Description

Fraser syndrome 1 homolog (human) [Source:MGI Symbol;Acc:MGI:2385368]

Location
INSDC coordinates

chromosome:GRCm38:CM000998.2:96373955:96784728:1

Transcripts



This gene has 1 transcript (splice variant) Show transcript tableHide transcript table

NameTranscript IDbpProteinBiotypeCCDSUniProtRefSeqFlags
Fras1-201ENSMUST00000036019158484010 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS19450Q80T14 NM_175473
NP_780682
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 [04-09-2014]
Glossary entry for APPRIS
APPRIS website

Gene-based displays