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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Nfictm1Rmg
targeted mutation 1, Richard M Gronostajski
MGI:2450153
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Nfictm1Rmg/Nfictm1Rmg either: (involves: 129P2/OlaHsd * 129S6/SvEvTac) or (involves: 129P2/OlaHsd * Black Swiss) or (involves: 129P2/OlaHsd * C57BL/6) MGI:4999865
hm2
Nfictm1Rmg/Nfictm1Rmg involves: 129P2/OlaHsd * C57BL/6 MGI:3713844


Genotype
MGI:4999865
hm1
Allelic
Composition
Nfictm1Rmg/Nfictm1Rmg
Genetic
Background
either: (involves: 129P2/OlaHsd * 129S6/SvEvTac) or (involves: 129P2/OlaHsd * Black Swiss) or (involves: 129P2/OlaHsd * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nfictm1Rmg mutation (0 available); any Nfic mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice reared on standard lab chow died prematurely due to a feeding impairment
• however, a soft-dough diet allowed all mice to survive >3 months and into adulthood

behavior/neurological
• mice reared on standard lab chow displayed compromised feeding due to tooth defects

growth/size/body
• molars dislodged during skull preparations of adult maxillae and mandibles, unlike in wild-type controls
• adult molar tooth sockets were shallow and contained an unorganized mesh of bony spicules
• at P15, no alveolar bone formation was seen in molar tooth sockets, unlike in wild-type controls
• thin and highly disorganized mandibular (lower) incisors, frequently showing scattered pockets of differentiated tissue
• grossly asymmetric maxillary incisors with near-normal labial dentin and enamel deposition but nearly absent lingual dentin deposition
• overgrown, thin maxillary (upper) incisors
• mice exhibited virtually no mandibular (lower) incisors
• all adult molar teeth had normal crowns but no roots
• all adult molar teeth lacked roots
• lack of roots was observed bilaterally
• mice displayed abnormal incisor and molar root development, associated with reduced tooth-specific gene expression
• at P14, molar roots failed to form, unlike in wild-type controls; however, molar crown formation was normal
• no structural changes were observed in the jaw, suggesting failure at either the initial outgrowth of the epithelial sheath or during early extension of the molar root
• maxillary incisors showed near-normal labial dentin deposition but displayed near absent lingual dentin deposition
• thin and brittle mandibular incisors
• weakened abnormal maxillary incisors
• mice reared on standard lab chow became severely runted after weaning
• continued rearing on standard lab chow resulted in further runting and premature death

craniofacial
• molars dislodged during skull preparations of adult maxillae and mandibles, unlike in wild-type controls
• adult molar tooth sockets were shallow and contained an unorganized mesh of bony spicules
• at P15, no alveolar bone formation was seen in molar tooth sockets, unlike in wild-type controls
• thin and highly disorganized mandibular (lower) incisors, frequently showing scattered pockets of differentiated tissue
• grossly asymmetric maxillary incisors with near-normal labial dentin and enamel deposition but nearly absent lingual dentin deposition
• overgrown, thin maxillary (upper) incisors
• mice exhibited virtually no mandibular (lower) incisors
• all adult molar teeth had normal crowns but no roots
• all adult molar teeth lacked roots
• lack of roots was observed bilaterally
• mice displayed abnormal incisor and molar root development, associated with reduced tooth-specific gene expression
• at P14, molar roots failed to form, unlike in wild-type controls; however, molar crown formation was normal
• no structural changes were observed in the jaw, suggesting failure at either the initial outgrowth of the epithelial sheath or during early extension of the molar root
• maxillary incisors showed near-normal labial dentin deposition but displayed near absent lingual dentin deposition
• thin and brittle mandibular incisors
• weakened abnormal maxillary incisors
• mandibles were ~10% smaller than normal
• however, size of maxillae was normal

skeleton
• molars dislodged during skull preparations of adult maxillae and mandibles, unlike in wild-type controls
• adult molar tooth sockets were shallow and contained an unorganized mesh of bony spicules
• at P15, no alveolar bone formation was seen in molar tooth sockets, unlike in wild-type controls
• thin and highly disorganized mandibular (lower) incisors, frequently showing scattered pockets of differentiated tissue
• grossly asymmetric maxillary incisors with near-normal labial dentin and enamel deposition but nearly absent lingual dentin deposition
• overgrown, thin maxillary (upper) incisors
• mice exhibited virtually no mandibular (lower) incisors
• all adult molar teeth had normal crowns but no roots
• all adult molar teeth lacked roots
• lack of roots was observed bilaterally
• mice displayed abnormal incisor and molar root development, associated with reduced tooth-specific gene expression
• at P14, molar roots failed to form, unlike in wild-type controls; however, molar crown formation was normal
• no structural changes were observed in the jaw, suggesting failure at either the initial outgrowth of the epithelial sheath or during early extension of the molar root
• maxillary incisors showed near-normal labial dentin deposition but displayed near absent lingual dentin deposition
• thin and brittle mandibular incisors
• weakened abnormal maxillary incisors
• mandibles were ~10% smaller than normal
• however, size of maxillae was normal

reproductive system
N
• well-nourished mice fed a soft-dough diet mated successfully and produced litters of normal size




Genotype
MGI:3713844
hm2
Allelic
Composition
Nfictm1Rmg/Nfictm1Rmg
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nfictm1Rmg mutation (0 available); any Nfic mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• at P17, mice showed normal cerebellar development relative to controls





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory