Gene Details



TTPA and homologs in 3 species are found in 323 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 MP 70 Genes GS163321: MP:0010240 decreased skeletal muscle size
Expand Tier I Mouse MP 389 Genes GS167918: MP:0000955 abnormal spinal cord morphology
Expand Tier I Human 13 Genes GS173504: HP:0200036 Skin nodule
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Mouse MP 1111 Genes GS166412: MP:0002118 abnormal lipid homeostasis
Expand Tier I Mouse 378 Genes GS136480: plasmacytoma susceptibility 2 (Pcyts2, Published QTL Chr 4)
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 Mouse 325 Genes GS136209: lupus BXSB x NZW 1 (Lxw1, Published QTL Chr 4)
Expand Tier I Human CTD 42 Genes GS127261: lipopolysaccharide, E coli O55-B5 interacting genes (MeSH:C482199) in CTD
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human CTD 419 Genes GS121514: Paraquat interacting genes (MeSH:D010269) in CTD
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 Mouse GO 8630 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse GO 8650 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse GO 1822 Genes GS190997: GO:0044281 small molecule metabolic process
Expand Tier I Mouse MP 396 Genes GS170108: MP:0003727 abnormal retinal layer morphology
Expand Tier I Mouse 348 Genes GS135284: "alcohol preference locus 8, female specific" (Alcp8, Published QTL Chr 4)
Expand Tier I Mouse MP 172 Genes GS170561: MP:0003991 arteriosclerosis
Expand Tier I Human CTD 2424 Genes GS123265: Estradiol interacting genes (MeSH:D004958) in CTD
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 GO 5400 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Mouse MP 7 Genes GS169934: MP:0001908 abnormal somatosensory cortex physiology
Expand Tier I Human GO 115 Genes GS201152: GO:0001890 placenta development
Expand Tier I Mouse GO 2 Genes GS182504: GO:0090212 negative regulation of establishment of blood-brain barrier
Expand Tier I Human GO 2661 Genes GS207797: GO:0030154 cell differentiation
Expand Tier I Human GO 4070 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human GO 4024 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Rat DRG 4920 Genes GS86494: Table S1: Hippocampus 17 K microarray data. [DRG]
Expand Tier I Mouse MP 3019 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier I Mouse MP 2057 Genes GS169835: MP:0005389 reproductive system phenotype
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human CTD 2013 Genes GS126646: Carbon Tetrachloride interacting genes (MeSH:D002251) in CTD
Expand Tier I Mouse MP 20 Genes GS166085: MP:0011521 decreased placental labyrinth size
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 Mouse MP 161 Genes GS164030: MP:0004817 abnormal skeletal muscle mass
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier I Mouse GO 2994 Genes GS186215: GO:0048519 negative regulation of biological process
Expand Tier I Mouse GO 8406 Genes GS177404: GO:0005737 cytoplasm
Expand Tier I Mouse GO 3080 Genes GS177265: GO:0048731 system development
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Mouse GO 3597 Genes GS188142: GO:0048856 anatomical structure development
Expand Tier I Human GO 1010 Genes GS196988: GO:0045595 regulation of cell differentiation
Expand Tier I Mouse GO 348 Genes GS181267: GO:0048568 embryonic organ development
Expand Tier I Mouse GO 4001 Genes GS183543: GO:0051179 localization
Expand Tier I Mouse 325 Genes GS136959: weight adult 1 (Wta1, Published QTL Chr 4)
Expand Tier I Human GO 25 Genes GS204418: GO:0009268 response to pH
Expand Tier I Mouse MP 814 Genes GS163226: MP:0003312 abnormal locomotor coordination
Expand Tier I Mouse MP 474 Genes GS169176: MP:0000759 abnormal skeletal muscle morphology
Expand Tier I Human 416 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Human GO 5 Genes GS196105: GO:0060856 establishment of blood-brain barrier
Expand Tier I Mouse MP 507 Genes GS166591: MP:0004087 abnormal muscle fiber morphology
