RGD:125268862 Rat Genome Database

Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)

Variant: RGD:125268862 -  Rattus norvegicus

RGD ID: 125268862
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: Mtfr2  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
Rnor_6.0 1 15,835,926
JBrowse: View Region in Genome Browser (JBrowse)
Model




Gene Symbol:Mtfr2
Accession:NM_001290110
Location:EXON
Amino Acid Prediction: P to R (nonsynonymous)
Amino Acid Position: 17
Polyphen Predictions
Prediction Basis Effect Site Score1 Score2 Diff Number Observed Structures Protein ID PDB ID Inverted
probably damaging alignment   NO -1.590 -3.625 +2.035 23   NP_001277039   +
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MQRDGTNEQCFLELASRMSFILNILRNMLAYFGVPVDQDLLIFQNKDYGSARSIVRVIGRMLPLEPCRRPRFELTPPANA
KEVDDYELAVPSFADVLCVADDGEAGCLRFRHSLWKKAEGKAALFHPSKLPWDLSSPALSQNRTVADDLPVSEAAIKKIA
ALEDELTSLRAQIAAIVAMQDLGGGGETGFISLSDGPSMEQVPPSSATARLSVEPDHVPSVVLSPPPLPPPPPPLPPPQF
SLQPPSSLPVPPGSANTRGIDNLAAEMKKRPSGVKKTDGSHHSESQRVSDVPNMLDVLKDMNKVKLRPVERSPGGRPIQK
RRRQSSQWDPVSLISNALKQKFAFQDDSFDSENRSWQGSPFSSPETSRNGSRF*
ACI/N (MCW) BN/SsN (MCW) M520/N (MCW) MR/N (MCW) WKY/N (MCW)