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Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: PFN1 ENSG00000108518

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Description

profilin 1 [Source:HGNC Symbol;Acc:8881]

Gene Synonyms

ALS18

Location

Chromosome 17: 4,848,947-4,852,356 reverse strand.

GRCh37:CM000679.1

About this gene

This gene has 3 transcripts (splice variants), 2 paralogues and is associated with 2 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000225655.5	PFN1-001	1291	140aa	ENSP00000225655.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS11061	P07737	NM_005022.3	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000574872.1	PFN1-002	1173	104aa	ENSP00000465019.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		K7EJ44	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000572383.1	PFN1-003	539	165aa	ENSP00000460363.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		I3L3D5	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,

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Summary

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