Expand Tier I Mouse GO 8414 Genes GS185585: GO:0044710 single-organism metabolic process
Expand Tier I Mouse 350 Genes GS136311: NZB and NZW autoimmunity 2 (Nbwa2, Published QTL Chr 4)
Expand Tier I Mouse MP 63 Genes GS163407: MP:0004019 abnormal vitamin homeostasis
Expand Tier I Human GO 899 Genes GS201125: GO:0009790 embryo development
Expand Tier I Human CTD 19 Genes GS122957: Niacin interacting genes (MeSH:D009525) in CTD
Expand Tier I Mouse MP 93 Genes GS168454: MP:0009400 decreased skeletal muscle fiber size
Expand Tier I Human GO 806 Genes GS197478: GO:0009628 response to abiotic stimulus
Expand Tier I Mouse MP 262 Genes GS164126: MP:0001388 abnormal stationary movement
Expand Tier I Human GO 1319 Genes GS208126: GO:0009605 response to external stimulus
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 370 Genes GS195515: GO:0031667 response to nutrient levels
Expand Tier I Mouse MP 380 Genes GS165261: MP:0001393 ataxia
Expand Tier I Mouse MP 29 Genes GS165729: MP:0002730 head shaking
Expand Tier I Human GO 6769 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Mouse MP 153 Genes GS169046: MP:0009398 abnormal skeletal muscle fiber size
Expand Tier I Mouse GO 1064 Genes GS179401: GO:0005215 transporter activity
Expand Tier I Human 202 Genes GS175171: HP:0001315 Reduced tendon reflexes
Expand Tier I Mouse MP 4592 Genes GS165537: MP:0005376 homeostasis/metabolism phenotype
Expand Tier I Mouse GO 903 Genes GS184317: GO:0009790 embryo development
Expand Tier I Mouse MP 54 Genes GS169125: MP:0005400 abnormal vitamin level
Expand Tier I Mouse MP 176 Genes GS165640: MP:0002269 muscular atrophy
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Mouse 325 Genes GS136640: salmonella enteritidis susceptibility 8 (Ses8, Published QTL Chr 4)
Expand Tier I Mouse MP 574 Genes GS167217: MP:0001325 abnormal retina morphology
Expand Tier I Mouse GO 2192 Genes GS178913: GO:0042221 response to chemical stimulus
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Mouse MP 3543 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier II Mouse 351 Genes GS84155: METH responses for climbing (Published QTL, Chr 4)
Expand Tier I Mouse MP 875 Genes GS168958: MP:0003492 abnormal involuntary movement
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse MP 278 Genes GS165604: MP:0008503 abnormal spinal cord grey matter morphology
Expand Tier II Mouse 30 Genes GS34393: Striatum Gene expression correlates of Novel environment rears 15-30 min in the center in Females BXD
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human CTD 24 Genes GS127046: Gliotoxin interacting genes (MeSH:D005912) in CTD
Expand Tier III Mouse 8003 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampal tissue
Expand Tier I Mouse GO 441 Genes GS180207: GO:0045596 negative regulation of cell differentiation
Expand Tier I Human GO 2511 Genes GS207903: GO:0044281 small molecule metabolic process
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 GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Mouse 370 Genes GS136965: weight loss response 3 (Wtlr3, Published QTL Chr 4)
Expand Tier I Mouse MP 576 Genes GS168750: MP:0002191 abnormal artery morphology
Expand Tier I Human GO 537 Genes GS205331: GO:0051093 negative regulation of developmental process
Expand Tier I Human 15 Genes GS175473: HP:0200034 Skin papules
Expand Tier I Human CTD 113 Genes GS126885: Chromium interacting genes (MeSH:D002857) in CTD
Expand Tier I Mouse 378 Genes GS135376: body length 6 (Bdln6, Published QTL Chr 4)
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Mouse MP 1130 Genes GS163227: MP:0003313 abnormal locomotor activation
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Mouse MP 29 Genes GS170394: MP:0005112 abnormal spinal cord ventral horn morphology
Expand Tier I Mouse 325 Genes GS136868: triglyceride QTL 1 (Triglq1, Published QTL Chr 4)
Expand Tier I Human GO 5452 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human 313 Genes GS176642: HP:0011355 Localized skin lesion
