Strain Name:

C3H/HeJ-Mgrn1md-2J/J

Stock Number:

000809

Availability:

Repository-Cryopreserved

Description

Strain Information

Former Names C3H/HeJ-md2J    (Changed: 15-DEC-04 )
Type Coisogenic; Mutant Strain; Spontaneous Mutation;
Additional information on Genetically Engineered Mutant Mice.
Specieslaboratory mouse
Generation+N1F2N1

Development
Mahoganoid 2 Jackson (Mgrnmd-2J) arose spontaneously in strain C3H/HeJ at F157 at The Jackson Laboratory. The mutation was maintained by sibling matings with md-2J segregating. At F157+F15 it was backcrossed once to C3H/HeJ. It was cryopreserved in 1984 by mating homozygous males at generation F157+F15N1F2 to C3H/HeJ females.

Related Strains

Strains carrying other alleles of Mgrn1
000001   B6.C3 A/a Mgrn1md/J
000309   B6.C3-Mgrn1md/J
000223   C3H/HeJ-Mgrn1md/J
001277   STOCK Mgrn1md Igl-1b Igl1-rlo/J
View Strains carrying other alleles of Mgrn1     (4 strains)

Phenotype

Phenotype Information

View Mammalian Phenotype Terms

Mammalian Phenotype Terms
      assigned by genotype

Mgrn1md-2J/Mgrn1md-2J

        C3H/HeJ-Mgrn1md-2J
  • pigmentation phenotype
  • abnormal coat color (MGI Ref ID J:119125)
    • have dark backs but some agouti hairs on their flanks
  • skin/coat/nails phenotype
  • abnormal coat color (MGI Ref ID J:119125)
    • have dark backs but some agouti hairs on their flanks

The following phenotype information may relate to a genetic background differing from this JAX® Mice strain.

Mgrn1md-2J/Mgrn1md-2J

        involves: 129S1/SvImJ * C3H/HeJ
  • lethality-prenatal/perinatal
  • perinatal lethality (MGI Ref ID J:116645)
    • 60% of homozygote die before birth or during the first 3 weeks of life
  • prenatal lethality (MGI Ref ID J:116645)
    • 60% of homozygote die before birth or during the first 3 weeks of life
  • lethality-postnatal
  • postnatal lethality (MGI Ref ID J:116645)
    • 60% of homozygote die before birth or during the first 3 weeks of life
  • growth/size phenotype
  • left pulmonary isomerism (MGI Ref ID J:116645)
    • in some 12.5-18.5 d.p.c. homozygous embryos
  • situs inversus (MGI Ref ID J:116645)
    • found in a very small proportion (<1%) of adult homozygous mice
  • cardiovascular system phenotype
  • abnormal artery morphology (MGI Ref ID J:116645)
    • malposition of the great artery of the heart in 12.5-18.5 d.p.c. homozygous embryo
    • abnormal coronary artery morphology (MGI Ref ID J:116645)
      • unroofed coronary sinus in 12.5-18.5 d.p.c. homozygous embryos
    • abnormal subclavian artery morphology (MGI Ref ID J:116645)
      • retroesophageal left subclavian artery in 12.5-18.5 d.p.c. homozygous embryo
    • right aortic arch (MGI Ref ID J:116645)
      • in 12.5-18.5 d.p.c. homozygous embryos
  • abnormal atrial septum morphology (MGI Ref ID J:116645)
    • in 12.5-18.5 d.p.c. homozygous embryos
  • abnormal ventricular septum morphology (MGI Ref ID J:116645)
    • in 12.5-18.5 d.p.c. homozygous embryos
  • congestive heart failure (MGI Ref ID J:116645)
    • in some 12.5-18.5 d.p.c. homozygous embryos caused by congenital heart defects
  • dextrocardia (MGI Ref ID J:116645)
    • in some 12.5-18.5 d.p.c. homozygous embryos
  • double outlet right ventricle (MGI Ref ID J:116645)
    • in 12.5-18.5 d.p.c. homozygous embryos
  • hemorrhage (MGI Ref ID J:116645)
    • in 12.5-18.5 d.p.c. homozygous embryos
  • mesocardia (MGI Ref ID J:116645)
    • n some 12.5-18.5 d.p.c. homozygous embryos
  • pericardial effusion (MGI Ref ID J:116645)
    • pericardial and pleural effusion in some 12.5-18.5 d.p.c. homozygous embryos
  • thin myocardial wall (MGI Ref ID J:116645)
    • in 12.5-18.5 d.p.c. homozygous embryos
  • muscle phenotype
  • thin myocardial wall (MGI Ref ID J:116645)
    • in 12.5-18.5 d.p.c. homozygous embryos
  • respiratory system phenotype
  • abnormal lung morphology (MGI Ref ID J:116645)
    • reversed lung situs in some 12.5-18.5 d.p.c. homozygous embryos
    • left pulmonary isomerism (MGI Ref ID J:116645)
      • in some 12.5-18.5 d.p.c. homozygous embryos
  • embryogenesis phenotype
  • abnormal left-right axis patterning (MGI Ref ID J:116645)
    • embryonic lethality resulted from congenital heart defects due to defective establishment and/or maintenance of the left-right axis
View Research Applications

