Gene Details



SNRPN and homologs in 3 species are found in 469 GeneSets:


- Entrez   - Ensembl   - GeneNetwork   - STRING   - 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.
GS164791: MP:0009546 absent gastric milk in neonates
GS171926: HP:0007018 Attention deficit hyperactivity disorder
GS36467: Whole Brain Gene expression correlates of Morphine - Severity of ptosis in Females & Males BXD
GS171644: HP:0011842 Abnormality of skeletal morphology
GS173418: HP:0000144 Decreased fertility
GS190158: GO:0005686 U2 snRNP
GS175130: HP:0000750 Delayed speech and language development
GS175316: HP:0000565 Esotropia
GS169830: MP:0005384 cellular phenotype
GS175897: HP:0000939 Osteoporosis
GS174979: HP:0011061 Abnormality of dental structure
GS172294: HP:0001510 Growth delay
GS173392: HP:0003330 Abnormal bone structure
GS136807: tuberculosis resistance 3 (Tbrs3, Published QTL Chr 7)
GS165382: MP:0001260 increased body weight
GS128584: Rotarod Baseline Chr# 7
GS171187: HP:0000140 Abnormality of the menstrual cycle
GS136309: New Zealand Black autoimmunity 3 (Nba3, Published QTL Chr 7)
GS1229: Differential gene expression among both the Heroin and Cocaine Abusers
GS171596: HP:0000164 Abnormality of the teeth
GS136498: proteoglycan induced arthritis 3 (Pgia3, Published QTL Chr 7)
GS176153: HP:0100820 Glomerulopathy
GS172701: HP:0002650 Scoliosis
GS172363: HP:0004324 Increased body weight
GS175411: HP:0100871 Abnormality of the palm
GS176107: HP:0000929 Abnormality of the skull
GS172293: HP:0001511 Intrauterine growth retardation
GS165839: MP:0009701 abnormal birth body size
GS135631: collagen induced arthritis 41 (Cia41, Published QTL Chr 7)
GS174906: HP:0000545 Myopia
GS175332: HP:0000032 Abnormality of male external genitalia
GS172821: HP:0000213 Thin lips
GS126646: Carbon Tetrachloride interacting genes (MeSH:D002251) in CTD
GS36508: Cerebellum Gene expression correlates of Morphine - wet dog shakes in Males BXD
GS171083: HP:0001328 Specific learning disability
GS176098: HP:0000927 Abnormality of skeletal maturation
GS171718: HP:0002808 Kyphosis
GS172054: HP:0001507 Growth abnormality
GS201251: GO:0044424 intracellular part
GS172060: HP:0001508 Failure to thrive
GS203908: GO:0016070 RNA metabolic process
GS170024: MP:0011086 partial postnatal lethality
GS172570: HP:0000341 Narrow forehead
GS170243: MP:0011085 complete postnatal lethality
GS171126: HP:0000022 Abnormality of male internal genitalia
GS174338: HP:0002719 Recurrent infections
GS175907: HP:0004349 Reduced bone mineral density
GS166660: MP:0001731 abnormal postnatal growth
GS176242: HP:0004207 Abnormality of the 5th finger
GS172350: HP:0000135 Hypogonadism
GS135740: dsRNA-induced UCM 1 (Ducm1, Published QTL Chr 7)
GS171436: HP:0000077 Abnormality of the kidney
GS163824: MP:0001259 abnormal body weight
GS172933: HP:0003745 Sporadic
GS178733: GO:0030532 small nuclear ribonucleoprotein complex
GS175909: HP:0004348 Abnormality of bone mineral density
GS136250: mean corpuscular volume QTL 1 (Mcvq1, Published QTL Chr 7)
GS174857: HP:0200006 Slanting of the palpebral fissure
GS173355: HP:0002205 Recurrent respiratory infections
GS175601: HP:0002086 Abnormality of the respiratory system
GS173152: HP:0002236 Frontal upsweep of hair
GS176203: HP:0000478 Abnormality of the eye
GS127931: Olfactory bulb - Allen Mouse Brain Atlas
GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
GS173484: HP:0000876 Oligomenorrhea
