Microphthalmia: a morphogenetic lethal mutation of the campbelli hamster (Phodopus campbelli). 1998

A Wada, and M Tsudzuki
Department of Laboratory Animal Science, College of Agriculture, Osaka Prefecture University, Japan.

Microphthalmia is a new mutation of the campbelli hamster (Phodopus campbelli) that is controlled by an incomplete dominant autosomal gene Mi. The dorsal coat of the heterozygote had dark markings on a white background. The dark markings appear on the head, back, and rump. Their color is very similar to that of the wild type, but slightly lighter. The pupil and iris of the heterozygote are black with reddish tinge. The homozygote has pure white fur all over the body and shows a smaller body size than the wild type and heterozygote. Moreover, the homozygote is characterized by small eyes with unopened eyelids and loss of the incisors. The pupil and iris are colorless and transparent or show a faint reddish tinge when the eyelid is artificially opened. In addition to these abnormalities, individual bones of the homozygote show dwarfism. The parietal and frontal region of the skull are thin and their symphysis is incomplete. The distal regions of the vertebral ribs show swelling. The homozygote is basically lethal within 3 weeks of age. A very few survivors are sterile.

UI MeSH Term Description Entries
D008297 Male Males
D009154 Mutation Any detectable and heritable change in the genetic material that causes a change in the GENOTYPE and which is transmitted to daughter cells and to succeeding generations. Mutations
D001842 Bone and Bones A specialized CONNECTIVE TISSUE that is the main constituent of the SKELETON. The principal cellular component of bone is comprised of OSTEOBLASTS; OSTEOCYTES; and OSTEOCLASTS, while FIBRILLAR COLLAGENS and hydroxyapatite crystals form the BONE MATRIX. Bone Tissue,Bone and Bone,Bone,Bones,Bones and Bone,Bones and Bone Tissue,Bony Apophyses,Bony Apophysis,Condyle,Apophyses, Bony,Apophysis, Bony,Bone Tissues,Condyles,Tissue, Bone,Tissues, Bone
D005260 Female Females
D005804 Genes, Lethal Genes whose loss of function or gain of function MUTATION leads to the death of the carrier prior to maturity. They may be essential genes (GENES, ESSENTIAL) required for viability, or genes which cause a block of function of an essential gene at a time when the essential gene function is required for viability. Alleles, Lethal,Allele, Lethal,Gene, Lethal,Lethal Allele,Lethal Alleles,Lethal Gene,Lethal Genes
D006200 Hair Color Color of hair or fur. Color, Hair,Colors, Hair,Hair Colors
D006224 Cricetinae A subfamily in the family MURIDAE, comprising the hamsters. Four of the more common genera are Cricetus, CRICETULUS; MESOCRICETUS; and PHODOPUS. Cricetus,Hamsters,Hamster
D000015 Abnormalities, Multiple Congenital abnormalities that affect more than one organ or body structure. Multiple Abnormalities
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D012376 Rodent Diseases Diseases of rodents of the order RODENTIA. This term includes diseases of Sciuridae (squirrels), Geomyidae (gophers), Heteromyidae (pouched mice), Castoridae (beavers), Cricetidae (rats and mice), Muridae (Old World rats and mice), Erethizontidae (porcupines), and Caviidae (guinea pigs). Disease, Rodent,Diseases, Rodent,Rodent Disease

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