Alternative titles; symbols
Cytogenetic location: 17p13.1 Genomic coordinates (GRCh38): 17:6,500,001-10,800,000
| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
|---|---|---|---|---|
| 17p13.1 | {Migraine with or without aura, susceptibility to, 10} | 610208 | Autosomal dominant | 2 |
For a phenotypic description and discussion of genetic heterogeneity of migraine headaches, see MGR1 (157300).
Since migraine is a syndrome instead of a clearly differentiated disease, Anttila et al. (2006) hypothesized that individual clinical components of migraine (i.e., traits such as pulsating pain and photophobia, among others) might represent reflections of specific rather than shared loci and thus independently contribute to susceptibility to migraine. To test this hypothesis, they used individual traits and trait groups of the International Headache Society (IHS) criteria as phenotypes for genomewide linkage analysis in the same dataset of 50 Finnish families used to establish the MGR1 locus (Wessman et al., 2002). In addition to confirming the MGR1 locus on 4q24, Anttila et al. (2006) found significant evidence of linkage between the pulsation trait and marker D17S945, where a 2-point highest lod score under locus heterogeneity (hlod) score of 4.65 was detected. They fine-mapped the region with 9 additional markers to provide a map interval of 1.7 cM on chromosome 17p13.1.
Anttila, V., Kallela, M., Oswell, G., Kaunisto, M. A., Nyholt, D. R., Hamalainen, E., Havanka, H., Ilmavirta, M., Terwilliger, J., Sobel, E., Peltonen, L., Kaprio, J., Farkkila, M., Wessman, M., Palotie, A. Trait components provide tools to dissect the genetic susceptibility of migraine. Am. J. Hum. Genet. 79: 85-99, 2006. [PubMed: 16773568] [Full Text: https://doi.org/10.1086/504814]
Wessman, M., Kallela, M., Kaunisto, M. A., Marttila, P., Sobel, E., Hartiala, J., Oswell, G., Leal, S. M., Papp, J. C., Hamalainen, E., Broas, P., Joslyn, G., and 11 others. A susceptibility locus for migraine with aura, on chromosome 4q24. Am. J. Hum. Genet. 70: 652-662, 2002. [PubMed: 11836652] [Full Text: https://doi.org/10.1086/339078]