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Gene: Rab38ru (Rab38, member of RAS oncogene family, ruby allele) Rattus norvegicus
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Symbol: Rab38ru
Name: Rab38, member of RAS oncogene family, ruby allele
Description: The Met1Ile mutation in the Rab38 gene abolishes the translation of the gene resulting in a hypopigmentation phenotype
ASSOCIATED WITH abnormal platelet dense granule number; abnormal surfactant secretion; dilated respiratory conducting tubes; ASSOCIATED WITH Hermansky-Pudlak syndrome
Type: allele  of Rab38  
Also known as: R; R_mapped; Rab38ru; red eyed dilution; Ruby; Ruby or red eyed dilution; ruby or red eyed dilution (mapped)
Is Marker For: Strains:   FH   TM/Kyo  
Latest Assembly: Rnor_6.0 - RGSC Genome Assembly v6.0
Position:
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Cytogenetic Map1q32RGD


Disease Annotations
Phenotype Annotations
References - curated

Genomics

Related Rat Strains

Expression


Sequence

Nucleotide Sequences

Additional Information

External Database Links
RGD Curation Notes
 
More on Rab38ru
Alliance Gene
NCBI Gene
Ensembl Gene
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1600311
Created: 2007-03-07
Species: Rattus norvegicus
Last Modified: 2007-03-07
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.