Gene Details



PLOD1 and homologs in 4 species are found in 542 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 Mouse MP 159 Genes GS168313: MP:0000767 abnormal smooth muscle morphology
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human GO 1684 Genes GS204629: GO:1901564 organonitrogen compound metabolic process
Expand Tier I Mouse 713 Genes GS136518: phospholipid transfer protein inducibility QTL 1 (Pltiq1, Published QTL Chr 4)
Expand Tier I Mouse MP 19 Genes GS166687: MP:0009865 abnormal aorta smooth muscle morphology
Expand Tier I Mouse MP 1055 Genes GS166120: MP:0002106 abnormal muscle physiology
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Mouse 772 Genes GS135221: aromatase activity QTL 2 (Aaiq2, Published QTL Chr 4)
Expand Tier I Mouse 772 Genes GS135220: aromatase activity QTL 1 (Aaiq1, Published QTL Chr 4)
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 537 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Human 282 Genes GS175900: HP:0009118 Aplasia/Hypoplasia of the mandible
Expand Tier I Mouse GO 2260 Genes GS189855: GO:0043168 anion binding
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Mouse GO 5588 Genes GS193061: GO:0044444 cytoplasmic part
Expand Tier I Human 174 Genes GS172015: HP:0000969 Edema
Expand Tier I Mouse GO 8630 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse GO 73 Genes GS181665: GO:0048029 monosaccharide binding
Expand Tier I Human 203 Genes GS175802: HP:0003272 Abnormality of the hip bone
Expand Tier I Mouse GO 8650 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier I Human 17 Genes GS176999: HP:0001290 Generalized hypotonia
Expand Tier I Mouse GO 3537 Genes GS192041: GO:0043169 cation binding
Expand Tier I Human 61 Genes GS175897: HP:0000939 Osteoporosis
Expand Tier I Human GO 2940 Genes GS210507: GO:0006950 response to stress
Expand Tier I Human 181 Genes GS175391: HP:0011004 Abnormality of the systemic arterial tree
Expand Tier I Human 269 Genes GS172261: HP:0000357 Abnormal location of ears
Expand Tier I Human GO 434 Genes GS202416: GO:0044711 single-organism biosynthetic process
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 Mouse GO 919 Genes GS178388: GO:0055114 oxidation-reduction process
Expand Tier I Human CTD 2424 Genes GS123265: Estradiol interacting genes (MeSH:D004958) in CTD
Expand Tier I Mouse GO 2223 Genes GS179830: GO:0006464 cellular protein modification process
Expand Tier I Human 189 Genes GS176004: HP:0100656 Thoracoabdominal wall defects
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Human 117 Genes GS173868: HP:0002143 Abnormality of the spinal cord
Expand Tier I Human GO 566 Genes GS194646: GO:0042803 protein homodimerization activity
Expand Tier I Human 379 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human 374 Genes GS175815: HP:0011025 Abnormality of cardiovascular system physiology
Expand Tier I Human GO 4070 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human 198 Genes GS175538: HP:0011276 Vascular skin abnormality
Expand Tier I Human 360 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human 56 Genes GS174818: HP:0007495 Prematurely aged appearance
Expand Tier I Human 30 Genes GS176144: HP:0001787 Abnormal delivery
Expand Tier I Human 602 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Mouse GO 735 Genes GS181962: GO:0016491 oxidoreductase activity
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 GO 4024 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Mouse MP 1628 Genes GS163852: MP:0001544 abnormal cardiovascular system physiology
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 264 Genes GS173014: HP:0010936 Abnormality of the lower urinary tract
Expand Tier I Human 639 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human 43 Genes GS173159: HP:0002239 Gastrointestinal hemorrhage
Expand Tier I Rat DRG 4920 Genes GS86494: Table S1: Hippocampus 17 K microarray data. [DRG]
Expand Tier I Human 490 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Human 81 Genes GS172726: HP:0000268 Dolichocephaly
Expand Tier I Human GO 5223 Genes GS207857: GO:0009058 biosynthetic process
Expand Tier I Human 141 Genes GS174906: HP:0000545 Myopia
Expand Tier I Human 426 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Mouse 750 Genes GS136608: colon tumor susceptibility 11 (Scc11, Published QTL Chr 4)
Expand Tier I Human 324 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Mouse 713 Genes GS136443: peak bone mineral density 3 (Pbmd3, Published QTL Chr 4)
Expand Tier I Mouse GO 4 Genes GS180175: GO:0070815 peptidyl-lysine 5-dioxygenase activity