Expand Tier I Human 344 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Mouse GO 4588 Genes GS177309: GO:1901363 heterocyclic compound binding
Expand Tier I Mouse GO 588 Genes GS184318: GO:0009792 embryo development ending in birth or egg hatching
Expand Tier I Mouse GO 2710 Genes GS192471: GO:0048869 cellular developmental process
Expand Tier I Mouse MP 79 Genes GS169923: MP:0009458 abnormal skeletal muscle size
Expand Tier I Mouse GO 9049 Genes GS180166: GO:0008152 metabolic process
Expand Tier I Mouse MP 647 Genes GS164446: MP:0005195 abnormal posterior eye segment morphology
Expand Tier I Human GO 520 Genes GS201126: GO:0009792 embryo development ending in birth or egg hatching
Expand Tier I Mouse MP 3716 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Mouse DRG 1187 Genes provisional GS87137: Table S2: List of probe-sets of genes differentially expressed among the four inbred strains of mice. Gene Ranks [DRG]
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 4144 Genes GS200341: GO:0051179 localization
Expand Tier I Mouse MP 30 Genes GS166914: MP:0005323 dystonia
Expand Tier I Human GO 157 Genes GS210474: GO:0005770 late endosome
Expand Tier I Mouse GO 8386 Genes GS189751: GO:0050794 regulation of cellular process
Expand Tier I Mouse GO 4637 Genes GS177382: GO:0097159 organic cyclic compound binding
Expand Tier I Mouse GO 124 Genes GS184345: GO:0001890 placenta development
Expand Tier I Mouse 120 Genes GS136085: keratinocyte stem cell locus 2 (Ksc2, Published QTL Chr 4)
Expand Tier I Human 399 Genes GS171100: HP:0000759 Abnormality of the peripheral nervous system
Expand Tier I Mouse GO 85 Genes GS184343: GO:0001892 embryonic placenta development
Expand Tier I Human GO 2741 Genes GS195668: GO:0042221 response to chemical stimulus
Expand Tier I Mouse 348 Genes GS135283: "alcohol preference locus 7, male specific" (Alcp7, Published QTL Chr 4)
Expand Tier I Human GO 396 Genes GS199644: GO:0009991 response to extracellular stimulus
Expand Tier II Mouse 377 Genes GS84156: METH responses for body temperature (Published QTL, Chr 4)
Expand Tier I Mouse MP 1013 Genes GS164724: MP:0001516 abnormal motor coordination/ balance
Expand Tier I Mouse GO 72 Genes GS187382: GO:0006766 vitamin metabolic process
Expand Tier I Mouse GO 3211 Genes GS192509: GO:0006810 transport
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human 16 Genes GS176886: HP:0100261 Abnormal tendon morphology
Expand Tier I Mouse MP 2406 Genes GS169391: MP:0002066 abnormal motor capabilities/coordination/movement
Expand Tier I Mouse MP 1476 Genes GS169531: MP:0005391 vision/eye phenotype
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 Mouse GO 51 Genes GS183131: GO:0006775 fat-soluble vitamin metabolic process
Expand Tier I Human 699 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Mouse GO 8942 Genes GS185492: GO:0050789 regulation of biological process
Expand Tier I Mouse MP 153 Genes GS163062: MP:0005031 abnormal trophoblast layer morphology
Expand Tier I Human GO 1 Genes GS199301: GO:0090210 regulation of establishment of blood-brain barrier
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 1138 Genes GS193812: GO:0006629 lipid metabolic process
Expand Tier I Mouse GO 5892 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier I Mouse MP 1825 Genes GS168956: MP:0003491 abnormal voluntary movement
Expand Tier I Human GO 8622 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Mouse MP 592 Genes GS165809: MP:0002864 abnormal ocular fundus morphology
Expand Tier I Mouse GO 549 Genes GS183491: GO:0060284 regulation of cell development
Expand Tier I Human 588 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Mouse 378 Genes GS136620: sucrose consumption 1 (Scon1, Published QTL Chr 4)
Expand Tier I Human GO 3 Genes GS196817: GO:0008431 vitamin E binding
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse MP 3924 Genes GS163934: MP:0001764 abnormal homeostasis