Research Applications
This mouse can be used to support research in many areas including:

Mgrn1md-2J related

Dermatology Research
Color and White Spotting Defects
Skin and Hair Texture Defects

Genes & Alleles

Gene & Allele Information

Allele Symbol Mgrn1md-2J
Allele Name mahoganoid 2 Jackson
Allele Type Spontaneous
Common Name(s) md2J;
Strain of OriginC3H/HeJ
Gene Symbol and Name Mgrn1, mahogunin, ring finger 1
Chromosome 16
Gene Common Name(s) 2610042J20Rik; KIAA0544; N28182; RGD1311862; RIKEN cDNA 2610042J20 gene; RNF156; expressed sequence N28182; mKIAA0544; mahoganoid; md; nc; non-agouti curly; non-agouti-curly;
General Note Genbank ID for this allele: AF532997, AF532998
Molecular Note The mutation in md2J has been attributed to an 8 kb retroviral insertion within exon 12. Northern analysis and RT-PCR indicate that the expression of transcript is greatly reduced in these mice. [MGI Ref ID J:80182]

Genotyping

Genotyping Information

This strain will not have a genotyping protocol or one is not currently available.

Helpful Links

Optimizing PCR Protocols

References

References

Additional References

Mgrn1md-2J related

Bagher P; Jiao J; Owen Smith C; Cota CD; Gunn TM. 2006. Characterization of Mahogunin Ring Finger-1 expression in mice. Pigment Cell Res 19(6):635-43. [PubMed: 17083490]  [MGI Ref ID J:119125]

Cota CD; Bagher P; Pelc P; Smith CO; Bodner CR; Gunn TM. 2006. Mice with mutations in Mahogunin ring finger-1 (Mgrn1) exhibit abnormal patterning of the left-right axis. Dev Dyn 235(12):3438-47. [PubMed: 17075880]  [MGI Ref ID J:116645]

Phan LK; Lin F; LeDuc CA; Chung WK; Leibel RL. 2002. The mouse mahoganoid coat color mutation disrupts a novel C3HC4 RING domain protein. J Clin Invest 110(10):1449-59. [PubMed: 12438443]  [MGI Ref ID J:80182]

Sweet HO; Davisson MT. 1995. Remutations at The Jackson Laboratory (Update to Mouse Genome 1993; 91:862-5 - J16313) Mouse Genome 93(4):1030-4.  [MGI Ref ID J:30778]

Health & husbandry

Health & Colony Maintenance Information

Currently there no information available for this strain. This may be due to the supply level of this strain.

Purchasing information

Pricing, Supply Level & Notes, Controls, General Terms & Conditions

Pricing

Pricing for USA, Canada and Mexico shipping destinations View International pricing
Price*
Cryorecovery Fee $1900.00
*Price(s) in US dollars ($)

Additional Supply Details

Pricing for International shipping destinations View USA Canada and Mexico pricing
Price*
Cryorecovery Fee $2470.00
*Price(s) in US dollars ($)

Additional Supply Details

Supply Details

Standard SupplyRepository-Cryopreserved. Must Be Recovered. Please refer to pricing and supply notes for further information.
Supply Notes
  • Cryorecovery - Standard.
    At least two mice that carry the mutation (if it is a mutant strain) will be provided. The total number of animals provided, their gender and genotype will vary. Please inquire if larger numbers of animals with specific genotypes and genders are needed. IMPORTANT NOTE: The genotypes of the animals provided may not reflect the mating scheme utilized by The Jackson Laboratory prior to cryopreservation, or that discussed in the strain description. Please inquire for possible genotypes for this specific strain. Animals typically ship within 13 to 16 weeks from your order. If a second cryorecovery is needed in order to provide the minimum number of animals, animals will typically ship within 25 weeks.

    Cryorecovery to establish a Dedicated Supply for greater quantities of mice.
    One to two pairs will be recovered to establish a Dedicated Supply of mice. Price by quotation. For more information on Dedicated Supply, please contact JAX® Services, Tel: 1-800-422-6423 or 1-207-288-5845.

  • Genomic DNA is available for this strain from the Mouse DNA Resource.

General Terms and Conditions


See Terms of Use


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Terms of Use

Terms of Use


General Terms and Conditions


Contact information

General inquiries

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fax:207-288-6655

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