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier II Mouse 519 Genes GS84164: cocaine related behavior (Published QTL, Chr 4)
Expand Tier I Human 149 Genes GS176098: HP:0000927 Abnormality of skeletal maturation
Expand Tier I Human GO 2464 Genes GS196595: GO:0006464 cellular protein modification process
Expand Tier I Human 157 Genes GS171718: HP:0002808 Kyphosis
Expand Tier I Human 114 Genes GS174412: HP:0007477 Abnormal dermatoglyphics
Expand Tier II Mouse 558 Genes GS84163: alcohol preference 3 QTL (Ap3q, Published QTL, Chr 4)
Expand Tier I Mouse GO 3548 Genes GS184566: GO:0019538 protein metabolic process
Expand Tier I Human GO 2625 Genes GS196343: GO:0036094 small molecule binding
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 72 Genes GS175808: HP:0011028 Abnormality of blood circulation
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 8406 Genes GS177404: GO:0005737 cytoplasm
Expand Tier I Mouse GO 3080 Genes GS177265: GO:0048731 system development
Expand Tier I Human GO 339 Genes GS195494: GO:0006520 cellular amino acid metabolic process
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 1 Genes GS197085: GO:0046946 hydroxylysine metabolic process
Expand Tier I Mouse 762 Genes GS136559: QTL for body weight independent of sex 1 (Qbis1, Published QTL Chr 4)
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human GO 772 Genes GS196729: GO:0005789 endoplasmic reticulum membrane
Expand Tier I Mouse GO 3597 Genes GS188142: GO:0048856 anatomical structure development
Expand Tier I Mouse GO 3442 Genes GS181533: GO:0046872 metal ion binding
Expand Tier I Mouse 758 Genes GS135839: femoral bone trait QTL 2 (Fbtq2, Published QTL Chr 4)
Expand Tier I Mouse GO 82 Genes GS185827: GO:0051213 dioxygenase activity
Expand Tier I Human 392 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Human 275 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier I Mouse 794 Genes GS136046: insulin dependent diabetes susceptibility 25 (Idd25, Published QTL Chr 4)
Expand Tier I Human 68 Genes GS175207: HP:0000978 Bruising susceptibility
Expand Tier I Human 184 Genes GS175907: HP:0004349 Reduced bone mineral density
Expand Tier I Mouse 713 Genes GS135460: bone mineral density 6 (Bomd6, Published QTL Chr 4)
Expand Tier I Mouse 767 Genes GS135509: body weight at 8 weeks QTL 2 (Bw8q2, Published QTL Chr 4)
Expand Tier I Human 174 Genes GS171806: HP:0005656 Positional foot deformities
Expand Tier I Human 65 Genes GS175131: HP:0000023 Inguinal hernia
Expand Tier I Human GO 953 Genes GS202555: GO:0043436 oxoacid metabolic process
Expand Tier I Human GO 168 Genes GS197078: GO:0005506 iron ion binding
Expand Tier I Human 101 Genes GS171997: HP:0001762 Talipes equinovarus
Expand Tier I Human 246 Genes GS175909: HP:0004348 Abnormality of bone mineral density
Expand Tier I Human 187 Genes GS173355: HP:0002205 Recurrent respiratory infections
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 103 Genes GS173741: HP:0100699 Scarring
Expand Tier I Mouse 713 Genes GS135245: adiposity 12 (Adip12, Published QTL Chr 4)
Expand Tier I Human 41 Genes GS176789: HP:0100872 Abnormality of the plantar skin of foot
Expand Tier I Human GO 1281 Genes GS196726: GO:0005783 endoplasmic reticulum
Expand Tier I Mouse 760 Genes GS135770: ear healing QTL 2 (Earheal2, Published QTL Chr 4)
Expand Tier I Human 397 Genes GS173137: HP:0011821 Abnormality of facial skeleton
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 Mouse 553 Genes GS135917: graft-versus-host disease 2 (Gvhd2, Published QTL Chr 4)
Expand Tier I Human 260 Genes GS170933: HP:0001288 Gait disturbance
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 806 Genes GS197478: GO:0009628 response to abiotic stimulus
Expand Tier I Human 9 Genes GS176415: HP:0100678 Premature skin wrinkling
Expand Tier I Mouse GO 3 Genes GS180628: GO:0008475 procollagen-lysine 5-dioxygenase activity
Expand Tier I Human 28 Genes GS172164: HP:0001182 Tapered finger
Expand Tier I Human 78 Genes GS174649: HP:0000954 Single transverse palmar crease
Expand Tier I Human 492 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Mouse 764 Genes GS135330: autoimmune renal vasculitis 2 (Arvm2, Published QTL Chr 4)
Expand Tier I Human 72 Genes GS175809: HP:0011029 Internal hemorrhage
Expand Tier I Mouse GO 79 Genes GS192384: GO:0016701 oxidoreductase activity, acting on single donors with incorporation of molecular oxygen
Expand Tier I Human GO 1771 Genes GS196284: GO:0012505 endomembrane system
