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

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Gene: CD93 ENSG00000125810

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Description

CD93 molecule [Source:HGNC Symbol;Acc:HGNC:15855]

Gene Synonyms

C1QR(P), C1QR1, C1QRP, CDW93, DJ737E23.1, ECSM3, MXRA4

Location

Chromosome 20: 23,065,139-23,086,324 reverse strand.

GRCh38:CM000682.2

About this gene

This gene has 5 transcripts (splice variants), 263 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000246006.5	CD93-201	6681	652aa	ENSP00000246006.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS13149	Q9NPY3	NM_012072.4	The Matched Annotation from NCBI and EMBL-EBI is a collaboration between Ensembl/GENCODE and RefSeq. The MANE Select is a default transcript per human gene that is representative of biology, well-supported, expressed and highly-conserved. This transcript set matches GRCh38 and is 100% identical between RefSeq and Ensembl/GENCODE for 5' UTR, CDS, splicing and 3'UTR.MANE Select, 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, GENCODE Primary represents a minimal set that contains MANE Select, MANE Plus Clinical and Ensembl Canonical transcripts and transcripts containing any conserved exons and common alternative splicing events (including exons skips) that are absent from the MANE and Ensembl Canonical transcripts for protein-coding genes. Other biotypes will have the GENCODE Primary flag added to the Ensembl Canonical transcript and for lncRNA genes only this will be the transcripts with the longest genomic span.GENCODE Primary, A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1, TSL 1: A transcript where all splice junctions 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, based on the type and quality of the alignments used to annotate the transcript. TSL:1,
ENST00000850633.1	CD93-203	3008	652aa	ENSP00000520912.1	Nonsense mediated decay	CCDS13149	-	-	-
ENST00000850635.1	CD93-205	2549	652aa	ENSP00000520914.1	Nonsense mediated decay	CCDS13149	-	-	-
ENST00000850634.1	CD93-204	2472	652aa	ENSP00000520913.1	Nonsense mediated decay	CCDS13149	-	-	-
ENST00000799105.1	CD93-202	489	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-

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Summary

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