GS171226: HP:0000812 Abnormal internal genitalia
GS170733: MP:0000188 abnormal circulating glucose level
GS173822: HP:0100720 Hypoplasia of the ear cartilage
GS173449: HP:0002683 Abnormality of the calvaria
GS174756: HP:0011947 Respiratory tract infection
GS166390: MP:0008877 abnormal DNA methylation
GS174214: HP:0009466 Radial deviation of finger
GS176639: HP:0011356 Regional abnormality of skin
GS136966: weight loss response 4 (Wtlr4, Published QTL Chr 7)
GS186744: GO:0043226 organelle
GS182835: GO:0005622 intracellular
GS168268: MP:0003122 maternal imprinting
GS135395: body growth early QTL 5 (Bgeq5, Published QTL Chr 7)
GS173740: HP:0009485 Radial deviation of the hand or of fingers of the hand
GS169075: MP:0002078 abnormal glucose homeostasis
GS136523: platelet quantitative locus 2 (Pltq2, Published QTL Chr 7)
GS174326: HP:0003199 Decreased muscle mass
GS127934: Retrohippocampal region - Allen Mouse Brain Atlas
GS194111: GO:0097159 organic cyclic compound binding
GS174057: HP:0100738 Abnormal eating behavior
GS176653: HP:0000058 Abnormality of the labia
GS171645: HP:0011843 Abnormality of skeletal physiology
GS173019: HP:0000819 Diabetes mellitus
GS175896: HP:0000938 Osteopenia
GS125190: Atenolol interacting genes (MeSH:D001262) in CTD
GS166590: MP:0002873 normal phenotype
GS171815: HP:0001574 Abnormality of the integument
GS170791: HP:0010978 Abnormality of immune system physiology
GS173375: HP:0010832 Abnormality of pain sensation
GS181473: GO:0005488 binding
GS175526: HP:0000005 Mode of inheritance
GS184445: GO:0044428 nuclear part
GS197734: GO:0006396 RNA processing
GS171647: HP:0011844 Abnormal appendicular skeleton morphology
GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
GS186251: GO:0003723 RNA binding
GS164264: MP:0002082 postnatal lethality
GS163601: MP:0002089 abnormal postnatal growth/weight/body size
GS201249: GO:0044428 nuclear part
GS197244: GO:0044237 cellular metabolic process
GS135448: bone length and organs 4 (Bod4, Published QTL Chr 7)
GS173436: HP:0005968 Temperature instability
GS194088: GO:0003676 nucleic acid binding
GS165527: MP:0005378 growth/size phenotype
GS175158: HP:0011747 Abnormality of the anterior pituitary
GS175529: HP:0000001 All
GS135882: femur geometry 6 (Fmgty6, Published QTL Chr 7)
GS171634: HP:0008050 Abnormality of the palpebral fissures
GS127938: Striatum - Allen Mouse Brain Atlas
GS135657: cocaine induced activation 9 (Cocia9, Published QTL Chr 7)
GS176660: HP:0000050 Hypoplastic genitalia
GS186740: GO:0043229 intracellular organelle
GS175333: HP:0000035 Abnormality of the testis
GS171609: HP:0011339 Abnormality of upper lip vermillion
GS173329: HP:0000682 Abnormality of dental enamel
GS173017: HP:0007015 Poor gross motor coordination
GS176568: HP:0000486 Strabismus
GS208012: GO:0044464 cell part
GS87380: Table S1: Additional data file 1 is a table listing the results of two-way ANOVA (FDR < 1%). (Whole Table) [DRG]
GS201239: GO:0046483 heterocycle metabolic process
GS865: Sey_Pax6_Age_Reduced_Linear_Incr
GS175164: HP:0011927 Short digit
GS34991: Cerebellum Gene expression correlates of Open Field - Total time in perimeter less corner in Females BXD
GS176101: HP:0000924 Abnormality of the skeletal system
GS176771: HP:0001000 Abnormality of skin pigmentation
GS174330: HP:0002714 Downturned corners of mouth
GS174385: HP:0002088 Abnormality of the lung
GS167020: MP:0003956 abnormal body size
GS135814: ether anesthesia 1 (Etan1, Published QTL Chr 7)
