier I Mouse 537 Genes GS136603: spinal bone mineral density 1 (Sbmd1, Published QTL Chr 2)
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 Human 8 Genes GS173407: HP:0002680 J-shaped sella turcica
Expand Tier I Human 47 Genes GS173284: HP:0000311 Round face
Expand Tier I Human 49 Genes GS173605: HP:0004426 Abnormality of the cheeks
Expand Tier I Human GO 2317 Genes GS209215: GO:0007166 cell surface receptor signaling pathway
Expand Tier I Human 374 Genes GS175815: HP:0011025 Abnormality of cardiovascular system physiology
Expand Tier I Human 150 Genes GS175411: HP:0100871 Abnormality of the palm
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human 119 Genes GS172170: HP:0003196 Short nose
Expand Tier I Human 19 Genes GS173843: HP:0002777 Tracheal stenosis
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 639 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human 89 Genes GS174323: HP:0004414 Abnormality of the pulmonary artery
Expand Tier I Human 490 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Rat 438 Genes GS128037: Alcohol consumption QTL 8 (Alc8, Published QTL, Chr 3)
Expand Tier I Human 44 Genes GS175611: HP:0002092 Pulmonary hypertension
Expand Tier I Mouse GO 3311 Genes GS192279: GO:0007166 cell surface receptor signaling pathway
Expand Tier I Mouse GO 40 Genes GS187392: GO:0030512 negative regulation of transforming growth factor beta receptor signaling pathway
Expand Tier I Human 81 Genes GS172821: HP:0000213 Thin lips
Expand Tier I Mouse GO 588 Genes GS189483: GO:0023057 negative regulation of signaling
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 Human 20 Genes GS171556: HP:0001387 Joint stiffness
Expand Tier I Human GO 2033 Genes GS201132: GO:0010646 regulation of cell communication
Expand Tier I Mouse 543 Genes GS136612: colon tumor susceptibility 2 (Scc2, Published QTL Chr 2)
Expand Tier I Human 11 Genes GS173408: HP:0002681 Deformed sella turcica
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Mouse GO 1833 Genes GS184324: GO:0010646 regulation of cell communication
Expand Tier I Mouse 247 Genes GS129114: collagen induced arthritis QTL 4 (Cia4 Published QTL Chr 2)
Expand Tier I Mouse GO 69 Genes GS177223: GO:0017015 regulation of transforming growth factor beta receptor signaling pathway
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 Human 165 Genes GS171654: HP:0003121 Limb joint contracture
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human 20 Genes GS172151: HP:0002673 Coxa valga
Expand Tier I Human 21 Genes GS173291: HP:0000319 Smooth philtrum
Expand Tier I Mouse GO 3442 Genes GS181533: GO:0046872 metal ion binding
Expand Tier II Mouse 456 Genes GS84122: ethanol conditioned taste aversion (Published QTL, Chr 2)
Expand Tier II Mouse 457 Genes GS84123: METH responses for climbing (Published QTL, Chr 2)
Expand Tier I Human 12 Genes GS175022: HP:0001620 High pitched voice
Expand Tier I Human 275 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier I Human GO 165 Genes GS210361: GO:0090092 regulation of transmembrane receptor protein serine/threonine kinase signaling pathway
Expand Tier I Human 184 Genes GS175907: HP:0004349 Reduced bone mineral density
Expand Tier I Mouse GO 548 Genes GS188289: GO:0009968 negative regulation of signal transduction
Expand Tier I Mouse GO 1828 Genes GS189485: GO:0023051 regulation of signaling
Expand Tier I Human GO 1998 Genes GS203688: GO:0008270 zinc ion binding
Expand Tier I Human 111 Genes GS173580: HP:0011994 Abnormality of the atrial septum
Expand Tier I Human 246 Genes GS175909: HP:0004348 Abnormality of bone mineral density
Expand Tier I Human GO 781 Genes GS206190: GO:0048585 negative regulation of response to stimulus
Expand Tier I Human 210 Genes GS174857: HP:0200006 Slanting of the palpebral fissure
