Gene: FCGR1A ENSG00000150337

Description

Fc fragment of IgG, high affinity Ia, receptor (CD64) [Source:HGNC Symbol;Acc:3613]

Gene Synonyms

CD64, CD64A, CD64b, FCG1, FCGR1, FCRI, IGFR1, IGFRB

Location

Chromosome 1: 149,754,227-149,764,074 forward strand.

GRCh37:CM000663.1

View alleles of this gene on alternative sequences

About this gene

This gene has 4 transcripts (splice variants), 1 gene allele and 14 paralogues.

Transcripts

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Transcript ID	Name	bp	Protein	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000369168.4	FCGR1A-001	2180	374aa	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS933	P12314	NM_000566.3	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, A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic,
ENST00000444948.1	FCGR1A-003	795	240aa	Gene/transcipt that contains an open reading frame (ORF).Protein coding		C9JSN8	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENST00000489479.1	FCGR1A-004	829	No protein	Gene/transcript that doesn't contain an open reading frame (ORF).Processed transcript		-	-	-
ENST00000489704.1	FCGR1A-002	477	No protein	Gene/transcript that doesn't contain an open reading frame (ORF).Processed transcript		-	-	-

Genomic alignments

As of the latest update in March 2020 we are not supporting data for species other than human on this GRCh37 site and the view you wish to use is disabled.

You can read more about why we have done this on our blog.

You can still view this page on the following archive resources:

1. The Ensembl 75 archive represents a code and data freeze taken in February 2014.

2. The GRCh37 archive represents a code and data freeze taken in January 2019.

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Gene: FCGR1A ENSG00000150337

Genomic alignments