Gene Details



SNRPN and homologs in 3 species are found in 492 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 II Mouse 278 Genes GS36467: Whole Brain Gene expression correlates of Morphine - Severity of ptosis in Females & Males BXD
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Mouse GO 2 Genes GS190158: GO:0005686 U2 snRNP
Expand Tier I Human 99 Genes GS175130: HP:0000750 Delayed speech and language development
Expand Tier I Mouse MP 3631 Genes GS169830: MP:0005384 cellular phenotype
Expand Tier I Human 61 Genes GS175897: HP:0000939 Osteoporosis
Expand Tier I Human 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 322 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier I Mouse 730 Genes GS136807: tuberculosis resistance 3 (Tbrs3, Published QTL Chr 7)
Expand Tier I Mouse MP 521 Genes GS165382: MP:0001260 increased body weight
Expand Tier I Mouse 907 Genes GS128584: Rotarod Baseline Chr# 7
Expand Tier I Human 72 Genes GS171187: HP:0000140 Abnormality of the menstrual cycle
Expand Tier I Mouse 612 Genes GS136309: New Zealand Black autoimmunity 3 (Nba3, Published QTL Chr 7)
Expand Tier III Human 735 Genes GS1229: Differential gene expression among Heroin Abusers
Expand Tier I Human 379 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Mouse 612 Genes GS136498: proteoglycan induced arthritis 3 (Pgia3, Published QTL Chr 7)
Expand Tier I Human 67 Genes GS176153: HP:0100820 Glomerulopathy
Expand Tier I Human 360 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human 157 Genes GS172363: HP:0004324 Increased body weight
Expand Tier I Human 150 Genes GS175411: HP:0100871 Abnormality of the palm
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 Mouse MP 257 Genes GS165839: MP:0009701 abnormal birth body size
Expand Tier I Mouse 312 Genes GS135631: collagen induced arthritis 41 (Cia41, Published QTL Chr 7)
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 III Mouse 327 Genes GS216879: Co-expression cluster of haloperidol-induced catalepsy genes in striatum of HS mice short term selected lines. Blue Cluster
Expand Tier I Human 81 Genes GS172821: HP:0000213 Thin lips
Expand Human 42 Genes GS221286: http://www.broadinstitute.org/gsea/msigdb/cards/SPLICEOSOME
Expand Tier I Human CTD 2013 Genes GS126646: Carbon Tetrachloride interacting genes (MeSH:D002251) in CTD
Expand Tier II Mouse 243 Genes GS36508: Cerebellum Gene expression correlates of Morphine - wet dog shakes in Males BXD
Expand Tier I Human 44 Genes GS171083: HP:0001328 Specific learning disability
Expand Tier I Human 149 Genes GS176098: HP:0000927 Abnormality of skeletal maturation
Expand Tier I Human 157 Genes GS171718: HP:0002808 Kyphosis
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human 283 Genes GS172060: HP:0001508 Failure to thrive
Expand Tier I Human GO 3917 Genes GS203908: GO:0016070 RNA metabolic process
Expand Tier I Mouse MP 792 Genes GS170024: MP:0011086 partial postnatal lethality
Expand Tier I Human 46 Genes GS172570: HP:0000341 Narrow forehead
Expand Tier I Mouse MP 680 Genes GS170243: MP:0011085 complete postnatal lethality
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 Human 184 Genes GS175907: HP:0004349 Reduced bone mineral density
Expand Tier I Mouse MP 1082 Genes GS166660: MP:0001731 abnormal postnatal growth
Expand Tier I Human 202 Genes GS176242: HP:0004207 Abnormality of the 5th finger
Expand Tier I Human 72 Genes GS172350: HP:0000135 Hypogonadism
Expand Tier I Mouse 473 Genes GS135740: dsRNA-induced UCM 1 (Ducm1, Published QTL Chr 7)
Expand Tier I Human 456 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Mouse MP 2357 Genes GS163824: MP:0001259 abnormal body weight
Expand Tier I Human 51 Genes GS172933: HP:0003745 Sporadic
Expand Tier I Mouse GO 24 Genes GS178733: GO:0030532 small nuclear ribonucleoprotein complex
Expand Tier I Human 246 Genes GS175909: HP:0004348 Abnormality of bone mineral density
Expand Tier I Mouse 413 Genes GS136250: mean corpuscular volume QTL 1 (Mcvq1, Published QTL Chr 7)
Expand Tier I Human 210 Genes GS174857: HP:0200006 Slanting of the palpebral fissure
Expand Tier I Human 187 Genes GS173355: HP:0002205 Recurrent respiratory infections
Expand Tier I Human 741 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 5 Genes GS173152: HP:0002236 Frontal upsweep of hair
