Gene Details



MESP2 and homologs in 3 species are found in 554 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 Human GO 1050 Genes GS202082: GO:0051254 positive regulation of RNA metabolic process
Expand Tier I Human 99 Genes GS172242: HP:0004930 Abnormality of the pulmonary vasculature
Expand Tier I Human 146 Genes GS171320: HP:0100360 Contractures of the joints of the upper limbs
Expand Tier I Mouse MP 127 Genes GS166501: MP:0003189 fused joints
Expand Tier I Mouse GO 1018 Genes GS185261: GO:0051254 positive regulation of RNA metabolic process
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human GO 1171 Genes GS203018: GO:0045935 positive regulation of nucleobase-containing compound metabolic process
Expand Tier I Mouse MP 599 Genes GS164506: MP:0001698 decreased embryo size
Expand Tier I Mouse MP 3631 Genes GS169830: MP:0005384 cellular phenotype
Expand Tier I Human 269 Genes GS172261: HP:0000357 Abnormal location of ears
Expand Tier I Human 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Mouse MP 10 Genes GS167779: MP:0002632 vestigial tail
Expand Tier I Mouse 907 Genes GS128584: Rotarod Baseline Chr# 7
Expand Tier I Mouse 612 Genes GS136309: New Zealand Black autoimmunity 3 (Nba3, Published QTL Chr 7)
Expand Tier I Human 178 Genes GS176151: HP:0000256 Macrocephaly
Expand Tier I Mouse 612 Genes GS136498: proteoglycan induced arthritis 3 (Pgia3, Published QTL Chr 7)
Expand Tier I Mouse MP 242 Genes GS167156: MP:0000459 abnormal presacral vertebrae morphology
Expand Tier I Human 360 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Mouse GO 4619 Genes GS191019: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Mouse MP 679 Genes GS170021: MP:0011087 complete neonatal lethality
Expand Tier I Human 533 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Human 786 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 177 Genes GS172293: HP:0001511 Intrauterine growth retardation
Expand Tier I Human 264 Genes GS173014: HP:0010936 Abnormality of the lower urinary tract
Expand Tier I Mouse GO 3776 Genes GS187887: GO:0080090 regulation of primary metabolic process
Expand Tier I Human 639 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Mouse MP 67 Genes GS169484: MP:0000729 abnormal myogenesis
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 GO 5223 Genes GS207857: GO:0009058 biosynthetic process
Expand Tier I Mouse 312 Genes GS135631: collagen induced arthritis 41 (Cia41, Published QTL Chr 7)
Expand Tier I Mouse GO 3311 Genes GS192279: GO:0007166 cell surface receptor signaling pathway
Expand Tier I Human 426 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Mouse MP 3019 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier I Mouse MP 8 Genes GS167059: MP:0004683 absent intervertebral disk
Expand Tier I Mouse GO 2763 Genes GS189669: GO:2000112 regulation of cellular macromolecule biosynthetic process
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 2896 Genes GS206108: GO:2001141 regulation of RNA biosynthetic process
Expand Tier I Human 157 Genes GS171718: HP:0002808 Kyphosis
Expand Tier I Mouse GO 13 Genes GS187058: GO:0042074 cell migration involved in gastrulation
Expand Tier I Mouse GO 4353 Genes GS192017: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human 121 Genes GS172789: HP:0001537 Umbilical hernia
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Mouse 613 Genes GS135251: adiposity 3 (Adip3, Published QTL Chr 7)
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier I Mouse MP 67 Genes GS168298: MP:0003651 abnormal axon outgrowth
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human GO 4169 Genes GS207925: GO:0034645 cellular macromolecule biosynthetic process
Expand Tier I Mouse GO 3599 Genes GS186227: GO:0090304 nucleic acid metabolic process
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Mouse GO 3865 Genes GS193238: GO:0031323 regulation of cellular metabolic process
Expand Tier I Mouse MP 870 Genes GS168593: MP:0002088 abnormal embryonic growth/weight/body size
Expand Tier I Human 165 Genes GS171654: HP:0003121 Limb joint contracture
Expand Tier I Human GO 208 Genes GS201404: GO:0009952 anterior/posterior pattern specification
Expand Tier I Human GO 3917 Genes GS203908: GO:0016070 RNA metabolic process
Expand Tier I Mouse GO 2955 Genes GS181893: GO:0048522 positive regulation of cellular process
Expand Tier I Human GO 4811 Genes GS204612: GO:0019222 regulation of metabolic process
Expand Tier I Mouse GO 3597 Genes GS188142: GO:0048856 anatomical structure development
