Mapping Data Summary

• Symbol: Mid2
• Name: midline 2
• ID: MGI:1344333
• Chromosome: X

3 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSB)	X	J:56619 Buchner G, et al., MID2, a homologue of the Opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during development. Hum Mol Genet. 1999 Aug;8(8):1397-407
CROSS	Cross Type: Backcross Mapping Panel: EUCIB (BSS)	X	J:60299 Perry J, et al., FXY2/MID2, a gene related to the X-linked Opitz syndrome gene FXY/MID1, maps to Xq22 and encodes a FNIII domain-containing protein that associates with microtubules. Genomics. 1999 Dec 15;62(3):385-94
TEXT-Physical Mapping		X	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