- abnormal startle reflex / IMPC
- increased startle reflex / IMPC
- limb grasping / IMPC
- decreased heart weight / IMPC
- decreased hemoglobin content / IMPC
- decreased erythrocyte cell number / IMPC
- abnormal locomotor activation / IMPC
- increased lean body mass / IMPC
- decreased lean body mass / IMPC
- increased blood urea nitrogen level / IMPC
- increased circulating amylase level / IMPC
- decreased prepulse inhibition / IMPC
- increased total body fat amount / IMPC
- increased bone mineral content / IMPC
- preweaning lethality, complete penetrance / IMPC
C3H.C-MecomJbo/H
Status | Available to order |
EMMA ID | EM:00091 |
International strain name | C3H.C-MecomJbo/H |
Alternative name | GENA251 |
Strain type | Induced Mutant Strains : Chemically-induced |
Allele/Transgene symbol | MecomJbo |
Gene/Transgene symbol | Mecom |
Information from provider
Provider | Nick Parkinson |
Provider affiliation | MRC Mammalian Genetics Unit |
Phenotypic information | These mice have late onset deafness, an extra digit, reduced body weight and craniofacial defects |
References |
|
Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
MGI allele-associated human disease models
Orphanet associated rare diseases, based on orthologous gene matching
- Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome / Orphanet_71289
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- abnormal locomotor activation / IMPC
- abnormal startle reflex / IMPC
- decreased erythrocyte cell number / IMPC
- decreased prepulse inhibition / IMPC
- limb grasping / IMPC
- thrombocytopenia / IMPC
- decreased hemoglobin content / IMPC
- increased startle reflex / IMPC
- preweaning lethality, complete penetrance / IMPC
- decreased heart weight / IMPC
- increased lean body mass / IMPC
- decreased lean body mass / IMPC
- increased blood urea nitrogen level / IMPC
- increased circulating amylase level / IMPC
- increased bone mineral content / IMPC
- increased total body fat amount / IMPC
MGI phenotypes (allele matching)
- abnormal craniofacial morphology / MGI
- polydactyly / MGI
- decreased body weight / MGI
- increased susceptibility to otitis media / MGI
- deafness / MGI
- respiratory system inflammation / MGI
- abnormal neutrophil differentiation / MGI
- abnormal miscarriage rate / MGI
- immune system phenotype / MGI
- abnormal tympanic membrane morphology / MGI
- tympanic membrane perforation / MGI
- abnormal pinna reflex / MGI
- hearing/vestibular/ear phenotype / MGI
- impaired hearing / MGI
- middle ear polyps / MGI
- middle ear effusion / MGI
- distended pericardium / MGI
- abnormal forebrain morphology / MGI
- brachydactyly / MGI
- abnormal limb development / MGI
- perinatal lethality, incomplete penetrance / MGI
- embryonic lethality during organogenesis, incomplete penetrance / MGI
- perinatal lethality, complete penetrance / MGI
MGI phenotypes (gene matching)
- malocclusion / MGI
- kyphosis / MGI
- increased leukocyte cell number / MGI
- decreased leukocyte cell number / MGI
- abnormal heart morphology / MGI
- abnormal heart looping / MGI
- overriding aortic valve / MGI
- double outlet right ventricle / MGI
- enlarged pericardium / MGI
- distended pericardium / MGI
- trabecula carnea hypoplasia / MGI
- abnormal craniofacial morphology / MGI
- polydactyly / MGI
- abnormal myotome development / MGI
- weakness / MGI
- abnormal forebrain morphology / MGI
- abnormal diencephalon morphology / MGI
- small embryonic telencephalon / MGI
- abnormal spinal nerve morphology / MGI
- abnormal cranial ganglia morphology / MGI
- small trigeminal ganglion / MGI
- abnormal superior glossopharyngeal ganglion morphology / MGI
- abnormal superior vagus ganglion morphology / MGI
- decreased body weight / MGI
- weight loss / MGI
- decreased body size / MGI
- abnormal pinna reflex / MGI
- incomplete somite formation / MGI
- decreased embryo size / MGI
- pale yolk sac / MGI
- postnatal growth retardation / MGI
- edema / MGI
- skin edema / MGI
- increased susceptibility to otitis media / MGI
- hemorrhage / MGI
- deafness / MGI
- neoplasm / MGI
- no abnormal phenotype detected / MGI
- abnormal bone marrow cell morphology/development / MGI
- respiratory system inflammation / MGI
- abnormal neutrophil differentiation / MGI
- brachydactyly / MGI
- persistent truncus arteriosis / MGI
- abnormal immune system organ morphology / MGI
- abnormal pharyngeal arch morphology / MGI
- thrombocytopenia / MGI
- abnormal vitelline vasculature morphology / MGI
- nervous system phenotype / MGI
- pharyngeal arch hypoplasia / MGI
- interrupted aortic arch / MGI
- abnormal miscarriage rate / MGI
- pale placenta / MGI
- abnormal platelet morphology / MGI
- abnormal hematopoietic stem cell morphology / MGI
- decreased hematopoietic stem cell number / MGI
- decreased B cell number / MGI