Expand Tier I Mouse GO 64 Genes GS187973: GO:0061053 somite development
Expand Tier I Human 486 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Mouse 615 Genes GS135471: blood pressure QTL 7 (Bpq7, Published QTL Chr 7)
Expand Tier I Mouse GO 4001 Genes GS183543: GO:0051179 localization
Expand Tier I Human 392 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Human GO 4 Genes GS204184: GO:0008078 mesodermal cell migration
Expand Tier I Mouse MP 533 Genes GS164258: MP:0002084 abnormal developmental patterning
Expand Tier I Mouse GO 827 Genes GS189835: GO:0051674 localization of cell
Expand Tier I Mouse MP 1571 Genes GS164133: MP:0005076 abnormal cell differentiation
Expand Tier I Mouse GO 4114 Genes GS193414: GO:0044249 cellular biosynthetic process
Expand Tier I Human 239 Genes GS174066: HP:0100737 Abnormality of the hard palate
Expand Tier I Mouse MP 50 Genes GS169928: MP:0004173 abnormal intervertebral disk morphology
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human GO 3573 Genes GS203607: GO:0034654 nucleobase-containing compound biosynthetic process
Expand Tier I Mouse GO 500 Genes GS185033: GO:0048598 embryonic morphogenesis
Expand Tier I Mouse MP 25 Genes GS169781: MP:0000737 abnormal myotome development
Expand Tier I Mouse MP 1038 Genes GS169114: MP:0004196 abnormal prenatal growth/weight/body size
Expand Tier I Mouse GO 8414 Genes GS185585: GO:0044710 single-organism metabolic process
Expand Tier I Mouse GO 763 Genes GS178922: GO:0003700 sequence-specific DNA binding transcription factor activity
Expand Tier I Mouse GO 1832 Genes GS187708: GO:0009893 positive regulation of metabolic process
Expand Tier I Human GO 899 Genes GS201125: GO:0009790 embryo development
Expand Tier I Human GO 1008 Genes GS204232: GO:0001071 nucleic acid binding transcription factor activity
Expand Tier I Mouse 324 Genes GS135926: hepatocarcinogenesis susceptibility 1 (Hcs1, Published QTL Chr 7)
Expand Tier I Mouse MP 994 Genes GS168502: MP:0002058 neonatal lethality
Expand Tier I Mouse MP 261 Genes GS168497: MP:0001256 abnormal body length
Expand Tier I Human 741 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Mouse MP 272 Genes GS167805: MP:0000150 abnormal rib morphology
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Mouse MP 105 Genes GS164406: MP:0004609 vertebral fusion
Expand Tier I Mouse 221 Genes GS127940: Cerebellum only - Allen Mouse Brain Atlas
Expand Tier I Human 34 Genes GS170804: HP:0003298 Spina bifida occulta
Expand Tier I Human 492 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human GO 1244 Genes GS196080: GO:0040011 locomotion
Expand Tier I Human GO 1393 Genes GS193937: GO:0006366 transcription from RNA polymerase II promoter
Expand Tier I Human 403 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 7 Genes GS175186: HP:0010772 Anomalous pulmonary venous return
Expand Tier I Mouse MP 1183 Genes GS166409: MP:0002114 abnormal axial skeleton morphology
Expand Tier I Mouse GO 5111 Genes GS189484: GO:0023052 signaling
Expand Tier I Human GO 2332 Genes GS195643: GO:0003677 DNA binding
Expand Tier I Human GO 1842 Genes GS198572: GO:0010604 positive regulation of macromolecule metabolic process
Expand Tier I Human 235 Genes GS175523: HP:0000008 Abnormality of female internal genitalia
Expand Tier I Mouse GO 903 Genes GS184317: GO:0009790 embryo development
Expand Tier I Human 129 Genes GS172916: HP:0003312 Abnormal form of the vertebral bodies
Expand Tier I Human GO 306 Genes GS209956: GO:0003002 regionalization
Expand Tier I Human GO 999 Genes GS195340: GO:0045893 positive regulation of transcription, DNA-dependent
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Mouse MP 221 Genes GS168408: MP:0000585 kinked tail
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Mouse GO 75 Genes GS181035: GO:0001704 formation of primary germ layer
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier II Mouse 489 Genes GS84192: ethanol conditioned taste aversion (Published QTL, Chr 7)
Expand Tier I Mouse MP 138 Genes GS166438: MP:0002231 abnormal primitive streak morphology
Expand Tier I Human GO 466 Genes GS204511: GO:0048729 tissue morphogenesis
Expand Tier I Mouse 324 Genes GS135395: body growth early QTL 5 (Bgeq5, Published QTL Chr 7)
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human GO 3118 Genes GS206544: GO:2000112 regulation of cellular macromolecule biosynthetic process
Expand Tier III Mouse 8003 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampal tissue
Expand Tier I Mouse GO 3021 Genes GS182703: GO:0051171 regulation of nitrogen compound metabolic process