GS176478: HP:0002119 Ventriculomegaly
GS177051: HP:0001155 Abnormality of the hand
GS173083: HP:0000492 Abnormality of the eyelid
GS173815: HP:0000736 Short attention span
GS127928: Lateral septal complex - Allen Mouse Brain Atlas
GS197016: GO:0032991 macromolecular complex
GS178448: GO:0005634 nucleus
GS168646: MP:0001429 dehydration
GS199635: GO:0005622 intracellular
GS171633: HP:0008373 Puberty and gonadal disorders
GS171461: HP:0011121 Abnormality of skin morphology
GS175125: HP:0000028 Cryptorchidism
GS127935: Striatum dorsal region - Allen Mouse Brain Atlas
GS171381: HP:0001558 Decreased fetal movement
GS136203: lung tumor shape-determining 5 (Ltsd5, Published QTL Chr 7)
GS171397: HP:0000177 Abnormality of upper lip
GS136660: skin tumor susceptibility 1 (Skts1, Published QTL Chr 7)
GS168265: MP:0003121 genetic imprinting
GS174075: HP:0009121 Abnormal axial skeleton morphology
GS196941: GO:0008150 biological_process
GS171388: HP:0001557 Prenatal movement abnormality
GS172711: HP:0000219 Thin upper lip vermilion
GS201256: GO:0044422 organelle part
GS176233: HP:0004209 Clinodactyly of the 5th finger
GS201431: GO:0005515 protein binding
GS135381: bone density traits 4 (Bdt4, Published QTL Chr 7)
GS175594: HP:0011014 Abnormal glucose homeostasis
GS128573: Ethanol Induced Hypothermia Chr# 7
GS168128: MP:0010024 increased total body fat amount
GS193059: GO:0044446 intracellular organelle part
GS135787: "early growth rate, maternal effect 3" (Egrm3, Published QTL Chr 7)
GS209564: GO:0043231 intracellular membrane-bounded organelle
GS174247: HP:0000539 Abnormality of refraction
GS172542: HP:0000830 Anterior hypopituitarism
GS171274: HP:0100543 Cognitive impairment
GS172285: HP:0000826 Precocious puberty
GS172793: HP:0001531 Failure to thrive in infancy
GS174606: HP:0001608 Abnormality of the voice
GS205047: GO:0006807 nitrogen compound metabolic process
GS172871: HP:0010490 Abnormality of the palmar creases
GS176186: HP:0000079 Abnormality of the urinary system
GS175149: HP:0009179 Deviation of the 5th finger
GS173993: HP:0000506 Telecanthus
GS172544: HP:0000834 Abnormality of the adrenal glands
GS174504: HP:0000709 Psychosis
GS170236: MP:0005452 abnormal adipose tissue amount
GS168931: MP:0001431 abnormal eating behavior
GS171621: HP:0100851 Abnormal emotion/affect behavior
GS170601: MP:0005621 abnormal cell physiology
GS172805: HP:0000789 Infertility
GS169095: MP:0004924 abnormal behavior
GS166718: MP:0002169 no abnormal phenotype detected
GS175602: HP:0002087 Abnormality of the upper respiratory tract
GS170965: HP:0000153 Abnormality of the mouth
GS195490: GO:0030532 small nuclear ribonucleoprotein complex
GS172667: HP:0011805 Abnormality of muscle morphology
GS174879: HP:0002104 Apnea
GS169396: MP:0002069 abnormal eating/drinking behavior
GS174331: HP:0002715 Abnormality of the immune system
GS164742: MP:0001732 postnatal growth retardation
GS166375: MP:0001436 abnormal suckling behavior
GS127924: Cerebral cortex - Allen Mouse Brain Atlas
GS127925: Hippocampal formation - Allen Mouse Brain Atlas
GS171995: HP:0001764 Small feet
GS175304: HP:0000290 Abnormality of the forehead
GS177356: GO:0003674 molecular_function
GS203590: GO:0043229 intracellular organelle
GS176245: HP:0011443 Abnormality of coordination
GS177309: GO:1901363 heterocyclic compound binding
GS172272: HP:0001197 Abnormality of prenatal development or birth
GS136787: TallyHo associated body weight (Tabw, Published QTL Chr 7)
