Description

fibroblast growth factor 21 [Source:HGNC Symbol;Acc:HGNC:3678]

Location
INSDC coordinates

chromosome:GRCh38:CM000681.2:48755559:48758330:1

About this gene

This gene has 2 transcripts (splice variants), 47 orthologues, 2 paralogues, is a member of 1 Ensembl protein family and is associated with 37 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
FGF21-001ENST000005937561312209aaENSP00000471477
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS12734Q9NSA1 -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 PI1APPRIS principal isoform
Glossary entry for APPRIS
APPRIS website
FGF21-201ENST00000222157885209aaENSP00000222157
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS12734Q9NSA1 NM_019113
NP_061986
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 PI1APPRIS principal isoform
Glossary entry for APPRIS
APPRIS website

Gene-based displays