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Mouse 3319 Genes GS127931: Olfactory bulb - Allen Mouse Brain Atlas
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human 7 Genes GS173484: HP:0000876 Oligomenorrhea
Expand Tier I Human 492 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Mouse MP 632 Genes GS170733: MP:0000188 abnormal circulating glucose level
Expand Tier I Human 8 Genes GS173822: HP:0100720 Hypoplasia of the ear cartilage
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 49 Genes GS166390: MP:0008877 abnormal DNA methylation
Expand Tier I Human 179 Genes GS174214: HP:0009466 Radial deviation of finger
Expand Tier I Human 157 Genes GS176639: HP:0011356 Regional abnormality of skin
Expand Tier I Mouse 730 Genes GS136966: weight loss response 4 (Wtlr4, Published QTL Chr 7)
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Mouse MP 32 Genes GS168268: MP:0003122 maternal imprinting
Expand Tier I Mouse 324 Genes GS135395: body growth early QTL 5 (Bgeq5, Published QTL Chr 7)
Expand Tier I Human 186 Genes GS173740: HP:0009485 Radial deviation of the hand or of fingers of the hand
Expand Tier I Mouse MP 990 Genes GS169075: MP:0002078 abnormal glucose homeostasis
Expand Tier I Mouse 531 Genes GS136523: platelet quantitative locus 2 (Pltq2, Published QTL Chr 7)
Expand Tier I Human 12 Genes GS174326: HP:0003199 Decreased muscle mass
Expand Tier I Mouse 2963 Genes GS127934: Retrohippocampal region - Allen Mouse Brain Atlas
Expand Tier I Human GO 5452 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human 11 Genes GS174057: HP:0100738 Abnormal eating behavior
Expand Tier I Human 23 Genes GS176653: HP:0000058 Abnormality of the labia
Expand Tier I Human 266 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier I Human 174 Genes GS173019: HP:0000819 Diabetes mellitus
Expand Tier I Human 54 Genes GS175896: HP:0000938 Osteopenia
Expand Tier I Human CTD 23 Genes GS125190: Atenolol interacting genes (MeSH:D001262) in CTD
Expand Tier I Mouse MP 1966 Genes GS166590: MP:0002873 normal phenotype
Expand Human 1421 Genes GS221020: http://www.broadinstitute.org/gsea/msigdb/cards/NUCLEUS
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 403 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Human 17 Genes GS173375: HP:0010832 Abnormality of pain sensation
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 Mouse GO 1777 Genes GS184445: GO:0044428 nuclear part
Expand Tier I Human GO 655 Genes GS197734: GO:0006396 RNA processing
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 GO 780 Genes GS186251: GO:0003723 RNA binding
Expand Tier I Mouse MP 1460 Genes GS164264: MP:0002082 postnatal lethality
Expand Tier I Mouse MP 3437 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Human GO 2486 Genes GS201249: GO:0044428 nuclear part
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 3 Genes GS173436: HP:0005968 Temperature instability
Expand Tier I Human GO 3310 Genes GS194088: GO:0003676 nucleic acid binding
Expand Tier I Mouse MP 4173 Genes GS165527: MP:0005378 growth/size phenotype
Expand Tier I Human 73 Genes GS175158: HP:0011747 Abnormality of the anterior pituitary
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Mouse 445 Genes GS135882: femur geometry 6 (Fmgty6, Published QTL Chr 7)
Expand Tier I Human 253 Genes GS171634: HP:0008050 Abnormality of the palpebral fissures
Expand Human 1183 Genes GS219899: http://www.broadinstitute.org/gsea/msigdb/cards/INTRACELLULAR_ORGANELLE_PART
Expand Tier I Mouse 3267 Genes GS127938: Striatum - Allen Mouse Brain Atlas
Expand Tier I Mouse 413 Genes GS135657: cocaine induced activation 9 (Cocia9, Published QTL Chr 7)
Expand Tier I Human 201 Genes GS176660: HP:0000050 Hypoplastic genitalia
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Human 384 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human 61 Genes GS171609: HP:0011339 Abnormality of upper lip vermillion
Expand Tier I Human 89 Genes GS173329: HP:0000682 Abnormality of dental enamel
Expand Tier I Human 3 Genes GS173017: HP:0007015 Poor gross motor coordination
Expand Tier I Human 315 Genes GS176568: HP:0000486 Strabismus
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 5369 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier III Mouse 1964 Genes GS865: Sey_Pax6_Age_Reduced_Linear_Incr