GS173666: HP:0005978 Type II diabetes mellitus
GS87137: Table S2: List of probe-sets of genes differentially expressed among the four inbred strains of mice. Gene Ranks [DRG] provisional
GS171832: HP:0000118 Phenotypic abnormality
GS203072: GO:0090304 nucleic acid metabolic process
GS177382: GO:0097159 organic cyclic compound binding
GS207972: GO:0030529 ribonucleoprotein complex
GS127937: Striatum-like amygdalar nuclei - Allen Mouse Brain Atlas
GS176941: HP:0002791 Hypoventilation
GS163103: MP:0000003 abnormal adipose tissue morphology
GS173827: HP:0002916 Abnormality of chromosome segregation
GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
GS176560: HP:0001010 Hypopigmentation of the skin
GS168956: MP:0003491 abnormal voluntary movement
GS173787: HP:0002813 Abnormality of limb bone morphology
GS176171: HP:0001250 Seizures
GS195214: GO:0009987 cellular process
GS123538: testosterone enanthate interacting genes (MeSH:C004648) in CTD
GS136590: radiation induced gastroschisis 1 (Rigs1, Published QTL Chr 7)
GS163934: MP:0001764 abnormal homeostasis
GS184452: GO:0044422 organelle part
GS172295: HP:0001513 Obesity
GS200648: GO:0044260 cellular macromolecule metabolic process
GS176586: HP:0001270 Motor delay
GS165525: MP:0010768 mortality/aging
GS175673: HP:0100022 Abnormality of movement
GS173081: HP:0000494 Downslanted palpebral fissures
GS202209: GO:0008380 RNA splicing
GS203642: GO:0006725 cellular aromatic compound metabolic process
GS207923: GO:0034641 cellular nitrogen compound metabolic process
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] provisional
GS165539: MP:0005375 adipose tissue phenotype
GS167206: MP:0003787 abnormal imprinting
GS176115: HP:0000540 Hypermetropia
GS198263: GO:0005488 binding
GS171309: HP:0000252 Microcephaly
GS194040: GO:1901360 organic cyclic compound metabolic process
GS36028: Hippocampus Gene expression correlates of Light-Dark Box Total seconds spent in dark compartment in Males BXD
GS165524: MP:0010769 abnormal survival
GS175423: HP:0010461 Abnormality of the male genitalia
GS136216: mandible shape 10 (Manh10, Published QTL Chr 7)
GS84194: alcohol preference locus (Published QTL, Chr 7)
GS165243: MP:0010770 preweaning lethality
GS176258: HP:0004370 Abnormality of temperature regulation
GS194267: GO:0043170 macromolecule metabolic process
GS172362: HP:0004325 Decreased body weight
GS175597: HP:0011013 Abnormality of carbohydrate metabolism/homeostasis
GS127939: Thalamus - Allen Mouse Brain Atlas
GS174706: HP:0000553 Abnormality of the uvea
GS171413: HP:0004097 Deviation of finger
GS171637: HP:0008872 Feeding difficulties in infancy
GS172637: HP:0010460 Abnormality of the female genitalia
GS83977: cocaine induced activation 9 (Cocia9, Published QTL, Chr 7)
GS1228: Expression patterns of the 77 genes that differentially expressed between brains of wild-type and nAChR beta-4 subunit deficient mice
GS174453: HP:0001438 Abnormality of the abdomen
GS171554: HP:0001385 Hip dysplasia
GS177357: GO:0003676 nucleic acid binding
GS168995: MP:0009642 abnormal blood homeostasis
GS176333: HP:0007319 Morphological abnormality of the central nervous system
GS136592: reactive oxygen species QTL 1 (Rosq1, Published QTL Chr 7)
GS174026: HP:0002033 Poor suck
GS205255: GO:0044238 primary metabolic process
GS171833: HP:0000119 Abnormality of the genitourinary system
GS180236: GO:0032991 macromolecular complex
GS136254: modifier of muscularity 3 (Mdmsc3, Published QTL Chr 7)