Expand Tier I Human GO 1256 Genes GS210178: GO:0031328 positive regulation of cellular biosynthetic process
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 32 Genes GS176375: HP:0000269 Prominent occiput
Expand Tier I Mouse MP 983 Genes GS166244: MP:0002752 abnormal somatic nervous system morphology
Expand Tier I Human 281 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human GO 1214 Genes GS198360: GO:0006357 regulation of transcription from RNA polymerase II promoter
Expand Tier I Human GO 2050 Genes GS203406: GO:0009653 anatomical structure morphogenesis
Expand Tier I Mouse GO 4500 Genes GS186790: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Mouse 531 Genes GS136523: platelet quantitative locus 2 (Pltq2, Published QTL Chr 7)
Expand Tier I Human GO 5452 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human GO 1198 Genes GS199501: GO:0051173 positive regulation of nitrogen compound metabolic process
Expand Tier I Human 403 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Mouse MP 12 Genes GS162830: MP:0008530 abnormal rostral-caudal patterning of the somites
Expand Tier I Mouse MP 70 Genes GS166437: MP:0002230 abnormal primitive streak formation
Expand Tier I Mouse GO 588 Genes GS184318: GO:0009792 embryo development ending in birth or egg hatching
Expand Tier I Human GO 4151 Genes GS206329: GO:0060255 regulation of macromolecule metabolic process
Expand Tier I Mouse 786 Genes GS136762: soft tissue heal 6 (Stheal6, Published QTL Chr 7)
Expand Tier I Human GO 5948 Genes GS195199: GO:0005634 nucleus
Expand Tier I Mouse GO 1232 Genes GS193234: GO:0031328 positive regulation of cellular biosynthetic process
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 Human 446 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier I Human GO 4144 Genes GS200341: GO:0051179 localization
Expand Tier I Mouse MP 101 Genes GS166581: MP:0004599 abnormal vertebral arch morphology
Expand Tier I Mouse GO 2540 Genes GS189240: GO:2001141 regulation of RNA biosynthetic process
Expand Tier I Mouse MP 384 Genes GS165361: MP:0004624 abnormal thoracic cage morphology
Expand Tier I Mouse MP 80 Genes GS164488: MP:0005225 abnormal vertebrae development
Expand Tier I Mouse GO 1149 Genes GS186178: GO:0045935 positive regulation of nucleobase-containing compound metabolic process
Expand Tier I Mouse GO 8386 Genes GS189751: GO:0050794 regulation of cellular process
Expand Tier I Mouse MP 1420 Genes GS163052: MP:0000266 abnormal heart morphology
Expand Tier I Mouse GO 5654 Genes GS182325: GO:0051716 cellular response to stimulus
Expand Tier I Mouse GO 92 Genes GS192057: GO:0007219 Notch signaling pathway
Expand Tier I Mouse MP 134 Genes GS163872: MP:0000961 abnormal dorsal root ganglion morphology
Expand Tier I Mouse GO 2588 Genes GS187343: GO:0006351 transcription, DNA-dependent
Expand Tier II Mouse 168 Genes GS35425: Whole Brain Gene expression correlates of Distance traveled (cm) during the second five minute bin after saline in Females & Males BXD
Expand Tier I Human 148 Genes GS172906: HP:0003319 Abnormality of the cervical spine
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
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 MP 13 Genes GS164859: MP:0004604 abnormal vertebral pedicle morphology
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier I Mouse MP 12 Genes GS167741: MP:0004206 abnormal dermomyotome development
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 1087 Genes GS192345: GO:0010628 positive regulation of gene expression
Expand Tier I Human GO 8622 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human GO 3401 Genes GS200312: GO:0019219 regulation of nucleobase-containing compound metabolic process
Expand Tier I Mouse GO 713 Genes GS177859: GO:0045944 positive regulation of transcription from RNA polymerase II promoter
Expand Tier I Mouse GO 1147 Genes GS191150: GO:0010557 positive regulation of macromolecule biosynthetic process
Expand Tier I Mouse GO 58 Genes GS181034: GO:0001707 mesoderm formation
Expand Tier II Mouse 145 Genes GS35430: Whole Brain Gene expression correlates of Distance traveled (cm) during the second five minute bin after saline in Females BXD
Expand Tier I Mouse MP 48 Genes GS165365: MP:0004620 cervical vertebral fusion
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 Mouse MP 176 Genes GS168687: MP:0000592 short tail
Expand Tier I Mouse 502 Genes GS135848: femoral cross-sectional area 6 (Fcsa6, Published QTL Chr 7)
Expand Tier I Human GO 4314 Genes GS204746: GO:0080090 regulation of primary metabolic process