Expand Tier I Human 187 Genes GS173355: HP:0002205 Recurrent respiratory infections
Expand Tier I Mouse 537 Genes GS136522: platelet quantitative locus 1 (Pltq1, Published QTL Chr 2)
Expand Tier I Mouse 459 Genes GS135533: cobblestone area-forming cell number QTL 1 (Cafcnq1, Published QTL Chr 2)
Expand Tier I Human 41 Genes GS174482: HP:0010579 Cone-shaped epiphysis
Expand Tier I Human GO 4034 Genes GS208978: GO:0043169 cation binding
Expand Tier I Human 741 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 489 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 678 Genes GS206354: GO:0023057 negative regulation of signaling
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human GO 2139 Genes GS210214: GO:0005576 extracellular region
Expand Tier I Mouse 548 Genes GS136471: periosteal circumference and femur length 1 (Pcfm1, Published QTL Chr 2)
Expand Tier I Human 281 Genes GS171204: HP:0011314 Abnormality of long bone morphology
Expand Tier I Human 530 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Mouse GO 377 Genes GS179537: GO:0031012 extracellular matrix
Expand Tier I Human 94 Genes GS174879: HP:0002104 Apnea
Expand Tier I Mouse 548 Genes GS135816: ethanol induced ataxia 3 (Etax3, Published QTL Chr 2)
Expand Tier I Human 197 Genes GS174756: HP:0011947 Respiratory tract infection
Expand Tier I Human 60 Genes GS174088: HP:0003366 Abnormality of the femoral neck and head region
Expand Tier I Human 151 Genes GS174920: HP:0000766 Abnormality of the sternum
Expand Tier I Human GO 267 Genes GS204628: GO:0007178 transmembrane receptor protein serine/threonine kinase signaling pathway
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Mouse GO 5111 Genes GS189484: GO:0023052 signaling
Expand Tier I Human 558 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Human 41 Genes GS172655: HP:0001792 Small nail
Expand Tier I Human 129 Genes GS172916: HP:0003312 Abnormal form of the vertebral bodies
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human GO 89 Genes GS193946: GO:0017015 regulation of transforming growth factor beta receptor signaling pathway
Expand Tier I Human 212 Genes GS174189: HP:0001597 Abnormality of the nail
Expand Tier III Mouse 6105 Genes GS213074: Genes with suggestive difference in (B6PF1) vs (PB6F1 + B6 + PWD) comparison
Expand Tier I Human 97 Genes GS174919: HP:0000767 Pectus excavatum
Expand Tier I Human 124 Genes GS171102: HP:0006493 Aplasia/Hypoplasia involving bones of the lower limbs
Expand Tier I Human 25 Genes GS173340: HP:0003368 Abnormality of the femoral head
Expand Tier I Mouse GO 1341 Genes GS186836: GO:0008270 zinc ion binding
Expand Tier I Human 114 Genes GS174643: HP:0005120 Abnormality of cardiac atrium
Expand Tier I Human 17 Genes GS173461: HP:0001650 Aortic valve stenosis
Expand Tier I Human 249 Genes GS176844: HP:0000429 Abnormality of the nasal alae
Expand Tier I Human 579 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 2833 Genes GS198684: GO:0048523 negative regulation of cellular process
Expand Tier I Human GO 8137 Genes GS202316: GO:0050789 regulation of biological process
Expand Tier I Human 112 Genes GS173465: HP:0001654 Abnormality of the heart valves
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human 599 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human 281 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human GO 360 Genes GS210217: GO:0005578 proteinaceous extracellular matrix
Expand Tier I Human 50 Genes GS171995: HP:0001764 Small feet
Expand Tier I Human 251 Genes GS171793: HP:0000377 Abnormality of the pinna
Expand Tier I Human 67 Genes GS172588: HP:0001831 Short toe
Expand Tier I Human 27 Genes GS171097: HP:0006499 Abnormality of femoral epiphyses
