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Gene: Gh1sdr (null) Rattus norvegicus
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Symbol: Gh1sdr
Name:
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.


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Phenotype Annotations
References - curated

Genomics

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Expression


Sequence

Nucleotide Sequences

Additional Information

 
More on Gh1sdr
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Ensembl Gene
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CRRD Object Information
CRRD ID: 12880380
Created: 2017-05-04
Species: Rattus norvegicus
Last Modified: 2017-05-04
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.