GS190159: GO:0005685 U1 snRNP
GS191064: GO:0030529 ribonucleoprotein complex
GS172260: HP:0000356 Abnormality of the outer ear
GS127930: Midbrain - Allen Mouse Brain Atlas
GS127933: Pons - Allen Mouse Brain Atlas
GS173476: HP:0002311 Incoordination
GS175965: HP:0200005 Abnormal shape of the palpebral fissure
GS171258: HP:0011138 Abnormality of skin adnexa
GS173167: HP:0100491 Abnormality of the joints of the lower limbs
GS176003: HP:0100651 Type I diabetes mellitus
GS176836: HP:0000422 Abnormality of the nasal bridge
GS203097: GO:0003723 RNA binding
GS167188: MP:0001264 increased body size
GS173032: HP:0007513 Generalized hypopigmentation
GS176433: HP:0000044 Hypogonadotrophic hypogonadism
GS174646: HP:0000951 Abnormality of the skin
GS171930: HP:0007010 Poor fine motor coordination
GS208954: GO:0006139 nucleobase-containing compound metabolic process
GS172666: HP:0011804 Abnormality of muscle physiology
GS170962: HP:0000159 Abnormality of the lip
GS175107: HP:0003808 Abnormal muscle tone
GS192624: GO:0043231 intracellular membrane-bounded organelle
GS175802: HP:0003272 Abnormality of the hip bone
GS186743: GO:0043227 membrane-bounded organelle
GS135897: granular brain lesions (Gbrln, Published QTL Chr 7)
GS176999: HP:0001290 Generalized hypotonia
GS173384: HP:0002750 Delayed skeletal maturation
GS174612: HP:0001600 Abnormality of the larynx
GS174488: HP:0000525 Abnormality of the iris
GS136413: osteosarcoma susceptibility 1 (Ossc1, Published QTL Chr 7)
GS193268: GO:0005575 cellular_component
GS194039: GO:1901363 heterocyclic compound binding
GS1250: High-density microarray analysis of hippocampal gene expression following experimental brain injury
GS127923: Cerebellum - Allen Mouse Brain Atlas
GS175963: HP:0000060 Clitoral hypoplasia
GS176657: HP:0000054 Micropenis
GS172358: HP:0003117 Abnormality of circulating hormone level
GS176718: HP:0000078 Abnormality of the genital system
GS176817: HP:0011446 Abnormality of higher mental function
GS136636: salmonella enteritidis susceptibility 2 (Ses2, Published QTL Chr 7)
GS165522: MP:0009674 decreased birth weight
GS172032: HP:0000366 Abnormality of the nose
GS173372: HP:0011297 Abnormality of the digits
GS172726: HP:0000268 Dolichocephaly
GS172801: HP:0000752 Hyperactivity
GS26229: Cerebellum Gene expression correlates of Thermal Nociception Hot Plate Avg of 2Trials in Females BXD
GS173707: HP:0000846 Adrenal insufficiency
GS201023: GO:0071704 organic substance metabolic process
GS174412: HP:0007477 Abnormal dermatoglyphics
GS171893: HP:0011458 Abdominal symptom
GS170964: HP:0000152 Abnormality of head and neck
GS164681: MP:0004262 abnormal physical strength
GS191106: GO:0044464 cell part
GS173290: HP:0011354 Generalized abnormality of skin
GS170981: HP:0011361 Congenital abnormal hair pattern
GS172941: HP:0000786 Primary amenorrhea
GS175957: HP:0000066 Labial hypoplasia
GS176364: HP:0008034 Abnormal iris pigmentation
GS176241: HP:0010935 Abnormality of the upper urinary tract
GS174187: HP:0001595 Abnormality of the hair
GS174292: HP:0011968 Feeding difficulties
GS167833: MP:0001784 abnormal fluid regulation
GS176655: HP:0000056 Abnormality of the clitoris
GS171277: HP:0100547 Abnormality of the forebrain
GS176435: HP:0000046 Scrotal hypoplasia
GS176514: HP:0007328 Impaired pain sensation
GS174016: HP:0000717 Autism
GS135926: hepatocarcinogenesis susceptibility 1 (Hcs1, Published QTL Chr 7)