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Mouse GO 5225 Genes GS189860: GO:0043167 ion binding
Expand Tier I Human 266 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier I Human 403 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Mouse 469 Genes GS136890: voluntary alcohol consumption QTL 4 (Vacq4, Published QTL Chr 2)
Expand Tier I Mouse GO 2190 Genes GS191129: GO:0016787 hydrolase activity
Expand Tier I Mouse 469 Genes GS135820: ethanol consumption 1 (Etohc1, Published QTL Chr 2)
Expand Tier I Mouse 448 Genes GS136889: voluntary alcohol consumption QTL 3 (Vacq3, Published QTL Chr 2)
Expand Tier I Human 54 Genes GS175896: HP:0000938 Osteopenia
Expand Tier I Human 263 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier I Human 46 Genes GS171463: HP:0004279 Short palm
Expand Tier I Human GO 638 Genes GS205146: GO:0009968 negative regulation of signal transduction
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 446 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier I Human GO 5810 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human 80 Genes GS175083: HP:0008386 Aplasia/Hypoplasia of the nails
Expand Tier I Mouse GO 8386 Genes GS189751: GO:0050794 regulation of cellular process
Expand Tier I Mouse GO 5654 Genes GS182325: GO:0051716 cellular response to stimulus
Expand Tier I Human 551 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 150 Genes GS175074: HP:0001156 Brachydactyly syndrome
Expand Tier I Human 263 Genes GS176692: HP:0009815 Aplasia/Hypoplasia of the extremities
Expand Tier I Mouse 3115 Genes GS128575: Ethanol induced LORR Chr# 2
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 426 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Mouse GO 8942 Genes GS185492: GO:0050789 regulation of biological process
Expand Tier I Human 403 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier I Human 75 Genes GS172096: HP:0000581 Blepharophimosis
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 266 Genes GS175823: HP:0002093 Respiratory insufficiency
Expand Tier I Human GO 8622 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human 47 Genes GS175664: HP:0006505 Abnormality involving the epiphyses of the limbs
Expand Tier I Mouse GO 5103 Genes GS192512: GO:0003824 catalytic activity
Expand Tier I Human 221 Genes GS171139: HP:0005288 Abnormality of the nares
Expand Tier I Human 588 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 112 Genes GS171616: HP:0100490 Camptodactyly of finger
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 616 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human 68 Genes GS172110: HP:0002983 Micromelia
Expand Tier I Human 232 Genes GS173288: HP:0000316 Hypertelorism
Expand Tier I Human GO 4983 Genes GS199124: GO:0051716 cellular response to stimulus
Expand Tier I Human 84 Genes GS172316: HP:0003026 Short long bones
Expand Tier I Human 128 Genes GS171035: HP:0002620 Systemic artery abnormality
Expand Tier I Mouse 338 Genes GS129163: proteoglycan induced spondylitis 2 (Pgis2 Published QTL Chr 2)
Expand Tier I Human 2 Genes GS177012: HP:0010446 Tricuspid stenosis
Expand Tier I Human 10 Genes GS176969: HP:0005003 Aplasia/Hypoplasia of the capital femoral epiphysis
Expand Tier I Mouse GO 75 Genes GS189382: GO:0090101 negative regulation of transmembrane receptor protein serine/threonine kinase signaling pathway
Expand Tier I Human GO 3104 Genes GS203058: GO:0048519 negative regulation of biological process
Expand Tier I Human 266 Genes GS172415: HP:0002240 Hepatomegaly
Expand Tier I Human GO 558 Genes GS205544: GO:0070011 peptidase activity, acting on L-amino acid peptides
Expand Tier I Human 421 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Mouse 446 Genes GS135721: variability in response to cholestrol enriched atherogenic diet (Diet1, Published QTL Chr 2)
