rs65978719 Marker Search Result - Rat Genome Database

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Marker: rs65978719

Symbol: rs65978719
Previously known as: ENSRNOSNP2727507; ENSRNOSNP2801895; ENSEMBL|tmpshr3215864; 
RGD ID: 7394842
Type: SNV
Expected Size: 0 (bp)
Notes A/G
Position
Rat AssemblyChrPosition (strand)SourceJBrowse
Rnor_6.01761,355,300 - 61,355,300RGDRnor6.0
Rnor_5.01763,128,836 - 63,128,836RGDRnor5.0
RGSC_v3.41765,022,528 - 65,022,528RGDRGSC3.4
Celera1757,695,835 - 57,695,835RGD
Is Marker For: QTLs:   Memor18   Bp406  


Annotation


References - curated
# Reference Title Reference Citation
1. Dahl (S x R) rat congenic strain analysis confirms and defines a chromosome 17 spatial navigation quantitative trait locus to <10 Mbp. Herrera VL, etal., PLoS One. 2013;8(2):e58280. doi: 10.1371/journal.pone.0058280. Epub 2013 Feb 28.
2. Systems biology with high-throughput sequencing reveals genetic mechanisms underlying the metabolic syndrome in the Lyon hypertensive rat. Wang J, et al., Circ Cardiovasc Genet. 2015 Apr;8(2):316-26. doi: 10.1161/CIRCGENETICS.114.000520. Epub 2015 Jan 8.

Strains and Sequence


Region

Nucleotide Sequences


Additional Information

Database Acc Id Source(s)
dbSNP (RS) rs65978719
dbSNP (SS) ss179360053
  ss196022369
  ss87375640
Ensembl Transcript rs65978719