Expand Tier I Mouse GO 377 Genes GS179537: GO:0031012 extracellular matrix
Expand Tier I Human 403 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 197 Genes GS174756: HP:0011947 Respiratory tract infection
Expand Tier I Mouse MP 112 Genes GS170197: MP:0005592 abnormal vascular smooth muscle morphology
Expand Tier I Human GO 3885 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier I Human 102 Genes GS177035: HP:0001928 Abnormality of coagulation
Expand Tier I Human GO 4 Genes GS196952: GO:0070815 peptidyl-lysine 5-dioxygenase activity
Expand Tier I Human 157 Genes GS176639: HP:0011356 Regional abnormality of skin
Expand Tier I Human 47 Genes GS175737: HP:0001238 Slender finger
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Human GO 35 Genes GS204137: GO:0009066 aspartate family amino acid metabolic process
Expand Tier I Mouse MP 3543 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Mouse 761 Genes GS136202: lung tumor shape-determining 4 (Ltsd4, Published QTL Chr 4)
Expand Tier I Mouse GO 188 Genes GS184450: GO:0044420 extracellular matrix part
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human 170 Genes GS173988: HP:0000501 Glaucoma
Expand Tier II Mouse 40 Genes GS35272: Hippocampus Gene expression correlates of Maximum startle response to 85 db in Females BXD
Expand Tier III Mouse 8003 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampal tissue
Expand Tier I Human GO 2511 Genes GS207903: GO:0044281 small molecule metabolic process
Expand Tier I Human 579 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 5 Genes GS170923: HP:0005294 Arterial dissection
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 Human 313 Genes GS176642: HP:0011355 Localized skin lesion
Expand Tier I Mouse GO 152 Genes GS191271: GO:0018205 peptidyl-lysine modification
Expand Tier I Mouse MP 281 Genes GS163997: MP:0011655 abnormal systemic artery morphology
Expand Tier I Mouse GO 6 Genes GS179652: GO:0018126 protein hydroxylation
Expand Tier I Human GO 186 Genes GS200970: GO:0031406 carboxylic acid binding
Expand Tier I Mouse 762 Genes GS135856: femoral bone morphometry 5 (Fembm5, Published QTL Chr 4)
Expand Tier I Human GO 4097 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human 10 Genes GS172435: HP:0002647 Aortic dissection
Expand Tier I Human 282 Genes GS172572: HP:0000347 Micrognathia
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 Mouse 794 Genes GS136772: SGC/Knj cross B6 QTL 1 (Sxbq1, Published QTL Chr 4)
Expand Tier I Human GO 211 Genes GS208505: GO:0030198 extracellular matrix organization
Expand Tier I Mouse MP 242 Genes GS170668: MP:0000272 abnormal aorta morphology
Expand Tier I Mouse GO 154 Genes GS180298: GO:0005506 iron ion binding
Expand Tier I Mouse GO 78 Genes GS192382: GO:0016702 oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen
Expand Tier I Human 4 Genes GS171676: HP:0003834 Shoulder dislocation
Expand Tier I Human 364 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Mouse 772 Genes GS135350: Alzheimer's disease modifier 2 (Azdm2, Published QTL Chr 4)
Expand Tier I Mouse MP 2406 Genes GS169391: MP:0002066 abnormal motor capabilities/coordination/movement
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 53 Genes GS174719: HP:0000774 Narrow chest
Expand Tier I Human 403 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Human 544 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 84 Genes GS202664: GO:0051213 dioxygenase activity
Expand Tier I Human 512 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Human 95 Genes GS176573: HP:0008065 Aplasia/Hypoplasia of the skin
Expand Tier I Human 266 Genes GS175823: HP:0002093 Respiratory insufficiency
Expand Tier I Mouse GO 5892 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier I Mouse GO 5103 Genes GS192512: GO:0003824 catalytic activity
Expand Tier I Mouse MP 21 Genes GS164732: MP:0008438 abnormal cutaneous collagen fibril morphology
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier III Mouse 5726 Genes GS213077: Genes with suggestive difference in (PWD) vs (PB6F1 + B6PF1 + B6) comparison
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 Mouse 713 Genes GS136191: light induced retinal degeneration 2 (Lrdg2, Published QTL Chr 4)
Expand Tier I Human 35 Genes GS176775: HP:0001004 Lymphedema
Expand Tier I Human 4 Genes GS171762: HP:0007517 Palmoplantar cutis laxa
Expand Tier I Human GO 47 Genes GS203663: GO:0005791 rough endoplasmic reticulum
Expand Tier I Mouse MP 1104 Genes GS169389: MP:0002060 abnormal skin morphology
