|
GS185131: GO:0044699 single-organism process
|
|
GS176836: HP:0000422 Abnormality of the nasal bridge
|
|
GS136711: susceptibility to lung cancer 12 (Sluc12, Published QTL Chr 12)
|
|
GS174646: HP:0000951 Abnormality of the skin
|
|
GS201949: GO:0044699 single-organism process
|
|
GS172666: HP:0011804 Abnormality of muscle physiology
|
|
GS171644: HP:0011842 Abnormality of skeletal morphology
|
|
GS175107: HP:0003808 Abnormal muscle tone
|
|
GS33864: Striatum Gene expression correlates of Difference in distance traveled (cm) during the first five min (saline-ethanol) in Males BXD
|
|
GS135735: delta power in slow-wave sleep 2 (Dps2, Published QTL Chr 12)
|
|
GS135566: cytokine deficiency colitis susceptibility 8 (Cdcs8, Published QTL Chr 12)
|
|
GS193268: GO:0005575 cellular_component
|
|
GS193046: GO:0050953 sensory perception of light stimulus
|
|
GS135713: diabesity 3 (Dbsty3, Published QTL Chr 12)
|
|
GS136399: organ weight 8 (Org8, Published QTL Chr 12)
|
|
GS172358: HP:0003117 Abnormality of circulating hormone level
|
|
GS173206: HP:0003241 Genital hypoplasia
|
|
GS195583: GO:0019953 sexual reproduction
|
|
GS171968: HP:0000405 Conductive hearing impairment
|
|
GS172363: HP:0004324 Increased body weight
|
|
GS174075: HP:0009121 Abnormal axial skeleton morphology
|
|
GS176718: HP:0000078 Abnormality of the genital system
|
|
GS196941: GO:0008150 biological_process
|
|
GS176817: HP:0011446 Abnormality of higher mental function
|
|
GS171900: HP:0011452 Functional abnormality of the middle ear
|
|
GS176107: HP:0000929 Abnormality of the skull
|
|
GS135531: Cyp7a1 mRNA level QTL (C7mlq, Published QTL Chr 12)
|
|
GS172032: HP:0000366 Abnormality of the nose
|
|
GS128594: Average rotarod training latency Chr# 12
|
|
GS175539: HP:0007256 Abnormality of pyramidal motor function
|
|
GS175332: HP:0000032 Abnormality of male external genitalia
|
|
GS135390: body growth early QTL 11 (Bgeq11, Published QTL Chr 12)
|
|
GS172843: HP:0000481 Abnormality of the cornea
|
|
GS176613: HP:0000271 Abnormality of the face
|
|
GS173753: HP:0000510 Retinitis pigmentosa
|
|
GS173147: HP:0011283 Abnormality of the metencephalon
|
|
GS175594: HP:0011014 Abnormal glucose homeostasis
|
|
GS170964: HP:0000152 Abnormality of head and neck
|
|
GS187160: GO:0044707 single-multicellular organism process
|
|
GS175674: HP:0007360 Aplasia/Hypoplasia of the cerebellum
|
|
GS175016: HP:0001626 Abnormality of the cardiovascular system
|
|
GS172054: HP:0001507 Growth abnormality
|
|
GS173290: HP:0011354 Generalized abnormality of skin
|
|
GS175990: HP:0000463 Anteverted nares
|
|
GS135254: adiposity 6 (Adip6, Published QTL Chr 12)
|
|
GS1072: ZM_ACTIVITY_Chr12_98.000000-112.000000
|
|
GS135262: acute functional tolerance to ethanol QTL 1 (Afteq1, Published QTL Chr 12)
|
|
GS172031: HP:0000364 Hearing abnormality
|
|
GS210485: GO:0007601 visual perception
|
|
GS176616: HP:0000662 Night blindness
|
|
GS171274: HP:0100543 Cognitive impairment
|
|
GS171126: HP:0000022 Abnormality of male internal genitalia
|
|
GS174860: HP:0010549 Paralysis due to lesions of the principle motor tracts
|
|
GS136679: skull morphology 18 (Skull18, Published QTL Chr 12)
|
|
GS171848: HP:0000598 Abnormality of the ear
|
|
GS172516: HP:0001347 Hyperreflexia
|
|
GS174378: HP:0000518 Cataract
|
|
GS192290: GO:0007600 sensory perception
|
|
GS204021: GO:0044707 single-multicellular organism process
|
|
GS209225: GO:0007600 sensory perception
|
|
GS84266: METH responses for home cage activity (Published QTL, Chr 12)
|
|
GS172553: HP:0100689 Decreased corneal thickness
|
|
