MP:0000497 | abnormal small intestine placement | "different location or arrangement of the small intestinal tract" [J:40203] |
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Allelic Composition: Abcc2tm2b(KOMP)Wtsi/Abcc2tm2b(KOMP)Wtsi Genetic Background: C57BL/6N-Abcc2tm2b(KOMP)Wtsi/H
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MP:0000602 | enlarged sinusoidal spaces | "larger than normal sized cavities in the liver " [J:23170] |
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Allelic Composition: Abcc2tm2b(KOMP)Wtsi/Abcc2tm2b(KOMP)Wtsi Genetic Background: C57BL/6N-Abcc2tm2b(KOMP)Wtsi/H
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MP:0001015 | small superior cervical ganglion | "reduced size of the group of neurons that is the largest of the ganglia of the sympathetic trunk; normally lies at the base of the skull and innervates the head and neck" [J:23882] |
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Allelic Composition: Abcc2tm2b(KOMP)Wtsi/Abcc2tm2b(KOMP)Wtsi Genetic Background: C57BL/6N-Abcc2tm2b(KOMP)Wtsi/H
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MP:0002169 | no phenotype detected | "normal, viable and fertile appearance and behavior; indistinguishable from controls" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Abcc2tm2b(KOMP)Wtsi/Abcc2tm2b(KOMP)Wtsi Genetic Background: C57BL/6N-Abcc2tm2b(KOMP)Wtsi/H
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MP:0003020 | decreased circulating chloride level | "reduced concentration of chlorine salts in the circulation" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, RGD:Rat Genome Database submission] |
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Allelic Composition: A830005F24Riktm1.1(KOMP)Mbp/A830005F24Rik+ Genetic Background: C57BL/6N-A830005F24Riktm1.1(KOMP)Mbp/Ucd
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MP:0003826 | abnormal Mullerian duct morphology | "malformation of the transient embryonic tubes that empty into the cloaca and in the female develop into the oviducts, uterus, and vagina" [smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Abcc2tm2b(KOMP)Wtsi/Abcc2tm2b(KOMP)Wtsi Genetic Background: C57BL/6N-Abcc2tm2b(KOMP)Wtsi/H
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MP:0003888 | liver hemorrhage | "bleeding within the liver" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator] |
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Allelic Composition: Abcc2tm2b(KOMP)Wtsi/Abcc2tm2b(KOMP)Wtsi Genetic Background: C57BL/6N-Abcc2tm2b(KOMP)Wtsi/H
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MP:0004666 | absent stapedial artery | "absence of the small artery that passes through the ring of the stapes" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Abcc2tm2b(KOMP)Wtsi/Abcc2tm2b(KOMP)Wtsi Genetic Background: C57BL/6N-Abcc2tm2b(KOMP)Wtsi/H
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MP:0005272 | abnormal temporal bone morphology | "anomalous structure of the large, irregular bone located at the base and side of the skull; consists of three parts at birth: squamous, tympanic, and petrous" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Abcc2tm2b(KOMP)Wtsi/Abcc2tm2b(KOMP)Wtsi Genetic Background: C57BL/6N-Abcc2tm2b(KOMP)Wtsi/H
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MP:0008499 | increased IgG1 level | "greater than normal immunoglobulin class G1 level" [MGI:tmeehan "Terry Meehan, Mouse Genome Informatics Curator"] |
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Allelic Composition: Baxtm1Dlo/Baxtm1Dlo Genetic Background: involves: 129P2/OlaHsd
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MP:0009571 | abnormal right lung accessory lobe morphology | |
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Allelic Composition: Abcc2tm2b(KOMP)Wtsi/Abcc2tm2b(KOMP)Wtsi Genetic Background: C57BL/6N-Abcc2tm2b(KOMP)Wtsi/H
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MP:0010418 | perimembraneous ventricular septal defect | "abnormal communications between the two lower chambers of the heart, occurring in the membranous septum with defects in the adjacent muscular portion of the septum; it is generally located in the LV outflow tract just below the aortic valve, associated with pouches or aneurysms of the septal leaflet of the tricuspid valve, which may partially or completely close the defect; an LV-to-RA shunt may also be associated with this defect" [http://emedicine.medscape.com] |
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Allelic Composition: Abcc2tm2b(KOMP)Wtsi/Abcc2tm2b(KOMP)Wtsi Genetic Background: C57BL/6N-Abcc2tm2b(KOMP)Wtsi/H
