Description

coagulation factor II (thrombin) receptor-like 2 [Source:HGNC Symbol;Acc:HGNC:3539]

Synonyms

PAR3

Location
INSDC coordinates

chromosome:GRCh38:CM000667.2:76615482:76623434:1

About this gene

This gene has 2 transcripts (splice variants), 71 orthologues, 12 paralogues, is a member of 1 Ensembl protein family and is associated with 66 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
F2RL2-001ENST000002966413429374aaENSP00000296641
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS4031O00254 NM_004101
NP_004092
TSL:1

TSL1: All splice junctions of the transcript are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS PI3APPRIS candidate principal isoform (earliest CCDS)
Glossary entry for APPRIS
APPRIS website
F2RL2-002ENST000005048991387352aaENSP00000426703
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS58959O00254 NM_001256566
NP_001243495
TSL:2

TSL2: The best supporting mRNA is flagged as suspect or the support is from multiple ESTs.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS ALT2APPRIS candidate principal isoform that appears to be conserved in fewer than three tested non-primate species
Glossary entry for APPRIS
APPRIS website

Gene-based displays