Expand Tier I Human 211 Genes GS175164: HP:0011927 Short digit
Expand Human 1188 Genes GS219988: http://www.broadinstitute.org/gsea/msigdb/cards/ORGANELLE_PART
Expand Tier II Mouse 104 Genes GS34991: Cerebellum Gene expression correlates of Open Field - Total time in perimeter less corner in Females BXD
Expand Human 1183 Genes GS219682: http://www.broadinstitute.org/gsea/msigdb/cards/INTRACELLULAR_ORGANELLE_PART
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 232 Genes GS176771: HP:0001000 Abnormality of skin pigmentation
Expand Tier I Human 40 Genes GS174330: HP:0002714 Downturned corners of mouth
Expand Tier I Human 545 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Mouse MP 3110 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Mouse 324 Genes GS135814: ether anesthesia 1 (Etan1, Published QTL Chr 7)
Expand Tier I Human 163 Genes GS176478: HP:0002119 Ventriculomegaly
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 49 Genes GS173815: HP:0000736 Short attention span
Expand Tier I Mouse 3096 Genes GS127928: Lateral septal complex - Allen Mouse Brain Atlas
Expand Tier I Human GO 3861 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Mouse GO 5247 Genes GS178448: GO:0005634 nucleus
Expand Tier I Mouse MP 104 Genes GS168646: MP:0001429 dehydration
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 161 Genes GS171633: HP:0008373 Puberty and gonadal disorders
Expand Tier I Human 489 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human 285 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier I Mouse 2918 Genes GS127935: Striatum dorsal region - Allen Mouse Brain Atlas
Expand Tier I Human 38 Genes GS171381: HP:0001558 Decreased fetal movement
Expand Tier I Mouse 330 Genes GS136203: lung tumor shape-determining 5 (Ltsd5, Published QTL Chr 7)
Expand Tier I Human 139 Genes GS171397: HP:0000177 Abnormality of upper lip
Expand Tier I Mouse 415 Genes GS136660: skin tumor susceptibility 1 (Skts1, Published QTL Chr 7)
Expand Tier I Mouse MP 71 Genes GS168265: MP:0003121 genetic imprinting
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 36 Genes GS172711: HP:0000219 Thin upper lip vermilion
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human 150 Genes GS176233: HP:0004209 Clinodactyly of the 5th finger
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
Expand Tier I Mouse 728 Genes GS135381: bone density traits 4 (Bdt4, Published QTL Chr 7)
Expand Tier I Human 287 Genes GS175594: HP:0011014 Abnormal glucose homeostasis
Expand Tier I Mouse 2087 Genes GS128573: Ethanol Induced Hypothermia Chr# 7
Expand Tier I Mouse MP 121 Genes GS168128: MP:0010024 increased total body fat amount
Expand Tier I Mouse GO 4224 Genes GS193059: GO:0044446 intracellular organelle part
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 189 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier I Human 47 Genes GS172542: HP:0000830 Anterior hypopituitarism
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 28 Genes GS172285: HP:0000826 Precocious puberty
Expand Tier I Human 5 Genes GS172793: HP:0001531 Failure to thrive in infancy
Expand Tier I Human 132 Genes GS174606: HP:0001608 Abnormality of the voice
Expand Human 42 Genes GS221037: http://www.broadinstitute.org/gsea/msigdb/cards/SPLICEOSOME
Expand Tier I Human GO 5962 Genes GS205047: GO:0006807 nitrogen compound metabolic process
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 150 Genes GS175149: HP:0009179 Deviation of the 5th finger
Expand Tier I Human 63 Genes GS173993: HP:0000506 Telecanthus
Expand Tier I Human 87 Genes GS172544: HP:0000834 Abnormality of the adrenal glands
Expand Tier I Human 33 Genes GS174504: HP:0000709 Psychosis
Expand Tier I Mouse MP 642 Genes GS170236: MP:0005452 abnormal adipose tissue amount
Expand Tier I Mouse MP 563 Genes GS168931: MP:0001431 abnormal eating behavior
Expand Human 1188 Genes GS219898: http://www.broadinstitute.org/gsea/msigdb/cards/ORGANELLE_PART
Expand Tier I Human 203 Genes GS171621: HP:0100851 Abnormal emotion/affect behavior
Expand Tier I Mouse MP 3494 Genes GS170601: MP:0005621 abnormal cell physiology
Expand Tier I Human 16 Genes GS172805: HP:0000789 Infertility
Expand Tier I Mouse MP 3543 Genes GS169095: MP:0004924 abnormal behavior