Expand Tier I Mouse GO 4073 Genes GS180034: GO:0032502 developmental process
Expand Tier I Mouse MP 88 Genes GS163064: MP:0005033 abnormal trophoblast giant cells
Expand Tier I Mouse GO 136 Genes GS179304: GO:0009636 response to toxin
Expand Tier I Human GO 1195 Genes GS196168: GO:0005215 transporter activity
Expand Tier I Human GO 3104 Genes GS203058: GO:0048519 negative regulation of biological process
Expand Tier I Mouse GO 2 Genes GS182505: GO:0090210 regulation of establishment of blood-brain barrier
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Mouse MP 175 Genes GS170151: MP:0001716 abnormal placenta labyrinth morphology
Expand Tier I Human GO 3513 Genes GS193991: GO:0048731 system development
Expand Tier I Mouse MP 1688 Genes GS168174: MP:0001919 abnormal reproductive system physiology
Expand Tier I Human CTD 531 Genes GS122992: nitrosobenzylmethylamine interacting genes (MeSH:C014707) in CTD
Expand Tier I Mouse DRG 2537 Genes provisional GS86906: Table S1: Additional data file 1 is a table listing the results of two-way ANOVA (FDR < 1%). Lists of probe sets and gene names altered by strain (3457). [DRG]
Expand Tier I Human GO 305 Genes GS197822: GO:0001701 in utero embryonic development
Expand Tier I Mouse MP 29 Genes GS166964: MP:0009413 skeletal muscle fiber atrophy
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier III Rat 3441 Genes GS135132: bHR vs bLR genes different in Nucleus Acumbens
Expand Tier I Human GO 5558 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Mouse GO 583 Genes GS190900: GO:0043009 chordate embryonic development
Expand Tier I Human GO 4 Genes GS204834: GO:0042360 vitamin E metabolic process
Expand Tier I Rat DRG 4920 Genes GS86932: Table S3: CORTEX 17K MICROARRAY [DRG]
Expand Tier I Mouse GO 122 Genes GS188395: GO:0019842 vitamin binding
Expand Tier I Mouse MP 4 Genes GS168955: MP:0011231 abnormal vitamin E level
Expand Tier I Human 416 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Mouse GO 6947 Genes GS192918: GO:0050896 response to stimulus
Expand Tier I Human CTD 1291 Genes GS125402: Diethylnitrosamine interacting genes (MeSH:D004052) in CTD
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Mouse MP 466 Genes GS163138: MP:0005253 abnormal eye physiology
Expand Tier I Human GO 137 Genes GS205251: GO:0019842 vitamin binding
Expand Tier III Rat 3441 Genes GS135133: bHR vs bLR genes different in Hippocampus
Expand Tier I Mouse GO 939 Genes GS190471: GO:0005829 cytosol
Expand Tier I Human CTD 794 Genes GS125548: Doxorubicin interacting genes (MeSH:D004317) in CTD
Expand Tier I Human 6 Genes GS176643: HP:0010732 Nodular changes affecting the eyelids
Expand Tier I Mouse MP 239 Genes GS169262: MP:0003084 abnormal skeletal muscle fiber morphology
Expand Tier I Human GO 493 Genes GS200286: GO:0060284 regulation of cell development
Expand Tier I Human 6 Genes GS175288: HP:0010604 Cysts of the eyelid
Expand Tier I Human GO 58 Genes GS199931: GO:0006775 fat-soluble vitamin metabolic process
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Mouse GO 487 Genes GS191180: GO:0005768 endosome
Expand Tier I Mouse MP 44 Genes GS169136: MP:0005401 abnormal fat-soluble vitamin level
Expand Tier I Mouse 355 Genes GS135623: cholesterol 8 (Chol8, Published QTL Chr 4)
Expand Tier I Mouse GO 3 Genes GS187976: GO:0042360 vitamin E metabolic process
Expand Tier I Mouse MP 86 Genes GS169944: MP:0004142 abnormal muscle tone
Expand Tier I Mouse GO 7552 Genes GS180452: GO:0044237 cellular metabolic process
Expand Tier I Mouse GO 105 Genes GS181530: GO:0010721 negative regulation of cell development
Expand Tier I Human GO 6585 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Mouse MP 15 Genes GS170145: MP:0001715 placental labyrinth hypoplasia
Expand Tier I Mouse GO 108 Genes GS193529: GO:0005770 late endosome
Expand Tier I Mouse 378 Genes GS136016: heart failure modifier 3 (Hrtfm3, Published QTL Chr 4)
Expand Tier I Mouse MP 164 Genes GS163724: MP:0000436 abnormal head movements
