GEPHE SUMMARY
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									Gephebase Gene
					
		
	
									Entry Status
					
		
													Published
					
	
									GepheID
					
		
													GP00000415
					
	
									Main curator
					
		
													Martin
					
	
            		PHENOTYPIC CHANGE
            	            
	                
	
									Trait Category
					
		
	
									Trait
					
		
	
									Trait State in Taxon A
					
		
													Homo sapiens - Sardinia
					
	
									Trait State in Taxon B
					
		
													Homo sapiens - Sardinia
					
	
									Ancestral State
					
		
													Data not curated
					
	
									Taxonomic Status
					
		
	Taxon A
					
									Latin Name
					
		
	
									Common Name
					
		
																			human
					
	
									Synonyms
					
		
																			human; man; Homo sapiens Linnaeus, 1758; Home sapiens; Homo sampiens; Homo sapeins; Homo sapian; Homo sapians; Homo sapien; Homo sapience; Homo sapiense; Homo sapients; Homo sapines; Homo spaiens; Homo spiens; Humo sapiens
					
	
									Rank
					
		
																			species
					
	
		Lineage
	
	
															
				Show more ... 
						opterygii; Dipnotetrapodomorpha; Tetrapoda; Amniota; Mammalia; Theria; Eutheria; Boreoeutheria; Euarchontoglires; Primates; Haplorrhini; Simiiformes; Catarrhini; Hominoidea; Hominidae; Homininae; Homo
			
			
							Parent
					
		
	
							NCBI Taxonomy ID
					
		
	
									is Taxon A an Infraspecies?
					
		
																													No
					
	Taxon B
					
									Latin Name
					
		
	
									Common Name
					
		
																			human
					
	
									Synonyms
					
		
																			human; man; Homo sapiens Linnaeus, 1758; Home sapiens; Homo sampiens; Homo sapeins; Homo sapian; Homo sapians; Homo sapien; Homo sapience; Homo sapiense; Homo sapients; Homo sapines; Homo spaiens; Homo spiens; Humo sapiens
					
	
									Rank
					
		
																			species
					
	
		Lineage
	
	
															
				Show more ... 
						opterygii; Dipnotetrapodomorpha; Tetrapoda; Amniota; Mammalia; Theria; Eutheria; Boreoeutheria; Euarchontoglires; Primates; Haplorrhini; Simiiformes; Catarrhini; Hominoidea; Hominidae; Homininae; Homo
			
			
							Parent
					
		
	
							NCBI Taxonomy ID
					
		
	
									is Taxon B an Infraspecies?
					
		
																													No
					
	
            GENOTYPIC CHANGE
            	            
	                
	
									Generic Gene Name
					
		
																			GHR
					
	
									Synonyms
					
		
																			GHBP; GHIP
					
	
									String
					
		
	
									Sequence Similarities
					
		
																			Belongs to the type I cytokine receptor family. Type 1 subfamily.
					
	
							GO - Molecular Function
						
						
																														GO:0042802 : identical protein binding
							
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							GO - Biological Process
						
						
					
							GO - Cellular Component
						
						
																														GO:0016021 : integral component of membrane
							
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									UniProtKB
																							
Homo sapiens
						
					Homo sapiens
									Presumptive Null
					
		
	
									Molecular Type
					
		
	
									Aberration Type
					
		
	
									SNP Coding Change
					
		
													Nonsense
					
	
									Molecular Details of the Mutation
					
		
													Arg61*
					
	
									Experimental Evidence
					
		
	| Taxon A | Taxon B | Position | |
|---|---|---|---|
| Codon | - | - | - | 
| Amino-acid | Arg | STP | 61 | 
				Authors
	
	
									Zoledziewska M; Sidore C; Chiang CWK; Sanna S; Mulas A; Steri M; Busonero F; Marcus JH; et al.
									
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							Abstract
					
		
																			We report sequencing-based whole-genome association analyses to evaluate the impact of rare and founder variants on stature in 6,307 individuals on the island of Sardinia. We identify two variants with large effects. One variant, which introduces a stop codon in the GHR gene, is relatively frequent in Sardinia (0.87% versus <0.01% elsewhere) and in the homozygous state causes Laron syndrome involving short stature. We find that this variant reduces height in heterozygotes by an average of 4.2 cm (-0.64 s.d.). The other variant, in the imprinted KCNQ1 gene (minor allele frequency (MAF) = 7.7% in Sardinia versus <1% elsewhere) reduces height by an average of 1.83 cm (-0.31 s.d.) when maternally inherited. Additionally, polygenic scores indicate that known height-decreasing alleles are at systematically higher frequencies in Sardinians than would be expected by genetic drift. The findings are consistent with selection for shorter stature in Sardinia and a suggestive human example of the proposed 'island effect' reducing the size of large mammals. 
					
	
				Additional References
	
	
            RELATED GEPHE
        
	
								Related Haplotypes
					
					
													No matches found.
											
				
            EXTERNAL LINKS
        
    
            COMMENTS
        
	
					Stop codon variant relatively frequent in Sardinia (0.87% versus <0.01% elsewhere) and can cause Laron-type dwarfism at the homozygous state
				
			
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