Characterization of Seven Gene Transcripts Selected as Preferentially Expressed in Brain
| GENX[i] | Sequence similarity[ii] | [iii]GenBank, SWISS-PROT* accession no. | Genexpress clone (1NIB) name | IMAGE clone ID | GenBank/ EMBL accession no. | Insert size (kb) | Transcript size (kb) | Chromosomal localization | Orphan neurologic pathologies[iv] |
| 465 | RELRattus norvegicus calcium- independent α-latrotoxin receptor | U72487 U78105 O09026 * O35818 * | c-0obo3 | 34591 | Z42577 F02089 | 1.4 | 7.5 | 4q12 | |
| 769 | ID clone 23682 mRNA sequence ID clone 24440 mRNA sequence ID mRNA for KIAA0513 protein | U79288 AF055005 AB011085 | c-08e08 | 57147 | Z42089 F01625 | 1.7 | 7.5 | 16q24.3 | |
| 3809 | ID protein Armadillo multigene family (Hatzfeld and Natchtsheim 1996) | X81889 Q99569 * | c-01d10 | 31734 | Z42486 Z38681 | 1.5 | 4.6 | 2q22.3–q24.2 | |
| 3960 | ID visinin-like protein1 (Polymeropoulos et al. 1995) | U14747 P42323 * | c-11h05 | 49279 | F06242 F02525 | 1.5 | 2 | 2 | |
| 4044 | REL mouse and cattle cyclin-dependent kinase regulatory subunit P35 | S73375 S82819 | c-0ge07 | 26501 | Z42350 Z38574 | 1.8 | 4.2 | 17p11.2–q12 | DFNB3 DDPAC |
| 4858 | ID human DNA sequence Chr22 | Z99716 Z82192 | c-03a10 | 32335 | Z41917 Z38211 | 1.8 | 6.0/2.6 | 22q13.1–q13.3 | |
| 200991 | ID clone 23876 neuronal olfactomedin-related ER localized protein mRNA | U79299 AF035301 Q99784 * | c-0oa03 | 34458 | F05835 F02082 | 1.4 | 2.6 | 9q34.1–34.3 | ALS4 |
[i] GENX number refers to the Genexpress Index 2 cluster of cDNA clones, sequences, and ESTS markers.
[ii] Classification of each GENX cluster is based on data base similarities. Sequences were classified as known (ID) if identical to a human sequence and related (REL) if having a partial similarity to a sequence in another species.
[iii] When a significant sequence similarity was found, the GenBank or SWISS-PROT (with an asterisk) accession no. is reported.
[iv] (DFNB3) Neurosensory recessive deafness 3; (DDPAC) frontotemporal dementia with parkinsonism with variable phenotypes; ALS4) familial ALS.