GS83982: cocaine related behavior 13 (Cocrb13, Published QTL, Chr 12)
|
|
GS136071: insulin QTL 10 (Insq10, Published QTL Chr 12)
|
|
GS196811: GO:0032504 multicellular organism reproduction
|
|
GS173146: HP:0011282 Abnormality of the hindbrain
|
|
GS173703: HP:0000842 Hyperinsulinemia
|
|
GS173741: HP:0100699 Scarring
|
|
GS173091: HP:0004374 Hemiplegia/hemiparesis
|
|
GS172134: HP:0000639 Nystagmus
|
|
GS207582: GO:0007276 gamete generation
|
|
GS129193: tibia bone quality traits 3 (Tbqt3 Published QTL Chr 12)
|
|
GS176203: HP:0000478 Abnormality of the eye
|
|
GS202899: GO:0050877 neurological system process
|
|
GS175373: HP:0011486 Abnormality of corneal thickness
|
|
GS36797: Whole Brain Gene expression correlates of Zero Maze - total time in open quadrants in Females & Males BXD
|
|
GS206696: GO:0044702 single organism reproductive process
|
|
GS84265: nicotine sensitivity (Published QTL, Chr 12)
|
|
GS172030: HP:0000365 Hearing impairment
|
|
GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
|
|
GS26217: Neocortex Gene expression correlates of Thermal Nociception Hargreaves' Test in Females & Males BXD
|
|
GS171226: HP:0000812 Abnormal internal genitalia
|
|
GS173024: HP:0000811 Abnormal external genitalia
|
|
GS135368: B.burgdorferi-associated arthritis 6 (Bbaa6, Published QTL Chr 12)
|
|
GS175492: HP:0000512 Abnormal electroretinogram
|
|
GS135680: Crhr1 transcript abundance QTL 2 (Crhr1taq2, Published QTL Chr 12)
|
|
GS135608: circulating hormone level QTL 17 (Chlq17, Published QTL Chr 12)
|
|
GS172360: HP:0004323 Abnormality of body weight
|
|
GS171168: HP:0000234 Abnormality of the head
|
|
GS207720: GO:0048609 multicellular organismal reproductive process
|
|
GS196808: GO:0032501 multicellular organismal process
|
|
GS171708: HP:0000359 Abnormality of the inner ear
|
|
GS209960: GO:0003008 system process
|
|
GS171047: HP:0008736 Hypoplasia of penis
|
|
GS172372: HP:0000648 Optic atrophy
|
|
GS193540: GO:0007601 visual perception
|
|
GS136274: multigenic obesity QTL 3 (Mobq3, Published QTL Chr 12)
|
|
GS136846: thymic lymphoma suppressor region 6 (Tlsr6, Published QTL Chr 12)
|
|
GS207991: GO:0000003 reproduction
|
|
GS173988: HP:0000501 Glaucoma
|
|
GS176844: HP:0000429 Abnormality of the nasal alae
|
|
GS36802: Whole Brain Gene expression correlates of Zero Maze - total time in open quadrants in Females BXD
|
|
GS174131: HP:0002011 Abnormality of the central nervous system
|
|
GS176231: HP:0010938 Abnormality of the external nose
|
|
GS176744: HP:0000987 Atypical scarring of skin
|
|
GS196196: GO:0022414 reproductive process
|
|
GS176988: HP:0008046 Abnormality of the retinal vasculature
|
|
GS177356: GO:0003674 molecular_function
|
|
GS174217: HP:0005105 Abnormal nasal morphology
|
|
GS171631: HP:0008051 Abnormality of the retinal pigment epithelium
|
|
GS205650: GO:0048232 male gamete generation
|
|
GS173019: HP:0000819 Diabetes mellitus
|
|
GS173666: HP:0005978 Type II diabetes mellitus
|
|
GS171855: HP:0000597 Ophthalmoparesis
|
|
GS171832: HP:0000118 Phenotypic abnormality
|
|
GS135565: cytokine deficiency colitis susceptibility 7 (Cdcs7, Published QTL Chr 12)
|
|
GS171946: HP:0002269 Abnormality of neuronal migration
|
|
GS175500: HP:0000517 Abnormality of the lens
|
|
GS173079: HP:0000496 Abnormality of eye movement
|
|
GS135771: ear healing QTL 3 (Earheal3, Published QTL Chr 12)
|
|
GS203862: GO:0007283 spermatogenesis
|
|
GS171251: HP:0003549 Abnormality of connective tissue
|
|
GS135991: Hfe modifier 4 (Hfem4, Published QTL Chr 12)
|
|
GS135681: Crh transcript abundance QTL 2 (Crhtaq2, Published QTL Chr 12)
|
|
GS173991: HP:0000505 Visual impairment