Expand Tier I Human GO 82 Genes GS197825: GO:0001704 formation of primary germ layer
Expand Tier I Mouse MP 3437 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Mouse 324 Genes GS135448: bone length and organs 4 (Bod4, Published QTL Chr 7)
Expand Tier I Human 53 Genes GS173835: HP:0003422 Vertebral segmentation defect
Expand Tier I Human GO 3626 Genes GS198456: GO:0019438 aromatic compound biosynthetic process
Expand Tier I Mouse MP 247 Genes GS163546: MP:0001688 abnormal somite development
Expand Tier I Mouse 445 Genes GS135609: circulating hormone level QTL 18 (Chlq18, Published QTL Chr 7)
Expand Tier I Mouse GO 2907 Genes GS181667: GO:0019438 aromatic compound biosynthetic process
Expand Tier I Mouse GO 583 Genes GS190900: GO:0043009 chordate embryonic development
Expand Tier I Mouse MP 60 Genes GS164514: MP:0001690 failure of somite differentiation
Expand Tier I Human GO 3310 Genes GS194088: GO:0003676 nucleic acid binding
Expand Tier I Human 298 Genes GS174145: HP:0005918 Abnormality of phalanx of finger
Expand Tier I Mouse GO 3090 Genes GS188511: GO:0010468 regulation of gene expression
Expand Tier I Mouse GO 290 Genes GS193014: GO:0003002 regionalization
Expand Tier I Mouse MP 4173 Genes GS165527: MP:0005378 growth/size phenotype
Expand Tier I Mouse 531 Genes GS135257: anti-erythrocyte autoantibody modifier 2 (Aem2, Published QTL Chr 7)
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 Mouse MP 14 Genes GS165364: MP:0004621 lumbar vertebral fusion
Expand Tier I Mouse 445 Genes GS135882: femur geometry 6 (Fmgty6, Published QTL Chr 7)
Expand Tier I Human 130 Genes GS173970: HP:0009473 Joint contracture of the hand
Expand Tier I Mouse GO 994 Genes GS178589: GO:0045893 positive regulation of transcription, DNA-dependent
Expand Tier I Mouse GO 933 Genes GS178813: GO:0046983 protein dimerization activity
Expand Tier III Mouse 8392 Genes GS128199: Alcohol Preference union of 86 Gene Sets
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Mouse GO 2947 Genes GS193236: GO:0031326 regulation of cellular biosynthetic process
Expand Tier I Human 397 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human GO 63 Genes GS207813: GO:0048332 mesoderm morphogenesis
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 Mouse MP 91 Genes GS167503: MP:0003054 spina bifida
Expand Tier I Mouse GO 3382 Genes GS191021: GO:0034645 cellular macromolecule biosynthetic process
Expand Tier I Human GO 3487 Genes GS199499: GO:0051171 regulation of nitrogen compound metabolic process
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Human 17 Genes GS171717: HP:0005108 Abnormality of the intervertebral disk
Expand Tier I Human 384 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human 137 Genes GS171202: HP:0100627 Displacement of the external urethral meatus
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human GO 493 Genes GS201848: GO:0048598 embryonic morphogenesis
Expand Tier I Mouse 605 Genes GS129144: insulin dependent diabetes susceptibility 27 (Idd27 Published QTL Chr 7)
Expand Tier I Human 221 Genes GS172288: HP:0000358 Posteriorly rotated ears
Expand Tier I Human 39 Genes GS172815: HP:0000337 Broad forehead
Expand Tier I Mouse MP 181 Genes GS169017: MP:0002932 abnormal joint morphology
Expand Tier I Mouse 324 Genes GS136234: mandible length 8 (Manln8, Published QTL Chr 7)
Expand Tier I Mouse GO 3978 Genes GS188506: GO:0010467 gene expression
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Mouse MP 248 Genes GS166029: MP:0000960 abnormal sensory ganglion morphology
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 518 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human GO 2875 Genes GS195291: GO:0006355 regulation of transcription, DNA-dependent
Expand Tier I Human GO 5369 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier I Human 28 Genes GS173311: HP:0010651 Abnormality of the meninges
Expand Tier I Human GO 3344 Genes GS205369: GO:0010468 regulation of gene expression
Expand Tier I Mouse GO 1204 Genes GS188763: GO:0009888 tissue development
Expand Tier I Mouse GO 4218 Genes GS192073: GO:1901576 organic substance biosynthetic process
Expand Tier I Mouse GO 7644 Genes GS188399: GO:0044238 primary metabolic process
Expand Tier I Mouse GO 2984 Genes GS188762: GO:0009889 regulation of biosynthetic process
Expand Tier I Human GO 7689 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier I Human 76 Genes GS172219: HP:0010301 Spinal dysraphism
Expand Tier I Human GO 1179 Genes GS208060: GO:0010557 positive regulation of macromolecule biosynthetic process