GS175898: HP:0010535 Sleep apnea
GS171999: HP:0001760 Abnormality of the foot
GS175220: HP:0009887 Abnormality of hair pigmentation
GS174649: HP:0000954 Single transverse palmar crease
GS164126: MP:0001388 abnormal stationary movement
GS176488: HP:0010720 Abnormal hair pattern
GS172360: HP:0004323 Abnormality of body weight
GS86977: Table S1: All transcripts significantly different in abundance between the majority of heroin subjects and their matched controls [DRG] provisional
GS175523: HP:0000008 Abnormality of female internal genitalia
GS127926: Hippocampal region - Allen Mouse Brain Atlas
GS169828: MP:0005386 behavior/neurological phenotype
GS171047: HP:0008736 Hypoplasia of penis
GS84192: ethanol conditioned taste aversion (Published QTL, Chr 7)
GS202415: GO:0044710 single-organism metabolic process
GS127932: Pallidum - Allen Mouse Brain Atlas
GS171253: HP:0002817 Abnormality of the upper limb
GS176672: HP:0000980 Pallor
GS174048: HP:0000729 Autism spectrum disorder
GS195199: GO:0005634 nucleus
GS173404: HP:0000141 Amenorrhea
GS127114: Methylnitronitrosoguanidine interacting genes (MeSH:D008769) in CTD
GS165386: MP:0001262 decreased body weight
GS169391: MP:0002066 abnormal motor capabilities/coordination/movement
GS177031: HP:0011442 Abnormality of central motor function
GS172354: HP:0004328 Abnormality of the anterior segment of the eye
GS172175: HP:0002275 Poor motor coordination
GS135636: collagen induced arthritis autoantibody QTL 1 (Ciaaq1, Published QTL Chr 7)
GS176434: HP:0000045 Abnormality of the scrotum
GS170997: HP:0000080 Abnormality of genital physiology
GS173104: HP:0000670 Carious teeth
GS171608: HP:0011338 Abnormality of mouth shape
GS176170: HP:0001252 Muscular hypotonia
GS135848: femoral cross-sectional area 6 (Fcsa6, Published QTL Chr 7)
GS135609: circulating hormone level QTL 18 (Chlq18, Published QTL Chr 7)
GS175742: HP:0011733 Abnormality of adrenal physiology
GS127929: Medulla - Allen Mouse Brain Atlas
GS176408: HP:0000446 Narrow nasal bridge
GS172433: HP:0002644 Abnormality of pelvic girdle bone morphology
GS135257: anti-erythrocyte autoantibody modifier 2 (Aem2, Published QTL Chr 7)
GS176283: HP:0009830 Peripheral neuropathy
GS175459: HP:0009484 Deviation of the hand or of fingers of the hand
GS184447: GO:0044424 intracellular part
GS171394: HP:0000174 Abnormality of the palate
GS175191: HP:0002060 Abnormality of the cerebrum
GS207056: GO:0005681 spliceosomal complex
GS171448: HP:0000606 Abnormality of the periorbital region
GS136234: mandible length 8 (Manln8, Published QTL Chr 7)
GS210212: GO:0005575 cellular_component
GS174081: HP:0004322 Short stature
GS174390: HP:0007874 Almond-shaped palpebral fissure
GS173020: HP:0000818 Abnormality of the endocrine system
GS174377: HP:0005927 Aplasia/Hypoplasia involving bones of the hand
GS176801: HP:0001263 Global developmental delay
GS172098: HP:0000582 Upslanted palpebral fissure
GS174500: HP:0000707 Abnormality of the nervous system
GS171998: HP:0001939 Abnormality of metabolism/homeostasis
GS36477: Whole Brain Gene expression correlates of Morphine - Severity of ptosis in Males BXD
GS163888: MP:0005449 abnormal food intake
GS182834: GO:0005623 cell
GS87058: Table S2: Cocaine Regulation of H4 Acetylation. [DRG] provisional
GS175335: HP:0000036 Abnormality of the penis
GS174914: HP:0003011 Abnormality of the musculature
GS135308: angle of entrainment 4 (Angle4, Published QTL Chr 7)
GS168012: MP:0010832 lethality during fetal growth through weaning
