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Organism Name
B6J;B6N-Esrp2tm1(KOMP)Vlcg/RpcMmucd
RRID:MMRRC_068069-UCD RRID Copied  
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RRID:MMRRC_068069-UCD
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Organism Information

URL: https://www.mmrrc.org/catalog/sds.php?mmrrc_id=68069

Proper Citation: RRID:MMRRC_068069-UCD

Description: Mus musculus with name B6J;B6N-Esrp2tm1(KOMP)Vlcg/RpcMmucd from MMRRC.

Species: Mus musculus

Notes: Research areas: Developmental Biology, Models for Human Disease; Mutation Type: Targeted Mutation ; Collection:

Phenotype: absent premaxilla [MP:0000090]| nasal bone hypoplasia [MP:0000103]| cleft palate [MP:0000111]| decreased hair follicle number [MP:0000379]| abnormal mouth morphology [MP:0000452]| abnormal mandible morphology [MP:0000458]| mandible hypoplasia [MP:0000460]| short limbs [MP:0000547]| abnormal forelimb morphology [MP:0000550]| absent radius [MP:0000553]| syndactyly [MP:0000564]| abnormal liver development [MP:0000596]| abnormal liver morphology [MP:0000598]| abnormal hepatocyte morphology [MP:0000607]| absent salivary gland [MP:0000614]| absent lungs [MP:0001181]| shiny skin [MP:0001196]| thin skin [MP:0001199]| abnormal epidermal layer morphology [MP:0001216]| thin epidermis [MP:0001218]| impaired skin barrier function [MP:0002796]| small kidney [MP:0002989]| abnormal hair follicle development [MP:0003704]| dry skin [MP:0003853]| increased hepatocyte proliferation [MP:0003893]| abnormal fetal growth/weight/body size [MP:0004197]| absent humerus [MP:0004352]| absent mandibular coronoid process [MP:0004912]| cleft upper lip [MP:0005170]| decreased circulating serum albumin level [MP:0005419]| abnormal protein level [MP:0008469]| decreased fetal weight [MP:0009431]| palatal shelf hypoplasia [MP:0009883]| cleft primary palate [MP:0009893]| postnatal lethality [MP:0011085]| complete penetrance [MP:0012173]| short rostral-caudal axis [MP:0013545]| cleft hard palate [MP:0013546]

Affected Gene: Esrp2

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Data and Source Information

Source: Integrated Animals

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