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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: C1QA ENSG00000173372

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Description

complement component 1, q subcomponent, A chain [Source:HGNC Symbol;Acc:1241]

Location

Chromosome 1: 22,962,999-22,966,101 forward strand.

GRCh37:CM000663.1

About this gene

This gene has 3 transcripts (splice variants), 16 paralogues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000374642.3	C1QA-001	1143	245aa	ENSP00000363773.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS226	P02745	NM_015991.2	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,
ENST00000402322.1	C1QA-003	976	245aa	ENSP00000385564.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS226	P02745	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000438241.1	C1QA-002	768	220aa	ENSP00000416841.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		-	-	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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