Variant ID | 24694 |
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Entrez Gene ID | 5746 |
Gene | PTH2R (GeneCards) |
Location | hg19 2:210092145-210092145
hg38 2:209227421-209227421 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000002.11:g.210092145 C>A (Genome Assembly: GRCh37) |
Exon or Intron | NA |
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Position in protein | NA |
Amino acid changes in protein | NA > NA |
Position in cDNA | NA |
Changes in cDNA | NA > NA |
mRNA accession | NA |
mRNA length | NA |
Reference length | 243199373 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | 0.1536 |
CADD Raw score (version 1.3) | 0.673592 (Deleterious) |
FATHMM raw prediction score | 0.20296 (Tolerated) |
Deleterious probability by DeFine | 0.3286 (Neutral) |
Entrez Gene ID | 5746 (NCBI Gene) |
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Official Gene Symbol | PTH2R (GeneCards) |
Number of variants in PTH2R in this database | 13 (view all the variants) |
Full name | parathyroid hormone 2 receptor |
Band | 2q34 |
Other IDs | Vega: OTTHUMG00000132960 OMIM: 601469 HGNC: HGNC:9609 Ensembl: ENSG00000144407 |
Other names | PTHR2 |
Summary | The protein encoded by this gene is a member of the G-protein coupled receptor 2 family. This protein is a receptor for parathyroid hormone (PTH). This receptor is more selective in ligand recognition and has a more specific tissue distribution compared to parathyroid hormone receptor 1 (PTHR1). It is activated only by PTH and not by parathyroid hormone-like hormone (PTHLH) and is particularly abundant in brain and pancreas. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013] |
Individual ID | 29217587.02 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |