MP:0000602 | enlarged sinusoidal spaces | "larger than normal sized cavities in the liver " [J:23170] |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|
MP:0000681 | abnormal thyroid gland morphology | "anomalous structure of the endocrine gland located in the front and to the sides of the upper part of the trachea and which secretes thyroid hormone and calcitonin" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|
MP:0000759 | abnormal skeletal muscle morphology | "anomalous structure of any of the striated muscle fibers connected at either or both extremeties with the bony framework of the body" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|
MP:0000783 | abnormal forebrain morphology | "malformed or absent anterior primitive cerebral vesicle; most rostral of three primary vesicles of the embryonic neural tube" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:38857] |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|
MP:0001914 | hemorrhage | "loss of blood from the vascular compartment to the exterior or into nonvascular body space as a result of rupture or severance of the blood vessels" [Stedman s Medical Dictionary, 27th edition:ISBN 0-683-40008-8] |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|
MP:0002092 | abnormal eye morphology | "abnormal development of the eye tissues resulting in morphological abnormality or abnormal structure of the visual system" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|
MP:0003686 | abnormal eye muscle morphology | "malformation of the muscles of the eye" [smb:Susan M Bello, Mouse Genome Informatics Curator] |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|
MP:0004158 | right aortic arch | "the aortic arch lies to the right of the trachea and esophagus; results from persistance of the entire right dorsal arch and involution of a segment of the left arch" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator] |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|
MP:0004269 | abnormal optic cup morphology | "any structural anomaly of double walled stuctured formed by expansion and invagination of the distal end of the optic vesicle that develops into the pigmented and sensory layers of the retina while the mouth of the optic cup eventually forms the pupil of the eye" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|
MP:0004613 | fusion of vertebral arches | "improper union of the dorsal part of adjacent vertebra" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|
MP:0004846 | absent skeletal muscle | "absence of any of the striated muscle fibers connected at either or both extremities with the bony framework of the body" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|
MP:0004938 | dilated vasculature | "stretched or widened aperture of the luminal space of the network of tubes that carries blood through the body" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|
MP:0006093 | arteriovenous malformation | "fusion of an artery and vein without an intervening capillary bed" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:93125] |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|
MP:0006203 | eye hemorrhage | "bleeding into the eye" [smb:Susan M Bello, Mouse Genome Informatics Curator] |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|
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] |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|
MP:0010572 | persistent right dorsal aorta | "persistence of the right dorsal aorta after development; the right dorsal aorta normally regresses but when it persists, a double aortic arch develops; if the left dorsal aorta also regresses, a right aortic arch forms" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|
MP:0010602 | abnormal pulmonary valve cusp morphology | "any structural anomaly of the three fibrous triangular components and associated flap of the pulmonary valve" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|
MP:0011697 | vacuolated lens | "fluid filled cavities are present in the cytoplasm of the transparent structure of the eye responsible for focusing light" [MGI:llw2] |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|
MP:0013155 | decreased KLRG1+ CD8 alpha beta T cell number | "decrease in the number of CD8+ alpha beta T cells that express KLRG1, a marker of effector and memory T cells" [MGI:csmith] |
Show
Allelic Composition: Ppp3r2tm1.1(KOMP)Vlcg/Ppp3r2tm1.1(KOMP)Vlcg Genetic Background: C57BL/6N-Ppp3r2tm1.1(KOMP)Vlcg/Ucd
|
MP:0013826 | absent hypoglossal canal | "absence of the bony canal in the occipital bone through which the hypoglossal nerve emerges from the skull" [ISBN:0683400088] |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|
MP:0013835 | absent hypoglossal nerve | "absence of the motor nerve which innervates all the intrinsic and all but one of the extrinsic muscles of the tongue" [ISBN:0-683-40008-8] |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|
MP:0013836 | abnormal hypoglossal nerve topology | "abnormal position of the hypoglossal nerve " [MGI:csmith] |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|
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] |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|
MP:0013847 | retropleural edema | "accumulation of watery or serous fluid in the retropleural space" [MGI:csmith] |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|
MP:0013917 | persistent right 6th pharyngeal arch artery | |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|
MP:0013953 | left sided brachiocephalic trunk | "the brachiocephalic trunk arises on the left side of the body, often seen in conjunction with right aortic arch" [MGI:csmith] |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|
MP:0013986 | abnormal vitelline vein topology | "abnormal position of the paired veins that carry blood from the yolk sac back to the embryo" [MGI:csmith] |
Show
Allelic Composition: Esr2tm1.1Gust/Esr2tm1.1Gust Genetic Background: B6J.129X1(Cg)-Esr2tm1.1Gust
|