Description

retinol binding protein 2, cellular [Source:HGNC Symbol;Acc:HGNC:9920]

Synonyms

CRABP-II, CRBP2, CRBPII, RBPC2

INSDC coordinates

chromosome:GRCh38:CM000665.2:139452884:139480747:1

Transcripts



This gene has 3 transcripts (splice variants) Show transcript tableHide transcript table

NameTranscript IDbpProteinBiotypeCCDSUniProtRefSeqFlags
RBP2-001ENST00000232217694134 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS3109D6RB89 D6RGE6 P50120
NM_004164
NP_004155
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 PIAPPRIS principal isoform [01-09-2014]
Glossary entry for APPRIS
APPRIS website
RBP2-002ENST00000511956489103 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-D6RB89 D6RGE6 -CDS 3' incomplete3' truncation in transcript evidence prevents annotation of the end of the CDS.TSL:3

TSL3:The only support for this transcript is from a single EST.

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.

RBP2-003ENST0000050682518024 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-D6RGE6 -CDS 3' incomplete3' truncation in transcript evidence prevents annotation of the end of the CDS.TSL:5

TSL5: No single transcript (mRNA or EST) supports this transcript model's structure.

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.

Gene-based displays