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Gene: Gh1sdr (null) Rattus norvegicus
Symbol: Gh1sdr
Description: The G to A substitution at the end of the 3rd intron of the rat Growth hormone gene was identified as the cause of the dwarf phenotype in SDR rats. This spontaneous mutation affected the 3' splice/acceptor site causing 1-bp deletion in mRNA and resulting in pre-mature termination of translation.
ASSOCIATED WITH decreased growth hormone level; decreased prolactin level; ASSOCIATED WITH Dwarfism
Type: allele  of Gh1  
Also known as: Gh1sdr
Is Marker For: Strains:   SDR/Slc  
Latest Assembly: Rnor_6.0 - RGSC Genome Assembly v6.0
Position: No map positions available.

Disease Annotations
Phenotype Annotations
References - curated


Related Rat Strains



Nucleotide Sequences

Additional Information

More on Gh1sdr
Alliance Gene
Ensembl Gene
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 12880380
Created: 2017-05-04
Species: Rattus norvegicus
Last Modified: 2017-05-04
Status: ACTIVE


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