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MP:0011110 | partial preweaning lethality | "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms between fertilization and weaning age (Mus: approximately 3-4 weeks of age)" [MGI:csmith] |
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Allelic Composition: Abcc2tm2b(KOMP)Wtsi/Abcc2tm2b(KOMP)Wtsi Genetic Background: C57BL/6N-Abcc2tm2b(KOMP)Wtsi/H
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MP:0011683 | dual inferior vena cava | "presence of two inferior vena cavae, often resulting from the persistence of both supracardinal veins during development; the two structures may be symmetric or asymmetric but typically join together at the renal vein" [MGI:csmith, PMID:10835118] |
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Allelic Composition: Abcc2tm2b(KOMP)Wtsi/Abcc2tm2b(KOMP)Wtsi Genetic Background: C57BL/6N-Abcc2tm2b(KOMP)Wtsi/H
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MP:0013840 | absent segment of posterior cerebral artery | "absence of a portion of one of a pair of blood vessels that supplies oxygenated blood to the posterior aspect of the brain" [UBERON:0001636] |
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Allelic Composition: Abcc2tm2b(KOMP)Wtsi/Abcc2tm2b(KOMP)Wtsi Genetic Background: C57BL/6N-Abcc2tm2b(KOMP)Wtsi/H
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MP:0013847 | retropleural edema | "accumulation of watery or serous fluid in the retropleural space" [MGI:csmith] |
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Allelic Composition: Abcc2tm2b(KOMP)Wtsi/Abcc2tm2b(KOMP)Wtsi Genetic Background: C57BL/6N-Abcc2tm2b(KOMP)Wtsi/H
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MP:0013852 | abnormal Mullerian duct topology | "aberrant position of the transient embryonic drainage tubes of the embryonic kidney (mesonephric tubules) that empty into the cloaca and in the female develop into the oviducts, uterus, and vagina" [ISBN:0-683-40008-8] |
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Allelic Composition: Abcc2tm2b(KOMP)Wtsi/Abcc2tm2b(KOMP)Wtsi Genetic Background: C57BL/6N-Abcc2tm2b(KOMP)Wtsi/H
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MP:0013876 | absent ductus venosus valve | "absence of the valve present on the right side of the ductus venosus at the site of the junction with the inferior vena cava" [PMID:5438957] |
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Allelic Composition: Abcc2tm2b(KOMP)Wtsi/Abcc2tm2b(KOMP)Wtsi Genetic Background: C57BL/6N-Abcc2tm2b(KOMP)Wtsi/H
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MP:0013877 | abnormal ductus venosus valve morphology | "any structural anomaly of the valve present on the right side of the ductus venosus at the site of the junction with the inferior vena cava" [PMID:5438957] |
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Allelic Composition: Abcc2tm2b(KOMP)Wtsi/Abcc2tm2b(KOMP)Wtsi Genetic Background: C57BL/6N-Abcc2tm2b(KOMP)Wtsi/H
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MP:0013971 | blood in lymph vessels | |
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Allelic Composition: Abcc2tm2b(KOMP)Wtsi/Abcc2tm2b(KOMP)Wtsi Genetic Background: C57BL/6N-Abcc2tm2b(KOMP)Wtsi/H
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MP:0013985 | abnormal umbilical vein topology | "abnormal position of the umbilical vein in relationship to other umbilical cord structures" [MGI:csmith] |
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Allelic Composition: Abcc2tm2b(KOMP)Wtsi/Abcc2tm2b(KOMP)Wtsi Genetic Background: C57BL/6N-Abcc2tm2b(KOMP)Wtsi/H
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MP:0014001 | abnormal vertebral artery topology | "abnormal position of the first branch of the left and right subclavian arteries that merge to form the single midline basilar artery; branches of the vertebral arteries supply the musculature of the neck" [MGI:csmith] |
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Allelic Composition: Abcc2tm2b(KOMP)Wtsi/Abcc2tm2b(KOMP)Wtsi Genetic Background: C57BL/6N-Abcc2tm2b(KOMP)Wtsi/H
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MP:0014003 | additional anastomosis between intracranial vertebral arteries | |
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Allelic Composition: Abcc2tm2b(KOMP)Wtsi/Abcc2tm2b(KOMP)Wtsi Genetic Background: C57BL/6N-Abcc2tm2b(KOMP)Wtsi/H
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