Expand Tier I Mouse GO 4478 Genes GS184435: GO:0046483 heterocycle metabolic process
Expand Tier I Human 117 Genes GS170853: HP:0006261 Abnormality of phalangeal joints of the hand
Expand Tier I Mouse GO 765 Genes GS187370: GO:0001071 nucleic acid binding transcription factor activity
Expand Tier I Human 112 Genes GS171810: HP:0005651 Flexion contracture of finger
Expand Tier I Mouse MP 26 Genes GS170265: MP:0006029 abnormal sclerotome morphology
Expand Tier I Human GO 110 Genes GS203402: GO:0007498 mesoderm development
Expand Tier I Mouse MP 1416 Genes GS164261: MP:0002081 perinatal lethality
Expand Tier I Human 64 Genes GS175226: HP:0008713 Genitourinary tract malformation
Expand Tier I Mouse GO 3293 Genes GS186214: GO:0048518 positive regulation of biological process
Expand Tier I Human GO 907 Genes GS196918: GO:0048870 cell motility
Expand Tier I Human GO 3737 Genes GS194038: GO:1901362 organic cyclic compound biosynthetic process
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 Mouse MP 99 Genes GS167525: MP:0000154 rib fusion
Expand Tier I Human 262 Genes GS172033: HP:0000369 Low-set ears
Expand Tier I Human CTD 4423 Genes GS123718: Ethinyl Estradiol interacting genes (MeSH:D004997) in CTD
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 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 Mouse MP 1817 Genes GS168149: MP:0005508 abnormal skeleton morphology
Expand Tier I Human 37 Genes GS174317: HP:0010306 Short thorax
Expand Tier I Human 143 Genes GS174721: HP:0000772 Abnormality of the ribs
Expand Tier I Mouse MP 3110 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Mouse MP 2099 Genes GS165616: MP:0002127 abnormal cardiovascular system morphology
Expand Tier I Mouse MP 1615 Genes GS165789: MP:0005369 muscle phenotype
Expand Tier I Human GO 3324 Genes GS210180: GO:0031326 regulation of cellular biosynthetic process
Expand Tier I Mouse MP 1692 Genes GS169833: MP:0005380 embryogenesis phenotype
Expand Tier I Mouse 324 Genes GS135814: ether anesthesia 1 (Etan1, Published QTL Chr 7)
Expand Tier I Mouse 686 Genes GS135762: experimental allergic encephalomyelitis susceptibility 4 (Eae4, Published QTL Chr 7)
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 GO 3354 Genes GS205622: GO:0009889 regulation of biosynthetic process
Expand Tier I Mouse GO 4 Genes GS187327: GO:0008078 mesodermal cell migration
Expand Tier I Mouse GO 2835 Genes GS191151: GO:0010556 regulation of macromolecule biosynthetic process
Expand Tier I Human GO 1079 Genes GS209282: GO:0010628 positive regulation of gene expression
Expand Tier I Mouse GO 3757 Genes GS189460: GO:0060255 regulation of macromolecule metabolic process
Expand Tier I Mouse MP 108 Genes GS169785: MP:0000733 abnormal muscle development
Expand Tier I Human 189 Genes GS176745: HP:0010866 Abdominal wall defect
Expand Tier I Mouse MP 1989 Genes GS169530: MP:0005390 skeleton phenotype
Expand Tier I Mouse GO 5247 Genes GS178448: GO:0005634 nucleus
Expand Tier I Human 291 Genes GS175335: HP:0000036 Abnormality of the penis
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 110 Genes GS173939: HP:0006101 Finger syndactyly
Expand Tier I Mouse GO 18 Genes GS184118: GO:0023019 signal transduction involved in regulation of gene expression
Expand Tier I Mouse 314 Genes GS135308: angle of entrainment 4 (Angle4, Published QTL Chr 7)
Expand Tier I Mouse MP 2485 Genes GS168012: MP:0010832 lethality during fetal growth through weaning
Expand Tier I Mouse MP 710 Genes GS167922: MP:0000959 abnormal somatic sensory system morphology
Expand Tier I Human 112 Genes GS172569: HP:0000343 Long philtrum
Expand Tier I Human 285 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier I Human 378 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier I Human GO 59 Genes GS197824: GO:0001707 mesoderm formation
Expand Tier I Human GO 3199 Genes GS208061: GO:0010556 regulation of macromolecule biosynthetic process
Expand Tier I Mouse GO 2536 Genes GS178537: GO:0006355 regulation of transcription, DNA-dependent
Expand Tier I Mouse 330 Genes GS136203: lung tumor shape-determining 5 (Ltsd5, Published QTL Chr 7)
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Mouse 415 Genes GS136660: skin tumor susceptibility 1 (Skts1, Published QTL Chr 7)
Expand Tier I Mouse GO 5111 Genes GS187146: GO:0044700 single organism signaling
Expand Tier I Human GO 1178 Genes GS207161: GO:0006928 cellular component movement
Expand Tier I Mouse MP 574 Genes GS168379: MP:0002151 abnormal neural tube morphology/development