Expand Tier I Mouse MP 1963 Genes GS166718: MP:0002169 no abnormal phenotype detected
Expand Tier I Human 258 Genes GS175602: HP:0002087 Abnormality of the upper respiratory tract
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human GO 33 Genes GS195490: GO:0030532 small nuclear ribonucleoprotein complex
Expand Tier I Human 530 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human 94 Genes GS174879: HP:0002104 Apnea
Expand Tier I Mouse MP 722 Genes GS169396: MP:0002069 abnormal eating/drinking behavior
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Mouse MP 1007 Genes GS164742: MP:0001732 postnatal growth retardation
Expand Mouse 648 Genes GS218282: Brain Ignorome
Expand Tier I Mouse MP 132 Genes GS166375: MP:0001436 abnormal suckling behavior
Expand Tier I Mouse 3289 Genes GS127924: Cerebral cortex - Allen Mouse Brain Atlas
Expand Tier I Mouse 3384 Genes GS127925: Hippocampal formation - Allen Mouse Brain Atlas
Expand Tier I Human 50 Genes GS171995: HP:0001764 Small feet
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 344 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Mouse GO 4588 Genes GS177309: GO:1901363 heterocyclic compound binding
Expand Tier I Human 258 Genes GS172272: HP:0001197 Abnormality of prenatal development or birth
Expand Human 42 Genes GS219740: http://www.broadinstitute.org/gsea/msigdb/cards/SPLICEOSOME
Expand Tier I Mouse 493 Genes GS136787: TallyHo associated body weight (Tabw, Published QTL Chr 7)
Expand Tier I Human 85 Genes GS173666: HP:0005978 Type II diabetes mellitus
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 4446 Genes GS203072: GO:0090304 nucleic acid metabolic process
Expand Tier I Mouse GO 4637 Genes GS177382: GO:0097159 organic cyclic compound binding
Expand Tier I Human GO 553 Genes GS207972: GO:0030529 ribonucleoprotein complex
Expand Tier I Mouse 2944 Genes GS127937: Striatum-like amygdalar nuclei - Allen Mouse Brain Atlas
Expand Tier I Human 18 Genes GS176941: HP:0002791 Hypoventilation
Expand Tier I Mouse MP 833 Genes GS163103: MP:0000003 abnormal adipose tissue morphology
Expand Tier I Human 20 Genes GS173827: HP:0002916 Abnormality of chromosome segregation
Expand Tier I Human 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human 95 Genes GS176560: HP:0001010 Hypopigmentation of the skin
Expand Tier I Mouse MP 1825 Genes GS168956: MP:0003491 abnormal voluntary movement
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 616 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse 502 Genes GS136590: radiation induced gastroschisis 1 (Rigs1, Published QTL Chr 7)
Expand Tier I Mouse MP 3924 Genes GS163934: MP:0001764 abnormal homeostasis
Expand Tier I Mouse GO 4333 Genes GS184452: GO:0044422 organelle part
Expand Tier I Human GO 6651 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Mouse MP 5057 Genes GS165525: MP:0010768 mortality/aging
Expand Tier I Human 140 Genes GS173081: HP:0000494 Downslanted palpebral fissures
Expand Tier I Human GO 5379 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Human GO 5601 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
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 Mouse MP 845 Genes GS165539: MP:0005375 adipose tissue phenotype
Expand Tier I Human GO 5558 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Human 1421 Genes GS219689: http://www.broadinstitute.org/gsea/msigdb/cards/NUCLEUS
Expand Tier II Mouse 24 Genes GS36028: Hippocampus Gene expression correlates of Light-Dark Box Total seconds spent in dark compartment in Males BXD
Expand Tier II Mouse 392 Genes GS84194: alcohol preference locus (Published QTL, Chr 7)
Expand Tier I Human GO 7311 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human 394 Genes GS172362: HP:0004325 Decreased body weight
Expand Tier I Human 320 Genes GS175597: HP:0011013 Abnormality of carbohydrate metabolism/homeostasis
Expand Tier I Mouse 3315 Genes GS127939: Thalamus - Allen Mouse Brain Atlas
Expand Tier II Mouse 425 Genes GS83977: cocaine induced activation 9 (Cocia9, Published QTL, Chr 7)
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human 10 Genes GS171554: HP:0001385 Hip dysplasia
Expand Tier I Mouse GO 2595 Genes GS177357: GO:0003676 nucleic acid binding