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 CTD 4389 Genes GS123768: Cyclosporine interacting genes (MeSH:D016572) in CTD
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Mouse MP 1485 Genes GS166712: MP:0002161 abnormal fertility/fecundity
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Mouse GO 1378 Genes GS188287: GO:0048468 cell development
Expand Tier I Mouse MP 226 Genes GS169032: MP:0005551 abnormal eye electrophysiology
Expand Tier I Human GO 433 Genes GS196987: GO:0045596 negative regulation of cell differentiation
Expand Tier I Mouse 133 Genes GS135465: blood pressure QTL 22 (Bpq22, Published QTL Chr 4)
Expand Tier I Mouse GO 1463 Genes GS189746: GO:0050793 regulation of developmental process
Expand Tier I Human GO 8702 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Mouse MP 2644 Genes GS169829: MP:0005385 cardiovascular system phenotype
Expand Tier I Human GO 226 Genes GS196074: GO:0009636 response to toxin
Expand Tier I Human GO 1 Genes GS199300: GO:0090212 negative regulation of establishment of blood-brain barrier
Expand Tier I Human CTD 870 Genes GS123911: Ozone interacting genes (MeSH:D010126) in CTD
Expand Tier I Human 474 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Mouse DRG 2693 Genes GS87380: Table S1: Additional data file 1 is a table listing the results of two-way ANOVA (FDR < 1%). (Whole Table) [DRG]
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Mouse GO 3268 Genes GS177721: GO:0051234 establishment of localization
Expand Tier I Human GO 5369 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier I Mouse MP 2200 Genes GS165465: MP:0003633 abnormal nervous system physiology
Expand Tier I Human GO 7689 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier I Mouse GO 8072 Genes GS184218: GO:0071704 organic substance metabolic process
Expand Tier I Mouse GO 4478 Genes GS184435: GO:0046483 heterocycle metabolic process
Expand Tier I Mouse MP 20 Genes GS166969: MP:0011519 abnormal placenta labyrinth size
Expand Tier I Human 95 Genes GS170930: HP:0001284 Areflexia
Expand Tier I Human GO 124 Genes GS204243: GO:0006766 vitamin metabolic process
Expand Tier I Mouse GO 369 Genes GS181032: GO:0001701 in utero embryonic development
Expand Tier I Mouse GO 2439 Genes GS179580: GO:0036094 small molecule binding
Expand Tier I Human GO 1456 Genes GS205144: GO:0048468 cell development
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human CTD 4423 Genes GS123718: Ethinyl Estradiol interacting genes (MeSH:D004997) in CTD
Expand Tier I Mouse 98 Genes GS136172: leishmaniasis resistance 9 (Lmr9, Published QTL Chr 4)
Expand Tier I Human CTD 1601 Genes GS123916: Aflatoxin B1 interacting genes (MeSH:D016604) in CTD
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human GO 514 Genes GS207807: GO:0043009 chordate embryonic development
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 743 Genes GS168294: MP:0003699 abnormal female reproductive system physiology
Expand Tier I Mouse MP 2099 Genes GS165616: MP:0002127 abnormal cardiovascular system morphology
Expand Tier I Mouse MP 1615 Genes GS165789: MP:0005369 muscle phenotype
Expand Tier I Mouse GO 24 Genes GS187553: GO:0009268 response to pH
Expand Tier I Mouse MP 1692 Genes GS169833: MP:0005380 embryogenesis phenotype
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Mouse MP 376 Genes GS168021: MP:0000745 tremors
Expand Tier I Human 13 Genes GS175483: HP:0000991 Xanthomatosis
Expand Tier I Mouse GO 553 Genes GS188475: GO:0051093 negative regulation of developmental process
Expand Tier I Human 411 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human GO 118 Genes GS198320: GO:0010721 negative regulation of cell development
Expand Tier I Mouse DRG 613 Genes provisional GS87058: Table S2: Cocaine Regulation of H4 Acetylation. [DRG]
Expand Tier I Human GO 329 Genes GS198056: GO:0048568 embryonic organ development
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Mouse MP 476 Genes GS169227: MP:0001405 impaired coordination