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 GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Mouse MP 14488 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Mouse MP 366 Genes GS166192: MP:0009937 abnormal neuron differentiation
Expand Tier I Mouse MP 1108 Genes GS166117: MP:0002108 abnormal muscle morphology
Expand Tier I Mouse MP 122 Genes GS164105: MP:0003047 abnormal thoracic vertebrae morphology
Expand Tier I Human 49 Genes GS173398: HP:0000776 Congenital diaphragmatic hernia
Expand Tier I Human 245 Genes GS176694: HP:0009810 Abnormality of the joints of the upper limbs
Expand Tier I Mouse GO 478 Genes GS187648: GO:0048729 tissue morphogenesis
Expand Tier I Mouse GO 72 Genes GS186079: GO:0035282 segmentation
Expand Tier I Mouse GO 3136 Genes GS187045: GO:0016070 RNA metabolic process
Expand Tier I Human GO 4593 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Human GO 4377 Genes GS210182: GO:0031323 regulation of cellular metabolic process
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 Human GO 6 Genes GS207964: GO:0007509 mesoderm migration involved in gastrulation
Expand Tier I Human 470 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Mouse MP 65 Genes GS166947: MP:0001683 absent mesoderm
Expand Tier I Human 64 Genes GS176161: HP:0100589 Urogenital fistula
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Mouse 2087 Genes GS128573: Ethanol Induced Hypothermia Chr# 7
Expand Tier I Mouse GO 2981 Genes GS177761: GO:0044271 cellular nitrogen compound biosynthetic process
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 409 Genes GS175670: HP:0007364 Aplasia/Hypoplasia of the cerebrum
Expand Tier I Mouse GO 3605 Genes GS190682: GO:0007275 multicellular organismal development
Expand Tier I Human 210 Genes GS175990: HP:0000463 Anteverted nares
Expand Tier I Mouse GO 1684 Genes GS181783: GO:0010604 positive regulation of macromolecule metabolic process
Expand Tier I Mouse GO 107 Genes GS183345: GO:0001667 ameboidal cell migration
Expand Tier I Mouse MP 8 Genes GS164863: MP:0004600 abnormal vertebral transverse process morphology
Expand Tier I Human GO 1880 Genes GS210181: GO:0031325 positive regulation of cellular metabolic process
Expand Tier I Mouse 324 Genes GS135787: "early growth rate, maternal effect 3" (Egrm3, Published QTL Chr 7)
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human GO 2957 Genes GS202080: GO:0051252 regulation of RNA metabolic process
Expand Tier I Mouse MP 141 Genes GS166579: MP:0005221 abnormal rostral-caudal axis patterning
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Mouse 796 Genes GS136153: limb length QTL 3 (Lmblgq3, Published QTL Chr 7)
Expand Tier II Mouse 490 Genes GS84193: alcohol preference locus 11, male specific (Alcp11, Published QTL, Chr 7)
Expand Tier I Mouse MP 1307 Genes GS170198: MP:0001614 abnormal blood vessel morphology
Expand Tier I Human 180 Genes GS175902: HP:0003468 Abnormality of the vertebrae
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Mouse MP 953 Genes GS165160: MP:0006207 embryonic lethality during organogenesis
Expand Tier I Mouse MP 344 Genes GS170107: MP:0003720 abnormal neural tube closure
Expand Tier I Human GO 1981 Genes GS204568: GO:0009893 positive regulation of metabolic process
Expand Tier I Mouse MP 26 Genes GS169156: MP:0004704 short vertebral column
Expand Tier I Mouse GO 6 Genes GS191057: GO:0007509 mesoderm migration involved in gastrulation
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Mouse MP 210 Genes GS163825: MP:0001258 decreased body length
Expand Tier I Human 237 Genes GS171395: HP:0000175 Cleft palate
Expand Tier I Human 545 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I 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 Mouse GO 6204 Genes GS184629: GO:0005515 protein binding
Expand Tier I Mouse MP 6 Genes GS164858: MP:0004605 abnormal vertebral lamina morphology
Expand Tier I Mouse MP 1692 Genes GS169603: MP:0001672 abnormal embryogenesis/ development
Expand Tier I Human 737 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Mouse MP 513 Genes GS166404: MP:0002113 abnormal skeleton development
Expand Tier I Human 8 Genes GS172183: HP:0011718 Abnormality of the pulmonary veins
Expand Tier I Human CTD 5725 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
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 Mouse GO 9323 Genes GS180152: GO:0065007 biological regulation
Expand Tier I Mouse GO 193 Genes GS184601: GO:0009952 anterior/posterior pattern specification
Expand Tier I Mouse MP 1211 Genes GS165536: MP:0005371 limbs/digits/tail phenotype