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Mouse 730 Genes GS136592: reactive oxygen species QTL 1 (Rosq1, Published QTL Chr 7)
Expand Tier I Human 12 Genes GS174026: HP:0002033 Poor suck
Expand Tier I Human GO 8702 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 990 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Human 1183 Genes GS219989: http://www.broadinstitute.org/gsea/msigdb/cards/INTRACELLULAR_ORGANELLE_PART
Expand Tier I Mouse GO 563 Genes GS191064: GO:0030529 ribonucleoprotein complex
Expand Tier I Mouse 3343 Genes GS127930: Midbrain - Allen Mouse Brain Atlas
Expand Tier I Mouse 3329 Genes GS127933: Pons - Allen Mouse Brain Atlas
Expand Tier I Human 172 Genes GS173476: HP:0002311 Incoordination
Expand Human 1183 Genes GS221019: http://www.broadinstitute.org/gsea/msigdb/cards/INTRACELLULAR_ORGANELLE_PART
Expand Tier I Human 567 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human 27 Genes GS176003: HP:0100651 Type I diabetes mellitus
Expand Tier I Human 387 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Human GO 853 Genes GS203097: GO:0003723 RNA binding
Expand Tier I Mouse MP 545 Genes GS167188: MP:0001264 increased body size
Expand Tier I Human 17 Genes GS173032: HP:0007513 Generalized hypopigmentation
Expand Tier I Human 17 Genes GS176433: HP:0000044 Hypogonadotrophic hypogonadism
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human 4 Genes GS171930: HP:0007010 Poor fine motor coordination
Expand Tier I Human GO 5216 Genes GS208954: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 275 Genes GS170962: HP:0000159 Abnormality of the lip
Expand Tier I Human 537 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Mouse GO 8630 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
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 Mouse 445 Genes GS135897: granular brain lesions (Gbrln, Published QTL Chr 7)
Expand Tier I Human 17 Genes GS176999: HP:0001290 Generalized hypotonia
Expand Tier I Human 125 Genes GS173384: HP:0002750 Delayed skeletal maturation
Expand Tier I Human 182 Genes GS174612: HP:0001600 Abnormality of the larynx
Expand Tier I Human 170 Genes GS174488: HP:0000525 Abnormality of the iris
Expand Tier I Mouse 417 Genes GS136413: osteosarcoma susceptibility 1 (Ossc1, Published QTL Chr 7)
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 III Rat 181 Genes GS1250: High-density microarray analysis of hippocampal gene expression following experimental brain injury
Expand Tier I Mouse 3109 Genes GS127923: Cerebellum - Allen Mouse Brain Atlas
Expand Tier I Human 6 Genes GS175963: HP:0000060 Clitoral hypoplasia
Expand Tier I Human 70 Genes GS176657: HP:0000054 Micropenis
Expand Tier I Human 120 Genes GS172358: HP:0003117 Abnormality of circulating hormone level
Expand Tier I Human 602 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Mouse 612 Genes GS136636: salmonella enteritidis susceptibility 2 (Ses2, Published QTL Chr 7)
Expand Tier I Mouse MP 115 Genes GS165522: MP:0009674 decreased birth weight
Expand Tier I Human 639 Genes GS172032: HP:0000366 Abnormality of the nose
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 80 Genes GS172801: HP:0000752 Hyperactivity
Expand Tier II Mouse 173 Genes GS26229: Cerebellum Gene expression correlates of Thermal Nociception Hot Plate Avg of 2Trials in Females BXD
Expand Tier I Human 37 Genes GS173707: HP:0000846 Adrenal insufficiency
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human 114 Genes GS174412: HP:0007477 Abnormal dermatoglyphics
Expand Tier I Human 473 Genes GS171893: HP:0011458 Abdominal symptom
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Human 1183 Genes GS221268: http://www.broadinstitute.org/gsea/msigdb/cards/INTRACELLULAR_ORGANELLE_PART
Expand Tier I Mouse MP 332 Genes GS164681: MP:0004262 abnormal physical strength
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier I Human 739 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human 69 Genes GS170981: HP:0011361 Congenital abnormal hair pattern
Expand Tier I Human 29 Genes GS172941: HP:0000786 Primary amenorrhea
Expand Tier I Human 16 Genes GS175957: HP:0000066 Labial hypoplasia
Expand Tier I Human 48 Genes GS176364: HP:0008034 Abnormal iris pigmentation