|
|
GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
|
|
GS171815: HP:0001574 Abnormality of the integument
|
|
GS177031: HP:0011442 Abnormality of central motor function
|
|
GS172354: HP:0004328 Abnormality of the anterior segment of the eye
|
|
GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
|
|
GS174836: HP:0001098 Abnormality of the fundus
|
|
GS180036: GO:0032501 multicellular organismal process
|
|
GS171139: HP:0005288 Abnormality of the nares
|
|
GS36782: Whole Brain Gene expression correlates of Zero Maze - Time in Closed Arms in Females & Males BXD
|
|
GS176171: HP:0001250 Seizures
|
|
GS136529: prion disease incubation time 4 (Prdt4, Published QTL Chr 12)
|
|
GS172295: HP:0001513 Obesity
|
|
GS176170: HP:0001252 Muscular hypotonia
|
|
GS176989: HP:0008047 Abnormality of the vasculature of the eye
|
|
GS136123: life span 3 (Lifespan3, Published QTL Chr 12)
|
|
GS175714: HP:0011389 Functional abnormality of the inner ear
|
|
GS136064: immunoregulatory 6 (Im6, Published QTL Chr 12)
|
|
GS122992: nitrosobenzylmethylamine interacting genes (MeSH:C014707) in CTD
|
|
GS171512: HP:0007703 Abnormal retinal pigmentation
|
|
GS175169: HP:0001317 Abnormality of the cerebellum
|
|
GS192918: GO:0050896 response to stimulus
|
|
GS174650: HP:0001133 Constricted visual fields
|
|
GS186067: GO:0050877 neurological system process
|
|
GS175529: HP:0000001 All
|
|
GS176955: HP:0000431 Wide nasal bridge
|
|
GS170971: HP:0000407 Sensorineural hearing impairment
|
|
GS175423: HP:0010461 Abnormality of the male genitalia
|
|
GS193018: GO:0003008 system process
|
|
GS171657: HP:0000613 Photophobia
|
|
GS172899: HP:0011815 Cephalocele
|
|
GS172100: HP:0000587 Abnormality of the optic nerve
|
|
GS175597: HP:0011013 Abnormality of carbohydrate metabolism/homeostasis
|
|
GS173810: HP:0002597 Abnormality of the vasculature
|
|
GS209863: GO:0050896 response to stimulus
|
|
GS172353: HP:0004329 Abnormality of the posterior segment of the eye
|
|
GS36787: Whole Brain Gene expression correlates of Zero Maze - Time in Closed Arms in Females BXD
|
|
GS176660: HP:0000050 Hypoplastic genitalia
|
|
GS180164: GO:0008150 biological_process
|
|
GS136023: hereditary spherocytosis modifer 1 (Hsm1, Published QTL Chr 12)
|
|
GS175333: HP:0000035 Abnormality of the testis
|
|
GS176333: HP:0007319 Morphological abnormality of the central nervous system
|
|
GS136424: pulmonary adenoma resistance 3 (Par3, Published QTL Chr 12)
|
|
GS171833: HP:0000119 Abnormality of the genitourinary system
|
|
GS135873: femur geometry 10 (Fmgty10, Published QTL Chr 12)
|
|
GS176202: HP:0000479 Abnormality of the retina
|
|
GS173020: HP:0000818 Abnormality of the endocrine system
|
|
GS135498: BSB obesity 4 (Bsbob4, Published QTL Chr 12)
|
|
GS209987: GO:0050953 sensory perception of light stimulus
|
|
GS135978: wound healing/regeneration 5 (Heal5, Published QTL Chr 12)
|
|
GS174379: HP:0002084 Encephalocele
|
|
GS176101: HP:0000924 Abnormality of the skeletal system
|
|
GS136450: postnatal body weight growth 12 (Pbwg12, Published QTL Chr 12)
|
|
GS174449: HP:0001123 Visual field defect
|
|
GS171791: HP:0000370 Abnormality of the middle ear
|
|
GS136930: vertebral trabecular bone trait 14 (Vtbt14, Published QTL Chr 12)
|
|
GS172195: HP:0000504 Abnormality of vision
|
|
GS174500: HP:0000707 Abnormality of the nervous system
|
|
GS171998: HP:0001939 Abnormality of metabolism/homeostasis
|
|
GS135226: antibody mediated myocarditis (Abmm, Published QTL Chr 12)
|
|
GS175335: HP:0000036 Abnormality of the penis
|
|
GS174914: HP:0003011 Abnormality of the musculature
|