Description

fibroblast growth factor 2 (basic) [Source:HGNC Symbol;Acc:HGNC:3676]

Synonyms

FGFB

INSDC coordinates

chromosome:GRCh38:CM000666.2:122826708:122898236:1

About this gene

This gene has 3 transcripts (splice variants), 53 orthologues, 1 paralogue, is a member of 1 Ensembl protein family and is associated with 31 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
FGF2-001ENST000002644986775288aaENSP00000264498
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS34059A0A087WUF6 -TSL:1

Transcript Support Level 1, when transcripts 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).
FGF2-201ENST000006140106774288aaENSP00000478620
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS34059A0A087WUF6 NM_002006
NP_001997
TSL:1

Transcript Support Level 1, when transcripts 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).
FGF2-002ENST000006084783880155aaENSP00000477134
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-D9ZGF5 P09038 -TSL:1

Transcript Support Level 1, when transcripts 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 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