Expand Tier I Mouse 830 Genes GS129104: bone mineral density 7 (Bmd7 Published QTL Chr 4)
Expand Tier I Human 128 Genes GS171035: HP:0002620 Systemic artery abnormality
Expand Tier I Human 534 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Human GO 422 Genes GS207919: GO:0044283 small molecule biosynthetic process
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 709 Genes GS198755: GO:0016491 oxidoreductase activity
Expand Tier I Human GO 3513 Genes GS193991: GO:0048731 system development
Expand Tier I Human 302 Genes GS176029: HP:0009116 Aplasia/Hypoplasia involving bones of the skull
Expand Tier I Mouse 772 Genes GS136689: skull morphology 6 (Skull6, Published QTL Chr 4)
Expand Tier I Human 73 Genes GS176571: HP:0008067 Abnormally lax or hyperextensible skin
Expand Tier I Human 55 Genes GS171548: HP:0001388 Joint laxity
Expand Tier I Mouse 760 Genes GS135803: elevated serum gp70 1 (Elsgp1, Published QTL Chr 4)
Expand Tier I Mouse GO 1041 Genes GS184451: GO:0044421 extracellular region part
Expand Tier I Human 240 Genes GS172433: HP:0002644 Abnormality of pelvic girdle bone morphology
Expand Tier I Mouse 758 Genes GS136823: triglyceride QTL 3 (Tgq3, Published QTL Chr 4)
Expand Tier I Mouse GO 122 Genes GS188395: GO:0019842 vitamin binding
Expand Tier I Mouse GO 1825 Genes GS193270: GO:0005576 extracellular region
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human CTD 999 Genes GS124711: Genistein interacting genes (MeSH:D019833) in CTD
Expand Tier I Human GO 3934 Genes GS198323: GO:0046872 metal ion binding
Expand Tier I Human 30 Genes GS170949: HP:0005616 Accelerated skeletal maturation
Expand Tier I Human 253 Genes GS171634: HP:0008050 Abnormality of the palpebral fissures
Expand Tier I Human GO 1 Genes GS197083: GO:0046947 hydroxylysine biosynthetic process
Expand Tier I Human CTD 794 Genes GS125548: Doxorubicin interacting genes (MeSH:D004317) in CTD
Expand Tier I Human 42 Genes GS175822: HP:0002090 Pneumonia
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Human GO 2392 Genes GS206737: GO:0043168 anion binding
Expand Tier I Human 3 Genes GS173945: HP:0005952 Decreased pulmonary function
Expand Tier I Human 93 Genes GS170972: HP:0001933 Subcutaneous hemorrhage
Expand Tier I Human 397 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Mouse MP 86 Genes GS169944: MP:0004142 abnormal muscle tone
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 CTD 308 Genes GS123854: Cyclophosphamide interacting genes (MeSH:D003520) in CTD
Expand Tier I Human GO 16 Genes GS198488: GO:0030867 rough endoplasmic reticulum membrane
Expand Tier I Human 13 Genes GS172297: HP:0001519 Disproportionate tall stature
Expand Tier I Mouse GO 2303 Genes GS177598: GO:0043412 macromolecule modification
Expand Tier I Human GO 2545 Genes GS203335: GO:0048513 organ development
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Human 63 Genes GS173367: HP:0005257 Thoracic hypoplasia
Expand Tier I Human 86 Genes GS174858: HP:0200007 Abnormal size of the palpebral fissures
Expand Tier I Mouse 767 Genes GS135416: beta-carboline-induced seizures 1 (Bis1, Published QTL Chr 4)
Expand Tier I Human 46 Genes GS175267: HP:0001166 Arachnodactyly
Expand Tier I Human 384 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human GO 2373 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human 221 Genes GS172288: HP:0000358 Posteriorly rotated ears
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 Mouse GO 2223 Genes GS182234: GO:0036211 protein modification process
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 269 Genes GS196679: GO:0030246 carbohydrate binding
Expand Tier I Human GO 6151 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 28 Genes GS173311: HP:0010651 Abnormality of the meninges
Expand Tier I Mouse 759 Genes GS136148: lithogenic gene 8 (Lith8, Published QTL Chr 4)
Expand Tier I Mouse GO 1204 Genes GS188763: GO:0009888 tissue development
Expand Tier I Human 388 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Mouse GO 7644 Genes GS188399: GO:0044238 primary metabolic process
Expand Tier I Mouse 553 Genes GS135315: alcohol preference 3 QTL (Ap3q, Published QTL Chr 4)
Expand Tier I Human GO 3409 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Mouse 565 Genes GS135831: fluctuating asymmetry QTL 1 (Faq1, Published QTL Chr 4)
Expand Tier I Human GO 72 Genes GS198454: GO:0048029 monosaccharide binding
Expand Tier III Mouse 2289 Genes GS216489: Genes that are binding sites of CREB and zif268, transcription factors mediating neuronal activity and plasticity, in Mus musculus.
