The TSHR gene homepage

General information
Gene symbol TSHR
Gene name thyroid stimulating hormone receptor
Chromosome 14
Chromosomal band q24-q31
Imprinted Unknown
Genomic reference NG_009206.1
Transcript reference NM_000369.2
Associated with diseases CHNG1, hyperthyroidism, familial gestational, Hyperthyroidism, nonautoimmune
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 84
Unique public DNA variants reported 65
Individuals with public variants 6
Hidden variants 2
Date created September 13, 2012
Date last updated November 15, 2023
Version TSHR:231115

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 12373
Entrez Gene 7253
PubMed articles TSHR
OMIM - Gene 603372
OMIM - Diseases CHNG1 (hypothyroidism, congenital, nongoitrous, type 1 (CHNG1))
hyperthyroidism, familial gestational
Hyperthyroidism, nonautoimmune
HGMD TSHR
GeneCards TSHR
GeneTests TSHR
Orphanet TSHR


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000371 14 transcript variant 1 NM_000369.2 NP_000360.2 84


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