Our efforts to clone the CLN5 gene, mutated in a severe children's brain di
sease, variant late infantile neuronal ceroid lipofuscinosis (vLINCL, MIM25
6731), resulted in large-scale sequencing of genomic clones flanking the cr
itical chromosomal region on 13q22. Computational and traditional transcrip
t identification analyses of the resulting sequence were used to identify t
he disease gene. In addition to the identification of the CLN5 gene, this e
ffort produced a large amount of genomic sequence data. Here, we report a t
ranscription map of the 107 kb sequence in the CLN5 region, based on tradit
ional and computational gene identification strategies. Several transcripts
were identified in this sequence. Queries against the database of expresse
d sequence tags proved to be the most powerful tool for gene identification
from large-scale sequence.