Expand Tier I Human GO 556 Genes GS195139: GO:0055114 oxidation-reduction process
Expand Tier I Mouse GO 2439 Genes GS179580: GO:0036094 small molecule binding
Expand Tier I Human GO 251 Genes GS201011: GO:0036293 response to decreased oxygen levels
Expand Tier I Mouse 759 Genes GS135544: corpus callosum hemisphere surface size 2 (Ccrs2, Published QTL Chr 4)
Expand Tier I Mouse MP 729 Genes GS165612: MP:0002128 abnormal blood circulation
Expand Tier I Human GO 1439 Genes GS205623: GO:0009888 tissue development
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 262 Genes GS172033: HP:0000369 Low-set ears
Expand Tier I Mouse GO 2926 Genes GS183803: GO:0044267 cellular protein metabolic process
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
Expand Tier I Human 7 Genes GS175753: HP:0000015 Bladder diverticula
Expand Tier I Human 414 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human GO 248 Genes GS200142: GO:0001666 response to hypoxia
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 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human 9 Genes GS175318: HP:0000563 Keratoconus
Expand Tier I Mouse MP 1777 Genes GS164263: MP:0002083 premature death
Expand Tier I Mouse MP 2099 Genes GS165616: MP:0002127 abnormal cardiovascular system 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 II Mouse 522 Genes GS84321: pentobarbital withdrawal Chr4 (Published QTL)
Expand Tier I Human GO 82 Genes GS209317: GO:0016702 oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen
Expand Tier I Human GO 18 Genes GS204136: GO:0009067 aspartate family amino acid biosynthetic process
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
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 Human CTD 211 Genes GS124295: Polychlorinated Biphenyls interacting genes (MeSH:D011078) in CTD
Expand Tier I Human 33 Genes GS174067: HP:0002904 Hyperbilirubinemia
Expand Tier I Human 189 Genes GS176745: HP:0010866 Abdominal wall defect
Expand Tier II Mouse 519 Genes GS84165: ethanol conditioned taste aversion (Published QTL, Chr 4)
Expand Tier I Human 46 Genes GS173617: HP:0011220 Prominent forehead
Expand Tier I Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human GO 61 Genes GS208235: GO:0008652 cellular amino acid biosynthetic process
Expand Tier I Human 489 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human 56 Genes GS175070: HP:0000973 Cutis laxa
Expand Tier II Mouse 739 Genes GS83998: cocaine and amphetamine-regulated transcript QTL 2 (Crq2, Published QTL, Chr 4)
Expand Tier I Human 285 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier I Human 38 Genes GS171381: HP:0001558 Decreased fetal movement
Expand Tier I Human 378 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier I Human GO 212 Genes GS195507: GO:0043062 extracellular structure organization
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Mouse 759 Genes GS136150: "lupus in MRL and B6 F2 cross, QTL 1" (Lmb1, Published QTL Chr 4)
Expand Tier I Human 86 Genes GS174810: HP:0001635 Congestive heart failure
Expand Tier I Human GO 3 Genes GS197428: GO:0008475 procollagen-lysine 5-dioxygenase activity
Expand Tier I Human 132 Genes GS173792: HP:0002815 Abnormality of the knees
Expand Tier I Mouse MP 2199 Genes GS165244: MP:0010771 integument phenotype
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 Human 58 Genes GS171388: HP:0001557 Prenatal movement abnormality
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Mouse 759 Genes GS136705: systemic lupus erythmatosus suppressor 2 (Sles2, Published QTL Chr 4)
Expand Tier I Mouse MP 14488 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Mouse MP 1108 Genes GS166117: MP:0002108 abnormal muscle morphology
Expand Tier I Mouse MP 11 Genes GS166730: MP:0004044 aortic dissection
Expand Tier I Human GO 260 Genes GS195145: GO:0016053 organic acid biosynthetic process
Expand Tier I Mouse 695 Genes GS135567: cytokine deficiency colitis susceptibility 9 (Cdcs9, Published QTL Chr 4)
Expand Tier I Human 245 Genes GS176694: HP:0009810 Abnormality of the joints of the upper limbs
Expand Tier I Mouse 553 Genes GS136621: sucrose consumption 2 (Scon2, Published QTL Chr 4)
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Mouse MP 582 Genes GS168151: MP:0001914 hemorrhage
Expand Tier I Human 525 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Human 2 Genes GS176961: HP:0001020 Soft, thin skin
Expand Tier I Human 122 Genes GS173563: HP:0000692 Misalignment of teeth
