UC Santa Cruz maintains a publicly available MySQL genetic database you can query from your own browser.
Go to this page here:
UCSC Genome Browser
genome.ucsc.edu
and look on the left hand side of the page, there's a convenient list of all the species that are catalogued. Just click on any of them to see what's available.
At the bottom of each page are download options, or you can use any MySql browser or get in from Python or R with username "genome", then you can list all the tables (there's like 53,000 of them) or query any table (obviously it's read only).
For example "Mouse" is a good one to look at, you can see under "Assembly Details" that it covers chromosomes 1-19 and the mitochondrial DNA. Whenever we prepare a new knockout strain that's missing a BBB membrane protein or something, we have to compare it against this database to make sure we've done the right thing. Verification takes about 15 min on a fast PC.
The blood brain barrier is very interesting, it's like a filter that keeps red and white blood cells and other things out of the cerebrospinal fluid. We can knock out specific proteins to make the filter porous and thereby change the brain's electrical behavior, calcium and magnesium pumps are examples. If there is an infarction we can tell where it happened using imagery like in the previous post. We want to do this BEFORE we slice up the mouse's brain because we're testing behavior.
So for example in my case, I can knock out one of the MAP proteins to make the blood brain barrier permeable to the JC virus, which causes PML (or the mouse equivalent). What happens is you get little bubbles on the walls of the capillaries, and when several nearby bubbles burst simultaneously you get an infarction, which allows small molecules and viruses to come rushing in. Similar work is being done on Mad Cow disease (CJV), which is actually a prion, it's even smaller than y'r average virus.
Normally the brain keeps viruses out, because it has internal virus-like behaviors that are vital for proper brain function. However some of these viruses have found ways to attack the cell membranes of the capillary wall. They can work from inside as well as outside - if an internal virus mutates and attacks its own capillaries we call it an autoimmune disorder, but the mechanisms are similar in many cases.
This kind of science requires comparisons across species because we're trying to get to the underlying mechanisms. If we know that calcium channel knockouts and microtubule associated protein knockouts both result in the same set of symptoms we start getting a pretty good idea of what's going on. Then we can find some other species that has a different sequence for one or the other and predict whether it's susceptible to a virus. Ultimately, once we understand all this stuff we can fabricate a protein that prevents the virus from entering while at the same time leaving normal function intact - because if the virus attacks a calcium pump we can't stop the pump just to inhibit the virus.