Expand Tier I Human 120 Genes GS171607: HP:0011337 Abnormality of mouth size
Expand Tier I Human 62 Genes GS174139: HP:0005914 Aplasia/Hypoplasia involving the metacarpal bones
Expand Tier I Human 311 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier I Human GO 93 Genes GS206245: GO:0090101 negative regulation of transmembrane receptor protein serine/threonine kinase signaling pathway
Expand Tier I Human 111 Genes GS174806: HP:0001631 Defect in the atrial septum
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Mouse GO 1041 Genes GS184451: GO:0044421 extracellular region part
Expand Tier I Human 56 Genes GS176099: HP:0000926 Platyspondyly
Expand Tier I Human 7 Genes GS175938: HP:0100830 Round ear
Expand Tier I Mouse 333 Genes GS135244: adiposity 10 (Adip10, Published QTL Chr 2)
Expand Tier I Human GO 4593 Genes GS206355: GO:0023052 signaling
Expand Tier I Human 298 Genes GS174145: HP:0005918 Abnormality of phalanx of finger
Expand Tier I Mouse GO 6947 Genes GS192918: GO:0050896 response to stimulus
Expand Tier I Mouse GO 1825 Genes GS193270: GO:0005576 extracellular region
Expand Tier I Human 9 Genes GS171748: HP:0001718 Mitral stenosis
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 4084 Genes GS209199: GO:0007165 signal transduction
Expand Tier I Human 118 Genes GS172076: HP:0001163 Abnormality of the metacarpal bones
Expand Tier I Human 65 Genes GS171559: HP:0000388 Otitis media
Expand Tier I Human GO 2353 Genes GS208037: GO:0016787 hydrolase activity
Expand Tier I Human GO 3934 Genes GS198323: GO:0046872 metal ion binding
Expand Tier I Human 253 Genes GS171634: HP:0008050 Abnormality of the palpebral fissures
Expand Tier I Human GO 4719 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human 130 Genes GS173970: HP:0009473 Joint contracture of the hand
Expand Tier I Human 47 Genes GS174089: HP:0003367 Abnormality of the femoral neck
Expand Tier I Human 112 Genes GS176480: HP:0009826 Hypoplasia involving bones of the extremities
Expand Tier I Human GO 167 Genes GS204627: GO:0007179 transforming growth factor beta receptor signaling pathway
Expand Tier I Human 358 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Mouse 539 Genes GS136035: induction of brown adipocytes 6 (Iba6, Published QTL Chr 2)
Expand Tier I Mouse 542 Genes GS136087: lean body mass 1 (Lbm1, Published QTL Chr 2)
Expand Tier I Human 384 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Human GO 6585 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human GO 105 Genes GS199822: GO:0004222 metalloendopeptidase activity
Expand Tier I Human GO 2027 Genes GS206356: GO:0023051 regulation of signaling
Expand Tier I Human 62 Genes GS173692: HP:0001646 Abnormality of the aortic valve
Expand Tier I Mouse GO 113 Genes GS187767: GO:0007179 transforming growth factor beta receptor signaling pathway
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 Human 76 Genes GS176150: HP:0003019 Abnormality of the wrist
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Human 86 Genes GS174858: HP:0200007 Abnormal size of the palpebral fissures
Expand Tier I Human 236 Genes GS174257: HP:0000309 Abnormality of the midface
Expand Tier I Human 94 Genes GS171105: HP:0006494 Aplasia/Hypoplasia involving bones of the feet
Expand Tier I Human 49 Genes GS175305: HP:0000293 Full cheeks
Expand Tier I Human 474 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Human 53 Genes GS174451: HP:0006705 Abnormality of the atrioventricular valves
Expand Tier I Human 32 Genes GS176416: HP:0100679 Lack of skin elasticity
Expand Tier I Human 250 Genes GS172246: HP:0001371 Flexion contracture
Expand Tier I Mouse GO 710 Genes GS189324: GO:0048585 negative regulation of response to stimulus