Expand Tier I Mouse GO 13 Genes GS191852: GO:0008198 ferrous iron binding
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Mouse 767 Genes GS135893: gastritis type A susceptibility locus 1 (Gasa1, Published QTL Chr 4)
Expand Tier II Mouse 41 Genes GS35262: Hippocampus Gene expression correlates of Maximum startle response to 80 db in Females BXD
Expand Tier I Mouse 549 Genes GS128576: Ethanol induced LORR Chr# 4
Expand Tier I Mouse GO 219 Genes GS179910: GO:0030246 carbohydrate binding
Expand Tier I Human 44 Genes GS172038: HP:0000963 Thin skin
Expand Tier I Human CTD 5075 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Mouse MP 52 Genes GS166790: MP:0009873 abnormal aorta tunica media morphology
Expand Tier I Human 60 Genes GS171207: HP:0000098 Tall stature
Expand Tier I Mouse 781 Genes GS136719: susceptibility to lung cancer 21 (Sluc21, Published QTL Chr 4)
Expand Tier I Mouse GO 87 Genes GS181440: GO:0005581 collagen
Expand Tier I Human 9 Genes GS172309: HP:0100692 Increased corneal curvature
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Human 90 Genes GS174101: HP:0001018 Abnormal palmar dermatoglyphics
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Mouse GO 3605 Genes GS190682: GO:0007275 multicellular organismal development
Expand Tier I Mouse 637 Genes GS135899: granulosa cell tumorigenesis 1 (Gct1, Published QTL Chr 4)
Expand Tier I Mouse GO 19 Genes GS188459: GO:0031418 L-ascorbic acid binding
Expand Tier I Human 173 Genes GS175117: HP:0001883 Talipes
Expand Tier I Human GO 3307 Genes GS195110: GO:0071842 cellular component organization at cellular level
Expand Tier I Mouse 772 Genes GS135775: epistatic circling B C57L/J (Eclb, Published QTL Chr 4)
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 189 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier I Human 50 Genes GS175148: HP:0010511 Long toe
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human GO 162 Genes GS202464: GO:0016705 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
Expand Tier II Mouse 519 Genes GS84166: METH responses for climbing (Published QTL, Chr 4)
Expand Tier I Mouse MP 1307 Genes GS170198: MP:0001614 abnormal blood vessel morphology
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Mouse GO 45 Genes GS190971: GO:0016706 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, 2-oxoglutarate as one donor, and incorporation of one atom each of oxygen into both donors
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human GO 260 Genes GS200383: GO:0046394 carboxylic acid biosynthetic process
Expand Tier I Human GO 846 Genes GS204326: GO:0019752 carboxylic acid metabolic process
Expand Tier I Human 545 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human 160 Genes GS175096: HP:0000286 Epicanthus
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 5962 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human 78 Genes GS172553: HP:0100689 Decreased corneal thickness
Expand Tier I Human 88 Genes GS172871: HP:0010490 Abnormality of the palmar creases
Expand Tier I Human 737 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human GO 2241 Genes GS209291: GO:0046914 transition metal ion binding
Expand Tier I Human CTD 48 Genes GS123568: 4-hydroxy-equilenin interacting genes (MeSH:C065250) in CTD
Expand Tier I Mouse GO 2 Genes GS184443: GO:0017185 peptidyl-lysine hydroxylation
Expand Tier I Human CTD 5725 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Mouse 695 Genes GS136860: thermal pain response 1 (Tpnr1, Published QTL Chr 4)
Expand Tier I Human GO 858 Genes GS194645: GO:0042802 identical protein binding
Expand Tier I Mouse 761 Genes GS136730: susceptibility to lung cancer 6 (Sluc6, Published QTL Chr 4)
Expand Tier I Human 148 Genes GS171552: HP:0001382 Joint hypermobility
Expand Tier I Mouse 553 Genes GS135480: bone response to mechanical loading 13 (Brml13, Published QTL Chr 4)
Expand Tier I Human 319 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Mouse GO 2279 Genes GS186488: GO:0048513 organ development
Expand Tier I Human 81 Genes GS172248: HP:0001373 Joint dislocation
Expand Tier I Human 212 Genes GS176185: HP:0100790 Hernia
Expand Tier I Human GO 455 Genes GS194627: GO:0008544 epidermis development
Expand Tier I Mouse GO 1572 Genes GS192354: GO:0046914 transition metal ion binding
Expand Tier I Mouse MP 3543 Genes GS169095: MP:0004924 abnormal behavior