- abnormal amnion morphology / MGI
- hearing/vestibular/ear phenotype / MGI
- immune system phenotype / MGI
- hematopoietic system phenotype / MGI
- abnormal tympanic membrane morphology / MGI
- abnormal limb development / MGI
- absent sclerotome / MGI
- impaired hearing / MGI
- abnormal common myeloid progenitor cell morphology / MGI
- abnormal mesonephros morphology / MGI
- increased sensitivity to xenobiotic induced morbidity/mortality / MGI
- pulmonary vascular congestion / MGI
- ventricular septal defect / MGI
- abnormal hematopoietic stem cell physiology / MGI
- postnatal lethality, complete penetrance / MGI
- perinatal lethality, complete penetrance / MGI
- perinatal lethality, incomplete penetrance / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- lethality throughout fetal growth and development, complete penetrance / MGI
- embryonic lethality during organogenesis, incomplete penetrance / MGI
- abnormal fetal liver hematopoietic progenitor cell morphology / MGI
- lethality, complete penetrance / MGI
- absent paraxial mesoderm / MGI
- abnormal liver bud morphology / MGI
- absent myotome / MGI
- small forelimb buds / MGI
- absent hindlimb buds / MGI
- abnormal hematopoietic precursor cell number / MGI
- middle ear polyps / MGI
- middle ear effusion / MGI
- tympanic membrane perforation / MGI
Literature references
- A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse.;Nolan P M, Peters J, Strivens M, Rogers D, Hagan J, Spurr N, Gray I C, Vizor L, Brooker D, Whitehill E, Washbourne R, Hough T, Greenaway S, Hewitt M, Liu X, McCormack S, Pickford K, Selley R, Wells C, Tymowska-Lalanne Z, Roby P, Glenister P, Thornton C, Thaung C, Stevenson J A, Arkell R, Mburu P, Hardisty R, Kiernan A, Erven A, Steel K P, Voegeling S, Guenet J L, Nickols C, Sadri R, Nasse M, Isaacs A, Davies K, Browne M, Fisher E M, Martin J, Rastan S, Brown S D, Hunter J, ;2000;Nature genetics;25;440-3; 10932191
- Mutation at the Evi1 locus in Junbo mice causes susceptibility to otitis media.;Parkinson Nicholas, Hardisty-Hughes Rachel E, Tateossian Hilda, Tsai Hsun-Tien, Brooker Debra, Morse Sue, Lalane Zuzanna, MacKenzie Francesca, Fray Martin, Glenister Pete, Woodward Anne-Marie, Polley Sian, Barbaric Ivana, Dear Neil, Hough Tertius A, Hunter A Jackie, Cheeseman Michael T, Brown Steve D M, ;2006;PLoS genetics;2;e149; 17029558
- Chronic otitis media is initiated by a bulla cavitation defect in the FBXO11 mouse model.;Del-Pozo Jorge, MacIntyre Neil, Azar Ali, Glover James, Milne Elspeth, Cheeseman Michael, ;2019;Disease models & mechanisms;12;3564-3577; 30898767
- The EDA-deficient mouse has Zymbal's gland hypoplasia and acute otitis externa.;Del-Pozo Jorge, Headon Denis J, Glover James D, Azar Ali, Schuepbach-Mallepell Sonia, Bhutta Mahmood F, Riddell Jon, Maxwell Scott, Milne Elspeth, Schneider Pascal, Cheeseman Michael, ;2022;Disease models & mechanisms;15;985214; 35107126
- Ectodysplasin signalling deficiency in mouse models of hypohidrotic ectodermal dysplasia leads to middle ear and nasal pathology.;Azar Ali, Piccinelli Chiara, Brown Helen, Headon Denis, Cheeseman Michael, ;2016;Human molecular genetics;25;95-112.e18; 27378689
- Trans-cortical vessels in the mouse temporal bulla bone are a means to recruit myeloid cells in chronic otitis media and limit peripheral leukogram changes.;Azar Ali, Bhutta Mahmood F, Del-Pozo Jorge, Milne Elspeth, Cheeseman Michael, ;2022;Frontiers in genetics;13;69-79; 36246635
- Limb development genes underlie variation in human fingerprint patterns.;Li Jinxi, Glover James D, Zhang Haiguo, Peng Meifang, Tan Jingze, Mallick Chandana Basu, Hou Dan, Yang Yajun, Wu Sijie, Liu Yu, Peng Qianqian, Zheng Shijie C, Crosse Edie I, Medvinsky Alexander, Anderson Richard A, Brown Helen, Yuan Ziyu, Zhou Shen, Xu Yanqing, Kemp John P, Ho Yvonne Y W, Loesch Danuta Z, Wang Lizhong, Li Yingxiang, Tang Senwei, Wu Xiaoli, Walters Robin G, Lin Kuang, Meng Ruogu, Lv Jun, Chernus Jonathan M, Neiswanger Katherine, Feingold Eleanor, Evans David M, Medland Sarah E, Martin Nicholas G, Weinberg Seth M, Marazita Mary L, Chen Gang, Chen Zhengming, Zhou Yong, Cheeseman Michael, Wang Lan, Jin Li, Headon Denis J, Wang Sijia, ;2022;Cell;185;29-46; 34995520
- A new model for non-typeable Haemophilus influenzae middle ear infection in the Junbo mutant mouse.;Hood Derek, Moxon Richard, Purnell Tom, Richter Caroline, Williams Debbie, Azar Ali, Crompton Michael, Wells Sara, Fray Martin, Brown Steve D M, Cheeseman Michael T, ;2016;Disease models & mechanisms;9;; 26611891
- Non-Typeable Haemophilus influenzae Infection of the Junbo Mouse.;Cheeseman Michael T, Hood Derek W, ;2017;Current protocols in mouse biology;7;; 28252201
Information on how we integrate external resources can be found here
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).