Expand Tier I Human 486 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human 453 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human 237 Genes GS174292: HP:0011968 Feeding difficulties
Expand Tier I Mouse MP 749 Genes GS167833: MP:0001784 abnormal fluid regulation
Expand Tier I Human 35 Genes GS176655: HP:0000056 Abnormality of the clitoris
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human 22 Genes GS176435: HP:0000046 Scrotal hypoplasia
Expand Human 570 Genes GS219684: http://www.broadinstitute.org/gsea/msigdb/cards/NUCLEAR_PART
Expand Tier I Human 17 Genes GS176514: HP:0007328 Impaired pain sensation
Expand Tier I Human 39 Genes GS174016: HP:0000717 Autism
Expand Tier I Mouse 324 Genes GS135926: hepatocarcinogenesis susceptibility 1 (Hcs1, Published QTL Chr 7)
Expand Tier I Human 11 Genes GS175898: HP:0010535 Sleep apnea
Expand Tier I Human 489 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human 56 Genes GS175220: HP:0009887 Abnormality of hair pigmentation
Expand Tier I Human 78 Genes GS174649: HP:0000954 Single transverse palmar crease
Expand Tier I Mouse MP 262 Genes GS164126: MP:0001388 abnormal stationary movement
Expand Tier I Human 72 Genes GS176488: HP:0010720 Abnormal hair pattern
Expand Tier I Human 534 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human DRG 911 Genes provisional GS86977: Table S1: All transcripts significantly different in abundance between the majority of heroin subjects and their matched controls [DRG]
Expand Tier I Human 235 Genes GS175523: HP:0000008 Abnormality of female internal genitalia
Expand Tier I Mouse 3136 Genes GS127926: Hippocampal region - Allen Mouse Brain Atlas
Expand Tier I Mouse MP 3543 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier I Human 179 Genes GS171047: HP:0008736 Hypoplasia of penis
Expand Tier II Mouse 489 Genes GS84192: ethanol conditioned taste aversion (Published QTL, Chr 7)
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Mouse 3289 Genes GS127932: Pallidum - Allen Mouse Brain Atlas
Expand Tier I Human 579 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human 123 Genes GS176672: HP:0000980 Pallor
Expand Tier I Human 39 Genes GS174048: HP:0000729 Autism spectrum disorder
Expand Tier I Human GO 5948 Genes GS195199: GO:0005634 nucleus
Expand Tier I Human 42 Genes GS173404: HP:0000141 Amenorrhea
Expand Tier I Human CTD 148 Genes GS127114: Methylnitronitrosoguanidine interacting genes (MeSH:D008769) in CTD
Expand Human 1421 Genes GS221269: http://www.broadinstitute.org/gsea/msigdb/cards/NUCLEUS
Expand Tier I Mouse MP 1856 Genes GS165386: MP:0001262 decreased body weight
Expand Tier I Mouse MP 2406 Genes GS169391: MP:0002066 abnormal motor capabilities/coordination/movement
Expand Tier I Human 699 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human 544 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 6 Genes GS172175: HP:0002275 Poor motor coordination
Expand Tier I Mouse 433 Genes GS135636: collagen induced arthritis autoantibody QTL 1 (Ciaaq1, Published QTL Chr 7)
Expand Tier I Human 41 Genes GS176434: HP:0000045 Abnormality of the scrotum
Expand Tier I Human 98 Genes GS170997: HP:0000080 Abnormality of genital physiology
Expand Tier I Human 79 Genes GS173104: HP:0000670 Carious teeth
Expand Tier I Human 76 Genes GS171608: HP:0011338 Abnormality of mouth shape
Expand Tier I Human 534 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Mouse 502 Genes GS135848: femoral cross-sectional area 6 (Fcsa6, Published QTL Chr 7)
Expand Tier I Mouse 445 Genes GS135609: circulating hormone level QTL 18 (Chlq18, Published QTL Chr 7)
Expand Human 42 Genes GS219957: http://www.broadinstitute.org/gsea/msigdb/cards/SPLICEOSOME
Expand Tier I Human 62 Genes GS175742: HP:0011733 Abnormality of adrenal physiology
Expand Tier I Mouse 3395 Genes GS127929: Medulla - Allen Mouse Brain Atlas
Expand Tier I Human 15 Genes GS176408: HP:0000446 Narrow nasal bridge
Expand Tier I Human 240 Genes GS172433: HP:0002644 Abnormality of pelvic girdle bone morphology
Expand Tier I Mouse 531 Genes GS135257: anti-erythrocyte autoantibody modifier 2 (Aem2, Published QTL Chr 7)
Expand Tier I Human 207 Genes GS176283: HP:0009830 Peripheral neuropathy
Expand Human 1421 Genes GS219906: http://www.broadinstitute.org/gsea/msigdb/cards/NUCLEUS