Expand Tier I Mouse 758 Genes GS135477: bone response to mechanical loading 10 (Brml10, Published QTL Chr 4)
Expand Tier I Human 79 Genes GS175373: HP:0011486 Abnormality of corneal thickness
Expand Tier I Mouse 565 Genes GS135920: graft-versus host disease 5 (Gvhd5, Published QTL Chr 4)
Expand Tier I Human 601 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 438 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier I Human 174 Genes GS173901: HP:0002007 Frontal bossing
Expand Tier I Human GO 4567 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human 530 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human 14 Genes GS175066: HP:0000977 Soft skin
Expand Tier I Human GO 6769 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Mouse 772 Genes GS135741: dystrophic cardiac calcinosis 2 (Dyscalc2, Published QTL Chr 4)
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 Mouse MP 27 Genes GS168795: MP:0004144 hypotonia
Expand Tier I Human 558 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Human GO 5152 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier I Mouse GO 250 Genes GS177887: GO:0008544 epidermis development
Expand Tier I Human GO 47 Genes GS207879: GO:0016706 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, 2-oxoglutarate as one donor, and incorporation of one atom each of oxygen into both donors
Expand Tier I Human 37 Genes GS176719: HP:0000541 Retinal detachment
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human 67 Genes GS172844: HP:0000482 Microcornea
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human 1 Genes GS174090: HP:0008458 Progressive congenital scoliosis
Expand Tier I Mouse 211 Genes GS129084: atherosclerosis susceptibility QTL 1 (Athsq1 Published QTL Chr 4)
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human CTD 1122 Genes GS127166: bisphenol A interacting genes (MeSH:C006780) in CTD
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Mouse MP 576 Genes GS168750: MP:0002191 abnormal artery morphology
Expand Tier I Human 599 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human 100 Genes GS176744: HP:0000987 Atypical scarring of skin
Expand Tier I Human 80 Genes GS173498: HP:0001763 Pes planus
Expand Tier I Human 324 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 197 Genes GS204383: GO:0006575 cellular modified amino acid metabolic process
Expand Tier I Human 75 Genes GS174446: HP:0001120 Abnormality of corneal size
Expand Tier I Mouse 772 Genes GS136880: tooth shape 6 (Tshp6, Published QTL Chr 4)
Expand Tier I Human GO 2464 Genes GS199032: GO:0036211 protein modification process
Expand Tier I Mouse 759 Genes GS136757: startle response 2 (Start2, Published QTL Chr 4)
Expand Tier I Mouse 760 Genes GS136540: psoriasis susceptibility 6 (Psrs6, Published QTL Chr 4)
Expand Tier I Human 398 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human 39 Genes GS174374: HP:0005922 Abnormal hand morphology
Expand Tier I Human 196 Genes GS172034: HP:0000368 Low-set, posteriorly rotated ears
Expand Tier I Human 15 Genes GS175044: HP:0006532 Recurrent pneumonia
Expand Tier I Mouse 760 Genes GS135607: circulating hormone level QTL 16 (Chlq16, Published QTL Chr 4)
Expand Tier I Human 258 Genes GS172272: HP:0001197 Abnormality of prenatal development or birth
Expand Tier I Human 263 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier I Human GO 2558 Genes GS194336: GO:0043412 macromolecule modification
Expand Tier I Mouse GO 9049 Genes GS180166: GO:0008152 metabolic process
Expand Tier I Mouse 772 Genes GS135394: body growth early QTL 3 (Bgeq3, Published QTL Chr 4)
Expand Tier I Human 31 Genes GS175063: HP:0000974 Hyperextensible skin
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Mouse GO 561 Genes GS182740: GO:0018193 peptidyl-amino acid modification
Expand Tier I Human GO 645 Genes GS204631: GO:1901566 organonitrogen compound biosynthetic process
Expand Tier I Mouse GO 1149 Genes GS179957: GO:0005783 endoplasmic reticulum
Expand Tier I Mouse 760 Genes GS136580: red blood cell QTL 2 (Rbcq2, Published QTL Chr 4)
Expand Tier I Human 33 Genes GS174652: HP:0001131 Corneal dystrophy
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 Mouse 760 Genes GS136916: vertebral morphology and mechanical traits 4 (Vmmt4, Published QTL Chr 4)
Expand Tier III Rat 350 Genes GS37147: Gene expression change in the nucleus accumbens, following continuous alcohol consumption in alcohol preferring rats.