Expand Tier I Human GO 2368 Genes GS207365: GO:0005829 cytosol
Expand Tier I Mouse GO 621 Genes GS180679: GO:0009628 response to abiotic stimulus
Expand Tier I Mouse MP 903 Genes GS167075: MP:0001924 infertility
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Mouse MP 34 Genes GS169186: MP:0000754 paresis
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Mouse 333 Genes GS135304: angiogenesis due to FGF2 QTL 1 (Angfq1, Published QTL Chr 4)
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
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 GO 2538 Genes GS190893: GO:0030154 cell differentiation
Expand Tier I Mouse MP 167 Genes GS166604: MP:0005338 atherosclerotic lesions
Expand Tier I Mouse GO 8 Genes GS179338: GO:0060856 establishment of blood-brain barrier
Expand Tier I Human GO 564 Genes GS208092: GO:0005768 endosome
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human GO 244 Genes GS197390: GO:0007584 response to nutrient
Expand Tier I Human 6 Genes GS174571: HP:0001114 Xanthelasma
Expand Tier I Mouse MP 396 Genes GS165214: MP:0001711 abnormal placenta morphology
Expand Tier I Human 416 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier I Human GO 2824 Genes GS209411: GO:0048869 cellular developmental process
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Mouse GO 3605 Genes GS190682: GO:0007275 multicellular organismal development
Expand Tier I Mouse 129 Genes GS136954: weight 2 (Wght2, Published QTL Chr 4)
Expand Tier I Human 261 Genes GS176172: HP:0001251 Ataxia
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse MP 43 Genes GS165215: MP:0001713 decreased trophoblast giant cell number
Expand Tier I Mouse GO 1038 Genes GS180208: GO:0045595 regulation of cell differentiation
Expand Tier I Mouse MP 346 Genes GS167073: MP:0001926 female infertility
Expand Tier I Mouse MP 1307 Genes GS170198: MP:0001614 abnormal blood vessel morphology
Expand Tier I Mouse MP 692 Genes GS163620: MP:0002086 abnormal extraembryonic tissue morphology
Expand Tier I Human GO 74 Genes GS201150: GO:0001892 embryonic placenta development
Expand Tier I Human GO 3318 Genes GS209452: GO:0006810 transport
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Mouse MP 1672 Genes GS165260: MP:0001392 abnormal locomotor behavior
Expand Tier I Mouse MP 1692 Genes GS169603: MP:0001672 abnormal embryogenesis/ development
Expand Tier I Mouse MP 1385 Genes GS163971: MP:0002092 abnormal eye morphology
Expand Tier I Mouse GO 2 Genes GS180044: GO:0008431 vitamin E binding
Expand Tier I Human CTD 5725 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Mouse 285 Genes GS128590: Average rotarod training latency Chr# 4
Expand Tier I Human GO 3372 Genes GS194459: GO:0051234 establishment of localization
Expand Tier I Mouse MP 295 Genes GS169967: MP:0001408 stereotypic behavior
Expand Tier I Mouse MP 48 Genes GS168739: MP:0009417 skeletal muscle atrophy
Expand Tier I Mouse GO 9323 Genes GS180152: GO:0065007 biological regulation
Expand Tier I Human 7 Genes GS172867: HP:0200040 Skin cysts
Expand Tier I Mouse MP 148 Genes GS163024: MP:0004819 decreased skeletal muscle mass
Expand Tier I Mouse MP 574 Genes GS166743: MP:0002229 neurodegeneration
Expand Tier I Human 2 Genes GS177005: HP:0010874 Tendon xanthomatosis
Expand Tier I Mouse GO 2279 Genes GS186488: GO:0048513 organ development
Expand Tier I Mouse MP 123 Genes GS167220: MP:0001326 retinal degeneration
Expand Tier I Mouse MP 52 Genes GS165330: MP:0009403 increased variability of skeletal muscle fiber size
Expand Tier I Mouse MP 3543 Genes GS169095: MP:0004924 abnormal behavior
Expand Tier I Mouse MP 21 Genes GS170124: MP:0001328 disorganized retinal layers
Expand Tier I Mouse 378 Genes GS136715: susceptibility to lung cancer 18 (Sluc18, Published QTL Chr 4)
Expand Tier I Human GO 4567 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human GO 1434 Genes GS206618: GO:0050793 regulation of developmental process