Expand Tier I Human 224 Genes GS175459: HP:0009484 Deviation of the hand or of fingers of the hand
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Human 397 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human GO 145 Genes GS207056: GO:0005681 spliceosomal complex
Expand Tier I Human 474 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Mouse 324 Genes GS136234: mandible length 8 (Manln8, Published QTL Chr 7)
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 4 Genes GS174390: HP:0007874 Almond-shaped palpebral fissure
Expand Tier I Human 514 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human 175 Genes GS174377: HP:0005927 Aplasia/Hypoplasia involving bones of the hand
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
Expand Tier I Human 83 Genes GS172098: HP:0000582 Upslanted palpebral fissure
Expand Human 1188 Genes GS219681: http://www.broadinstitute.org/gsea/msigdb/cards/ORGANELLE_PART
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 II Mouse 219 Genes GS36477: Whole Brain Gene expression correlates of Morphine - Severity of ptosis in Males BXD
Expand Tier I Mouse MP 419 Genes GS163888: MP:0005449 abnormal food intake
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Mouse DRG 613 Genes provisional GS87058: Table S2: Cocaine Regulation of H4 Acetylation. [DRG]
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 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 Human 378 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 211 Genes GS173206: HP:0003241 Genital hypoplasia
Expand Tier I Mouse 433 Genes GS135313: aortic lesion size 2 (Aorls2, Published QTL Chr 7)
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 663 Genes GS163398: MP:0005266 abnormal metabolism
Expand Tier I Human 212 Genes GS171106: HP:0006496 Aplasia/Hypoplasia involving bones of the upper limbs
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 470 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Human 52 Genes GS177055: HP:0005599 Hypopigmentation of hair
Expand Tier I Human 90 Genes GS174101: HP:0001018 Abnormal palmar dermatoglyphics
Expand Tier I Human 409 Genes GS175670: HP:0007364 Aplasia/Hypoplasia of the cerebrum
Expand Tier I Human 17 Genes GS174402: HP:0001611 Nasal speech
Expand Tier I Mouse MP 256 Genes GS165811: MP:0009703 decreased birth body size
Expand Tier I Mouse MP 314 Genes GS169915: MP:0005560 decreased circulating glucose level
Expand Tier I Human 4 Genes GS175959: HP:0000064 Hypoplastic labia minora
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 90 Genes GS172611: HP:0003474 Sensory impairment
Expand Tier I Human 114 Genes GS173262: HP:0000864 Abnormality of the hypothalamus-pituitary axis
Expand Human 570 Genes GS219990: http://www.broadinstitute.org/gsea/msigdb/cards/NUCLEAR_PART
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Human 1421 Genes GS219991: http://www.broadinstitute.org/gsea/msigdb/cards/NUCLEUS
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 8 Genes GS175819: HP:0002591 Polyphagia
Expand Tier I Human 110 Genes GS175595: HP:0011017 Abnormality of cell physiology
Expand Tier I Human 77 Genes GS173703: HP:0000842 Hyperinsulinemia
Expand Tier II Mouse 24 Genes GS36058: Hippocampus Gene expression correlates of Light- Dark Box Total seconds spent in light compartment in Males BXD
Expand Tier I Human 72 Genes GS176656: HP:0000055 Abnormality of female external genitalia
Expand Tier III Human 2403 Genes GS137413: Supplementary Table 2. CNA Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Human 319 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Human 20 Genes GS173655: HP:0000823 Delayed puberty
Expand Tier I Mouse MP 2606 Genes GS165397: MP:0001265 decreased body size
Expand Tier I Human 9 Genes GS174398: HP:0001614 Hypernasal speech
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 Mouse 3375 Genes GS127927: Hypothalamus - Allen Mouse Brain Atlas
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 4713 Genes GS205364: GO:0010467 gene expression
Expand Tier I Mouse MP 115 Genes GS165509: MP:0009672 abnormal birth weight
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 Human 46 Genes GS175481: HP:0000992 Cutaneous photosensitivity
Expand Tier I Human 558 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Mouse 2121 Genes GS128593: Average rotarod training latency Chr# 7
