NOD.Cg Prkdc^scid-B2m^b/Dvs

Stock number: 002571
Research areas: Immunology, Inflammation and Autoimmunity Research, Internal/Organ Research, Research Tools, Virology Research

Development

NOD.CB17-Prkdc^scid at N10 was crossed with NOR/Lt to capture the B2m^b allele. This was followed by backcrossing 11 generations to NOD.CB17-Prkdc^scid then sibling mating to fix this congenic homozygous for B2m^b.

Allele

Symbol: Prkdc^scid
Name: severe combined immunodeficiency
MGI accession ID: MGI:1857113
Generation method: Spontaneous
Marker symbol: Prkdc
Marker name: protein kinase, DNA activated, catalytic polypeptide
Chromosome: 16
Strain of origin: C.BKa-Igh^b/Icr
Site of expression: T and B lymphocytes.
Molecular note: A T-to-A transversion point mutation at a position corresponding to codon 4046 (codon 4095 in transcript ENSMUST00000023352.8) created a premature stop codon (p.Y4046*).

Allele

Symbol: B2m^b
Name: b variant
MGI accession ID: MGI:6711994
Generation method: Spontaneous
Attributes: Not Applicable
Marker symbol: B2m
Marker name: beta-2 microglobulin
Chromosome: 2
Strain of origin: C57BL
Molecular note: The b variant is runs faster than the a variant on SDS PAGE and was found to have an alanine at amino acid position 85. This allele is found in the C57BL strain family including C57BL/6, C57BL/10, C57L/J, C57BR/cdJ, as well as CAST/Ei, but not in C58/J, which has the a variant.

Allele

MGI accession ID: MGI:88127
Marker symbol: B2m
Marker name: beta-2 microglobulin
Chromosome: 2