|
Symbol Name ID Chromosome |
Mid2
midline 2 MGI:1344333 X |
| 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 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/30/2024 MGI 6.23 |
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