Expand Tier I Human 319 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Mouse MP 2606 Genes GS165397: MP:0001265 decreased body size
Expand Tier I Mouse MP 3494 Genes GS170601: MP:0005621 abnormal cell physiology
Expand Tier I Human 212 Genes GS176185: HP:0100790 Hernia
Expand Tier I Mouse MP 21 Genes GS164624: MP:0004613 fusion of vertebral arches
Expand Tier I Human GO 110 Genes GS200141: GO:0001667 ameboidal cell migration
Expand Tier I Human 78 Genes GS175969: HP:0000069 Abnormality of the ureter
Expand Tier I Human 22 Genes GS173165: HP:0002435 Meningocele
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 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 GO 4713 Genes GS205364: GO:0010467 gene expression
Expand Tier I Human GO 907 Genes GS206715: GO:0051674 localization of cell
Expand Tier I Human 153 Genes GS175067: HP:0001159 Syndactyly
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Mouse MP 12 Genes GS168198: MP:0000963 fused dorsal root ganglion
Expand Tier I Human 229 Genes GS171908: HP:0004298 Abnormality of the abdominal wall
Expand Tier I Human 558 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Human GO 5152 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier I Mouse 613 Genes GS136396: organ weight 5 (Org5, Published QTL Chr 7)
Expand Tier I Mouse GO 4286 Genes GS190949: GO:0009058 biosynthetic process
Expand Tier I Mouse 2121 Genes GS128593: Average rotarod training latency Chr# 7
Expand Tier I Mouse GO 61 Genes GS190906: GO:0048332 mesoderm morphogenesis
Expand Tier I Mouse MP 63 Genes GS164392: MP:0003050 abnormal sacral vertebrae morphology
Expand Tier I Mouse GO 1176 Genes GS182705: GO:0051173 positive regulation of nitrogen compound metabolic process
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Mouse MP 46 Genes GS164244: MP:0001685 abnormal endoderm development
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 1279 Genes GS201265: GO:0009891 positive regulation of biosynthetic process
Expand Tier I Mouse 324 Genes GS136691: skull morphology 9 (Skull9, Published QTL Chr 7)
Expand Tier I Mouse GO 3005 Genes GS177308: GO:1901362 organic cyclic compound biosynthetic process
Expand Tier I Mouse MP 544 Genes GS166405: MP:0002111 abnormal tail morphology
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
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 Mouse GO 1260 Genes GS184461: GO:0009891 positive regulation of biosynthetic process
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 Mouse GO 1763 Genes GS178885: GO:0003677 DNA binding
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 70 Genes GS204831: GO:0061053 somite development
Expand Tier I Mouse GO 1466 Genes GS180001: GO:0048646 anatomical structure formation involved in morphogenesis
Expand Tier I Mouse GO 4588 Genes GS177309: GO:1901363 heterocyclic compound binding
Expand Tier I Human 398 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human 196 Genes GS172034: HP:0000368 Low-set, posteriorly rotated ears
Expand Tier I Mouse GO 2595 Genes GS188410: GO:0032774 RNA biosynthetic process
Expand Tier I Mouse 493 Genes GS136787: TallyHo associated body weight (Tabw, Published QTL Chr 7)
Expand Tier I Mouse GO 9049 Genes GS180166: GO:0008152 metabolic process
Expand Tier I Mouse GO 132 Genes GS185588: GO:0007369 gastrulation
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 137 Genes GS208994: GO:0007219 Notch signaling pathway
Expand Tier I Human GO 4446 Genes GS203072: GO:0090304 nucleic acid metabolic process
Expand Tier I Human 54 Genes GS176964: HP:0011217 Abnormal shape of the occiput
Expand Tier I Mouse GO 4637 Genes GS177382: GO:0097159 organic cyclic compound binding
Expand Tier I Mouse 623 Genes GS136867: T cell receptor induced activation 4 (Tria4, Published QTL Chr 7)
Expand Tier I Human GO 1006 Genes GS195678: GO:0003700 sequence-specific DNA binding transcription factor activity
Expand Tier I Human 551 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Mouse GO 36 Genes GS185659: GO:0090130 tissue migration
Expand Tier I Mouse GO 827 Genes GS180140: GO:0048870 cell motility
Expand Tier I Mouse MP 134 Genes GS164109: MP:0003048 abnormal cervical vertebrae morphology
Expand Tier I Human 426 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Mouse MP 286 Genes GS164509: MP:0001695 abnormal gastrulation
Expand Tier I Mouse GO 764 Genes GS188893: GO:0016477 cell migration
Expand Tier I Human 186 Genes GS171144: HP:0005280 Depressed nasal bridge
Expand Tier I Mouse MP 136 Genes GS164110: MP:0003049 abnormal lumbar vertebrae morphology