Expand Tier I Mouse MP 4592 Genes GS165537: MP:0005376 homeostasis/metabolism phenotype
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse 324 Genes GS136691: skull morphology 9 (Skull9, Published QTL Chr 7)
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
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 Human 599 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human 251 Genes GS171793: HP:0000377 Abnormality of the pinna
Expand Tier I Human CTD 1068 Genes GS121343: Flavonoids interacting genes (MeSH:D005419) in CTD
Expand Tier I Human 398 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human 5 Genes GS171673: HP:0004283 Narrow palm
Expand Tier II Mouse 32 Genes GS33872: Striatum Gene expression correlates of Difference in distance traveled (cm) during the first last min (saline-ethanol) in Males BXD
Expand Tier I Human 14 Genes GS173223: HP:0007730 Iris hypopigmentation
Expand Tier I Human 46 Genes GS171463: HP:0004279 Short palm
Expand Tier I Human 7 Genes GS176526: HP:0010721 Abnormal hair whorl
Expand Tier I Human 399 Genes GS171100: HP:0000759 Abnormality of the peripheral nervous system
Expand Tier I Human 150 Genes GS175074: HP:0001156 Brachydactyly syndrome
Expand Tier I Mouse MP 171 Genes GS168890: MP:0000746 weakness
Expand Tier I Mouse 473 Genes GS135318: alcohol preference 7 QTL (Ap7q, Published QTL Chr 7)
Expand Tier I Human 263 Genes GS176692: HP:0009815 Aplasia/Hypoplasia of the extremities
Expand Tier I Human 426 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Mouse 2962 Genes GS127936: Striatum ventral region - Allen Mouse Brain Atlas
Expand Tier I Human 20 Genes GS172286: HP:0000824 Growth hormone deficiency
Expand Tier I Human 263 Genes GS176477: HP:0002118 Abnormality of the cerebral ventricles
Expand Tier I Human 77 Genes GS171254: HP:0002360 Sleep disturbance
Expand Tier I Human 588 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human CTD 479 Genes GS123538: testosterone enanthate interacting genes (MeSH:C004648) in CTD
Expand Tier I Human 149 Genes GS172295: HP:0001513 Obesity
Expand Tier I Human 143 Genes GS176586: HP:0001270 Motor delay
Expand Tier I Human 543 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human GO 329 Genes GS202209: GO:0008380 RNA splicing
Expand Tier I Mouse MP 34 Genes GS167206: MP:0003787 abnormal imprinting
Expand Tier I Human 41 Genes GS176115: HP:0000540 Hypermetropia
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human 346 Genes GS171309: HP:0000252 Microcephaly
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 3815 Genes GS165243: MP:0010770 preweaning lethality
Expand Tier I Human 123 Genes GS176258: HP:0004370 Abnormality of temperature regulation
Expand Tier I Human 203 Genes GS174706: HP:0000553 Abnormality of the uvea
Expand Tier I Human 202 Genes GS171413: HP:0004097 Deviation of finger
Expand Tier I Human 199 Genes GS171637: HP:0008872 Feeding difficulties in infancy
Expand Tier I Human 271 Genes GS172637: HP:0010460 Abnormality of the female genitalia
Expand Tier III Mouse 75 Genes GS1228: Expression patterns of the 77 genes that differentially expressed between brains of wild-type and nAChR beta-4 subunit deficient mice
Expand Tier I Mouse MP 2663 Genes GS168995: MP:0009642 abnormal blood homeostasis
Expand Human 570 Genes GS219901: http://www.broadinstitute.org/gsea/msigdb/cards/NUCLEAR_PART
Expand Tier I Mouse GO 3583 Genes GS180236: GO:0032991 macromolecular complex
Expand Tier I Mouse 413 Genes GS136254: modifier of muscularity 3 (Mdmsc3, Published QTL Chr 7)
Expand Tier I Mouse GO 2 Genes GS190159: GO:0005685 U1 snRNP
Expand Tier I Human 433 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Human 4 Genes GS175965: HP:0200005 Abnormal shape of the palpebral fissure
Expand Tier I Human 289 Genes GS173167: HP:0100491 Abnormality of the joints of the lower limbs
Expand Tier I Mouse MP 87 Genes GS164791: MP:0009546 absent gastric milk in neonates
Expand Tier I Human 41 Genes GS171926: HP:0007018 Attention deficit hyperactivity disorder
Expand Tier I Human 55 Genes GS173418: HP:0000144 Decreased fertility
Expand Tier I Human 20 Genes GS175316: HP:0000565 Esotropia
Expand Tier I Human 154 Genes GS174979: HP:0011061 Abnormality of dental structure