Expand Tier I Human 433 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Mouse GO 146 Genes GS193417: GO:0090092 regulation of transmembrane receptor protein serine/threonine kinase signaling pathway
Expand Tier I Human 518 Genes GS174081: HP:0004322 Short stature
Expand Tier II Mouse 473 Genes GS84124: ethanol consumption (Published QTL, Chr 2)
Expand Tier I Human 8 Genes GS172165: HP:0001239 Wrist flexion contracture
Expand Tier I Human 567 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human GO 7689 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier I Human GO 5321 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Mouse 550 Genes GS136074: insulin QTL 7 (Insq7, Published QTL Chr 2)
Expand Tier I Mouse 459 Genes GS135441: bone marrow graft rejection 2 (Bmgr2, Published QTL Chr 2)
Expand Tier I Human 117 Genes GS170853: HP:0006261 Abnormality of phalangeal joints of the hand
Expand Tier I Human 211 Genes GS175164: HP:0011927 Short digit
Expand Tier I Human 11 Genes GS174480: HP:0010577 Absent epiphyses
Expand Tier I Human 112 Genes GS171810: HP:0005651 Flexion contracture of finger
Expand Tier I Human 1 Genes GS172520: HP:0006161 Short metacarpals with rounded proximal ends
Expand Tier I Human CTD 1541 Genes GS125445: Phenobarbital interacting genes (MeSH:D010634) in CTD
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 27 Genes GS175661: HP:0006500 Abnormality involving the epiphyses of the lower limbs
Expand Tier I Human 175 Genes GS174377: HP:0005927 Aplasia/Hypoplasia involving bones of the hand
Expand Tier I Human 14 Genes GS172154: HP:0002679 Abnormality of the sella turcica
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
Expand Tier I Human 220 Genes GS171791: HP:0000370 Abnormality of the middle ear
Expand Tier I Human 83 Genes GS172098: HP:0000582 Upslanted palpebral fissure
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 Human 56 Genes GS175733: HP:0010049 Short metacarpal
Expand Tier I Rat 418 Genes GS128039: Alcohol consumption QTL 19 (Alc19, Published QTL, Chr 3)
Expand Tier I Human 77 Genes GS172300: HP:0001991 Aplasia/Hypoplasia of the toes
Expand Tier I Mouse GO 592 Genes GS187168: GO:0010648 negative regulation of cell communication
Expand Tier I Human GO 375 Genes GS209907: GO:0004175 endopeptidase activity
Expand Tier I Human GO 65 Genes GS204254: GO:0030512 negative regulation of transforming growth factor beta receptor signaling pathway
Expand Tier I Mouse GO 571 Genes GS188685: GO:0070011 peptidase activity, acting on L-amino acid peptides
Expand Tier I Human 553 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human 411 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Mouse GO 230 Genes GS187768: GO:0007178 transmembrane receptor protein serine/threonine kinase signaling pathway
Expand Tier I Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Mouse GO 360 Genes GS192965: GO:0004175 endopeptidase activity
Expand Tier I Human 489 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human 112 Genes GS172569: HP:0000343 Long philtrum
Expand Tier I Human 378 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier I Human 8 Genes GS173132: HP:0003090 Hypoplasia of the capital femoral epiphysis
Expand Tier I Human 1 Genes GS173489: HP:0005041 Irregular capital femoral epiphysis
Expand Tier III Mouse 8107 Genes GS213076: Genes with suggestive difference in (B6) vs (B6PF1 + PB6F1 + PWD) comparison
Expand Tier I Mouse GO 5111 Genes GS187146: GO:0044700 single organism signaling
Expand Tier I Human 86 Genes GS174810: HP:0001635 Congestive heart failure
Expand Tier I Mouse 549 Genes GS136554: pentylenetetrazol induced seizure susceptibility 1b (Ptz1b, Published QTL Chr 2)
