Description

RAP2B, member of RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9862]

INSDC coordinates

chromosome:GRCh38:CM000665.2:153162270:153167173:1

About this gene

This gene has 1 transcript (splice variant), 41 orthologues, 11 paralogues, is a member of 1 Ensembl protein family and is associated with 24 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
RAP2B-001ENST000003235344904183aaENSP00000319096
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS3170P61225 NM_002886
NP_002877
TSL:NA

Transcript Support Level Not Analysed. Pseudogenes, single exon transcripts, HLA, T-cell receptor and Ig transcripts are not analysed and therefore not given any of the TSL categories.

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 P1

PRINCIPAL1 - APPRIS candidate principal isoform.

APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods.

Gene-based displays