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Organism Name
C.Cg-Msx1tm1Rilm/Mmucd
RRID:MMRRC_000068-UCD RRID Copied  
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Organism Information

URL: https://www.mmrrc.org/catalog/sds.php?mmrrc_id=68

Proper Citation: RRID:MMRRC_000068-UCD

Description: Mus musculus with name C.Cg-Msx1tm1Rilm/Mmucd from MMRRC.

Species: Mus musculus

Notes: Research areas: ; Mutation Type: Targeted Mutation ; Collection:

Phenotype: abnormal malleus morphology [MP:0000029]| abnormal neurocranium morphology [MP:0000074]| overlapping parietal bones [MP:0000082]| large anterior fontanelle [MP:0000085]| short mandible [MP:0000088]| absent premaxilla [MP:0000090]| absent alveolar process [MP:0000094]| short maxilla [MP:0000097]| abnormal frontal bone morphology [MP:0000107]| cleft palate [MP:0000111]| arrest of tooth development [MP:0000118]| growth retardation of molars [MP:0000128]| abnormal heart valve morphology [MP:0000285]| abnormal atrioventricular cushion morphology [MP:0000297]| decreased atrioventricular cushion size [MP:0000301]| decreased hair follicle number [MP:0000379]| absent maxillary shelf [MP:0000430]| absent palatine bone horizontal plate [MP:0000431]| abnormal cranium morphology [MP:0000438]| abnormal mandible morphology [MP:0000458]| abnormal mammary gland development [MP:0000628]| cyanosis [MP:0001575]| abnormal breathing pattern [MP:0001951]| abnormal tooth morphology [MP:0002100]| absent malleus processus brevis [MP:0003110]| absent tympanic ring [MP:0003138]| abnormal metopic suture morphology [MP:0003842]| small nasal bone [MP:0004470]| absent upper incisors [MP:0004790]| absent lower incisors [MP:0004791]| abnormal middle ear ossicle morphology [MP:0005105]| abnormal Meckel's cartilage morphology [MP:0005587]| decreased tympanic ring size [MP:0006020]| abnormal external auditory canal morphology [MP:0006033]| small malleus [MP:0008372]| short malleus [MP:0008373]| absent malleus manubrium [MP:0008377]| abnormal cardiac epithelial to mesenchymal transition [MP:0008825]| absent gastric milk in neonates [MP:0009546]| absent external auditory canal [MP:0009707]| abnormal palatal shelf fusion at midline [MP:0009887]| cleft secondary palate [MP:0009890]| atrial septal defect [MP:0010403]| neonatal lethality [MP:0011087]| complete penetrance [MP:0030154]| abnormal tympanic cavity morphology [MP:0030187]

Affected Gene: Msx1

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Data and Source Information

Source: Integrated Animals

Source Database: Mutant Mouse Resource and Research Center (MMRRC)