Expand Tier I Human 108 Genes GS171228: HP:0002823 Abnormality of the femur
Expand Tier I Human 52 Genes GS174808: HP:0001633 Abnormality of the mitral valve
Expand Tier I Human 941 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Mouse GO 577 Genes GS182069: GO:0007167 enzyme linked receptor protein signaling pathway
Expand Tier I Mouse GO 1575 Genes GS188290: GO:0009966 regulation of signal transduction
Expand Tier I Human GO 681 Genes GS204029: GO:0010648 negative regulation of cell communication
Expand Tier I Human 189 Genes GS176449: HP:0001671 Abnormality of the cardiac septa
Expand Tier I Human 245 Genes GS176694: HP:0009810 Abnormality of the joints of the upper limbs
Expand Tier I Human 212 Genes GS171106: HP:0006496 Aplasia/Hypoplasia involving bones of the upper limbs
Expand Tier I Human GO 4593 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
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 Human 44 Genes GS174688: HP:0004890 Elevated pulmonary artery pressure
Expand Tier I Human 215 Genes GS176973: HP:0001072 Thickened skin
Expand Tier I Human GO 2335 Genes GS206192: GO:0048583 regulation of response to stimulus
Expand Tier I Mouse 338 Genes GS135222: aromatase activity QTL 3 (Aaiq3, Published QTL Chr 2)
Expand Tier I Human GO 180 Genes GS199022: GO:0008237 metallopeptidase activity
Expand Tier I Mouse GO 600 Genes GS182209: GO:0008233 peptidase activity
Expand Tier I Mouse GO 98 Genes GS183020: GO:0004222 metalloendopeptidase activity
Expand Tier I Human GO 425 Genes GS196302: GO:0031012 extracellular matrix
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 210 Genes GS175990: HP:0000463 Anteverted nares
Expand Tier I Mouse 537 Genes GS136515: plasma plant sterol 2a (Plast2a, Published QTL Chr 2)
Expand Tier I Human GO 580 Genes GS199006: GO:0008233 peptidase activity
Expand Tier I Human GO 1097 Genes GS201255: GO:0044421 extracellular region part
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 189 Genes GS172253: HP:0001376 Limitation of joint mobility
Expand Tier I Human 310 Genes GS175805: HP:0003271 Visceromegaly
Expand Tier I Human 180 Genes GS175902: HP:0003468 Abnormality of the vertebrae
Expand Tier I Mouse 459 Genes GS136228: mandible length 2 (Manln2, Published QTL Chr 2)
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human 132 Genes GS174606: HP:0001608 Abnormality of the voice
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 545 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human 87 Genes GS173838: HP:0002778 Abnormality of the trachea
Expand Tier I Human GO 2241 Genes GS209291: GO:0046914 transition metal ion binding
Expand Tier I Mouse GO 5221 Genes GS179211: GO:0007154 cell communication
Expand Tier I Mouse GO 4725 Genes GS192265: GO:0007165 signal transduction
Expand Tier I Human GO 1776 Genes GS205147: GO:0009966 regulation of signal transduction
Expand Tier I Mouse GO 9323 Genes GS180152: GO:0065007 biological regulation
Expand Tier I Human 10 Genes GS171365: HP:0000391 Thickened helices
Expand Tier I Mouse 469 Genes GS135851: fecundity QTL 1 (Fecq1, Published QTL Chr 2)
Expand Tier I Human 487 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Mouse GO 1572 Genes GS192354: GO:0046914 transition metal ion binding
Expand Tier I Human 115 Genes GS171171: HP:0005607 Abnormality of the tracheobronchial system
Expand Tier I Human 578 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 258 Genes GS175602: HP:0002087 Abnormality of the upper respiratory tract
Expand Tier I Human 25 Genes GS173494: HP:0010574 Abnormality of the epiphysis of the femoral head
Expand Tier I Mouse GO 2030 Genes GS189326: GO:0048583 regulation of response to stimulus
Expand Tier I Human 601 Genes GS172021: HP:0001367 Abnormal joint morphology