Expand Tier I Mouse GO 4518 Genes GS187751: GO:0019222 regulation of metabolic process
Expand Tier I Human GO 14 Genes GS203921: GO:0042074 cell migration involved in gastrulation
Expand Tier I Mouse MP 684 Genes GS169663: MP:0004703 abnormal vertebral column morphology
Expand Tier I Human 162 Genes GS175958: HP:0000795 Abnormality of the urethra
Expand Tier I Human 136 Genes GS171627: HP:0000470 Short neck
Expand Tier I Human 221 Genes GS171139: HP:0005288 Abnormality of the nares
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human GO 838 Genes GS205758: GO:0016477 cell migration
Expand Tier I Mouse GO 1715 Genes GS193237: GO:0031325 positive regulation of cellular metabolic process
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse 502 Genes GS136590: radiation induced gastroschisis 1 (Rigs1, Published QTL Chr 7)
Expand Tier I Human GO 3201 Genes GS204204: GO:0006351 transcription, DNA-dependent
Expand Tier I Mouse GO 4073 Genes GS180034: GO:0032502 developmental process
Expand Tier I Human GO 4983 Genes GS199124: GO:0051716 cellular response to stimulus
Expand Tier I Human GO 6651 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 123 Genes GS171384: HP:0001551 Abnormality of the umbilicus
Expand Tier I Mouse MP 5057 Genes GS165525: MP:0010768 mortality/aging
Expand Tier I Mouse MP 750 Genes GS170442: MP:0010866 abnormal prenatal body size
Expand Tier I Human GO 688 Genes GS194602: GO:0045944 positive regulation of transcription from RNA polymerase II promoter
Expand Tier I Mouse GO 2598 Genes GS185259: GO:0051252 regulation of RNA metabolic process
Expand Tier I Human GO 5379 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Human 421 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human GO 85 Genes GS202909: GO:0035282 segmentation
Expand Tier I Human 60 Genes GS174720: HP:0000775 Abnormality of the diaphragm
Expand Tier I Human GO 5601 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human 346 Genes GS171309: HP:0000252 Microcephaly
Expand Tier I Human GO 5558 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Mouse MP 99 Genes GS169608: MP:0001675 abnormal ectoderm development
Expand Tier I Rat DRG 4920 Genes GS86932: Table S3: CORTEX 17K MICROARRAY [DRG]
Expand Tier I Human GO 4593 Genes GS206355: GO:0023052 signaling
Expand Tier I Mouse GO 6947 Genes GS192918: GO:0050896 response to stimulus
Expand Tier I Mouse GO 2917 Genes GS190067: GO:0018130 heterocycle biosynthetic process
Expand Tier I Mouse MP 4772 Genes GS165524: MP:0010769 abnormal survival
Expand Tier I Human 445 Genes GS175423: HP:0010461 Abnormality of the male genitalia
Expand Tier I Mouse 324 Genes GS136216: mandible shape 10 (Manh10, Published QTL Chr 7)
Expand Tier I Mouse MP 251 Genes GS169609: MP:0001674 abnormal triploblastic development
Expand Tier I Human GO 60 Genes GS202820: GO:0001756 somitogenesis
Expand Tier I Mouse MP 30 Genes GS167522: MP:0000153 rib bifurcation
Expand Tier II Mouse 392 Genes GS84194: alcohol preference locus (Published QTL, Chr 7)
Expand Tier I Human GO 3287 Genes GS205266: GO:0032774 RNA biosynthetic process
Expand Tier I Human GO 4719 Genes GS195977: GO:0007154 cell communication
Expand Tier I Mouse MP 438 Genes GS169234: MP:0000137 abnormal vertebrae morphology
Expand Tier I Mouse MP 3815 Genes GS165243: MP:0010770 preweaning lethality
Expand Tier I Mouse GO 55 Genes GS185983: GO:0001756 somitogenesis
Expand Tier I Human GO 7311 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human GO 5047 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Tier I Mouse GO 7552 Genes GS180452: GO:0044237 cellular metabolic process
Expand Tier I Mouse MP 160 Genes GS164247: MP:0001680 abnormal mesoderm development
Expand Tier I Mouse MP 18 Genes GS166593: MP:0005223 abnormal anterior-posterior polarity of the somites
Expand Tier I Human 271 Genes GS172637: HP:0010460 Abnormality of the female genitalia
Expand Tier I Human GO 969 Genes GS195570: GO:0046983 protein dimerization activity
Expand Tier I Human GO 3640 Genes GS206953: GO:0018130 heterocycle biosynthetic process
Expand Tier I Human GO 3446 Genes GS203057: GO:0048518 positive regulation of biological process
Expand Tier I Human CTD 766 Genes GS124457: Mustard Gas interacting genes (MeSH:D009151) in CTD
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human GO 3721 Genes GS194499: GO:0044271 cellular nitrogen compound biosynthetic process
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Mouse GO 2595 Genes GS177357: GO:0003676 nucleic acid binding
Expand Tier I