Mapping Data Summary

• Symbol: Epb42
• Name: erythrocyte membrane protein band 4.2
• ID: MGI:95402
• Chromosome: 2

21 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Intercross	2	J:38773 Gwynn B, et al., The gene encoding protein 4.2 is distinct from the mouse platelet storage pool deficiency mutation pallid. Genomics. 1997 Jun 15;42(3):532-5
CROSS	Cross Type: Backcross Mapping Panel: Copeland-Jenkins	2	J:59131 Hurlin PJ, et al., Mga, a dual-specificity transcription factor that interacts with Max and contains a T-domain DNA-binding motif. EMBO J. 1999 Dec 15;18(24):7019-28
CROSS	Cross Type: Backcross Mapping Panel: Copeland-Jenkins	2	J:48738 Kwon YT, et al., The mouse and human genes encoding the recognition component of the N-end rule pathway. Proc Natl Acad Sci U S A. 1998 Jul 7;95(14):7898-903
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSB)	2	J:32426 Zuberi AR, et al., A genetic linkage map of mouse chromosome 2 extending from thrombospondin to paired box gene 1, including the H3 minor histocompatibility complex. Genomics. 1996 Apr 1;33(1):75-84
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	2	J:32426 Zuberi AR, et al., A genetic linkage map of mouse chromosome 2 extending from thrombospondin to paired box gene 1, including the H3 minor histocompatibility complex. Genomics. 1996 Apr 1;33(1):75-84
RI	RI/RC Set: AKXD	2	J:51036 Nakamura T, et al., Molecular cloning, characterization, and chromosomal localization of FKBP23, a novel FK506-binding protein with Ca2+-binding ability. Genomics. 1998 Nov 15;54(1):89-98
RI	RI/RC Set: AKXD	2	J:2185 White RA, et al., The murine pallid mutation is a platelet storage pool disease associated with the protein 4.2 (pallidin) gene. Nat Genet. 1992 Sep;2(1):80-3
RI	RI/RC Set: BXD	2	J:2185 White RA, et al., The murine pallid mutation is a platelet storage pool disease associated with the protein 4.2 (pallidin) gene. Nat Genet. 1992 Sep;2(1):80-3
TEXT		2	J:38773 Gwynn B, et al., The gene encoding protein 4.2 is distinct from the mouse platelet storage pool deficiency mutation pallid. Genomics. 1997 Jun 15;42(3):532-5
TEXT		2	J:48583 Zuberi AR, et al., Expression screening of a yeast artificial chromosome contig refines the location of the mouse H3a minor histocompatibility antigen gene. J Immunol. 1998 Jul 15;161(2):821-8
TEXT-Cytogenetic Localization		2	J:32426 Zuberi AR, et al., A genetic linkage map of mouse chromosome 2 extending from thrombospondin to paired box gene 1, including the H3 minor histocompatibility complex. Genomics. 1996 Apr 1;33(1):75-84
TEXT-Genetic Cross		2	J:38773 Gwynn B, et al., The gene encoding protein 4.2 is distinct from the mouse platelet storage pool deficiency mutation pallid. Genomics. 1997 Jun 15;42(3):532-5
TEXT-Genetic Cross		2	J:48738 Kwon YT, et al., The mouse and human genes encoding the recognition component of the N-end rule pathway. Proc Natl Acad Sci U S A. 1998 Jul 7;95(14):7898-903
TEXT-Genetic Cross		2	J:2185 White RA, et al., The murine pallid mutation is a platelet storage pool disease associated with the protein 4.2 (pallidin) gene. Nat Genet. 1992 Sep;2(1):80-3
TEXT-Physical Mapping		2	J:71289 Grenard P, et al., Evolution of transglutaminase genes: identification of a transglutaminase gene cluster on human chromosome 15q15. structure of the gene encoding transglutaminase x and a novel gene family member, transglutaminase z. J Biol Chem. 2001 Aug 31;276(35):33066-78
TEXT-Physical Mapping		2	J:64907 Huang L, et al., The pallid gene encodes a novel, syntaxin 13-interacting protein involved in platelet storage pool deficiency. Nat Genet. 1999 Nov;23(3):329-32
TEXT-Physical Mapping		2	J:80000 The FANTOM Consortium and The RIKEN Genome Exploration Research Group Phase I & II Team, Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. Nature. 2002;420:563-573
TEXT-Physical Mapping		2	J:51335 Zuberi AR, et al., Positional cloning and molecular characterization of an immunodominant cytotoxic determinant of the mouse H3 minor histocompatibility complex. Immunity. 1998 Nov;9(5):687-98
TEXT-QTL		2	J:50271 Risinger FO, et al., Ethanol-induced conditioned taste aversion in BXD recombinant inbred mice. Alcohol Clin Exp Res. 1998 Sep;22(6):1234-44
TEXT-Radiation Hybrid		2	J:71289 Grenard P, et al., Evolution of transglutaminase genes: identification of a transglutaminase gene cluster on human chromosome 15q15. structure of the gene encoding transglutaminase x and a novel gene family member, transglutaminase z. J Biol Chem. 2001 Aug 31;276(35):33066-78
TEXT-Radiation Hybrid		2	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;