Description

sorting nexin 13 [Source:MGI Symbol;Acc:MGI:2661416]

Location
INSDC coordinates

chromosome:GRCm38:CM001005.2:35047189:35147469:1

Transcripts

This gene has 2 transcripts (splice variants) Show transcript tableHide transcript table

NameTranscript IDbpProteinBiotypeCCDSUniProtRefSeqFlags
Snx13-201ENSMUST000000485196218958 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS56837E9QNG6 Q6PHS6 Q80TT7
NM_001014973
NP_001014973
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
Glossary entry for APPRIS
APPRIS website
Snx13-202ENSMUST000001636773667777 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-E9Q7T4 -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).

Gene-based displays