| 1 | ECM2, FGD3, HSAN1, NINJ1, OGN, OMD, ROR2, SPTLC1 |
| SPTLC1 is mutated in hereditary sensory neuropathy, type 1. | |
| Bejaoui K, Wu C, Scheffler MD, Haan G, Ashby P, Wu L, de Jong P, Brown RH Jr. | |
| Nat Genet 27(3):261-2. 2001 | |
| 2 | ECM2 |
| Identification of a novel gene (ECM2) encoding a putative extracellular matrix protein expressed predominantly in adipose and female-specific tissues and its chromosomal localization to 9q22.3. | |
| Nishiu J, Tanaka T, Nakamura Y. | |
| Genomics 52 : 378-381. 1998 | |