GS176038: HP:0002795 Functional respiratory abnormality
GS196943: GO:0008152 metabolic process
GS173206: HP:0003241 Genital hypoplasia
GS135313: aortic lesion size 2 (Aorls2, Published QTL Chr 7)
GS199634: GO:0005623 cell
GS164136: MP:0000001 mammalian phenotype
GS163398: MP:0005266 abnormal metabolism
GS171106: HP:0006496 Aplasia/Hypoplasia involving bones of the upper limbs
GS176613: HP:0000271 Abnormality of the face
GS175928: HP:0000240 Abnormality of skull size
GS177055: HP:0005599 Hypopigmentation of hair
GS174101: HP:0001018 Abnormal palmar dermatoglyphics
GS175670: HP:0007364 Aplasia/Hypoplasia of the cerebrum
GS174402: HP:0001611 Nasal speech
GS165811: MP:0009703 decreased birth body size
GS169915: MP:0005560 decreased circulating glucose level
GS175959: HP:0000064 Hypoplastic labia minora
GS175981: HP:0000163 Abnormality of the oral cavity
GS172611: HP:0003474 Sensory impairment
GS173262: HP:0000864 Abnormality of the hypothalamus-pituitary axis
GS176100: HP:0000925 Abnormality of the vertebral column
GS171848: HP:0000598 Abnormality of the ear
GS175819: HP:0002591 Polyphagia
GS175595: HP:0011017 Abnormality of cell physiology
GS173703: HP:0000842 Hyperinsulinemia
GS36058: Hippocampus Gene expression correlates of Light- Dark Box Total seconds spent in light compartment in Males BXD
GS176656: HP:0000055 Abnormality of female external genitalia
GS174462: HP:0002648 Abnormality of calvarial morphology
GS173655: HP:0000823 Delayed puberty
GS165397: MP:0001265 decreased body size
GS174398: HP:0001614 Hypernasal speech
GS172021: HP:0001367 Abnormal joint morphology
GS173024: HP:0000811 Abnormal external genitalia
GS127927: Hypothalamus - Allen Mouse Brain Atlas
GS203594: GO:0043226 organelle
GS205364: GO:0010467 gene expression
GS165509: MP:0009672 abnormal birth weight
GS175067: HP:0001159 Syndactyly
GS171168: HP:0000234 Abnormality of the head
GS175481: HP:0000992 Cutaneous photosensitivity
GS175530: HP:0000002 Abnormality of body height
GS128593: Average rotarod training latency Chr# 7
GS165537: MP:0005376 homeostasis/metabolism phenotype
GS203593: GO:0043227 membrane-bounded organelle
GS136691: skull morphology 9 (Skull9, Published QTL Chr 7)
GS210000: GO:0044446 intracellular organelle part
GS174131: HP:0002011 Abnormality of the central nervous system
GS194087: GO:0003674 molecular_function
GS171424: HP:0002814 Abnormality of the lower limb
GS171793: HP:0000377 Abnormality of the pinna
GS121343: Flavonoids interacting genes (MeSH:D005419) in CTD
GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
GS171673: HP:0004283 Narrow palm
GS33872: Striatum Gene expression correlates of Difference in distance traveled (cm) during the first last min (saline-ethanol) in Males BXD
GS173223: HP:0007730 Iris hypopigmentation
GS171463: HP:0004279 Short palm
GS176526: HP:0010721 Abnormal hair whorl
GS171100: HP:0000759 Abnormality of the peripheral nervous system
GS175074: HP:0001156 Brachydactyly syndrome
GS168890: MP:0000746 weakness
GS135318: alcohol preference 7 QTL (Ap7q, Published QTL Chr 7)
GS176692: HP:0009815 Aplasia/Hypoplasia of the extremities
GS175268: HP:0001167 Abnormality of finger
GS127936: Striatum ventral region - Allen Mouse Brain Atlas
GS172286: HP:0000824 Growth hormone deficiency
GS176477: HP:0002118 Abnormality of the cerebral ventricles
GS171254: HP:0002360 Sleep disturbance
GS175098: HP:0000284 Abnormality of the ocular region