Expand Tier I Human 27 Genes GS176727: HP:0003043 Abnormality of the shoulder
Expand Tier I Human GO 21 Genes GS205315: GO:0031418 L-ascorbic acid binding
Expand Tier I Mouse MP 187 Genes GS169179: MP:0000753 paralysis
Expand Tier I Human 426 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Mouse 586 Genes GS135894: gastritis type A susceptibility locus 2 (Gasa2, Published QTL Chr 4)
Expand Tier I Human 157 Genes GS174877: HP:0001892 Abnormal bleeding
Expand Tier I Human CTD 183 Genes GS125960: Cholecalciferol interacting genes (MeSH:D002762) in CTD
Expand Tier I Human 75 Genes GS172096: HP:0000581 Blepharophimosis
Expand Tier I Mouse 761 Genes GS136100: lupus NZB x NZW 2 (Lbw2, Published QTL Chr 4)
Expand Tier I Human 51 Genes GS174123: HP:0100807 Long fingers
Expand Tier I Mouse GO 182 Genes GS182661: GO:0042277 peptide binding
Expand Tier II Mouse 474 Genes GS83985: cocaine related behavior 16 (Cocrb16, Published QTL, Chr 4)
Expand Tier I Human GO 83 Genes GS209319: GO:0016701 oxidoreductase activity, acting on single donors with incorporation of molecular oxygen
Expand Tier I Mouse MP 1825 Genes GS168956: MP:0003491 abnormal voluntary movement
Expand Tier I Human 144 Genes GS175754: HP:0000014 Abnormality of the bladder
Expand Tier I Human 186 Genes GS171144: HP:0005280 Depressed nasal bridge
Expand Tier I Mouse GO 8145 Genes GS190714: GO:0016020 membrane
Expand Tier I Human 4 Genes GS171715: HP:0007392 Excessive wrinkled skin
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 35 Genes GS172848: HP:0000488 Retinopathy
Expand Tier I Human 24 Genes GS176256: HP:0002783 Recurrent lower respiratory tract infections
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse GO 4073 Genes GS180034: GO:0032502 developmental process
Expand Tier I Human GO 4213 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human GO 6651 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 143 Genes GS176586: HP:0001270 Motor delay
Expand Tier I Mouse MP 5057 Genes GS165525: MP:0010768 mortality/aging
Expand Tier I Human 543 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human 3 Genes GS174321: HP:0010303 Abnormality of the spinal meninges
Expand Tier I Human 174 Genes GS171148: HP:0011218 Abnormal shape of the frontal region
Expand Tier I Human GO 266 Genes GS197236: GO:0070482 response to oxygen levels
Expand Tier I Human 421 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Mouse GO 165 Genes GS185632: GO:0016705 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
Expand Tier I Human 626 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Mouse 785 Genes GS136575: recognized antigen from MCA-induced tumor 1 (Ramt1, Published QTL Chr 4)
Expand Tier I Mouse GO 189 Genes GS189291: GO:0033218 amide binding
Expand Tier I Human 7 Genes GS176140: HP:0001788 Premature rupture of membranes
Expand Tier I Human GO 54 Genes GS194084: GO:0042398 cellular modified amino acid biosynthetic process